This is an HTML version of an attachment to the Official Information request 'ACC’s internal policies and procedures for impairment assessments and client reviews'.


Impairment Assessments Overview Service Page v23.0
Document 1
Summary
Objective
Clients who suffer a permanent or long-term impairment resulting from an injury are entitled to an impairment assessment to deter-
mine whether ACC should provide them with lump sum compensation or an independence allowance.
Owner
out of scope
Expert
out of scope
Procedure
1.0 What is an Impairment Assessment?
Clients who suffer a permanent or long-term impairment resulting from a covered injury may be entitled to lump sum compen-
sation or an independence allowance (IA). An impairment assessment is used to determine the client's entitlement.
Lump sum eligibility criteria Policy
Independence allowance eligibility criteria Policy
Impairment Assessments are completed by independent assessors following a referral from ACC. These assessors use the 
AMA guides and the ACC Handbook to rate the level of impairment for each of the client's covered injuries. Assessors deduct 
any impairment that has not resulted from the covered injury and provides ACC with a whole person impairment rating.
An Impairment Assessment does not determine diagnosis or causation. The key output from an Assessment is an Impairment 
Report. The whole person impairment rating is used to calculate a client’s entitlement to an IA and/or lump sum.
NOTE What is an Impairment?
The concept of impairment differs from the concepts of disability and work capacity. The testing of impairment deter-
mines the severity of the injury, not the impact the client’s impairment has on them personally (their disability), or their 
ability to work (work capacity).
2.0 Who refers for an Impairment Assessment?
A client can apply for an IA/Lump sum entitlement (or both) at any time. If the client meets the criteria (attached) ACC will ar-
range an Impairment Assessment to determine the level of impairment.
Client Eligibility to IA & LS.PNG
When a client wants to apply for a Lump Sum or Independence Allowance entitlement, ACC sends the client a Permanent 
Injury Compensation application pack. The application pack prompts the client to provide the required information to allow ACC 
to process their application for a Lump Sum or Independence Allowance. For more information on how to send a permanent 
injury compensation application pack, please refer to the process linked below.
The client will need to complete the ACC54 Application for independence allowance/lump sum and return this to ACC. A med-
ical practitioner will need to complete an ACC554 Medical certificate and return this to ACC.
Send a Permanent Injury Compensation application pack
Independence allowance & lump sum (IALS)
NOTE How can you notify Treatment and Support about your client?
You can refer your client to Treatment and Support by generating a 'Send LSIA Application Pack' task in Eos. This task 
will automatically be allocated to the appropriate Eos queue.
ACC > Claims Management > Manage Claims > Service Pages > Specialist Care and Rehabilitation > Vocational, Pain and Assessment Services > Impairment Assessments >
Impairment Assessments Overview Service Page
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NOTE What if the client is in prison?
Assessment and payment of lump sums are discretionary, there are decision making principles located in the Clients 
in prison policy. These principles will need to be applied before continuing with the assessment process. For Indepen-
dence Allowance ACC can assess the client’s impairment but payment cannot be made until after their release.
PROCESS Clients in Prison Policy
3.0 What are the requirements of an Impairment Assessment?
The Assessment Tool is used during an Impairment Assessment to provide an objective measure of a Client’s impairment for 
ACC. The ACC Handbook and Operational Guidelines sets out the procedures, formatting and other requirements for the 
Assessment and Impairment Report in full detail.
ACC Handbook
https://www.acc.co.nz/assets/provider/fe092baf01/acc716-ama4-handbook.pdf
Operational Guidelines - Impairment Assessment Service 2021
The Impairment Assessor must, but is not limited to:
• Introduce themselves to the client and provide an explanation of the Impairment Assessment process and what the assess-
ment involves.
• Obtain and review any additional information required for a comprehensive Assessment of the client.
• Complete a medical examination of the client (Note: Skype or paper based assessments may be completed).
• Completion an Impairment Report in accordance with the formatting and procedural requirements of the ACC Handbook, in-
cluding a whole-body impairment rating.
• Have a discussion with the client on the findings of the assessment.
Impairment Assessment Timeframes (Image below)
Assessment timeframes.PNG
4.0 Why does ACC peer review the Impairment Report?
ACC checks the quality of Impairment Reports and the impairment rating through a process of peer reviews. Peer reviews 
ensure the consistent and equitable provision of IA and lump sum entitlements to clients.
Not all Impairment Reports are peer reviewed. The IALS unit will determine if an Impairment Report requires a peer review. 
They will only peer review claims that meet a the criteria listed in the guidelines attached below.
Peer review guidelines - Reference
Peer Review Timeframes (Image below)
Peer review timeframes.PNG
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5.0 Telehealth
Telehealth may be used instead of in-person consultation on a case by case basis to meet Client need. This will be assessed 
by the Permanent Injury Compensation (PIC) unit, who will ensure this is in the best interest of the Client and that the Client 
provides informed consent. Services can be delivered by Telehealth, where clinically appropriate. Services delivered by Tele-
health must:
- be agreed in advance with the Permanent Injury Compensation unit to ensure that referrals accurately reflect the appropriate 
delivery method and other considerations related to the specific needs of Clients (sensitive claims and terminal illnesses for 
example);
- have Client or authorised representative consent (recorded in the clinical notes), and with the option of an in-person meeting 
if the Client prefers;
- be preceded by an initial risk assessment to ensure Client safety;
- meet the same required standards of care provided through an in-person consultation;
- have clinical records that meet ACC and professional body requirements;
- meet the requirements outlined in the standards/guidelines of the NZ Medical Council, if there is a difference between what 
the regulatory body states and what is stated in this contract, then the contract conditions take precedence;
- have both the Client receiving the Telehealth service, and the provider delivering the Telehealth service, physically present in 
New Zealand at the time the service is provided. Unless the Client is or will be overseas at the time of the assessment, in 
which case the assessment may be delivered by Telehealth if all other requirements of this clause are met.
All Telehealth assessments must be clinically appropriate i.e. a physical examination is not necessary. Treatment and Support 
Assessors must carefully consider all options and only utilise Telehealth when it is clinically appropriate and a better option for 
the Client than a face to face assessment. Face to face assessment remains the preferred option in most cases.
NOTE What is telehealth
Telehealth means the use of information or communication technologies to deliver health care when clients and care 
providers are not in the same physical location.
Telehealth relates to real-time videoconferencing interactions and telephone consultations. Telehealth excludes elec-
tronic messaging, e.g. texts and emails.
A Telehealth consultation is to replace an in-person visit, it does not include a quick triage or check-in phone calls 
(unless specified).
NOTE What does in-person mean?
In-person means the provider and client are physically present in the same room.
NOTE Service requirements
The Supplier will provide all equipment and technology necessary to deliver services by Telehealth and manage their 
own technical difficulties.
When using telehealth the Assessors must clearly document in their client’s clinical record if either a telephone or video confe-
rencing consultation was used.
NOTE Oversees clients
When assessing a Client who is overseas at the time of the assessment, the Provider is responsible for ensuring that 
its risk of providing those services is covered, in accordance with clause 17 of the Standard Terms and Conditions.
6.0 Claiming for Exceptional Circumstances - Code IA06
IA06 should be for seven or more injuries OR whose medical records exceed 150 pages;
• Where an assessment contains seven or more injuries AND whose medical records exceed 150 pages they may bill two units 
of IA06.
• Where an assessment contains an exceptional (seven or more injuries or whose medical records exceed 150 pages) mental 
AND physical assessment they may bill two units of IA06.
7.0 Useful information and tips
NOTE What is the Assessment Tool?
The Assessment Tool refers to the:
• The American Medical Association’s Guides to the Evaluation of Permanent Impairment 4th Edition (AMA4) (AMA 
Guides); and
• The ACC User Handbook to the AMA ‘Guides to the Evaluation of Permanent Impairment’ 4th Edition (ACC Hand-
book).
The AMA Guides are explicit, but not intuitive, and are designed to require training in their use and application, as well 
as clinical judgement and expertise. The AMA Guides provide a framework for minimising interobserver variation in as-
sessing impairment.
The interpretation and application of the AMA Guides are supported by the ACC Handbook, which provides additional 
material so that the AMA Guides are relevant to the New Zealand.
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Impairment Assessments Overview Service Page
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NOTE What qualifications does an Impairment Assessor need to have?
To be an ACC approved Impairment Assessor the Impairment Assessor must be a Medical Practitioner who has at 
least general registration with the New Zealand Medical Council (NZMC) and three years’ post-registration clinical 
experience.
They must hold a current annual practising certificate, ie it is renewed annually. ACC relies on the NZMC to assess the 
competence of a medical practitioner to hold a vocational annual practising certificate.
NOTE What training does an Impairment Assessor have to completed?
To complete Impairment Assessments for ACC, ACC requires an appropriately qualified Medical Practitioner to have 
satisfactorily completed ACC’s training courses on using the AMA Guides and the ACC Handbook.
Initial Training involves practice in using the AMA Guides, assessment methods, calculating impairment, and report 
formatting. An assessor must satisfactorily complete several sample case studies before they undertake assessments.
ACC Handbook
https://www.acc.co.nz/assets/provider/fe092baf01/acc716-ama4-handbook.pdf
Operational Guidelines
https://www.acc.co.nz/assets/contracts/b4ac64f075/imp-og.pdf
Independence Allowance and Lump Sum Policy pages
IA and Lump Sum - Process Pages
http://thesauce/team-spaces/chips/compensation/independence-allowance--lump-sum/process/index.htm
IA and Lump Sum - Reference Pages
http://thesauce/team-spaces/chips/compensation/independence-allowance--lump-sum/reference/index.htm
Operational Guidelines - Impairment Assessment Service 2021
Where can I find out more about the PIC application assessment process?
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Impairment Assessments Overview Service Page
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Impairment assessors Policy
Document 2
v9.0
Summary
Objective
ACC must appoint and pay an appropriate assessor in accordance with the Accident Compensation Act 2001, Schedule 1, part 3, 
clause 58.
Owner
out of scope
Expert
out of scope
Policy
1.0 Contracts
As per the contract specifications, approved Assessors must:
• be approved by ACC to provide the Assessment Service; and
• be Medical Practitioners with at least general registration and three years' post-registration clinical experience; and
• have satisfactorily completed ACC’s training course on the Assessment Tool and post-course test in the use and application
of the Assessment Tool.
The Assessment Tool is currently the AMA Guide to the Evaluation of Permanent Impairment (4th Edition) in conjunction with 
the The ACC User Handbook to AMA4, and any additional guidance promulgated in the ACC Operational Guidelines.
ACC’s initial training course encompasses correct interpretation and use of the Guides with the NZ-specific variations de-
scribed in the ACC Handbook.
Requirements for an assessor to perform an impairment assessment
Impairment Assessments - Service Schedule
2.0 AMA Guides
The AMA Guides are explicit but not intuitive, and are designed to require training in their use and application, as well as clin-
ical judgement and expertise. The Guides provide a framework for minimising interobserver variation in assessing impairment, 
so that compensation is awarded consistently, correctly, and equitably. The Guides provide assessment methods for the dif-
ferent body systems and the way that impairments can be ‘rated’ and combined so that a ‘whole person’ impairment rating can 
be achieved. There are also rules around how non-covered conditions, which may be contributing to overall impairment, can 
be accommodated and appropriately excluded from the final rating. Within the ACC context, the interpretation and application 
of the Guides are supported by the ACC Handbook, which provides additional material so that the Guides are relevant to the 
NZ situation. Impairment rating reports are also subject to ‘peer review’ by expert medical assessors as part of ACC’s quality 
assurance program.
3.0 Training and mentoring for assessors
The initial training is usually about eight hours of tuition and practice in using the AMA Guides, assessment methods, calcu-
lating impairment, and report formatting. An assessor must satisfactorily complete several sample case studies before they 
undertake assessments. The training is followed by a period of one-to-one support, when new assessors discuss their cases 
and reports with an experienced assessor and have regular quality reviews.
Initial training is followed by a period of mentorship and collegial oversight from ACC’s Senior Medical Advisor (SMA), who is 
independently trained in the use of the AMA Guides in Australia, and has experience in conducting, peer reviewing, and in-
structing doctors in the formal assessment of impairment and proportional attribution in New Zealand and Australia. The SMA 
provides support in the application of the Guides and Handbook/Guidelines to individual cases and advice on report formatting
until the assessor’s reports are consistently compliant with the Assessment Tool.
Subsequently, a proportion of all assessment reports are ‘peer reviewed’ by an experienced assessor to ensure compliance 
and quality, with direct feedback to assessors.
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4.0 Keeping up training
Annual ‘refresher’ training is provided for all assessors at regional meetings, at which assessors can raise issues for clari-
fication, and interval guidance on consistency of approach is provided via the publication of Operational Guidelines, and an 
ACC newsletter. The annual refresher training covers a whole day (about two hours each of physical and mental injury, plus 
two hours of ‘general’ themes).
The approved NZ trainers are currently three doctors who themselves have appropriate training and experience in the use of 
the ACC Handbook and the AMA Guides.
5.0 Types of assessment
Assessors may only carry out those types of assessment that they are listed as being able to undertake in Part A Clause 3.
The types of assessment are:
• General assessments for physical injury; and
• Chapter 14 assessments for behavioural and mental impairment.
Assessors must complete training in their listed assessment types and are listed with ACC as being able to provide impairment 
assessments under these vocational scopes.
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GOV-039784 - Document 3


E iti noa ana, na te aroha
Though my present be small, my love goes with it
1
 
   
   
 

2
 
   
   
 

Guideline highlights
Traumatic brain injury (TBI), an injury to the brain rather than an injury to the head, is identifi ed by confusion or 
disorientation, loss of consciousness, post-traumatic amnesia and other neurological abnormalities. Thousands 
of New Zealanders each year experience TBI. This comprehensive guideline outlines important aspects of the 
diagnosis, acute management and rehabilitation of children, young people and adults after TBI.
Guideline highlights include:
• a clear defi nition of TBI, explicitly describing the necessary criteria for this diagnosis
• a clear description of severity levels for TBI
• straightforward descriptions of who should be seen in the Emergency Department and with what urgency
• clear recommendations about who should receive a computed tomography (CT) scan as part of the initial 
work-up, for both adults and children and young people
• recommendations about when it is safe to discharge adults, and children and young people, from an initial 
medical presentation
• a description of the types of rehabilitation services available for people with TBI in New Zealand
• recommendations about the organisation of rehabilitation services and approaches to TBI rehabilitation
• where there is enough evidence and/or consensus, recommendations about which interventions for people
with TBI are appropriate
• sections dealing with specifi c issues for Ma¯ori, Pacifi c peoples, consumers and carers as well as a separate
chapter dealing solely with issues for children and young people after TBI.
The guideline also points to other resources that come with the guideline. These resources can be found at 
www.nzgg.org.nz and www.acc.co.nz.
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4
 
   
   
 

Contents
Purpose ..........................................................................................................................................................11
About the guideline ........................................................................................................................................12
Chapters
1.
Traumatic brain injury in New Zealand ......................................................................................................21
1.1 Defi ning traumatic brain injury ........................................................................................................ 21
1.2 
Estimates of the incidence of traumatic brain injury in New Zealand ................................................ 23
1.3 Hospital-based 
rehabilitation 
......................................................................................................... 24
1.4 Cost 
................................................................................................................................................ 25
1.5 
Demographic characteristics of the traumatic brain injury population ............................................. 25
1.6 
Causes of traumatic brain injury in New Zealand ............................................................................. 25
1.7 Prognostic 
factors ........................................................................................................................... 25
1.8 
Consequences of traumatic brain injury .......................................................................................... 27
1.9 
Current practice in New Zealand ...................................................................................................... 29
1.10  Major gaps identifi ed ...................................................................................................................... 34
2. Pre-hospital 
assessment, management and referral to hospital ...............................................................35
2.1 Pre-hospital 
assessment – acute .................................................................................................... 36
2.2 
Assessment of need for medical attention ...................................................................................... 37
2.3 
Referral to Emergency Department .................................................................................................. 42
2.4 
Assessment in hospital not required ............................................................................................... 43
2.5 First 
assessment – delayed ............................................................................................................. 44
2.6 No 
assessment 
............................................................................................................................... 44
2.7 
Advice to the community sector ...................................................................................................... 44
2.8 
Organisation of trauma services ...................................................................................................... 45
3.
Acute phase of traumatic brain injury care ...............................................................................................47
3.1 
Emergency Department assessment of people with a suspected traumatic brain injury ................... 48
3.2 
Primary investigation for people with a suspected traumatic brain injury ........................................ 51
3.3 
Non-accidental injury in children .................................................................................................... 57
3.4 
Imaging of people with a suspected traumatic brain injury .............................................................. 57
3.5 
Use of corticosteroids in acute traumatic brain injury ...................................................................... 57
3.6 Involving 
neurosurgical care ........................................................................................................... 58
3.7 
Transfer from secondary to tertiary care settings ............................................................................. 59
3.8 
Indications for hospital admission .................................................................................................. 61
3.9 
In-hospital observation of people with traumatic brain injury .......................................................... 62
3.10  In-hospital support for families/wha¯nau and carers ........................................................................ 64
3.11 Discharge 
from hospital .................................................................................................................. 65
3.12  Referral to rehabilitation in the acute phase after traumatic brain injury .......................................... 66
4. Rehabilitation 
services 
............................................................................................................................69
4.1 
The rehabilitation process .............................................................................................................. 69
4.2 
Stages of rehabilitation .................................................................................................................. 72
4.3 
Organisation of services ................................................................................................................. 73
4.4 Rehabilitation 
teams 
...................................................................................................................... 76
5.
Rehabilitation following clinically signifi cant traumatic brain injury – assessment ..................................79
5.1 
Non-neurological medical sequelae of traumatic brain injury .......................................................... 81
5.2 Differential 
diagnosis ..................................................................................................................... 82
5.3 Physical 
assessment 
...................................................................................................................... 82
5
5.4 Communicative 
assessment 
........................................................................................................... 83
5.5 Neuropsychological 
assessment 
..................................................................................................... 83
 
   
   
 

6.
Rehabilitation following clinically signifi cant traumatic brain injury – intervention ..................................87
6.1 Physical 
rehabilitation 
.................................................................................................................... 88
6.2 
Optimising performance in daily living tasks .................................................................................106
6.3 
Sleep and fatigue .........................................................................................................................110
6.4 Vocational 
rehabilitation 
..............................................................................................................110
6.5 Sexuality 
......................................................................................................................................113
6.6 
Leisure and recreation ..................................................................................................................116
6.7 Evaluating 
progress 
in rehabilitation .............................................................................................117
6.8 
Discharge from rehabilitation services ..........................................................................................117
7.
Complementary and alternative medicines .............................................................................................119
7.1 Biofeedback 
.................................................................................................................................119
7.2 Electroencephalographic 
biofeedback/neurofeedback .................................................................120
7.3 Homoeopathy 
...............................................................................................................................120
7.4 Manipulative 
therapies 
.................................................................................................................120
7.5 Herbal 
remedies 
...........................................................................................................................121
7.6 Dietary 
supplements ....................................................................................................................122
7.7 Acupuncture 
.................................................................................................................................122
7.8 Distant 
healing 
.............................................................................................................................122
8.
Management of persistent symptoms and activity limitation following mild traumatic brain injury ........125
8.1 
Symptoms of mild traumatic brain injury .......................................................................................125
8.2 
Characterisation of people with persistent symptoms following mild traumatic brain injury ...........126
8.3 
Prevention of persistent symptoms following mild traumatic brain injury ......................................127
8.4 
Assessment of people with persistent symptoms after mild traumatic brain injury ........................127
8.5 
Return to work or study .................................................................................................................128
9.
Post-discharge follow-up and support for people with traumatic brain injury .........................................129
9.1 Follow-up 
.....................................................................................................................................130
9.2 
Continuing care and support .........................................................................................................132
10. Ma¯ori and traumatic brain injury ............................................................................................................137
10.1  Epidemiology of traumatic brain injury in Ma¯ori ............................................................................138
10.2  Health perspective of Ma¯ori ..........................................................................................................139
10.3  Service delivery for Ma¯ori ..............................................................................................................140
10.4  Assessment of Ma¯ori with traumatic brain injury ...........................................................................141
10.5 Wha¯nau support ...........................................................................................................................141
11. Pacifi c peoples and traumatic brain injury ..............................................................................................143
11.1 Pacifi c peoples in New Zealand .....................................................................................................144
11.2  Perception of health for Pacifi c peoples ........................................................................................145
11.3  Access to and utilisation of health and disability services .............................................................145
11.4  Rehabilitation planning for Pacifi c peoples with traumatic brain injury ..........................................146
11.5 Research 
issues 
............................................................................................................................147
12. Children and young people and traumatic brain injury ...........................................................................149
12.1 Defi nitions....................................................................................................................................149
12.2  Effects of traumatic brain injury in children and young people .......................................................150
12.3  Rehabilitation of children and young people with traumatic brain injury ........................................150
13. Needs of carers ......................................................................................................................................157
13.1  Interventions for people with traumatic brain injury and their families/wha¯nau and carers ............158
13.2  Parents/carers of children and young people with traumatic brain injury .......................................162
6
 
   
   
 

14. Special issues ........................................................................................................................................165
14.1  Capacity and consent ...................................................................................................................166
14.2 Driving..........................................................................................................................................167
14.3  Drug and alcohol use and misuse .................................................................................................169
14.4  Mental health in adults with traumatic brain injury .......................................................................172
14.5  Repeated traumatic brain injury and traumatic brain injury in sports .............................................186
14.6  Violence and traumatic brain injury ..............................................................................................192
15. Implementation .....................................................................................................................................195
15.1 Implementation 
activities 
.............................................................................................................195
15.2 Performance 
indicators 
.................................................................................................................198
15.3  Potential impact of the guideline ..................................................................................................198
Appendices ...................................................................................................................................................201
A.
Objectives for future research on traumatic brain injury in New Zealand ........................................203
B. Guideline 
grading 
systems 
...........................................................................................................205
C. Glasgow 
Coma 
Scale 
.....................................................................................................................209
D.
Additional resources and supporting documents ..........................................................................211
Glossary .......................................................................................................................................................213
References ....................................................................................................................................................219
Recommendations and good practice points
Chapters
2.
Pre-hospital assessment, management and referral to hospital ..........................................35
2.1
Pre-hospital 
assessment – acute ......................................................................................... 36
2.2.1
Glasgow 
Coma 
Scale 
........................................................................................................... 37
2.2.2 
Loss of consciousness......................................................................................................... 38
2.2.3
Post-traumatic 
amnesia 
...................................................................................................... 38
2.2.4
Neurological 
signs 
.............................................................................................................. 39
2.2.5
Bleeding 
disorders and use of anticoagulants ..................................................................... 39
2.2.11 
Headache (good practice point only) ................................................................................... 41
2.8  
Organisation of trauma services .......................................................................................... 45
3.
Acute phase of traumatic brain injury care ..........................................................................47
3.1  
Emergency Department assessment of people with a suspected traumatic brain injury ........ 48
3.1.2
Alcohol 
............................................................................................................................... 51
3.2 
Primary investigation for people with a suspected traumatic brain injury ............................. 51
3.2.1 
Selection of adults for CT imaging of the head ..................................................................... 53
3.4 
Imaging of people with a suspected traumatic brain injury (good practice points only) ........ 57
3.5 
Use of corticosteroids in acute traumatic brain injury .......................................................... 57
3.7 
Transfer from secondary to tertiary care settings .................................................................. 59
3.8
Indications for hospital admission ...................................................................................... 61
3.9 
In-hospital observation of people with traumatic brain injury .............................................. 62
3.11
Discharge 
from 
hospital ...................................................................................................... 65
4.
Rehabilitation 
services 
.......................................................................................................69
4.3.2.1 Case 
coordination 
............................................................................................................... 75
4.4
Rehabilitation teams ........................................................................................................... 76
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5.
Rehabilitation following clinically signifi cant traumatic brain injury – assessment .............79

Rehabilitation following clinically signifi cant traumatic brain injury – assessment ............... 80
6.
Rehabilitation following clinically signifi cant traumatic brain injury – intervention ............87
6.1
Physical 
rehabilitation......................................................................................................... 88
6.1.1 
Motor control and function .................................................................................................. 90
6.1.3
Continence 
......................................................................................................................... 93
6.1.4
Sensory 
impairment 
............................................................................................................ 95
6.1.5 
Communication and language rehabilitation ....................................................................... 97
6.1.6
Cognitive 
rehabilitation 
....................................................................................................... 98
6.1.7
Psychosocial/Behavioural rehabilitation ...........................................................................103
6.2 
Optimising performance in daily living tasks .....................................................................106
6.4
Vocational 
rehabilitation 
...................................................................................................110
6.5
Sexuality 
...........................................................................................................................113
6.6 
Leisure and recreation .......................................................................................................116
8.
Management 
of persistent symptoms and activity limitations following
mild traumatic brain injury ...............................................................................................125
8.3 
Prevention of persistent symptoms following mild traumatic brain injury ...........................127
8.4 
Assessment of people with persistent symptoms after mild traumatic brain injury .............127
9.
Post-discharge follow-up and support for people with traumatic brian injury ....................129
9.1
Follow-up 
..........................................................................................................................130
9.2 
Continuing care and support .............................................................................................132
10.
Ma¯ori and traumatic brain injury ......................................................................................137
10
Ma¯ori and traumatic brain injury ........................................................................................137
11.
Pacifi c peoples and traumatic brain injury ........................................................................143
11
Pacifi c peoples and traumatic brain injury .........................................................................144
12.
Children and young people and traumatic brain injury ......................................................149
12.3.1
Transitions 
........................................................................................................................151
12.3.2
Provision of rehabilitation .................................................................................................153
13.
Needs of carers ................................................................................................................157
13
Needs 
of 
carers .................................................................................................................157
13.2 
Parents/Carers of children and young people with traumatic brain injury ...........................162
14.
Special 
issues 
..................................................................................................................165
14.1 
Capacity and consent ........................................................................................................166
14.2 
Driving (good practice point only) ......................................................................................167
14.3 
Drug and alcohol use and misuse .....................................................................................169
14.4 
Mental health in adults with traumatic brain injury ............................................................172
14.4.9.1 Diagnosis of post-traumatic brain injury depression (good practice points only) ................177
14.4.10.1 Diagnosis and management of post-traumatic stress disorder for people with
traumatic brain injury (good practice point only)................................................................181
14.4.10.2 Diagnosis and management of post-traumatic brain injury psychosis
(good practice point only) .................................................................................................182
14.4.10.3 
Pharmacotherapy for post-traumatic brain injury mental illness .........................................182
14.4.10.3.1  Pharmacotherapy for post-traumatic brain injury depression .............................................183
14.4.10.3.2 Psychotherapeutic 
approaches .........................................................................................185
14.5.2 
Immediate management of and return to play after sporting injuries .................................188
14.5.3 
Repeated traumatic brain injury in children (good practice points only) .............................192
14.6 
Violence and traumatic brain injury ...................................................................................192
8
 
   
   
 

List of tables
1.1 Criteria 
for 
classifying the severity of traumatic brain injury ............................................................. 23
1.2 
Intervention settings: the progression into residential rehabilitation ............................................... 31
7.1 
Summary of the evidence for complementary and alternative medicine in
treating adults with traumatic brain injury .....................................................................................122
List of fi gures
1.1 
Presentations and admissions for head injury at Christchurch Hospital
Emergency Department, 2004 ........................................................................................................ 23
3.1 
Diagnostic management and selection for imaging of children and
young people aged <17 years  ......................................................................................................... 56
4.1 
Interaction of concepts ................................................................................................................... 71
4.2 
‘Stages of rehabilitation’ model for people with traumatic brain injury ............................................ 72
4.3 
A functionally oriented model of community-based rehabilitation  .................................................. 73
14.1  Assessment of depression in traumatic brain injury ......................................................................180
14.2  Reasons for depression following traumatic brain injury ................................................................184
14.3  Algorithm: Safe steps to return to play after a possible traumatic brain injury ................................191
9
 
   
   
 

10
 
   
   
 

Purpose
This guideline provides evidence-based recommendations for best practice in the diagnosis, acute management 
and rehabilitation of children, young people and adults after traumatic brain injury (TBI). It is intended 
to support informed decision-making about acute management, care and rehabilitative approaches by 
practitioners working with people who have a TBI, their families/wha¯nau and carers.
This guideline is intended for use primarily by all practitioners involved in the acute management and 
rehabilitation of those with TBI, including Emergency Departments, primary and secondary care practitioners, 
rehabilitation and allied health practitioners, providers of residential care, private providers, and case managers 
and educationalists. 
The guideline will also be a resource for the Accident Compensation Corporation (ACC) and District Health Board 
(DHB) funders and planners as it identifi es the necessary aspects of care and services that should be provided. 
In addition, it identifi es where there is a need for targeted research to improve the evidence base. 
11
 
   
   
 

About the guideline
Foreword
The New Zealand Guidelines Group Incorporated (NZGG) is a not-for-profi t, independent organisation 
established to promote effective health and disability services. NZGG oversees the development and 
implementation of guidelines across the health and disability sectors in New Zealand. Guidelines make an 
effective contribution to this aim by reviewing the latest national and international studies and synthesising 
their fi ndings into practical recommendations for use in the New Zealand setting. 
The Traumatic Brain Injury Rehabilitation Guideline,1 published jointly in 1998 by ACC and the National 
Health Committee, describes essential features of a TBI rehabilitation service, but does not offer guidance 
on the management and rehabilitation of people with TBI. A Clinical Guideline for the Acute Management of 
Traumatic Brain Injury2 was developed in 2001, which defi nes TBI and provides the main principles for clinical 
management of acute TBI. However, the previous guideline did not cover the diagnosis, classifi cation or 
management of people with TBI after the acute phase. ACC is also currently developing generic guidelines for 
claims assessors, but these will not cover specialised assessments, such as those required for claimants with 
TBI. ACC commissioned the development of this new guideline for use in the management and care of people 
with TBI.
Scope
This guideline provides a diagnostic, acute management and rehabilitation framework for the care and 
management of TBI. It is intended to inform and guide: all TBI acute and rehabilitation treatment providers and 
specialists throughout New Zealand; funding agencies such as ACC and DHBs; and people with TBI and the 
people who care for them, including family/wha¯nau and unpaid carers. The guideline will also inform ACC’s 
purchasing strategy and the development of contracts.
This guideline addresses the acute care and post-acute rehabilitation for all levels of severity of TBI, for all ages, 
and in all locations of care (ie, pre-hospital, hospital and community-based assessment and management). 
For the purpose of this guideline, TBI is broadly defi ned as brain injury resulting from externally infl icted 
trauma, ie, due to head injury or post-surgical damage. Therefore, the guideline does not specifi cally address 
other categories of brain injury, including those resulting from poisoning and anoxia, or stroke and other 
cardiovascular events. (For current guidelines on brain injury secondary to stroke see Life after Stroke: a New 
Zealand guideline for management of stroke, available at www.nzgg.org.nz.)
This guideline also excludes pre- and peri-natal brain damage resulting from prenatal and birth-related events. 
The management of TBI-related issues including prevention, drug and alcohol abuse, and family violence is also 
outside the scope of this guideline. Where other guidelines have relevance to TBI management, they are cross-
referenced in the text.
This guideline is not a service framework and does not extend to a detailed analysis of the most effective 
service confi gurations to support the recommended assessment and rehabilitation strategies. The section on 
implementation is similarly intended as a broad conceptual guide. This edition does not specifi cally address the 
needs of all minority populations within New Zealand, although they may be considered in future reviews.
The guideline is informed by the International Classifi cation of Functioning, Disability and Health (ICF).3 
Therefore, there is a focus on the impact of the TBI on a person’s functioning and participation rather than 
specifi c impairments.
12
 
   
   
 

Terminology
The term ‘head trauma’ or ‘head injury’ is used throughout the guideline to mean the original injury. A head 
injury does not always cause an injury to the brain, and the terms ‘head’ and ‘brain’ are used to distinguish 
between the original injury to the head and consequent injury to the brain respectively. 
Terms routinely used to describe the severity of the injury, such as the term mild brain injury, may be 
unacceptable to people who have suffered a brain injury that falls within this category, as the impact on their 
health and functioning that they experience as a result of the injury may be far from ‘mild’. There are also 
anecdotal accounts that use of this term impacts on the interactions with case managers and health care 
professionals so that the injured person feels that the professionals are dismissive and do not accept the full 
extent of their problems. Although classifi cation of the initial severity of TBI is useful in the prediction of some 
short- and long-term outcomes, the relationship between initial severity of injury and medium- and long-term 
outcomes has been questioned.4 
Following recent international practice, the Guideline Development Team has used the terms mild, moderate or 
severe TBI to describe the initial severity of injury in a few sections of this guideline, particularly in Chapter 1 
where the size and impact of the problem of TBI are discussed.
In most other sections of the guideline, the Guideline Development Team has followed the convention of 
other recent international evidence-based guidelines, and used, where possible, clinically signifi cant TBI or 
symptomatic TBI to refer to TBI with a need for intervention or other care or support, irrespective of the initial 
severity of injury. Additional specifi c terminology used in this guideline is defi ned in the Glossary.
Background to the guideline
Current Practice Review
A number of aspects of the rehabilitation and support services delivered to TBI clients in New Zealand are 
uncertain. There are variations in content and quality for different services operating under the same contract 
across different regions of New Zealand (eg, urban compared with rural centres). There are also differences in 
terms of the volume of clients and in client mix (eg, solely TBI compared with TBI and other rehabilitation clients, 
clients from ethnic minority populations and clients with comorbid conditions, such as mental health disorder 
or drug abuse). There has been no systematic New Zealand study following large cohorts of people with TBI from 
onset, documenting the nature and extent of services provided such as would occur with a TBI register. Small-
scale studies have been conducted in Auckland, Hamilton and Wellington at various times in the past 10 years. 
As part of this guideline project, ACC commissioned a review of current practice in TBI rehabilitation from the 
perspective of TBI providers and consumers. This Current Practice Review was undertaken and completed during 
2004, and included a survey of both TBI providers and TBI consumers (people with TBI and carers) throughout 
New Zealand.5 The full report is available at www.nzgg.org.nz.
The evidence base
Many aspects of both adult and paediatric rehabilitation following a clinically signifi cant TBI lack a robust 
evidence base. For example, in the case of paediatric studies, many group a wide range of ages, where the 
participants may be at differing developmental stages. The lack of a robust evidence base is also partly 
due to the heterogeneous nature of the brain injuries and of the people who have suffered the injury. To 
perform robust randomly controlled trials of interventions would require very large numbers of people to 
eliminate the confounding effects of individual differences. Therefore, much of the evidential support for the 
recommendations in this guideline is necessarily drawn from less robust research study designs, or from closely 
related areas such as the stroke literature. Specifi c ‘gaps’ in the evidence have been identifi ed (see Appendix 
A) and it is suggested that research funding bodies consider supporting more research in these areas. It is also 
suggested that implementation of the guideline recommendations be evaluated to provide stronger evidence for 
13
future revisions.
 
   
   
 

The Wellington School of Medicine and Health Science’s Rehabilitation Medicine Department was 
commissioned by NZGG to conduct an evidence-based comparative review6 of psychometric testing and other 
tools commonly used in the initial assessment of TBI, and in the assessment of outcomes of rehabilitation. This 
review, TBI Tools Review for the Development of Guidelines on the Assessment, Management and Rehabilitation 
of Traumatic Brain Injury, 2005, is available as a separate document at www.nzgg.org.nz and provides the 
evidence base for the recommendations for diagnostic and outcomes assessment.
Guideline development process
The TBI Rehabilitation Guideline Development Team fi rst met in March 2004 to undergo training in the guideline 
development process, and to determine the main topics and questions to be covered by the guideline.
Results of a preliminary literature search (conducted to inform the scope of the guideline) made it apparent 
that a risk to the effectiveness of any guideline for rehabilitation from TBI would be the impact of treatment 
recommendations in the acute stage of management. This preliminary literature search also identifi ed a 
rigorous, evidence-based guideline for care of the acute stage of TBI: Head Injury: Triage, Assessment, 
Investigation and Early Management of Head Injury in Infants, Children and Adults, produced by the United 
Kingdom’s (UK) National Institute of Clinical Excellence (NICE) in 2003.7 ACC agreed that this guideline should 
be adapted for the New Zealand environment to produce a guideline that would cover the entire process of care 
and rehabilitation from the point of injury. A sub-group with a focus on the adaptation of the NICE guideline was 
formed from the main Guideline Development Team, with the addition of clinicians with expertise in emergency 
medicine and the acute phase of care.
Agreed principles underlying the development of the guideline were: 
• a consumer focus – evidence and recommendations should be considered in terms of outcomes that matter
to people with TBI, their families/wha¯nau and paid and informal carers
• consistency with the World Health Organization’s ICF3
• recommendations for diagnostic assessment and rehabilitative interventions should support national 
consistency in practice
• aspects of service structure and linkages between sectors and services necessary to support the guideline
recommendations should be identifi ed.
The specifi c topics to be covered by the guideline, in addition to those in the NICE acute care guideline, were 
agreed as follows:
• the epidemiology of TBI in New Zealand
• appropriate 
assessments 
(including neuropsychological testing) to confi rm diagnosis, classify severity
and identify people at high risk of long-term sequelae (including work loss), and to identify important early 
complications
• effective 
identifi cation of TBI in a variety of non-clinical settings, such as schools and prisons
• appropriate 
strategies 
that minimise subsequent disability and work loss and maximise quality of life,
including effective rehabilitative therapies and interventions appropriate to New Zealand clinical settings 
• the effectiveness of complementary and alternative medications and therapies, such as osteopathy and
acupuncture, in the rehabilitation of people with TBI
• appropriate management strategies for post-acute complications of TBI (including physical, cognitive,
behavioural impairments, spasticity, and intervention strategies) that are associated with improved
outcomes if recovery is slower than expected
• appropriate follow-up strategies for people with TBI or specifi c sub-groups of people with TBI
• the most appropriate TBI outcome measurements for New Zealand clinical settings, including assessment of 
when people can return to sporting, educational, work and leisure activities
14
 
   
   
 

• the effectiveness, in terms of improving outcomes for consumers, of:
– information provided to families, carers, people with TBI, the wider population and/or ACC staff 
– support provided to families and carers of people with TBI
– application of supported employment for people with TBI
– care coordination in enhancing the general functional status of people with TBI
• identifi cation of gaps in TBI services and processes to address these gaps, including the need for liaison with
mental health services, such as drug and alcohol services
• necessary elements of effective service delivery confi guration for the assessment and management of people
with TBI.
It was agreed that for each topic, consideration would be given to whether the evidence and recommendations 
would apply equally well to both adults and children, and to Ma¯ori and Pacifi c peoples, and to provide differing 
recommendations for these populations, where appropriate. 
These topics were operationalised as searchable questions by the NZGG research team, and a systematic 
hierarchical search for evidence was conducted. The search strategy for the guideline is available online at www.
nzgg.org.nz – select ‘Publications’ then ‘Guidelines’ then ’Neurology/Rehabilitation’ then the guideline title, 
then ‘Search Strategy’. 
Research identifi ed through the search was assessed for relevance by the NZGG research team, and papers 
identifi ed as potentially relevant were retained to be included in the critical appraisal process. 
A number of recent and rigorously produced ‘seed’ guidelines and syntheses of relevant evidence to inform the 
development of this guideline for New Zealand were identifi ed. The Guideline Development Team acknowledges 
the help and support received from the authors and editors of these works, which include:
1. Head Injury: Triage, Assessment, Investigation and Early Management of Head Injury in Infants, Children and
Adults, 2003. Produced by NICE and the National Collaborating Centre for Acute Care.7
2. Rehabilitation following Acquired Brain Injury: National Clinical Guidelines, 2003. Ed: Turner-Stokes L.
Produced by the Royal College of Physicians and British Society of Rehabilitation Medicine.8
3. Management and Prognosis of Severe Traumatic Brain Injury, 2000. Produced by Bullock MR, Chesnut RM,
Clifton GL, et al., for the Brain Trauma Foundation and American Association of Neurological Surgeons.9
4. Evidence Report on Rehabilitation of Persons with Traumatic Brain Injury, 1998. Produced by Chesnut RM,
Carney N, Maynard H, et al., of the Oregon Health Sciences University Agency for Health Care Policy and
Research.10
5. Rehabilitation for Traumatic Brain Injury in Children And Adolescents. Evidence report no. 2, supplement,
1999. Produced by Carney N, du Coudray H, Davis-O’Reilly C, et al., of Oregon Health Sciences University 
Agency for Health Care Policy and Research.11
6. Joint Framework and Guidelines on Vocational Assessment and Rehabilitation after Acquired Brain Injury,
2004. Produced by the Inter-Agency Advisory Group on Vocational Rehabilitation after Brain Injury and in
association with the British Society of Rehabilitation Medicine Working Party on Rehabilitation following
Acquired Brain Injury, British Society of Rehabilitation Medicine.12
7. Concise Guidance for the Use of Anti-depressant medication in Adults Undergoing Recovery or Rehabilitation
Following Acquired Brain Injury, 2005. Ed: Turner-Stokes L. Produced by the British Society of Rehabilitation
Medicine and the British Geriatrics Society with the Royal College of Physicians’ Clinical Effectiveness and
Evaluation Unit.13
15
 
   
   
 

Guideline Development Team
The following organisations were approached to nominate or endorse members of the multidisciplinary team 
who developed this guideline: 
The Australasian Faculty of Rehabilitation Medicine, The Royal Australasian College of Physicians (RACP)
The Australasian College for Emergency Medicine (ACEM)
The Paediatric Society of New Zealand
The Pasifi ka Medical Association
The Royal Australia and New Zealand College of Psychiatrists (RANZCP)
The New Zealand College of Clinical Psychologists (NZCCP)
The Royal New Zealand College of General Practitioners (RNZCGP)
The College of Nurses Aotearoa (NZ) Inc 
The New Zealand Society of Physiotherapists Inc (NZSP)
The New Zealand Speech-Language Therapy Association (NZSTA)
The New Zealand Association of Occupational Therapists (NZAOT)
Group Special Education in the Ministry of Education
The Head Injury Society of New Zealand (HISNZ)
The Brain Injury Association of New Zealand (BIANZ)
Carers NZ
Ranworth Healthcare 
Health Partners Limited
The Disability Resource Centre (DRC), Auckland
The Accident Compensation Corporation (ACC)
The Royal Australasian College of Surgeons
The Guideline Development Team members are:
Harry McNaughton (Chair)
 
Rehabilitation Physician, Capital and Coast DHB; Programme Director, Stroke/Rehabilitation Medical 
Research Institute of New Zealand Endorsed by the Australasian Faculty of Rehabilitation Medicine
Michael Ardagh 
 
Professor of Emergency Medicine, Christchurch School of Medicine and Health Sciences, University of Otago 
Endorsed by ACEM
Andrew Beattie 
 
Specialist Nurse and private provider, Goodwood Park Trust Nominated by ACC to represent private providers
Vijaya Dharan 
 
Senior Advisor, Professional Practice Unit, Ministry of Education Nominated by Group Special Education, 
Ministry of Education
Margaret Dudley 
 Neuropsychologist 
Nominated by ACC to represent Ma¯ori and endorsed by NZCCP
Chris Dyson 
 
Paediatric and adult neuropsychologist; provider of TBI rehabilitation therapy for children Endorsed by NZCCP
Monique Niumata-Faleafa 
 Clinical 
Psychologist/Pacifi c Clinical Advisor, University of Auckland Endorsed by NZCCP
Greg Finucane
 Neuropsychiatrist, 
provider of TBI rehabilitation Nominated by RANZCP
Beatrice Hale 
 
Social worker (retired); carers’ advocate Nominated by Carers NZ
Kate Hall
 
Paediatrician; provider of TBI rehabilitation Nominated by the Paediatric Society of  New Zealand
16
 
   
   
 

Matire Harwood
 
General Practitioner; Research Fellow, Medical Research Institute of New Zealand, representing Ma¯ori 
Endorsed by RNZCGP 
Brenda Kenworthy
 ex 
offi cio ACC Senior Improvement Analyst, Rehabilitation Improvement, ACC
Peter Larking 
 ex 
offi cio Project Manager Research, ACC 
Brigette Larkins
 Speech-Language 
Therapist; 
Project Manager, Canterbury DHB Senior Fellow, University of Canterbury 
Nominated by private providers
Janet Leathem
 
Professor of Neuropsychology, Massey University Endorsed by NZCCP
William Levack
 
Physiotherapist; Lecturer in Rehabilitation, Wellington School of Medicine and Health Sciences Endorsed by 
NZSP
Joan Limmer 
 Field 
Offi cer, Head Injury Society Waikato; consumer advocate Nominated by HISNZ
Kelly Lynch
 
Clinical nurse specialist: rehabilitation Nominated by the College of Nurses Aotearoa (NZ) Inc
Martin MacFarlane
 
Clinical Director, Department of Neurosurgery, Christchurch Hospital Endorsed by the Royal Australasian 
College of Surgeons 
John Mayhew
 
General Practitioner, former Medical Adviser NZ Rugby Football Union Nominated by RNZCGP
Jenny McClure
 Parent/Consumer 
advocate 
Endorsed by BIANZ
Siobhan Molloy 
 
Executive Director, NZAOT; Speech-Language Therapist Endorsed by NZSTA and NZAOT
Harley Pope 
 Consumer 
advocate 
Nominated by BIANZ
Sharon Reilly
 ex 
offi cio ACC Programme Manager, Specialised Services 
Elizabeth Rowland
 
Occupational Therapist, provider of TBI rehabilitation Nominated by NZAOT
Bernadette Ryan
 
Psychiatric Nurse, Disability Project Coordinator Nominated by DRC (Auckland)
Richard Siegert 
 Neuropsychologist; 
Associate 
Professor of Rehabilitation, Rehabilitation Teaching and Research Unit, 
Department of Medicine, Wellington School of Medicine and Health Sciences Endorsed by NZCCP
Peter Stormer
 
General Practitioner, provider of TBI rehabilitation; ex offi cio ACC Branch Medical Adviser Nominated by ACC
Plus, contributors to the early stages of development: 
Wendy Browne 
 ex 
offi cio Scheme Performance Nominated by ACC
Denise Udy
 ex 
offi cio Rehabilitation Adviser Nominated by ACC
17
 
   
   
 

NZGG staff
Rowena Cave 
 
Senior Project Manager, until September 2005
Rob Cook
 Medical 
Advisor
Naomi Brewer
 
Researcher, until September 2004
Rose Matthews
 
Researcher, until April 2005
Mark Ayson
Researcher, from October 2005
Declarations of competing interests 
Michael Ardagh is a member of the Christchurch Brain Research Group, which received funding for post-head 
injury assessment. He is also a member of the Emergency Care Research Foundation, a charitable trust which 
supports emergency care research
Harry McNaughton has received funding for research and fees for consulting from ACC 
Kate Hall received funding to attend the Epilepsy Symposium 2002 from Janssen-Cilag
Elizabeth Rowland is a director of a private limited company providing occupational therapy services 
Consultation
A draft of this guideline was widely circulated to more than 250 individuals/organisations for comment in 
June 2005 as part of the peer review process. Comments were received from the following organisations or 
individuals:
• Andrew 
Swain, 
ACEM
• Anna McRae, Auckland DHB
• Anne 
Smith, 
Wilson 
Centre
• Blair Donkin, Otago DHB
• Bridget Kool, University of Auckland
• Brigette Larkins, TBI Guideline Development Team
• Chris Milne, Anglesea Sports Medicine
• Colin McArthur, Auckland DHB
• Derek Keith Sage (Dr), Bay of Plenty DHB
• Dharan Vijaya, Ministry of Education
• Elizabeth Rowland, Capital and Coast DHB
• Garry Clearwater, Waitemata DHB
• Gillian Robb, University of Auckland, School of Population Health
• Helen Cosgrove, MidCentral Health
• Kathryn McPherson, Auckland University of Technology 
• Janis Henry, Integrated Partners in Health
• Jenni Coles, Counties Manukau DHB
• Jiff Stewart, Ministry for Social Development 
• Jocelyn Neutze, Kidzfi rst and Middlemore Hospital Emergency Department
• Jock Muir, Canterbury DHB
• John Clink, Canterbury DHB
• Judith Roessink-Berryman, Unimed, Grange House
18
 
   
   
 

•  Karen Gallagher, GAS Gallagher and Associates Limited
•  Katie Latimer, Waikato DHB
•  Kieran Hobbs (Dr), Cavit ABI Rehabilitation Wellington Branch
•  Lucy O’Hagan, Aspiring Medical Centre
•  Marcus Heitger, Christchurch School of Medicine, University of Otago
•  Margaret Anderson, Canterbury DHB
•  Mary Bonner, Waikato DHB
•  Nic Beets, Psychologist and Relationship Therapist
•  Occupational Therapists, Community Rehabilitation 
•  Paul Malpass, Bay of Plenty DHB
•  Phillipa Corby, Abano Rehabilitation
•  R C Freebairn (Dr), Joint Faculty of Intensive Care Medicine
•  Rehabilitation Team, MidCentral Health
•  Samir Anwar (Dr), FAFRM (RACP)
•  Sid Cuthbertson, Auckland City Hospital
• Steve 
Targett, 
Anglesea Sports Medicine 
•  Susan Freeman, College of Nurses Aotearoa (NZ) Inc
•  Valerie Smith, Ministry of Health
•  Wendy Browne, ACC, Porirua Branch
Expert peer review was provided by:
Kathryn McPherson, Professor, School of Education, College of Saint Rose, New York
Acknowledgements
NZGG and the Guideline Development Team would like to acknowledge, in particular, the help and support of 
the following people and organisations for provision of additional information and permission to include and 
adapt their work:
The UK NICE and the UK National Collaborating Centre for Acute Care 
Professor Kathleen Bell, Department of Rehabilitation Medicine, University of Washington, Seattle, USA
Dr Scott Bezeau, Department of Psychology, University of Victoria, Victoria, British Columbia, Canada
Professor R Chesnut and the Oregon Health Sciences University, Portland, USA 
Professor Lynne Turner-Stokes, the British Society of Rehabilitation Medicine and the UK Royal College of 
Physicians, London, UK 
Professor Mark Ylvisaker, School of Education, College of Saint Rose, Albany, New York, USA
Thanks to Dr Monique FaleafaDr Matire HarwoodDr Rob CookMargaret Dudley and Sarah Howard for their 
development of the chapters on TBI in Ma¯ori and Pacifi c populations. 
Funding
This guideline was funded by ACC and development and production was independently managed by NZGG. 
ACC staff members were co-opted onto the Guideline Development Team to provide advice about ACC internal 
processes. All evidence appraisal, reporting and formulation of recommendations is independent of ACC, and 
NZGG retains editorial independence.
19
 
   
   
 

Evidence and recommendation grading system
All studies relating to benefi ts or harms of interventions are graded for quality. Each study has been assigned an 
overall level of evidence (+~ or x). When applicable, the level is listed alongside the citation in the reference 
list. See Appendix B for details of the grading system. Study details and levels of evidence were summarised in 
evidence tables, which were used for the formulation of recommendations. Studies with an ‘x’ level of evidence 
had questionable validity and were not considered relevant to the formulation of recommendations. Descriptive 
research, included for information, was not graded for quality.
20
 
   
   
 

1
Chapter 1:
Traumatic brain injury in New Zealand
Overview
• A consumer survey suggests that people with TBI experience signifi cant health disadvantage, in terms of 
both physical and mental health, compared with their peers. TBI, an injury to the brain rather than an injury 
to the head, is identifi ed by confusion or disorientation, loss of consciousness, post-traumatic amnesia and
other neurological abnormalities.
• The Glasgow Coma Scale score and ‘duration of post-traumatic amnesia’ can be used to classify the severity 
of TBI.
• Accurate data on the incidence and prevalence of TBI and TBI sequelae is needed to aid the planning and
evaluation of service delivery.
• A number of pre-injury, injury-related and post-injury factors have been shown to be associated with better or
poorer outcomes.
• Some people with mild TBI will have effects lasting greater than 12 months, while in those with moderate
and severe TBI there may be a residual impact on functioning throughout the lifespan.
• Carers of individuals with TBI have a poorer quality of life and increased psychological morbidity compared
with the general population.
• Considerable 
variation currently exists in New Zealand TBI rehabilitation service provision.
• Rehabilitation services are provided by both DHBs and private providers.
• ACC funds a range of residential and non-residential rehabilitation services.
1.1 Defi ning traumatic brain injury
For the purposes of this guideline, the Guideline Development Team adopted a broad defi nition of TBI as an 
injury to the brain resulting from externally infl icted trauma. 
The main diffi culty with defi ning TBI is differentiating between those people who have had a head injury (a 
defi nite episode of external force to the head, including a deceleration force without actual impact to the head), 
and those who also have TBI. Most international defi nitions of TBI require some neurological symptoms or signs 
such as loss of consciousness, a period of amnesia and/or focal neurological defi cit.14
There is no ‘gold standard’ for the diagnosis of TBI, as some forms of radiological imaging are neither sensitive 
nor specifi c for TBI. There are also instances where individuals who do not meet low-threshold criteria for the 
diagnosis of TBI (those with no loss of consciousness, with a normal Glasgow Coma Scale score [see Section 
2.2.1 Glasgow Coma Scale for more details] and no amnesia) have evidence of injury to the brain, such as a 
contusion, on magnetic resonance imaging (MRI) scan.
The World Health Organization (WHO) Collaborating Centre Task Force on Mild Traumatic Brain Injury performed 
a systematic review of explicit case defi nitions to produce a working defi nition for TBI and then applied a 
specifi c defi nition for mild TBI.15 In the absence of a ‘gold standard’ diagnostic test, its defi nition of TBI is 
currently the best available, and it has been adapted by the Guideline Development Team to delineate the lower 
threshold of ‘defi nite TBI’.
21
 
   
   
 

The defi nition used in this guideline is: 
TBI is an acute brain injury resulting from mechanical energy to the head from external physical forces. 
Operational criteria for clinical identifi cation include one or more of the following:
•  confusion or disorientation
•  loss of consciousness
• post-traumatic 
amnesia
•  other neurological abnormalities, such as focal neurological signs, seizure and/or intracranial lesion.
These manifestations of TBI must not be due to drugs, alcohol or medications, caused by other injuries or 
treatment for other injuries (eg, systemic injuries, facial injuries or intubation), or caused by other problems (eg, 
psychological trauma, language barrier or co-existing medical conditions).
TBI can occur in the context of penetrating craniocerebral injuries but in this situation, focal neurological defi cits 
are generally more important than any diffuse element. 
1.1.1 Classifi cation of severity
Studies of TBI incidence and prevalence tend to classify the initial severity of injury as ‘mild’, ‘moderate’ and 
‘severe’. There are a number of criteria for assessing severity, including:
•  the Glasgow Coma Scale score
•  loss of consciousness or coma 
•  post-traumatic or retrograde amnesia.
The most commonly used criterion for classifying severity has been the Glasgow Coma Scale score. This is 
usually used for assessment when a person with suspected TBI presents to an Emergency Department or 
general practitioner.15
The scores are categorised as follows: ‘mild TBI’ 13 to 15 (of a maximum 15); ‘moderate TBI’ 9 to 12; and 
‘severe TBI’ 3 to 8 (with 3 being the minimum score).15 There is some evidence that people with an initial 
Glasgow Coma Scale score of 13 have worse outcomes than those with a Glasgow Coma Scale score of 14 to 
15,16 with those authors advocating a subset of ‘mild TBI’ called ‘high-risk mild TBI’ for people with an initial 
Glasgow Coma Scale score of 13 to 14 and/or radiological abnormalities. Nevertheless, current international 
consensus, including the recent WHO Task Force on Mild Traumatic Brain Injury,15 supports the severity 
classifi cation using the Glasgow Coma Scale as described here (ie, initial Glasgow Coma Scale of 13–15 = mild 
TBI).
See Chapter 2, Pre-hospital assessment, management and referral to hospital and Appendix C for more details 
about the adult and paediatric versions of the Glasgow Coma Scale.
Another useful indicator of the severity of a TBI is post-traumatic amnesia, as it is strongly related to 
outcomes.17–23 Post-traumatic amnesia is calculated from the time of the accident and includes any period of 
loss of consciousness or coma.
Assessment of post-traumatic amnesia can be inaccurate if trying to determine it retrospectively through clinical 
interview, and should commence before the resolution of post-traumatic amnesia, where possible.24 There is 
little difference between particular assessment measures of post-traumatic amnesia, although the Tools Review6 
concluded there were some qualitative advantages to the Modifi ed Oxford Post-traumatic Amnesia Scale 
(MOPTAS),25 which is similar to the widely-used Westmead Post Traumatic Amnesia Scale.26
22
 
   
   
 

1
In this guideline, unless otherwise stated, the defi nitions of severity of TBI used are those given in Table 1.1.
table 1.1:
criteria f or cl assif ying the severit y of traumatic brain injury*
gl asgow coma scale 
duration of post-
severit y of injury
score†
traumatic amnesia‡
Mild
13–15
<24 hours
Moderate
9–12
1–6 days
Severe
3–8
7 days or more
* If there is a discordance between the severity level for the Glasgow Coma Scale score and post-traumatic 
amnesia, it is appropriate to use the more severe category, eg, Glasgow Coma Scale of 14, but mild TBI, post-
traumatic amnesia two days = moderate TBI.
†  Teasdale, et al. Acta Neurochir (Wien) 1979; 28:13–16.
‡  Carroll LJ, et al. J Rehabil Med 2004(43 Suppl):113–25.
1.2  Estimates of the incidence of traumatic brain injury in New Zealand
The problem of inconsistent and inaccurate diagnosis of TBI has been demonstrated in coding of hospital 
discharges for TBI in New Zealand, with errors in both directions (ie, defi nite TBI not coded as such and coded 
TBI not meeting the criteria for defi nite TBI). Many people with possible TBI, generally at the ‘mild’ end of 
the spectrum, do not seek medical attention. This also means they are unlikely to make a claim to ACC, and 
therefore will not be identifi ed by ACC statistics. It is not currently possible to identify how many people, who 
visit an Emergency Department or general practitioner with an injury that is coded as a head injury, actually have 
TBI. Even so, in 2004, Christchurch Hospital Emergency Department recorded a total of 66,238 presentations,27 
including 2133 (3.2%) people with head injuries of all levels of severity, who were assessed and admitted as 
outlined in Figure 1.1.
figure 1.1:
presentations and admissions f or head injury at christchurch hospital emergency department, 2004
age 
head 
(years)
injuries
0–2
87
2133 head injuries
3–16
467
(including people with other injuries and conditions)
17–25
574
26–65
776
66–100
228
69% (1467) discharged
31% (666) admitted
31% (666) 
54% (359) 
admitted
wards
Reproduced from: MacFarlane, MC. Director, Department of Neurosurgery Christchurch Hospital, New Zealand.27
In the absence of prospectively acquired New Zealand hospital and community data with consistent criteria for 
the defi nition of TBI, the Guideline Development Team has been unable to determine the exact extent of TBI in 
New Zealand. These caveats need to be considered alongside the data in this section.
23
 
   
   
 

New Zealand data on hospital presentations for mild TBI found a rate of 437 per 100,000 per year for people 
aged 15 years and older, and 252 per 100,000 per year for those aged less than 15.28 It was estimated that for 
every 100 people seen at hospital, 60 were seen and managed by their general practitioner alone. Based on a 
current New Zealand population of four million, this would give a population estimate of ‘medically attended 
TBI’ of around 700 per 100,000 per year for those 15 years and older. Data from the United States of America 
(USA)29 provides a fi gure for ‘medically attended TBI’ of around 465 per 100,000 per year, which extrapolated to 
the New Zealand population would suggest a total of 19,000 medical attendances per year. 
A systematic review of the literature by the WHO Collaborating Centre Task Force on Mild Traumatic Brain Injury30 
concluded that a ‘true’ population-based rate of mild TBI would be more than 600 cases per 100,000 per year. 
Assuming this is true for New Zealand, this would give an estimate of more than 24,000 cases of mild TBI in 
New Zealand each year and approximately 60 per 100,000 per year of moderate to severe TBI (an estimated 
2400 cases per year in New Zealand). Therefore, the total TBI incidence (including all levels of severity) in New 
Zealand, projected from the WHO Task Force data, would be approximately 660 per 100,000 per year (ie, 26,400 
cases per year). 
In reviewing ACC data on TBI incidence, it is important to recognise that ACC uses operational defi nitions to 
classify severity. These defi nitions differ from the classifi cation of severity used in this guideline. An ACC 
classifi cation of ‘moderate to severe’ TBI thus refers to the need for extensive care, support and lifetime 
planning. Other categories are aggregated under the heading ‘concussion’. In 2003, ACC recorded 17,514 new 
cases of ‘concussion’ (about 437 cases per 100,000 per year) and 123 moderate to severe TBI cases in 2002. 
Assuming these fi gures are correct and the proportion of all TBI that is ‘moderate and severe’ is around 10%, 
there should be 2000 to 3000 cases of moderate and severe TBI per year. It seems probable that the majority 
of people with moderate and severe TBI are assessed at hospital, and the fi gure of 8.1% moderate to severe4,30 
seems conservatively realistic. 
Based on the national and international data available, the Guideline Development Team calculates that an 
estimate of hospital attendance with TBI in New Zealand for all ages would be in the range of 10,000 to 17,000 
cases per year, with 8% to 10% of those in the moderate to severe category.4,30 A signifi cant proportion (perhaps 
as high as 25%) of these people may have ‘suspected TBI’, not meeting the criteria for ‘defi nite TBI’. Our best 
estimate of all ‘medically attended TBI’ in New Zealand would be 16,000 to 22,500 per year with an even 
stronger caveat applied regarding the proportion of ‘defi nite TBI’ in this group. The best estimate of all TBI will, 
necessarily, have a large range. A total TBI incidence fi gure for New Zealand, including those people with TBI 
who do not seek medical attention, is likely to be in the range of 20,000 to 30,000 cases per year.
In order to plan and evaluate service delivery for people with TBI, and test interventions in a TBI population, 
accurate information about the incidence and prevalence of TBI in New Zealand, together with information about 
the consequences directly attributable to TBI for those people, is required. Currently that information is not 
available to a suffi cient level of accuracy. 
1.3 Hospital-based 
rehabilitation
In 1999, people with TBI made up 4% of admissions to comprehensive rehabilitation facilities in the USA.31 The 
mean age of individuals was 46 years and the mean length of stay in rehabilitation 23 days. Of this group, 80% 
were discharged to community settings, including supported and transitional living situations, while 9% were 
discharged to long-term care facilities. Accurate data to allow comparison with New Zealand is not available. 
24
 
   
   
 

1
1.4 Cost
In 2004, ACC fi gures indicated that it paid over $100 million a year for post-acute treatment and rehabilitation 
of claimants with concussion and TBI.32 This excludes costs incurred during the acute phase of care. ACC also 
supports the operation of Emergency Departments through funds to DHBs. However, it is not possible to identify 
the proportion of this funding that is used for treating people with TBI. In 2003, 17,514 new cases of concussion 
led to claim payments of $12,532,834 for that year alone while in 2002, the 132 new cases labelled moderate 
to severe TBI led to claim payments of $3,603,579 for that year. In 2003, there were 1477 ongoing cases of 
TBI (ie, people with claims originating more than a year previously), which led to claim payments of a further 
$93,728,240.
1.5  Demographic characteristics of the traumatic brain injury population
According to 2003 ACC fi gures, 61.9% of people with concussion were male, in broad agreement with 
international data suggesting a roughly 2:1 ratio for males:females with TBI.32 The incidence of TBI peaks in 
the 15 to 30 years age group and again in those aged 60 years or older. ACC fi gures32 show the highest rate 
of concussion and TBI occurred in those aged 15 to 19 years of age. In total, 14% of people with concussion 
identifi ed as New Zealand Ma¯ori and 5% as Pacifi c peoples; slightly less than the proportions of Ma¯ori and 
Pacifi c peoples in the New Zealand population as a whole (Ma¯ori 15%, Pacifi c peoples 6.5%).
1.6  Causes of traumatic brain injury in New Zealand
ACC data suggests that for people with more severe TBI, approximately 50% were involved in a car crash.33 This 
is in keeping with international data.29,30
In those aged under fi ve years at the time of injury, the causes of the injuries (ACC Injury Statistics, 2004)32 were 
as follows:
• 17% motor vehicle related
• 17.2% ‘other loss of balance/personal control’
• 16.1% resulting from being struck by a person, animal or object
• 43% of cases could not be classifi ed according to the criteria used or the cause was unclear.33
1.7 Prognostic 
factors
Prognostic factors are those features of the traumatic injury, and of the injured person’s life and functioning, 
which are related to better or poorer outcomes in terms of recovery and rehabilitation from TBI. Although there 
has been no rigorous analysis of these factors demonstrating their relative importance, consistent evidence has 
been identifi ed for a number of prognostic factors for adults and children.
1.7.1 Prognostic factors: adults and children and young people
Pre-injury factors 
• Pre-injury psychological morbidity is related to poorer outcomes.34
• Age: the likelihood of adverse outcomes increases in those over 35 years, and the risk in those aged 65 years 
or older is 10 times the risk for those aged 15 to 25 years. The very young and oldest groups have the poorest 
outcomes; outcomes for children are worst for those aged under seven years.11,35–37
• Sex: on balance, males with TBI have lower morbidity and better outcomes.38–40
Injury-related factors
• TBI resulting from physical abuse in both adults and children and young people is related to poorer
outcomes.41–43
25
 
   
   
 

•  Both adults and children and young people tend to have poorer outcomes from severe TBI (as measured by 
the Glasgow Coma Scale).11,44,45
•  Direct brain tissue damage in both adults and children and young people is related to poorer outcomes.46
• Somatosensory-evoked 
potentials* (SEPs)/cognitive event-related potentials* (ERPs): in severe TBI, SEPs 
may be useful in predicting severe negative outcomes, and ERPs are able to predict a wider range of negative 
outcomes. Both SEPs and ERPs may predict positive outcomes.47,48
Post-injury factors
•  Multiple TBIs: there is some evidence that multiple or repeated mild TBI, over an extended period of months 
or years, may in some cases result in cumulative neurological and cognitive defi cits. Very rarely, where the 
repeated mild TBIs occur within a period of hours, days or weeks, the outcomes can be severe or fatal.49,50
•  Social deprivation and lower socioeconomic status are related to poorer outcomes.51–53
•  Good or poor family functioning is related to better or poorer outcomes respectively.11,54 
1.7.2 Prognostic factors: adults
There are a number of additional factors associated with poorer or better outcomes in adults following TBI. 
These include pre-injury and post-injury factors, factors related to the injury, and personality and environmental 
factors. 
Pre-injury factors related to poorer outcomes
•  A history of alcohol and/or drug abuse.34,44,55
•  A history of childhood sexual abuse.56
•  Genetic vulnerability: people with the apolipoprotein E (ApoE) _4 allele are more likely to have a poorer 
outcome than those without the allele (OR 13.93; 95% CI: 1.45–133.97; p=0.02).57,58
Injury-related factors
•  Mechanism and type of injury infl uences outcome:59 people who have an injury where an object strikes their 
head have a poorer outcome compared with people whose heads strike an object; the type of injury (ie, 
motor vehicle collision, fall, assault, motor vehicle-pedestrian collision, falling object, sports/recreation) 
also has some effect on outcome – people whose injury results from being hit by a falling object, assault or a 
motor vehicle accident generally have poorer outcomes than people whose injury was due to other causes. 
•  Better cognitive status as assessed by cognitive testing during the acute stage (inpatient stay) is related to 
better outcomes.60 
•  In mild TBI, headache, dizziness and/or nausea acutely following injury (ie, in the Emergency Department) is 
strongly associated with the severity of post-traumatic sequelae six months post-injury.61
•  Serum markers: the specifi c serum markers S-100B and neurone-specifi c enolase (NSE) are thought to be 
markers of cell damage in the human central nervous system, and after damage to brain tissue, increased 
concentrations of NSE and S-100B can be measured in peripheral blood serum. In mild TBI, one small 
study found an increase in severity of forgetfulness, dizziness or headache after six months in people 
with increased early serum NSE or S-100B concentrations. All people with mild TBI without increased 
serum markers or symptoms in the Emergency Department were symptom free after six months.61 In TBI 
of all severities, a serum S-100B concentration of >0.32 mcg/L as measured acutely post-injury (ie, in the 
Emergency Department) has been shown to predict severe disability as measured by the Glasgow Outcome 
Scale (GOS <5) at one month post-injury, with a sensitivity of 93% (95% CI: 68–100%), a specifi city of 72% 
(54–79%), and a negative predictive value of 99% (93–100%).62 Although these results are interesting, the 
use of serum markers as a predictive tool is still part of ongoing research rather than of clinical utility.
Post-injury factors
•  Development of post-TBI mental illness, such as depression or anxiety, may be related to poorer outcomes.63
•  Better social support is related to better outcomes.34
26
* See 
Glossary
 
   
   
 

1
1.7.3 Prognostic factors: children and young people
For children alone:
• pre-injury behavioural problems are related to poorer outcomes53
• identifi cation of lactate acutely by proton magnetic resonance spectroscopy has a strong relationship with
poor, long-term cognitive outcomes.64 This is currently a research-only tool.
1.7.4 Factors not related to prognosis
There are a number of factors frequently assumed to be related to better or poorer long-term outcomes from TBI 
for which the evidence shows no relationship. These include the following:
• premorbid characteristics are not related to personality changes post-TBI65
• computed tomography (CT) scan results – in people with a mild TBI, there is no difference in neurophysical 
status and vocational outcome between those who had positive fi nding on CT and those who had negative
fi ndings59
• brief loss of consciousness does not appear to be related to long-term outcomes in people with mild TBI.59
1.8  Consequences of traumatic brain injury
1.8.1 Mortality from traumatic brain injury
Data for mortality from TBI in New Zealand is not available. NICE7 reports that in the UK, only 0.02% of people 
attending an Emergency Department with a TBI will die from the injury – about 6 to 10 per 100,000 population 
per annum. In Sweden, the mortality rate from TBI was found to be 0.7% annually (3.8 per 100,000 per year),66 
while in the USA the mortality has been reported as 19.3 per 100,000 per annum, although this fi gure also 
includes deaths from fi rearms.
1.8.2 Consequences of traumatic brain injury: adults
1.8.2.1 Mild traumatic brain injury 
A recent systematic review of the international literature67 found that in adults, cognitive defi cits and other 
symptoms are common in the acute stage for those who have had a mild TBI. Most people have recovered 
fully by somewhere between three and 12 months following the injury. However, in both children and adults a 
minority will have longer-lasting effects of the TBI. There is also some evidence that adults who sustained a TBI 
in childhood or adolescence may have psychological impairments in adulthood. For example, one study looking 
at the effects of TBI in college students found that those who had a ‘mild’ TBI in childhood or adolescence 
reported more distress in terms of their emotional and personal functioning than a control group.68
1.8.2.2 Moderate and severe traumatic brain injury
A USA National Institute of Health Expert Consensus panel evaluated a comprehensive report of the evidence 
on TBI. The panel concluded that a person who has had a TBI may have a complex set of neurological and 
psychological impairments, together with medical problems and physical disabilities that affect not only the 
person who has suffered the TBI, but also their family/wha¯nau, carers and the wider community. They reported 
that the consequences of severe TBI often persist in varying forms for the rest of the person’s life, and that new 
problems resulting from the injury may emerge as a result both of the aging process and of new demands on the 
person.69
An evidence report on rehabilitation of people with TBI stated that: 
…studies [have] demonstrated that survivors of severe TBI often lose friendships 
and social support, have limited opportunities to develop new social contacts and 
friends, have few leisure activities, and have high levels of anxiety and depression 
for prolonged periods of time. (p. 28)10
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The sequelae of severe TBI vary in individual people and according to the nature and location of the brain injury. 
The defi cits fi t broadly into four main categories:
1. physical, including motor and sensory impairment
2. cognitive, including impairment of memory attention, and judgement
3. behavioural, including emotional and mood problems, and inappropriate behaviour
4. communicative, including language expression and comprehension.
These defi cits limit the functioning of the person with clinically signifi cant TBI to differing degrees, depending 
on the severity and combination of the brain injury with consequent defi cits, presence of other injuries, and 
other circumstances such as the person’s intellectual background, environment, and family and social support. 
People who have had a clinically signifi cant TBI may have impairment in their ability to live independently, 
return to work, education and leisure activities, and maintain relationships. These impairments may impact not 
only on the injured person, but also on their family/wha¯nau and carers.8
Neurological recovery after a clinically signifi cant TBI may take months or years, and people may be left 
with permanent defi cits. Most people with ‘mild’ brain injuries recover completely over the subsequent few 
months.67 However, some may have symptoms which persist for longer than this, reporting headache, dizziness, 
concentration and memory problems, mood changes and irritability. 
People who have suffered a clinically signifi cant TBI are an extremely heterogeneous group. Thus, rehabilitative 
care needs to be tailored to the individual, with consideration of individual defi cits and rates of progress. 
Specifi c recommendations on rehabilitation are contained within Chapter 5, Rehabilitation following clinically 
signifi cant traumatic brain injury – assessment and Chapter 6, Rehabilitation following clinically signifi cant 
traumatic brain injury – intervention.
1.8.3 Consequences of traumatic brain injury: children and young people
1.8.3.1 Mild traumatic brain injury
The WHO Task Force systematic review on mild TBI found that children and young people who have a single mild 
TBI have a good prognosis; there is little evidence of residual defi cits, although there will be a minority who will 
have longer-lasting effects of the TBI.67
1.8.3.2 Moderate and severe traumatic brain injury
Children and adolescents who have a moderate or severe TBI are more likely to survive the injury than adults.11 
Many survivors of severe TBI will have a life-long need for support in various ways, so the burden of care and 
support for the child survivor with TBI is greater as they have more remaining life years. Between 50% and 90% 
of children and young people who have had a severe TBI will require help in bathing, dressing and walking, 
proportional to the number of functional defi cits they have, for varying periods of time after the injury.11 Of 
children and young people exhibiting four or more functional defi cits, 75% will have impairments in self-
feeding, cognition and behaviour; 67% will have speech impairments; 29% impaired vision; and 16% impaired 
hearing.11 International evidence about the provision of services for children and young people suggests that TBI 
is underreported and misidentifi ed; and that many interventions developed for other pathologies may be being 
inappropriately applied.11
A recent UK study of 526 children aged between 5 and 15 years with varying severity of TBI used the King’s 
Outcome Scale for Childhood Head Injury (KOSCHI) to assess outcomes at approximately two years post-injury. 
Frequent behavioural, emotional, memory and attention problems occurred in one-third of those who had 
sustained a severe TBI, one quarter of those who had had a moderate TBI, and in 10% to 18% of those who 
had had a mild TBI. Personality change after TBI was reported for 148 children (28% of the total, of whom 21% 
had a mild TBI, 46% a moderate TBI, and 69% a severe TBI). Signifi cant associations were noted between injury 
severity and KOSCHI outcomes, and between social deprivation and poorer outcomes.51
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1
There is some international evidence that children and young people may not have adequate post-TBI follow-up 
and treatment. A population study found that at around two years post-injury, 43% of those with mild TBI, 64% 
of those with moderate TBI and 69% of those with severe TBI had moderate disability (n=252), while 57% of 
those with mild TBI, 36% of those with moderate TBI and 22% of those with severe TBI made a good recovery 
(n=270).51 A total of 30% of children received follow-up, but whereas all of the children who had a severe 
disability (30%) received appropriate follow-up, 64% of children with moderate disability received no follow-
up.51 Although this study did not analyse the infl uence of pre-injury factors in measurement of outcomes, it is 
illustrative of the need for follow-up of children with less severe, as well as more severe TBI.
1.8.4 Consequences of traumatic brain injury for families and carers 
Carers of adults or children and young people with TBI are at risk of adverse consequences themselves, and 
have signifi cantly poorer quality of life and more psychiatric morbidity than the general population.70 For 
example, one study of adult carers of people with severe TBI found that at six months post-injury, about one-
third of carers reported clinically signifi cant symptoms of anxiety and depression, and poor social adjustment. 
By one year post-injury, the same proportion reported signifi cant anxiety and depression, and about a quarter 
continued to suffer poor social adjustment.71
Another study of carers in New Zealand found that in addition to distress, many carers reported health problems 
and a change in roles. Partners who were carers were more likely to report health problems, distress and 
changes in role than were parents who were carers.72 Similarly, a study in South Africa of the effects of caring 
for a partner with a TBI found that the injured person’s altered communication patterns affected interpersonal 
relationships and quality of life extensively and the carers had decreased income due to the low incidence of 
return to work.73 Carers also reported changes in family relationships, particularly between the injured person 
and their children, as well as a deterioration in marital relationships. Most carers reported feeling ‘tied down’ 
due to the dependence of the injured person, and loneliness predominated as a social consequence despite 
the support of pre-injury friendships.
Families who have a child with clinically signifi cant TBI frequently experience work loss and fi nancial diffi culties 
as a consequence of the care needs of the child.11 There is substantial evidence for a negative impact on family 
functioning when a child in the family has had a TBI, with deteriorating functioning associated with the severity 
of the child’s injury. Families with severely injured children have been shown to be more likely to actively seek 
help than families of children with less severe TBI, although the latter families are also likely to have need of 
help.11
1.9  Current practice in New Zealand
1.9.1 Acute phase services
Acute phase care for people with suspected TBI in New Zealand is currently provided by general practitioners, 
Emergency Departments, accident and medical services, ambulances, sports coaches, teachers at schools and 
others. Most people with suspected serious brain injury are assessed at the nearest hospital and/or transported 
(usually by helicopter) to the nearest large hospital providing facilities for assessment and treatment of the 
immediate consequences of the head injury.
A small number of very severely injured people are transported to tertiary care centres with neurosurgical 
services (Auckland, Hamilton, Wellington, Christchurch and Dunedin).
Many people with TBI who are assessed in an Emergency Department are not admitted or, if they are admitted, 
stay only a very short time in hospital (see Section 1.2, Estimates of the incidence of traumatic brain injury in 
New Zealand. Christchurch Hospital data).27
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1.9.2 Current traumatic brain injury rehabilitation practice 
For people requiring rehabilitation following TBI, various services are currently available. These range 
from intensive, residential rehabilitation to community rehabilitation aimed at specifi c issues, vocational 
rehabilitation programmes, and various support services. ACC contracts for these services with a per-claimant 
price-agreed fee for service, but with no set volumes.
Most children with TBI are admitted to paediatric wards in general hospitals and are managed by general 
paediatric teams. For children with severe TBI there is a single specialist residential rehabilitation service, the 
Wilson Home in Auckland, which accepts referrals from around New Zealand.
Services for people with TBI are available in all major centres in New Zealand. Service provision is restricted to 
providers who can show a high level of expertise and commitment to rehabilitation following TBI. The service 
providers tender for each of the services, and through this tendering process must demonstrate to ACC that 
they have the resources, competence/training and community links to provide rehabilitation matched to the 
particular needs of the relevant client group.
1.9.2.1 Non-residential rehabilitation services 
1.9.2.1.1 Services: mild traumatic brain injury
There is a wide range of non-residential rehabilitation services, from primarily assessment services to primarily 
intervention services, and from a single operator in a single discipline, to full multidisciplinary team operations. 
A mixture of DHB and non-DHB services aiming to support people in their own homes or similar ‘natural’ 
environments operates in New Zealand. Specifi c elements of non-residential programmes, including intensity 
and duration, are currently specifi ed by the ACC case manager, following independent assessment.
The mild TBI service is intended to provide early access and timely assessment and rehabilitation for people 
who have a mild TBI. The aim of this service is to rehabilitate people to maximum independence through case 
management and appropriate assessment and rehabilitation. It allows entry for people either early in the post-
acute stage of a mild TBI, or later on for people who have persisting symptoms following mild TBI. The service 
allows for the assessment of people who may have had a TBI and need assessment to establish cover and 
entitlement.
There are seven mild TBI clinics, sometimes known as ‘concussion clinics’, around New Zealand. Two further 
clinics provide specifi c care for children with TBI. The clinics provide a combination of specialist medical 
assessment, screening neuropsychological assessment, and assessment and intervention from an occupational 
therapist, although this is usually limited to a few sessions.
Users of this service fall into three main categories.
1. Those who have defi nitely suffered a mild TBI and need further assessment and rehabilitation following the
acute episode.
2. Those for whom it is unclear whether they have suffered a TBI and who need assessment to establish cover
and rehabilitation needs.
3. Those who have established symptoms of more than three months’ duration following a mild TBI who need
assessment and rehabilitation.
However, most services report also seeing a varying proportion of people with more severe injuries.
1.9.2.1.2 Services: moderate to severe traumatic brain injury
There is a wide range of non-residential services for people with more severe injuries. This range includes 
established providers, services that provide assessment and rehabilitation (including vocational rehabilitation), 
and individual providers of specifi c services (eg, neuropsychologists).
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1
 1.9.2.2 Residential rehabilitation
Residential rehabilitation funding for people following a TBI is provided by two main ACC service contracts. 
These are the Active Rehabilitation Services Contract and the Residential Support Services Contract. The two 
service contracts both provide services for rehabilitation, but serve different ranges of claimant need.
Rehabilitation can be provided in a person’s own home. Where residential rehabilitation options are being 
considered, the advantages and disadvantages of living at home, with appropriate inputs and support, need to 
be discussed. Particular consideration should be given to the needs of family and/or carers in this situation.
Residential rehabilitation services are defi ned by three features.
1. The person with TBI stays overnight in accommodation provided as part of a rehabilitation package of care.
2. The accommodation provides a ‘rehabilitation environment’ with an emphasis on education, problem-
solving and self-responsibility for the person with TBI, working towards higher levels of independence and
participation in the community.
3. In addition to 1 and 2 above, there is rehabilitation and clinician input with an expectation of improvement in
functioning over time (although this time-frame can be long).
Almost exclusively, people with TBI who are managed in residential rehabilitation services have had a severe 
TBI, and/or have a complication of the initial TBI or other injuries. Occasionally there may be signifi cant 
comorbidities (particularly mental health disorders) which, in addition to a less severe TBI, may require 
residential placement for rehabilitation. Table 1.2 provides an approximate outline of the current pathway into 
residential rehabilitation following severe TBI in New Zealand.
table 1.2:
intervention settings: the progression into residential rehabilitation 
phase
duration
location
1. Acute care
Few days up to few 
Acute hospital ward (generally 
months
neurosurgery or surgery)
2. Post-acute but medical problems
Few days to a few 
Stay on acute ward, OR transferred to 
weeks
inpatient rehabilitation ward
3. Post-acute, medically stable
Few weeks up to 
Dedicated residential rehabilitation, 
several months
usually in community rather than hospital 
setting
4. ‘Plateau’ phase, unable to live
Months to years
Community residential setting
independently unsupported
5. Independence or able to live in private
Years
Own home or similar
accommodation with suitable support 
package
A decade ago the residential rehabilitation services described were provided almost exclusively in hospitals. 
The 2004 Current Practice Review5 shows that a minority of people with TBI requiring residential rehabilitation 
are now managed in hospital environments. A common model for these services in 2005 is for small numbers of 
people with TBI to be managed in a privately owned ‘community house’, with 24-hour supervision and varying 
amounts of health-professional input. These environments are more ‘real life’ than hospital rehabilitation 
wards, and therefore may facilitate transition back to independent (or assisted) community living.
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Elements that vary between different residential rehabilitation environments in New Zealand are:5
•  the composition of a ‘core team’ that sees every referred person with TBI. This ranges from an occupational 
therapist and a nurse to a ‘full multidisciplinary team’ including specialist doctor, nurses, occupational 
therapist, physiotherapist, psychologist, speech-language therapist and social worker
•  hours per week of health-professional input
•  availability of 24-hour medical cover, which can delay discharge from an acute hospital to a community 
setting, for example, especially in Phase 2 (see Table 1.2)
•  staff who provide 24-hour supervision; generally registered nurses in hospital rehabilitation wards, but varies 
in community settings.
1.9.2.2.1 Active rehabilitation services
Active rehabilitation services provide rehabilitation for people following a serious injury. Residential services 
provide a community-based environment and fully inclusive rehabilitation for high-needs claimants by a 
specialist multidisciplinary rehabilitation team. The contracts for these services are usually held by private 
providers, although some DHBs also provide the service.
This service is designed for people who have suffered a moderate to severe TBI, and the emphasis on 
community-based care is to aid the person’s eventual re-integration into the community. People who receive 
this service usually have substantial cognitive and/or physical needs. From a clinical and rehabilitation 
management perspective, this client group presents a challenge in that they require 24-hour supervision and 
care, often with more than one person working with each person at any given time.
The key distinction between ‘active residential rehabilitation’ and ‘residential rehabilitation support’ (described 
in the following section) is the intensity of rehabilitation input, linked to expectations regarding speed of 
recovery. Where signifi cant functional gains are possible over weeks to a few months with appropriate input, 
active rehabilitation (ie, providing a rehabilitation environment and intensive [at least daily] rehabilitation) input 
is indicated.
1.9.2.2.2 Residential support services 
Where gains for people following serious injury are expected to be over a longer period of time (ie, a few to 
several months), a residential rehabilitation support programme is appropriate. This provides a rehabilitation 
environment and less intensive rehabilitation input (a few hours per week from rehabilitation clinicians). 
Residential support services aim to promote a level of independence in a safe environment for people who are 
unable to live safely, independently. The service provides rehabilitation and support in a home-for-life setting.
This service is aimed at a broad spectrum of people who have TBI long term, and provides community-based 
rehabilitation of serious injury claimants (most commonly TBI). These claimants may remain in the service in 
the long term. The service may rehabilitate the person who has had a serious injury into community living with 
appropriate support. People using this service generally have a need for ‘slower-stream’ rehabilitation. 
In residential support services, there is no necessary expectation of improving levels of independence and/
or participation in the community; there is monitoring to identify secondary problems, which may lead to 
deterioration and an ongoing need to provide suffi cient support to realise the person’s full ability to function. 
This includes provision of physical supports (eg, appropriate wheelchair, communication device), social 
supports (eg, day programmes) and emotional supports (eg, appropriate management of mood, interaction with 
family/wha¯nau or friends). 
A residential environment with people of similar age and interests should contribute to appropriate levels of 
social and emotional support. However, residential support programmes providing such an environment are 
not currently available in many parts of New Zealand. In addition, some people with severe TBI can be diffi cult 
to manage in existing residential support programmes, due to behavioural diffi culties in particular. Such issues 
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1
require careful consideration from appropriately trained rehabilitation clinicians, including trial placements, 
before long-term decisions are made.
Residential support services also provide for people who may not have suffered a serious injury, but are 
nonetheless unable to rehabilitate to the community (eg, an older person with a relatively minor injury but no 
carer). 
1.9.2.3 Review of current practice
Summary information from the 2004 Current Practice Review commissioned by ACC and completed in 2004 
is presented in this section.5 This review of TBI rehabilitation included a survey of providers and consumers 
(people with TBI and carers). The full report is available at www.nzgg.org.nz.
1.9.2.3.1 Provider survey
A total of 49 respondents to the survey of TBI service providers met the criterion of managing at least three 
people with TBI in the last year or 10 people with TBI in the last fi ve years. Thirty-six of the responses were from 
providers of non-residential rehabilitation services (managing a total of 4668 clients in the previous 12 months) 
and 13 were from providers of residential rehabilitation services (managing 452 clients in the previous 12 
months). 
Key fi ndings of the survey
• Providers were clearly attempting to provide the best possible service they could for people with TBI.
• A range of approaches and variations in structure, staffi ng and practice was evident. There appeared to be
many reasons for this variation including historical factors, local staff availability, contractual requirements 
and a desire to provide an optimum service.
• Providers supported a need for evidence-based guidelines to help develop best practice.
• There was little or no consistency in the use of standardised assessment and outcome measures and tools.
• Audit and quality improvement initiatives, where present, tended to be at the level of consumer satisfaction
and/or audit by funders to ensure contract compliance.
• There was a move away from DHB-provided services, with only 42% of residential clients and 9% of non-
residential clients being managed by DHB providers.
• Most providers of TBI services indicated that they provided services targeted to specifi c sub-groups of the TBI
population, such as Ma¯ori, Pacifi c peoples, people with mental health disorders, and people with alcohol or
drug abuse problems. However, the extent to which these services met these needs was uncertain.
• The lower age range for acceptance into both residential and non-residential rehabilitation programmes 
varied, from one specialist paediatric service to others where the lower age limit was between 14 years and
18 years. 
Residential TBI rehabilitation services
• Some of these were specialist TBI services (ie, managing clients with TBI only). However, the majority of 
TBI clients were managed in non-specialist environments (ie, with non-TBI clients as well). Overall, when
responses from providers managing across multiple sites were considered, services tended to be low
volume, averaging about 16 clients per year.
• TBI rehabilitation provision has been aggregated by a few organisations, often operating across different 
sites. This allows standardisation of management, staff skill mix and training.
Open-ended responses from providers about effective interventions, barriers to effectiveness, gaps in services 
and ideas for better services provided further information, and are presented as verbatim responses in the full 
report. The full report can be accessed at www.nzgg.org.nz.
 1.9.2.3.2 Consumer survey
The consumer survey elicited 420 responses from people with TBI and/or their carers across New Zealand. 
Carers were not separately surveyed. 
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Survey fi ndings
• About half of the respondents felt that people with TBI got a ‘good deal’ from TBI rehabilitation services, and
approximately 60% felt that TBI rehabilitation services focused on goals that were important for them.
• There was considerable support (76%) for the provision of specialist TBI rehabilitation centres in New
Zealand.
• In general, people surveyed were ‘happy’ with ACC services. A substantial minority (around 40%) were
‘unhappy’ with these services. Much of their discontent seemed to focus on the training and turnover of case
managers. 
• Health status of the consumers, measured by a standard instrument, the Short Form 12 (SF12), showed
mean values for ‘physical health’ and ‘mental health’ well below (around one standard deviation below the
mean) those expected for people of a similar age.
1.10 Major gaps identifi ed
Gaps in knowledge and between existing practice and best practice identifi ed from the Current Practice Review5 
and in developing this guideline include:
• TBI is a signifi cant health issue in New Zealand. The extent of the problem will remain uncertain until we have
better information from prospective studies in a New Zealand population. Such studies would require clear
criteria for distinguishing people with a blow to the head who do not meet criteria for TBI from those with
defi nite TBI. Such research should be a high priority for health research funders and ACC
• the consumer survey suggests that people with TBI experience signifi cant health disadvantage, in terms of 
both physical and mental health, compared with their peers
• there is no uniform approach to standardised assessment and outcome measures
• considerable 
variation 
exists in New Zealand TBI rehabilitation service provision, which is probably
unacceptable
• providers see a need for clear evidence-based guidelines to help develop best practice for TBI services in
New Zealand
• considerable gaps may exist between what is currently being provided and what might be considered to
meet the needs of differing groups of people (eg, different ethnic groups or people with specifi c comorbid
conditions, such as mental health disorders, or high drug and alcohol use)
• TBI rehabilitation services in New Zealand are not specialised. It is possible that one or more specialist TBI
centres for acute care and early rehabilitation could complement current community-based rehabilitation
centres.
Although there is little robust comparative evidence to demonstrate whether specialisation of services for TBI 
leads to better outcomes, strong evidence from related conditions and international expert opinion suggests 
that this would be the case.8 One issue that needs to be considered for New Zealand is whether specialist 
TBI rehabilitation services should be pursued, acknowledging that this would require centralisation and the 
potential disadvantages that might engender – particularly the diffi culties for family and other support. It should 
be noted that consumers supported the idea of a small number of expert TBI specialist units rather than the 
current widely dispersed services – that is, they preferred the ‘best possible treatment available’ over the ‘most 
convenient treatment option’. The ‘centralisation’ model has been applied to spinal injury services for the acute 
phase of spinal cord injury (SCI) treatment in New Zealand; however, SCI and TBI are not identical conditions.
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2
Chapter 2:
Pre-hospital assessment,
management and referral to hospital 
Overview
• Pre-hospital assessment can be undertaken by a range of trained health care professionals, in order to
establish whether a trauma to the brain has occurred and factors associated with serious complications of 
head trauma are present.
• There are limited, well designed studies on the effi cacy of pre-hospital intervention.
• There are a number of risk indicator assessment tools for acute complication of TBI, including the Glasgow
Coma Scale.
• The Glasgow Coma Scale is used for immediate, pre-hospital and hospital assessment of the acute
complication risk associated with TBI.
• People with symptoms/signs that are defi ned as risk factors for acute intracranial complications of TBI
should be promptly referred to an Emergency Department. Emergency transport services should also be used
if the signs of acute complications are more serious, if the person assessing has additional concerns, or for
some other circumstances, such as a lack of suitable transport.
• Rapid transfer to an Emergency Department using emergency services is appropriate if there is deterioration
in the person’s condition, a loss of consciousness, focal neurological defi cit, skull fracture or penetrating
head injury, seizure, or suspected neck injury.
• People with none of the signs or symptoms for Emergency Department assessment should seek further
medical assessment from a general practitioner or accident and medical clinic.
• There is consistent evidence that coordinated trauma systems reduce mortality for serious injury, including
serious neurotrauma. A coordinated system of trauma care for TBI that provides an organised and responsive
system of care for people is required.
This chapter deals with the pre-hospital phase of assessment and management for people with suspected TBI. 
It provides advice about who should be referred for an assessment at hospital and who should be transported 
by ambulance, along with recommendations about appropriate public health and educational material for the 
general public. 
This chapter is adapted and updated for New Zealand from the NICE Head Injury Guidelines.7
There are four important reasons for undertaking pre-hospital assessment, which are outlined below.
1. Identifying actual or potential hypotension and/or hypoxia, which untreated will magnify TBI effects.
2. Identifying risk factors for acute complications of TBI, which may require intervention, particularly bleeding
inside the skull and/or brain.
3. Identifying other injuries that may require urgent management.
4. Estimating the severity of any injury to the brain that has implications for subsequent management and
follow-up.
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2.1  Pre-hospital assessment – acute 
recommendations
grade
A person with a suspected traumatic brain injury should initially be assessed and managed 
C
according to clear principles and standard practice as embodied in the Advanced Trauma 
Life Support (ATLS)/Early Management of Severe Trauma (EMST) system and for children the 
Advanced Paediatric Life Support (APLS) system.
The fi rst priority for those administering immediate care is to treat the greatest threat to life 
C
and avoid further harm. 
A person who has sustained a suspected traumatic brain injury should have full cervical spine 
C
immobilisation attempted, unless they have all of the following: 
•  no alteration of consciousness
• no 
neck 
pain/tenderness
•  no focal neurological defi cit
•  no major distracting injury.
A person who has sustained a suspected traumatic brain injury should be transported directly 
C
to a centre where traumatic brain injury is managed in entirety. 
Where this type of facility is unavailable, the person should be transported to a centre that 
can stabilise the person’s condition prior to transfer to a centre where traumatic brain injury is 
managed in entirety.
It is expected that all acute hospitals accepting people who have sustained a suspected 
traumatic brain injury should have the resources to expeditiously assess and intervene to 
optimise outcome and that these resources should be appropriate for the person’s age.
Paramedics should be fully trained in the use of the adult and paediatric versions of the 
C
Glasgow Coma Scale and its derived score. 
Paramedics should have training in the detection of non-accidental injury and should pass 
C
this information to Emergency Department personnel when the relevant signs and symptoms 
arise. 
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
The fi rst assessment of a person suspected of having sustained a TBI may be performed by a general 
practitioner or other primary health care practitioner, a sports coach, an ambulance offi cer, a member of the 
public, or telephone operator for a telephone health ‘helpline’. The aim of this assessment is to establish 
whether trauma to the head has occurred and whether any of the factors associated with serious complications 
of head trauma are present.
When assessing a person with a suspected TBI who is apparently intoxicated, it should not be assumed that 
the signs and symptoms of the person’s injury are due to the intoxication from alcohol or drugs. There should 
be particular caution with people who are vomiting or who may be intoxicated, due to the risk of aspiration and 
consequent hypoxia.
There are specifi c questions regarding the very early management of people with severe head injuries (ie, 
Glasgow Coma Scale score of 8 or less). Recent systematic reviews have examined evidence on the management 
36
 
   
   
 

2
of TBI.7,74 These reviews found strong evidence for only a small number of interventions and concluded that 
there was a paucity of well designed studies examining the effi cacy of pre-hospital interventions in severe head 
injury. Management advice in this guideline is based on the UK’s NICE guideline recommendations7 informed by 
the New Zealand TBI Guideline Development Team.
A general principle in immediate management is that the fi rst priority for those administering immediate care 
is to treat the greatest threat to life and avoid further harm.7 See also Chapter 3, Acute phase of traumatic brain 
injury care.
2.2  Assessment of need for medical attention
This section details the evidence for using various assessment tools as risk indicators for acute complications of 
TBI, particularly intracranial bleeding. Factors that might indicate a high risk are also identifi ed. 
These tools and factors are used to assess whether a person with a suspected TBI requires assessment at an 
Emergency Department or other medical assessment and with what urgency.
Recommendations concerning the assessment itself are made in Chapter 5, Rehabilitation following clinically 
signifi cant traumatic brain injury – assessment.
2.2.1. Glasgow Coma Scale
recommendation
grade
The adult and paediatric versions of the Glasgow Coma Scale should be used to assess people 
C
with a head injury.
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
good practice point
A fall in the Glasgow Coma Scale score of two or more points, no matter what the original 

score, requires urgent investigation and/or referral.
This is the opinion of the Guideline Development Team, or feedback from consultation within New Zealand where no evidence is available.
The adult and paediatric versions of the Glasgow Coma Scale are widely used to assess and monitor people 
in the acute phase after a suspected TBI. The Glasgow Coma Scale score gives a useful indication of level of 
consciousness at a given point in time, allows for serial measurement and provides a useful shorthand for 
communicating information to ambulance or Emergency Department staff.6,7 It is also a familiar tool that enables 
the collection and comparison of data, both nationally and internationally. Recommended versions are included 
in Appendix C.
The risk of intracranial complications and the consequent need for surgery increases as the Glasgow Coma Scale 
score declines.7,75 A recent study calculated that the rate of clinically signifi cant brain injury in hospital attenders 
who had experienced some loss of consciousness and/or amnesia since their head injury, increased from 5% 
with an initial Glasgow Coma Scale score of 15, to 17% for a Glasgow Coma Scale score of 14, and to 41% for 
a Glasgow Coma Scale score of 13.7 A further study on paediatric head injury found that a Glasgow Coma Scale 
score of less than 13 was a signifi cant predictor of an abnormal CT scan in children with head injury aged 14 
years or younger.7
Any fall in a Glasgow Coma Scale score, after an initial recording, is of concern and may represent the 
development of intracranial bleeding, such as an extradural haematoma. A fall of two or more points, no matter 
37
 
   
   
 

what the original score, should mandate immediate further investigation and referral (see Section 3.2.1, 
Selection of adults for CT imaging of the head).
The Glasgow Coma Scale is composed of three separate responses: eye opening, verbal and motor. These 
are summed for a total Glasgow Coma Scale score out of 15. The following is a brief guide on how to use the 
Glasgow Coma Scale.
• Monitoring and exchange of information about individual people is based on the three separate responses 
on the Glasgow Coma Scale (eg, a score of 13 based on scores out of 4 for eye opening, 4 for verbal response
and 5 for motor response should be reported as E4, V4, M5).
• If a total score is recorded or communicated, it is based on a total possible score of 15, and this denominator
should be specifi ed (eg, 13/15) to avoid confusion.
• Describe the eye opening, verbal response and motor response components of the Glasgow Coma Scale in all 
communications and notes, which should always accompany the total score.
• For the paediatric version of the Glasgow Coma Scale, include a ‘grimace’ alternative to the verbal score to
facilitate scoring in pre-verbal or intubated infants or children (see Appendix C).
2.2.2 Loss of consciousness 
recommendation
grade
Any loss of, or alteration in, consciousness should be recorded and assessed in people with a 
C
suspected traumatic brain injury.
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
good practice point
People with altered consciousness should have their blood glucose levels checked routinely 

as part of their assessments.
This is the opinion of the Guideline Development Team, or feedback from consultation within New Zealand where no evidence is available.
A history of loss of or altered consciousness after a brain injury is associated with an increased risk of 
developing an intracranial complication, such as an expanding haematoma, although the absolute risk remains 
low.7 In most cases, a longer duration of loss of or altered consciousness is associated with greater severity of 
injury. Momentary loss of or altered consciousness is diffi cult to measure when no independent observer is 
available, and there is debate about its importance.
There is some evidence that intracranial complications can occur even when there has been no loss of or altered 
consciousness. However, as most studies in this area exclude people who have not experienced any loss of 
or altered consciousness, there is a lack of published research on this aspect of risk. Loss of, or change in, 
consciousness may have other causes, and blood glucose levels should be checked routinely in all people with 
loss of or altered consciousness. 
2.2.3 Post-traumatic amnesia 
recommendation
grade
Post-traumatic amnesia should be prospectively assessed and recorded when assessing 
C
people with a suspected traumatic brain injury, where possible. 
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
38
 
   
   
 

2
good practice point
Services assessing people with traumatic brain injury should choose one of the available 

validated post-traumatic amnesia measurement tools and ensure all staff are familiar with its 
use.
This is the opinion of the Guideline Development Team, or feedback from consultation within New Zealand where no evidence is available.
Post-traumatic amnesia, also known as anterograde amnesia, is the impaired memory for events after 
brain trauma. It is usually considered the most important amnesic disorder for assessing the risk of acute 
complications of TBI. However, a recent rigorous study has suggested that retrograde amnesia (ie, impairment of 
memories before the trauma) is a more important indicator of signifi cant injury.75
Even though post-traumatic amnesia is associated with an increased risk of intracranial complications, evidence 
on the length and type of amnesia is inconsistent.7,76 There is some evidence that the duration of post-traumatic 
amnesia is a more accurate predictor of longer-term outcomes than the Glasgow Coma Scale score.77 However, 
there is a lack of robust evidence to support the use of any particular form of assessment of post-traumatic 
amnesia.76,78 Assessing post-traumatic amnesia is less useful in infants and young children because it is diffi cult 
to measure. 
The Guideline Development Team recommends the assessment of post-traumatic amnesia in all people with 
suspected TBI. Measurement should commence prospectively (ie, before it has resolved) to increase accuracy.24 
The Tools Review identifi ed three measures of post-traumatic amnesia suitable for use in New Zealand: 
the Galveston Orientation and Amnesia Test (GOAT), the Westmead Post-traumatic Amnesia Scale, and the 
MOPTAS.6
The Tools Review concluded that while there is no strong empirical evidence to favour one of these measures of 
post-traumatic amnesia over another, qualitative arguments have been made in favour of the MOPTAS.6
2.2.4 Neurological signs
recommendation
grade
Neurological signs should be assessed and recorded when assessing people with a suspected 
C
traumatic brain injury.
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
Post-traumatic neurological signs, such as focal neurological defi cits or seizure, are highly associated with the 
risk of an intracranial complication.7,76 Consequently, people with these signs are commonly excluded from 
studies developing clinical decision rules for the management of acute brain injury.
2.2.5 Bleeding disorders and use of anticoagulants 
recommendation
grade
Coagulopathy and the use of anticoagulant medication, or medications and supplements 
C
with anticoagulant effect, should be considered when assessing people with a suspected 
traumatic brain injury. 
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
People with coagulopathy or who are on anticoagulant medication, such as warfarin, have an elevated risk of 
intracranial complications but there is no robust evidence that has established this relationship.7,76
39
 
   
   
 

Some commonly taken medications (such as aspirin) and supplements (such as Ginkgo biloba)79 also have 
an anticoagulant effect. Health care practitioners should be aware of this and ask the person about what 
alternative or complementary therapies they may be taking, including supplements, when checking their 
medication use (see Chapter 7, Complementary and alternative medicines).
2.2.6 Skull fracture 
The risk of intracranial complications is higher in people with a diagnosed skull fracture. The risk of developing 
an intracranial haematoma is approximately 12 times higher in people with a radiographically detected skull 
fracture than in people without this diagnosis. This calculation of risk is based on an estimate of 38% sensitivity 
and 95% specifi city reported from a meta-analysis on the value of the radiological diagnosis of skull fracture.80
There is variation in diagnostic practice for skull fracture. Some international guidelines advocate a skull X-ray 
for the diagnosis of skull fracture.81
Skull X-rays have limited effectiveness in the diagnosis of TBI. Skull X-rays will be normal in many people 
with clinically signifi cant acute complications of TBI. In addition, skull X-rays are associated with exposure 
to radiation, and come at a cost in terms of resources and time. Therefore, the routine use of skull X-ray as a 
decision-making tool cannot be recommended. However, the clinical assessment of signs of skull fracture, 
including signs of basal skull fracture, such as cerebrospinal fl uid leak, periorbital haematoma, depressed or 
open skull injury, and penetrating injury, should be undertaken.7  If an imaging study is indicated in people with 
suspected TBI, it should be a CT head scan (see Section 3.2, Primary investigation for people with suspected 
traumatic brain injury).
2.2.7 Seizure
A seizure alone, with no other neurological signs and full recovery, is almost never a sign of an intracranial 
haematoma. The diffi culty with seizures is that the person may become unconscious as a result of the seizure 
or from a drug, such as diazepam, used to stop the seizure. This alteration in consciousness level cannot be 
differentiated from that caused by an intracranial bleeding complication of TBI. Unless recovery is prompt and 
complete a (further) CT scan is necessary to exclude such a complication.
2.2.8 Mechanism of injury 
The widely differing nature of high-energy injury mechanisms makes it diffi cult to determine the infl uence on the 
risk of intracranial complications. Terms such as ‘assault’ or ‘road traffi c accident’ cover a great heterogeneity 
of circumstance. A recent study has proposed the following criteria as high-risk factors for clinically signifi cant 
brain injuries after head injury: a pedestrian struck by a motor vehicle, an occupant ejected from a motor 
vehicle, or a fall from a height of greater than three feet or more than fi ve stairs (or less in infants and children 
under fi ve years).75 
The height threshold for a high-risk fall is sometimes defi ned as three feet, and sometimes as one metre. For 
consistency, this guideline uses the term ‘one metre’. Falls from lower heights may be risk factors with infants 
and children less than fi ve years of age. 
A further study has defi ned ‘axial load to head’ as a high-risk factor for cervical spine injury after an accident.7  
This includes: diving; high-speed motor vehicle collision; rollover motor accident; ejection from a motor vehicle; 
accident involving motorised recreational vehicles; and bicycle collision. In addition, there are many other high-
energy mechanism injuries considered to be important which cannot be readily listed (eg, the variety of blunt 
instruments that could be used in an assault).7
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2
2.2.9 Age 
An exact age threshold for identifying people at high risk of intracranial complications following a suspected 
TBI has not been identifi ed, but it is clear that increasing age is associated with an increased risk and a poorer 
prognosis.7 Commonly used thresholds are 60 years7 and 65 years.7,75
This guideline adopts a standard age threshold of 65 years and over. An odds ratio of 4.1 (95% CI 2.8–6.1) 
for clinically signifi cant acute complication of TBI is associated with this threshold when the person has 
experienced loss of consciousness or amnesia.75
There is evidence that the incidence of intracranial complications in children and infants is much lower than 
in adults.7 In young infants (under 12 months) age is inversely related to the risk of intracranial complications 
requiring intervention, with those under two months old being at highest risk.82
2.2.10 Drug or alcohol intoxication 
Drug or alcohol intoxication can result in signs and symptoms that are also risk factors for intracranial 
complications (eg, vomiting, headache, amnesia, impaired consciousness). Excessive consumption of alcohol 
can also cause hypoglycaemia, which, in turn, can cause impaired consciousness. This makes a differential 
diagnosis diffi cult and could lead to an incorrect diagnosis of a developing intracranial complication. Drug 
and/or alcohol use have also been identifi ed as independent risk factors for poorer outcomes following TBI,7,76 
and may impact on rehabilitation from TBI (see Chapter 14, Special issues).
Although alcohol intoxication can reduce the Glasgow Coma Scale, it is always safer to assume that such signs 
are due to TBI or a complication of TBI rather than intoxication and proceed accordingly.
2.2.11 Headache 
good practice point
Strong analgesia for headache should be avoided, if possible, until a full assessment has 

been made in the Emergency Department.
This is the opinion of the Guideline Development Team, or feedback from consultation within New Zealand where no evidence is available.
Headache – any head pain either diffuse or localised – is a symptom that may be associated with raised 
intracranial pressure and is a risk factor for intracranial complications.76 Headache can, however, be diffi cult to 
defi ne in terms of duration and severity, particularly in infants and young children. 
Analgesic medications carry a risk of sedation or ‘masking’ symptoms of complications of TBI. If possible, strong 
analgesics should be avoided until the person has been fully assessed in the Emergency Department, so that an 
accurate measure can be made of consciousness and other neurological signs. For people with headache alone, 
simple analgesics, such as paracetamol, may be appropriate. There are situations where strong analgesics are 
required (eg, fractures) prior to hospital and their use should be clearly documented. 
2.2.12 Vomiting 
Vomiting is a symptom associated with raised intracranial pressure and is consistently identifi ed as a high risk 
factor for those with a TBI. However, there is some debate about the number of vomiting episodes required to 
identify high risk.7,75 
Vomiting is quite common in infants and children, and its predictive power is uncertain in this age group. It has 
been estimated that around 16% of infants and children aged 12 years or under vomit after relatively minor 
head injury, and the cause of vomiting may be related to individual intrinsic factors (eg, previous tendency to 
vomit) rather than specifi c features of the head injury.7 However, a recent rigorous systematic review concluded 
that any vomiting should be considered a risk factor for intracranial complications.
41
 
   
   
 

2.2.13 Irritability and altered behaviour 
Irritability and altered behaviour are non-specifi c terms which are sometimes used in clinical guidelines for 
acute head injury management with little empirical evidence to support their use.81 However, they are an 
important sign in young children, where other problems, such as amnesia or headache, cannot be detected.83 
Irritability and altered behaviour may also be early signs of deterioration, and should therefore be monitored 
carefully.  Where there is irritability or altered behaviour present, the Glasgow Coma Scale verbal response 
should be scored at most as 5 (ie, confused).  Appropriate action needs to be taken in relation to the overall 
Glasgow Coma Scale and any change in Glasgow Coma Scale (see recommendations in Chapter 3).
2.2.14  History of cranial neurosurgical interventions 
There is no evidence to indicate previous cranial neurosurgical intervention is a risk factor for intracranial 
complications. However, expert opinion considers that such intervention is likely to increase the risk of 
developing a subdural haematoma. Therefore, any intervention should be recorded, particularly if there has 
been cranial neurosurgery in the six weeks prior to injury, or if there is a shunt for hydrocephalus.7
2.3  Referral to Emergency Department
This section covers two clinical questions.
1.  For a person with suspected TBI, is assessment in the Emergency Department required?
2.  If ‘Yes’ to (1), is emergency service transport required?
Signs and symptoms that are risk factors for acute intracranial complications of TBI (see Section 2.1, Pre-
hospital assessment – acute) should initiate referral to the Emergency Department. Promptly transport the 
injured person to an Emergency Department by emergency services if:
•  there are more serious signs
•  the person assessing the injured person has concerns
•  there are other circumstances, such as the lack of suitable alternative transport.
RAPID TRANSFER TO EMERGENCY DEPARTMENT USING EMERGENCY SERVICES is appropriate if any of the 
following indicators are present.
•  Any deterioration in the injured person’s condition.
•  Unconsciousness, or lack of full consciousness (ie, Glasgow Coma Scale score <15).
•  Any focal neurological defi cit (ie, restricted to a particular part of the body or a particular activity) 
since the injury (eg, problems understanding, speaking, reading or writing; loss of feeling in part of 
the body; problems balancing; general weakness; any changes in eyesight; diffi culty walking).
•  Any suspicion of a skull fracture or penetrating head injury (eg, clear fl uid running from the ears or 
nose; black eye with no associated damage around the eye; bleeding from one or both ears; new 
deafness in one or both ears; bruising behind one or both ears; penetrating injury signs; visible 
trauma to the scalp or skull).
•  Any seizure (ie, ‘convulsion’ or ‘fi t’) since the injury.
•  A high-energy head injury (eg, pedestrian struck by motor vehicle; occupant ejected from motor 
vehicle; a fall from a height of greater than one metre or more than fi ve stairs, or less for infants and 
children aged under fi ve; diving accident; high-speed motor vehicle collision; rollover motor accident; 
accident involving motorised recreational vehicles; bicycle collision; or any other potentially high-
energy mechanism).
•  Suspected neck injury.
•  The injured person or their carer is unable to transport the injured person safely to the hospital 
Emergency Department without the use of ambulance services (providing any other risk factor 
indicating Emergency Department referral is present).
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2
In the absence of any of the indicators for emergency services transport, but where review in an Emergency 
Department is indicated, transport to the Emergency Department could be with a competent adult.7
EMERGENCY DEPARTMENT REVIEW NEEDED but TRANSPORT could be WITH COMPETENT ADULT if any of 
the following indicators are present.
• Any loss of consciousness (‘knocked out’) as a result of the injury, unless trivial, apparently resolved
and alternative observation available.
• Amnesia for events before or after the injury (‘problems with memory’).
Note: The assessment of amnesia will not be possible in pre-verbal children and is unlikely to be
possible in any child aged younger than fi ve years.
• Persistent headache since the injury.
• Irritability or altered behaviour (‘easily distracted’, ‘not themselves’, ‘no concentration’, ‘no interest 
in things around them’) particularly in infants and young children (ie, aged younger than fi ve years).
• Any vomiting episodes since the injury.
• History of bleeding or clotting disorder.
• Current anticoagulant therapy such as warfarin, or if the person is taking supplements, such as 
Ginkgo biloba, or other supplements with anticoagulant effects.
• Current drug or alcohol intoxication.
• Any previous cranial neurosurgical interventions (‘brain surgery’).
• Suspicion of non-accidental injury.
• Age 65 years and older; one year or younger.
• Concern about the cause of any symptoms by the person undertaking the assessment.
* Depending on local availability, assessment at an after hours medical clinic or accident and medical 
clinic may be appropriate for this group of people and this arrangement should be described in local 
ambulance and hospital protocols.
People who have none of the factors requiring Emergency Department review fall outside the defi nition of 
‘defi nite TBI’ used in this guideline (see Chapter 1, Traumatic brain injury in New Zealand). Some people whose 
presentation lies outside this defi nition, but who have one or more risk factors for acute complications (eg, aged 
65 years or older or alcohol intoxication) should also be reviewed in the Emergency Department. All people who 
meet the defi nition of ‘defi nite TBI’ should be referred for an Emergency Department assessment. 
2.4  Assessment in hospital not required
People who present with none of the indications for Emergency Department assessment should seek further 
medical assessment from a general practitioner or at an accident and medical clinic if there are: 
• adverse social factors (eg, no one is able to supervise the injured person at home)
• continuing concerns by the injured person or their carer about the diagnosis.7
People not meeting the criteria for Emergency Department or other further medical assessment can go home 
with an information sheet with details of when to seek medical help. The information sheet should state clearly:
• that there are some symptoms (eg, headaches, dizziness, fatigue, diffi culty with concentration) that occur
fairly commonly after an external force to the head, which resolve over the fi rst few hours and days up to a
few weeks 
• the 
specifi c symptoms and/or signs which, if they occur, indicate the need to seek prompt medical attention.
As these people do not meet the defi nition of ‘defi nite TBI’, there is no need to arrange routine general 
practitioner follow-up or to arrange time off regular activities, including work. People in whom symptoms 
43
persist, worsen or signifi cantly interfere with usual activities should be reassessed by their general practitioner 
(see Section 2.5, First assessment – delayed).
 
   
   
 

2.5  First assessment – delayed
Not all people who have had an episode of external force to the head present for medical attention on the day 
of injury. This section refers to anyone presenting to a general practitioner or an Emergency Department more 
than 24 hours after the injury. People may present weeks or months after the injury. When the fi rst presentation 
is delayed, it can be more diffi cult to identify a connection between the reported symptoms and an episode of 
external force to the head leading to suspicion of TBI. 
The key features of this assessment are to:
• document the episode of external force to the head
• document the current presenting symptoms and duration
• try to determine and document acute symptoms (see Sections 2.1, Pre-hospital assessment – acute and 2.2,
Assessment of need for medical attention)
• explain the possibility that some or all of the symptoms may be related to the injury
• if a diagnosis of TBI is probable, consider whether:
− any of the symptoms are suffi ciently serious to consider acute referral to hospital
− any specialist input is required (see Chapter 5, Rehabilitation following clinically signifi cant traumatic
brain injury – assessment and Chapter 6, Rehabilitation following clinically signifi cant traumatic brain
injury – intervention)
• if a diagnosis of TBI is uncertain, decide whether specialist referral or investigation is required to establish a
diagnosis
• consider appropriate management of symptoms (see Chapter 5, Rehabilitation following clinically signifi cant
traumatic brain injury – assessment and Chapter 6, Rehabilitation following clinically signifi cant traumatic
brain injury – intervention).
2.6 No 
assessment
Some people with defi nite TBI never present for an initial assessment. This may be due to a variety of reasons: 
• the effects of alcohol and other drugs
• an unwitnessed episode with amnesia of the event
• an accident in the context of sports
• unwitnessed or unreported falls in school playgrounds for children and young people
• unwitnessed or unreported falls for older people
• blows to the head where assault may go unreported (eg, a blow from a family member).
In 1991, one population-based survey of self-reported mild TBI in the USA indicated that 25% of those reporting 
a brain injury did not seek medical care.29
In a recent New Zealand study, prison inmates reported high rates of previous head injuries.84 Given the 
frequency with which TBI is thought to occur, a degree of suspicion that TBI may be implicated in some 
instances of otherwise unexplained poor performance is reasonable. However, in the absence of an appropriate 
initial assessment, it may prove diffi cult to substantiate such a link.
2.7  Advice to the community sector 
The Brain Injury Association of New Zealand provides useful information through its national 0800 helpline 
(0800 BRAINHELP, 0800 272 464).
New or worsening symptoms indicate a need for the person to seek immediate medical advice.
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2
2.8  Organisation of trauma services 
recommendations
grade
Each District Health Board in New Zealand should develop a plan for maximising the 
C
coordination of its trauma services to ensure the best possible care for people with severe 
traumatic brain injury, including timely referral to services provided by other District Health 
Boards.
A system and appropriate protocols for alerting the destination Emergency Department should 
C
be developed for all hospitals managing suspected traumatic brain injury.
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
There is consistent evidence that coordinated trauma systems reduce mortality in serious injury, including 
serious neurotrauma. For example, there is good consistent evidence that implementing trauma systems leads 
to considerable reduction in mortality (by 20–50%) from TBI.9 There is similar good evidence of harm; that the 
initial treatment of severely injured people at local hospitals without good trauma care capability, followed by 
transfer to ‘trauma centres’ doubles the mortality in both adult and paediatric populations.9 
A coordinated system of trauma care for TBI requires an organised, responsive system of care for people with 
severe TBI, which would include: 
• planning of pre-hospital management and triage
• transport directly to the trauma centre
• maintenance of appropriate call schedules for staff
• audit and quality improvement reviews
• staff participation in trauma education programmes.9
Trauma facilities for treating moderate to severe TBI should ideally include: 
• a specialist-led emergency medical service
• a neurosurgery service with a neurosurgeon readily and promptly available
• an in-house surgeon with trauma training
• a continuously staffed and available operating room, intensive care unit and laboratory equipped ‘for’
management of people with TBI
• a continuously staffed and available CT scanner and operating staff.9
In areas without access to a neurosurgeon, local surgeons should have competency in: 
• performing neurological assessment 
• immediate neurotrauma care
• surgical treatment of extracerebral haematoma for people whose condition is deteriorating.9
45
 
   
   
 

46
 
   
   
 

Chapter 3:
3
Acute phase of traumatic brain injury care
Overview
• Details of good practice and evidence-based guidance for emergency assessment of suspected TBI are
provided in this chapter.
• On arrival at the Emergency Department, the person with a suspected TBI should be assessed by a clinician
to determine the presence of TBI, and whether a CT scan is necessary. A range of data is needed to assess 
the person.
• Emergency Department assessment and management of people with a brain injury is focused on the
management or avoidance of hypotension and hypoxia, and on determining whether an imaging study is 
required.
• Early imaging, rather than admission and observation, will reduce the time to detection for life-threatening
complications and is associated with better outcomes.
• Skull X-rays are of limited value in determining the presence of acute complications of TBI.
• CT imaging of the head is the primary investigation for the detection of clinically signifi cant acute
complications of TBI.
• The Canadian CT Head Rule has been adapted as a guide for New Zealand.
• Early support can help the injured person’s family/wha¯nau or carer(s) prepare for the effects of TBI; can
reduce the psychological sequelae experienced by the carers; and can result in better outcomes for both the
injured person and their family/wha¯nau.
• Careful assessment of the need for rehabilitation during the acute management of people after TBI should
take place during hospital care, prior to discharge and if the person has continuing or emergent symptoms of 
signifi cant brain injury following discharge.
This chapter covers the acute phase of care for people with suspected TBI. 
It provides advice about Emergency Department assessment, including selection for CT scanning, and routine 
observation protocols. Indications for hospital admission and continuation of hospital stay are presented, along 
with guidance on family and carer support and rehabilitation in the acute phase. 
Specifi cally excluded from this chapter is discussion of the intensive care management of people with severe 
TBI, which is beyond the scope of this guideline.
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3.1  Emergency Department assessment of people with a suspected 
traumatic brain injury
recommendations
grade
Emergency Department assessments of people with suspected traumatic brain injury should 
C
focus on the identifi cation of actual or potential hypotension and/or hypoxia, clinically 
signifi cant brain injuries and appropriate referral for imaging.
Co-existing injuries and other concerns, such as possible non-accidental injury or non-
C
traumatic aetiology, should also receive attention.
Imaging (for those meeting selection criteria) should be done early, in preference to 
C
admission and observation for neurological deterioration.
Data to enable decisions to be made about the probability of traumatic brain injury and 
C
the necessity of referring for a CT scan should be collected on admission by a health care 
practitioner appropriately trained in emergency medicine.
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
48
 
   
   
 

good practice points
The priority for all people attending an Emergency Department is the stabilisation of airways, 

3
breathing and circulation (ABC) before attention to other injuries. 
Anyone presenting to an Emergency Department with a suspected traumatic brain injury 

should receive a triage assessment by a trained staff member on arrival. Part of this triage 
assessment should establish whether they are high or low risk for clinically signifi cant brain 
injury and/or cervical spine injury, using the CT rules in this guideline.
Anyone presenting to an Emergency Department with impaired consciousness (Glasgow Coma 

Scale score of less than 15) should be assessed immediately by a trained staff member (such 
as a triage nurse).
In people with a Glasgow Coma Scale score of 8 or less, there should be early involvement of 

an anaesthetist, emergency physician or critical care physician to provide appropriate airway 
management and assist with resuscitation.
Anyone found to be high risk on triage for clinically signifi cant traumatic brain injury should be 

assessed within 10 minutes by a health care practitioner with experience in the assessment of 
such people. 
Anyone assessed, on initial triage, as being at low risk for clinically signifi cant traumatic brain 
injury should be reassessed within a further hour by a doctor with appropriate experience. 
Junior doctors rostered to the Emergency Department should have training in the assessment 
of people with traumatic brain injury, and clear protocols detailing when to seek more senior 
assistance.
Assessment should establish the need to request CT imaging of the head. All Emergency 

Department health care practitioners involved in the assessment of people with suspected 
traumatic brain injury should be competent in assessing the presence or absence of risk 
factors used to select adults, infants and children appropriately for CT imaging. Training 
should be provided to ensure that this is the case.
In general, people with a suspected traumatic brain injury should not receive strong systemic 

analgesia until they have been fully assessed, so that an accurate measure can be made 
of consciousness and other neurological signs. Local anaesthetic should be delivered for 
fractured limbs or other painful injuries.
Throughout the hospital episode, all care professionals should use a standard ‘suspected 

traumatic brain injury’ proforma in their documentation when assessing and observing people 
with suspected traumatic brain injury.
This is the opinion of the Guideline Development Team, or feedback from consultation within New Zealand where no evidence is available.
Many of the people presenting to an Emergency Department with a suspected TBI will have had an initial 
assessment outside hospital (see Chapter 2, Pre-hospital assessment, management and referral to hospital). 
49
 
   
   
 

For these people there will be some factor present that indicates they need to be referred to an Emergency 
Department. Others may present without having had any pre-hospital assessment.
There are four important reasons for undertaking an Emergency Department assessment.
1. Identifying actual or potential hypotension and/or hypoxia, which if untreated will magnify TBI effects.
2. Identifying acute complications of TBI that may require intervention, particularly bleeding inside the skull 
and/or brain.
3. Identifying other injuries that may require urgent management, including injuries to the cervical spine.
4. Estimating the severity of any injury to the brain that has implications for subsequent management and
follow-up.
A main focus of Emergency Department assessment for people who have sustained a suspected TBI is the 
management or avoidance of hypotension and hypoxia, and deciding who needs an imaging study. Early 
imaging, rather than admission and observation for neurological deterioration, will reduce the time of detection 
for life-threatening complications and is associated with better outcomes.7 See Section 3.2.1, Selection of 
adults for CT imaging of the head and Section 3.2.2, Selection of infants and children and young people for CT 
imaging of the head).
The good practice outlined above should be followed during Emergency Department assessment. Proformas will 
be developed as part of post-guideline documentation to assist health care professionals when assessing and 
observing people with suspected TBI.
3.1.1 Data collection on presentation
When a person presents to the Emergency Department with a suspected TBI, a clinician who has appropriate 
training in emergency medicine should collect data to enable decisions to be made about the probability of TBI 
and the necessity of referring for a CT scan. This data should include: 
• age
• mechanism of injury
• vomiting since the injury
• presence of headache since the injury
• presence of seizures since the injury
• presence of anterograde amnesia since the injury or retrograde amnesia of greater than 30 minutes before
the injury
• Glasgow Coma Scale score (on presentation and two hours after injury)
• evidence of suspected or open skull fracture
• signs of basal skull fracture
• evidence of trauma above the clavicles
• evidence of drug or alcohol intoxication.6
50
 
   
   
 

3.1.2 Alcohol
recommendations
grade
3
Airways, breathing and circulation (ABC) should be stabilised before attention to other 
C
injuries.
Signs of possible traumatic brain injury should not be attributed to alcohol intoxication alone 
C
when assessing people with traumatic brain injury.
Blood alcohol levels should be tested and results recorded for all people with suspected 
C
traumatic brain injury and a Glasgow Coma Scale score of less than 15 and/or where alcohol 
intoxication is suspected.
People who present with a suspected traumatic brain injury who are intoxicated following 
C
drug or alcohol use should have this recorded as part of their assessment.
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
The number of people presenting with suspected TBI affected by alcohol has varied from around 40% to 70% in 
hospital-based studies.4,85 There is considerable similarity in the signs of alcohol intoxication and TBI, making 
the Glasgow Coma Scale unreliable in alcohol-intoxicated people, particularly where levels exceed about 40 
mmol/L.86 Conversely, if the blood alcohol concentration (BAC) is below about 40 mmol/L alteration in the 
conscious level should not be attributed to alcohol alone. Therefore, the presence of alcohol should signal 
caution in the assessment of people with possible TBI, and a lower threshold for CT scan and admission should 
be observed. 
Routine BAC testing in suspected TBI might allow more accurate risk stratifi cation and eventual diagnosis. An 
alternative is to use a decision point two hours from admission for people where it is suspected that intoxication 
may account for the symptoms. If the Glasgow Coma Scale has not returned to 15 by that point, a CT scan 
is indicated whether or not alcohol is involved.75 Any deterioration during the two hours would necessitate 
immediate intervention.
3.2  Primary investigation for people with a suspected traumatic brain injury
recommendations
grade
The diagnosis of intracranial haemorrhage should not be ruled out on the basis of negative 
C
skull X-rays.
The primary investigation of choice for the detection of clinically signifi cant acute 
A
complications of traumatic brain injury is CT imaging of the head.
Skull X-rays may be requested as part of skeletal surveys for the detection of non-accidental 
C
injury in children and in addition to a CT scan.
Skull X-rays in conjunction with high-quality inpatient observation have a role where CT 
C
scanning resources are unavailable. 
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
51
 
   
   
 

A 2004 systematic review of clinical decision rules for the selection of people who have sustained a suspected 
TBI for CT imaging of the head identifi ed skull X-rays as only being of limited value for three reasons.76
Firstly, skull X-rays are only of limited value in assisting the diagnosis of intracranial haemorrhage. A meta-
analysis found that the sensitivity and specifi city of a skull fracture for predicting the presence of intracranial 
haemorrhage were 38% and 95% respectively. A recent meta-analysis, in children, found a sensitivity of 59% 
and specifi city of 88%. The equivalent predictive values were 0.41 (positive predictive value) and 0.94 (negative 
predictive value). These fi gures imply that if there is a skull fracture diagnosed on radiography, the risk of an 
intracranial haemorrhage is elevated (about 4.9 times higher than before testing), but one cannot rule out an 
intracranial haemorrhage in people for whom a skull X-ray does not show a skull fracture. 
Secondly, the negative predictive power for a CT scan was 99.7%. People with a negative CT scan and no other 
body-system injuries or persistent neurological fi ndings can be considered for discharge as they are safe from 
the risk of having an intracranial haematoma at that time. However, it should be recognised that some of these 
individuals will be too unwell in terms of headache, vertigo, nausea/vomiting, impairment of cognition, motor 
performance and coordination to be discharged, despite a normal CT scan. It must also be recognised that there 
will be a small number (more often older people) who develop a chronic subdural haematoma over the ensuing 
four to six weeks after the injury.
Thirdly, a strategy of either 100% CT imaging of people who present with a head injury or high-quality inpatient 
observation for people who have sustained a mild head injury will be 100% sensitive for clinically important 
acute complications of TBI. Early imaging, rather than admission and observation for neurological deterioration, 
will reduce the time to detection for life-threatening complications and is associated with better outcomes. 
Therefore, the task is to derive a more sophisticated clinical decision rule for selection that will improve 
specifi city without impairing sensitivity.
The current primary investigation of choice for the detection of clinically signifi cant acute complications of TBI is 
CT imaging of the head. 
For safety, logistic and resource reasons, magnetic resonance imaging (MRI) is not currently indicated as a tool 
for primary investigation, although it is recognised that additional information of importance to the person’s 
prognosis can sometimes be detected using MRI.7
MRI is contraindicated in head investigations unless there is absolute certainty that the person does not harbour 
an incompatible device, implant or foreign body. There should be appropriate equipment for maintaining and 
monitoring the person within the MRI environment and all staff involved should be aware of the dangers and 
necessary precautions for working near an MRI scanner. MRI safety, availability and speed may improve in the 
future to the point where it becomes a realistic option for primary investigation for people with suspected TBI.7
52
 
   
   
 

3.2.1. Selection of adults for CT imaging of the head 
recommendations
grade
3
CT scans should be immediately requested for adults who have sustained a head injury, if 
B
they have any one of the following risk factors:
• any deterioration in condition
• a Glasgow Coma Scale score of less than 13 when assessed, irrespective of the time
elapsed since the injury
• a Glasgow Coma Scale score of 13 or 14 two hours after the injury 
• a suspected open or depressed skull fracture
• any sign of basal skull fracture (haemotympanum, ‘panda’ eyes, cerebrospinal fl uid
otorrhoea, Battle’s sign)
• post-traumatic 
seizure
• focal neurological defi cit
• more than one episode of vomiting
• amnesia for more than 30 minutes for events before the injury.
CT scanning should be immediately requested for adults with any of the following risk factors 
B
who have experienced an injury to the head with some loss of consciousness or amnesia 
since the injury: 
• age 65 years or older
• coagulopathy (history of bleeding, clotting disorder, current treatment with warfarin)
• high-risk mechanism of injury (a pedestrian struck by a motor vehicle, an occupant ejected
from a motor vehicle, or a fall from a height of greater than one metre or fi ve stairs).
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
A number of decision rules have been developed for CT imaging in an attempt to identify those at a high risk 
of TBI complications (usually intracranial haemorrhage).7 However, the purpose of scanning those who may be 
at high risk varies, from the wish to identify any injury requiring medical and/or surgical intervention, through 
to attempting to identify any injury to the brain of any degree of severity, sometimes for purposes other than 
determining appropriate treatment, such as support for litigation. 
For the purposes of this guideline, the Guideline Development Team has considered the balance of risks 
and benefi ts, and recommends that CT scanning be used to identify the need for medical and/or surgical 
intervention, or to confi rm, where there is doubt on clinical assessment, the safety of discharging a person with 
a head injury.
The UK’s NICE Head Injury Guideline Development Team based its decision rules for CT scanning following head 
injury on the seven-point Canadian CT Head Rule.75 The Canadian CT Head Rule reported a 50% (95% CI 48–51) 
specifi city rate for detecting clinically signifi cant brain injury. 
This section of the guideline is based on the NICE guideline.7 Since the NICE guideline, there has been further 
work on developing clinical decision criteria for determining those who require CT scanning following apparently 
mild TBI. One example of such work is the criteria identifi ed by the WHO Collaborating Centre Task Force on Mild 
Traumatic Brain Injury.
These criteria were derived from a systematic review of the literature on diagnostic procedures and selection 
rules for imaging of people with head injury.76 However, the WHO criteria were specifi cally developed to identify 
people who could be quickly and safely discharged from hospital Emergency Departments. 
53
 
   
   
 

The team developing this guideline for New Zealand considered that if the WHO criteria were adopted, it 
would result in a large increase in the number of people unnecessarily receiving CT scans. The public and peer 
consultation for this guideline confi rmed that these criteria were considered too broad and demanding of 
resources to be appropriate for the New Zealand setting. 
In order to provide comprehensive guidance, the seven-point Canadian CT Head Rule75 has been adapted for the 
New Zealand setting as follows:
• deterioration in condition at any time is a strong indicator for an immediate CT scan
• people with post-traumatic seizure, focal neurological defi cit or coagulopathy, meet selection criteria for CT
scanning
• drug or alcohol intoxication should not be assumed to be the cause of an altered Glasgow Coma Scale score.
The decision to CT scan should be applied regardless of the infl uence of intoxication
• people with non-symptomatic risk factors (ie, aged 65 years or older, coagulopathy, high-risk mechanism of 
injury) should at least have had an injury to the head and an instance of loss of consciousness or amnesia
(ie, the main signs and symptoms used to screen people for inclusion in the Canadian CT Head Rule study)
before receiving a CT scan. This is to prevent the possibility of people with no signs or symptoms receiving a
CT. For consistency, falls from three feet have been changed to falls from greater than one metre.
3.2.1.1 Observation of adults 
Some adults who have had an injury to the head may be observed in hospital for 24 hours as a safe alternative 
to a CT scan, although it should be remembered that early imaging (compared with observation) is associated 
with better outcomes.7
The Guideline Development Team acknowledges that for clinicians in rural centres with limited access to CT, it 
can be diffi cult to weigh up the pros and cons of transfer for a CT scan, when the risks of a complication of TBI 
are fairly low versus the very real diffi culties of managing such a complication at a distance from a neurosurgical 
centre. In some situations, observation for 24 hours rather than CT scan is a reasonable compromise.
People with the following factors must be referred for CT scan as observation may not be a safe and effective 
alternative for these people:
• any deterioration in condition
• a Glasgow Coma Scale score of less than 13 at time of assessment irrespective of time elapsed since the
injury or Glasgow Coma Scale score of 13 to 14 two hours after injury
• any sign of basal skull fracture (haemotympanum, ‘panda’ eyes, cerebrospinal fl uid otorrhoea, Battle’s sign)
• focal neurological defi cit.
People without these signs and symptoms, but with any other of the factors indicating a CT scan, may be 
admitted for observation for 24 hours, as an alternative to early CT scan.76 It is recommended that the presence 
of factors that would normally indicate a need for CT scanning (eg, post-traumatic seizure with full recovery and 
no focal signs; amnesia greater than 30 minutes; age of 65 years or older; high-risk mechanism of injury) be 
discussed with the relevant neurosurgical centre regarding the appropriateness of observation and possible 
need for transfer before making the decision not to transfer for CT scan.
3.2.2 Selection of infants and children and young people for CT imaging of the head 
There is some evidence that the prevalence of intracranial complications in children and infants is much 
lower than in adults,7 but it is important that any complications requiring neurosurgical intervention are 
detected as early as possible. CT scanning in infants and children carries a greater risk than for adults, both 
from the increased risk of lifetime fatal cancer from the radiation exposure (see Appendix D for a link to a 
supplementary resource) and from the sedation and anaesthesia frequently needed in younger children for 
the scanning procedure. Therefore, it is important to ensure that the balance of benefi ts and harms of CT 
54
 
   
   
 

scanning is considered. For this reason, the criteria in this section are aimed at detecting the possible need for 
neurosurgical intervention only and not to gain information about the existence of TBI.
There are several recent robust studies that have derived clinical decision rules from large study populations, 
3
which can be used to select candidates in the paediatric setting for imaging of the head.87,88 These include rules 
developed for use specifi cally with infants under the age of two years. 
Although at the time of writing none of these decision rules has been independently validated, there is 
considerable concordance between studies on the factors identifi ed, and therefore the validity of these factors 
can be inferred. 
Current evidence supports the following factors indicating a need for imaging in children aged 0 to 16 years 
(see Figure 3.1): 
• post-injury adverse events or signs, including focal neurological defi cits, seizures, loss of consciousness,
altered mental state, more than one episode of vomiting
• a paediatric Glasgow Coma Scale score of 13 or less, particularly an initial or ‘fi eld’ (pre-hospital) Glasgow
Coma Scale score of 13 or less, or any decrease in Glasgow Coma Scale score
• skull 
fracture, either obvious or suspected on the basis of clinical signs
• injury resulting from a fall from one metre or fi ve stairs, or less in the case of younger children
• non-accidental cause of injury
• younger 
age
• lethargy or irritability on examination.76,82,83,87–89
3.2.2.1 Infants aged 24 months or less
In infants aged two years or younger, there are additional risk factors for TBI indicating CT scanning, which 
include:
• soft tissue injury such as swelling or haematoma
• occipital or temporal/parietal location of injury 
• age under one year.
Taken together, these suggest a lower threshold for scanning if a large scalp swelling is present, if the 
haematoma is temporal/parietal or occipital rather than frontal, and the age is younger.
3.2.3 Skull X-rays in infants and children 
The literature on skull X-ray in children and infants indicates that, as with adults, the sensitivity of skull X-ray 
is too low to be the primary investigation (ie, the absence of skull fracture does not predict the absence of 
intracranial complications).7,87 In studies which have included both children and adults, there is evidence 
that adult rules for selection for X-ray can be safely applied to children, but these studies have suffered from 
statistical power problems.7 The evidence regarding the safety of adult rules with infants is inconclusive.7 
55
 
   
   
 

figure 3.1:
diagnostic management and selection f or imaging of children and young people aged <17 years 
History of trauma to head
• Injury resulting from a
CT scan§
Any
Scan +ve or GCS 
fall from 1m or 5 stairs or
13–14
more*
• Non-accidental cause of 
injury 
Admit to 
hospital and/or 
Post injury
neurosurgical 
• Any 
deterioration
consult
• Any seizure, except 
immediate
• Examination:†
− initial GCS score ≤13
Scan –ve and 
− GCS score that 
GCS = 15
decreases at any time
− obvious or suspected
skull fracture
− lethargy or irritability
− any focal neurological 
No
defi cits
None
Any non-surgical 
Observe and reassess
indicators for 
at 2 hours
GCS = 15?
Yes
paediatric 
Yes
Note: Any deterioration 
consult or 
– refer for scan immediately
admission?
Paediatric 
No
consult and/or 
admit to hospital 
Discharge with information to 
Recommended minimum 
home observation‡
observation period = 4 hours
* In younger children, falls from lesser heights may have a high risk of intracranial complications.
†  Use paediatric version of GCS.
‡  Children and young people with a head injury should only be discharged home if they have a responsible
adult who can observe them for any deterioration.
§
CT scanning of infants and children can be diffi cult and may require anaesthesia and pose a signifi cant
radiation risk. If uncertain about benefi ts of CT scan versus risks of scan, seek specialist advice (Emergency 
Department specialist, intensive care unit specialist, neurosurgeon, paediatrician) before scanning.
56
GCS = Glasgow Coma Scale
 
   
   
 

3.3  Non-accidental injury in children 
The acute management of non-accidental injury is outside the scope of this guideline. However, it is important 
that health practitioners are aware that the head injury examination is an important opportunity to identify this 
3
problem. There is evidence that a distinct pattern of brain injuries is associated with non-accidental injury in 
children. This results from the different mechanisms of injury in accidental versus non-accidental head injury. 
Non-accidental head injuries are more likely to involve inertial forces (eg, shaking) whereas accidental injuries 
are more likely to involve blunt trauma.7 
Due to the distinct pattern of injuries involved, skull X-ray as part of a series of plain X-rays (skeletal survey), 
along with other well established examinations (eg, ophthalmoscopic examination for retinal haemorrhage, 
examination for pallor, anaemia, tense fontanelle) and additional investigations (eg, CT and MRI imaging), has a 
role in detecting non-accidental head injuries in children (ie, aged less than 12 years).7 
Work on the derivation of clinical decision rules to predict non-accidental injury, based on imaging patterns, has 
recently started.90 However, decision rules in this area will require substantial validation before they can inform 
clinical practice. 
3.4  Imaging of people with a suspected traumatic brain injury
good practice points
All CT scans of the head should be reviewed by a clinician who has been deemed competent 

to review such images.
A full or interim written report for the person’s notes should be provided within an hour of all 

imaging procedures performed on people with head injury. 
Neurosurgical or anaesthetic referral for people with severe head injury should not be delayed 

for imaging of any kind.
This is the opinion of the Guideline Development Team, or feedback from consultation within New Zealand where no evidence is available.
It is assumed that clinicians will adhere to general principles of good practice in imaging as outlined by the 
Royal College of Radiologists.7 Where necessary, transport or transmission of images should be used to ensure 
that a competent clinician reviews the images.7 
There may be occasions where the CT scan needs to be repeated, in addition to the recommendation regarding 
imaging during observation. For example: 
• if an initial scan shows an abnormality, such as a small intracranial haematoma and there is clinical 
deterioration
• to check that an original small lesion has not progressed (often scan repeated the next day)
• to check that an initial small lesion has resolved spontaneously (often scan repeated a week or two later).
3.5  Use of corticosteroids in acute traumatic brain injury
recommendation
grade
Avoid corticosteroids in the management of people with acute traumatic brain injury of any 
A
severity.
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
57
 
   
   
 

A 2004 trial recruited 10,008 participants with acute TBI and a Glasgow Coma Scale of 14 or less in over 40 
countries. Participants were randomised to receive 48 hours of intravenous methylprednisolone or placebo. 
Results showed that two-week all-cause mortality was 18% higher in the methylprednisolone group. This is 
strong evidence to avoid corticosteroids in people with acute TBI of any severity.91
3.6  Involving neurosurgical care
Information in this section has been adapted for New Zealand from the NICE guideline on head injury.7 A small 
number of people with TBI will require an operation or invasive monitoring. Apart from situations where the 
person is far from a neurosurgical centre and has a life-threatening complication requiring urgent intervention, 
decisions about surgery will normally be made by, or in consultation with, a neurosurgeon. There are no 
absolute rules for deciding which people should be discussed with, and/or managed by, a neurosurgeon. Rules 
will vary depending on local availability, preference of neurosurgeons and other factors.
Although local centres will need to decide on their own criteria, in general, the person’s condition should be 
discussed with the nearest neurosurgeon, with a view to their taking over their care in the following clinical 
situations:
• the person is deteriorating, particularly regarding level of consciousness (documented Glasgow Coma Scale
score fall of two or more), has developed pupil dilation or other new neurological defi cit
• the person has had a severe TBI (Glasgow Coma Scale score 8 or less), especially if they have remained
unconscious from the time of injury
• the person has a signifi cant neurological defi cit following the TBI
• the person has a ‘surgically signifi cant lesion’ on imaging, which may include:
− a mass lesion with >1 cm midline shift or with acute hydrocephalus. Such lesions include acute extradural 
and acute subdural haematomas, cerebral contusions and traumatic intracerebral haematomas
− open/compound skull fracture
− obvious brain wounds visible at the bedside
− diffuse brain swelling/cerebral oedema.
A list of examples of abnormalities not considered ‘surgically signifi cant’ was produced by a survey of 
neuroradiologists and emergency physicians in Canada.75 However, a survey conducted in the UK in 2003 by the 
Society of British Neurological Surgeons found substantial concern about these Canadian criteria.7 
Further situations where a neurosurgeon should be consulted, not necessarily with a view to their taking over 
care, would be:
• a cerebrospinal fl uid leak
• defi nite or suspected penetrating injury
• a seizure without full recovery.
The exact nature and timing of the neurosurgical interventions are beyond the scope of this guideline. It is 
assumed that best practice will be followed once neurosurgeons have become involved with a particular 
person. Details of best practice in neurosurgical management for adults are given in an evidence-based 
guideline9 available from the Brain Trauma Foundation, at www2.braintrauma.org/guidelines/ and an 
evidence-based guideline for infants, children and adolescents92 is available from www.ohsu.edu/news/2003/
neuroGuidelines/.81
58
 
   
   
 

3.7  Transfer from secondary to tertiary care settings 
recommendations
grade
3
There should be designated consultants in both the referring hospital and the tertiary care 
C
facility (generally a neurosurgical unit but may be an adult or paediatric intensive care unit) 
with responsibility for the transfer and receipt of people (adults and children) with suspected 
traumatic brain injury. 
Local guidelines, consistent with national guidelines, on the transfer of people with suspected 
C
traumatic brain injury, including the transfer of the responsibility for care, should be drawn up 
between the referring hospital and the tertiary care facility.
Resuscitation and stabilisation of the injured person should be completed before transfer. 
C
A person persistently hypotensive despite resuscitation should not be transported until 
stabilised.
All people requiring transfer to tertiary care with Glasgow Coma Scale scores of 8 or less 
C
should be intubated and ventilated.
A person with suspected traumatic brain injury should be accompanied by a doctor with at 
C
least two years’ experience in an appropriate specialty, who should:
• be familiar with the pathophysiology of traumatic brain injury, drugs, equipment and
working in the ambulance or helicopter
• have received specialist training in the transfer of people with traumatic brain injury
• have an adequately trained assistant
• be provided with appropriate clothing and medical indemnity and personal insurance.
The transfer of a child or infant to a tertiary care facility should be undertaken by staff 
C
experienced in the transfer of critically ill children.
The transfer team should have a means of communication with their base hospital and the 
C
tertiary care facility during the transfer.
Appropriate resources for education, training and audit should be provided.
C
Continued…
59
 
   
   
 

recommendations
grade
Indications for intubation and ventilation in people with traumatic brain injury: immediately.
C
• Coma (Glasgow Coma Scale score of 8 or less).
• Loss of protective laryngeal refl exes.
• Ventilatory 
insuffi ciency:
− hypoxaemia (PaO  less than 65 mm Hg on air or less than 95 mm Hg on oxygen) or
2
− hypercarbia (PaCO  greater than 45 mm Hg).
2
• Spontaneous 
hyperventilation causing PaCO  less than 30 mm Hg.
2
• Respiratory 
arrhythmia.
Indications for intubation and ventilation in people with traumatic brain injury: before the 
C
journey.
• Signifi cantly deteriorating conscious level, even if not coma.
• Bilateral fractured mandible.
• Copious bleeding into mouth.
• Seizures.
Carers and family/wha¯nau should have as much access to the injured person during transfer 

as is practical.
Carers and family/wha¯nau should be fully informed about the transfer.
Service provision in the area of paediatric transfer to tertiary care should also follow these 
C
principles.
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
The risk of a further injury to people with TBI during transfer to tertiary care is well established.7
Recommendations in this section have been adapted for New Zealand from the NICE guideline on head injury.7
60
 
   
   
 

3.8  Indications for hospital admission
recommendations
grade
3
Criteria for admission to hospital following traumatic brain injury:
C
•  a deteriorating Glasgow Coma Scale score
• clinically 
signifi cant abnormalities on imaging
•  a Glasgow Coma Scale score of less than 15 after imaging 
•  when criteria for CT scanning are met but it is not possible
•  focal or abnormal neurological signs 
•  early post-traumatic seizure
• skull 
fracture
•  a major force of injury
•  continuing signs of concern to the clinician (eg, vomiting, severe headaches, amnesia) 
•  other reasons for clinician concern (eg, drug or alcohol intoxication, other injuries, shock, 
suspected non-accidental injury, meningism, cerebrospinal fl uid leak, where a scalp 
laceration overlies a fracture, or due to the injured person’s age)
•  when there is no responsible family member, caregiver or close friend under whose care 
the person could be discharged
•  ‘mild’ head injuries with symptoms such as headache, photophobia, nausea and vomiting, 
or amnesia requiring management.
People who require an extended period in a recovery setting due to the use of sedation or 
C
general anaesthetic during CT imaging should not normally require admission.
Resuscitation and stabilisation of the injured person should be completed before transfer. 
C
A person persistently hypotensive despite resuscitation should not be transported until 
stabilised.
People with multiple injuries should be admitted under the care of the team appropriate to 
C
their most severe and urgent problem.
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
The recommendations are based on the NICE guideline on head injury.7 Although most of the criteria concern 
injuries at the more severe end of the spectrum of TBI, a signifi cant number of people with ‘mild’ TBI may also 
need admission so as to better manage symptoms of headache, photophobia, nausea and vomiting, amnesia 
and other post-concussion sequelae. Admission allows for appropriate input and advice from a neurosurgeon, 
neurosciences nurses, and other members of the multidisciplinary team, including occupational therapists 
and social workers. Such input and help at this time can be of considerable assistance in the recovery and 
rehabilitation process and the benefi ts should not be underestimated.93 
This guideline places emphasis on the early diagnosis of clinically signifi cant brain injuries, using a sensitive 
and specifi c clinical decision rule with early imaging. Admission to hospital is intrinsically linked to imaging 
results, on the basis that people who do not require imaging are safe for discharge to the community (provided 
no other reasons for admission exist) and those who do require imaging can be discharged following negative 
imaging (again, provided no other reasons for admission exist). However, observation of the injured person 
still forms an important part of the acute management phase, for people with abnormal CT results who do not 
require surgery, and/or for people with unresolved neurological signs, and/or for some people with initially 
abnormal Glasgow Coma Scale scores who are observed, without CT, for two hours.
Neurosurgical and intensive care management of severe TBI is outside the scope of this guideline.
61
 
   
   
 

3.9  In-hospital observation of people with traumatic brain injury 
recommendations
grade
observation: general
In-hospital observation, including all Emergency Department observation, of a person with 
C
traumatic brain injury should be conducted only by health care practitioners competent in the 
assessment of traumatic brain injury. 
Observation of infants and young children with traumatic brain injury should only be 
C
performed by units (including normal paediatric observation settings) with staff trained and 
experienced in their observation. 
t ype and frequency of observations
Minimum documented neurological observations should be:
C
•  Glasgow Coma Scale score
•  pupil size and reactivity
• limb 
movements
• respiratory 
rate
• heart 
rate
• blood 
pressure
• temperature.
Observations should be performed and recorded every 15 minutes, or more frequently 
C
in some cases, until the person has achieved a Glasgow Coma Scale score of 15 on two 
consecutive occasions.
For people with an initial Glasgow Coma Scale score of 15, or who have returned to a Glasgow 
C
Coma Scale of 15 on two consecutive observations, the minimum frequency of observations 
following the initial assessment should be: 
•  half hourly for the fi rst two hours, then 
•  one hourly for four hours, then 
•  two hourly thereafter.
need f or reassessment/other action
If a person with a Glasgow Coma Scale score of 15 deteriorates at any time after the initial 
C
two-hour period, observations should revert to every 15 minutes or more frequently if 
necessary and follow the original frequency schedule.
An urgent reappraisal should be done by the supervising doctor if any of the following signs of 
C
neurological deterioration occur:
•  development of agitation or abnormal behaviour 
• a 
sustained 
(ie, 
≥30 minutes) drop of one point in the Glasgow Coma Scale score 
•  any drop of more than two points in the Glasgow Coma Scale score 
•  development of severe/increasing headache or persisting vomiting 
•  new or evolving neurological symptoms or signs.
62
 
   
   
 

recommendations
grade
need f or reassessment/other action continued
3
An immediate CT scan should be considered if any of the above signs of neurological 
C
deterioration occur.
Further CT or MRI scanning should be considered in the case of a person who has had a 
C
normal CT scan but who has not achieved a Glasgow Coma Scale score of 15 after 24 hours’ 
observation.
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
good practice point
t ype and frequency of observations

Post-traumatic amnesia and focal neurological signs should be assessed at regular intervals.
This is the opinion of the Guideline Development Team, or feedback from consultation within New Zealand where no evidence is available.
Observation should occur throughout the person’s stay in the Emergency Department or after admission 
following abnormal imaging results. All clinicians should use a standard ‘suspected TBI’ proforma in their 
documentation when assessing and observing people with suspected TBI. Separate adult-specifi c and child and 
infant-specifi c proformas should be used. The adult and paediatric Glasgow Coma Scale and derived scores (see 
Appendix C) should form the basis of observation, supplemented by other important observations. 
There is some evidence from the UK that Emergency Department observation wards are more effi cient than 
general acute wards in dealing with people admitted for short-stay observation, with more senior supervision, 
fewer tests and shorter stays.7 There have also been concerns about the experience and skills of staff on 
general and orthopaedic acute wards in head injury care.7 This resulted in a recommendation by the Royal 
College of Surgeons of England in 1999 that adults needing a period of observation be admitted to a dedicated 
observation ward within or adjacent to an Emergency Department.7
Where the optimal management of other injuries necessitates management in an orthopaedic or general 
surgical ward, the observations and responses described in the recommendations must continue. 
It is recommended that in-hospital observation of people with a TBI, including all Emergency Department 
observation, should only be conducted by professionals competent in the assessment of TBI.7 The service 
confi guration and training arrangements required to ensure that this occurs are beyond the scope of this 
guideline, but best practice demands that this issue be addressed by future policy. 
Observation of infants and young children (ie, those aged less than fi ve years) is a diffi cult exercise and 
therefore should only be performed by units with staff experienced in the observation of infants and young 
children with a head injury. Infants and young children may be observed in normal paediatric observation 
settings, as long as staff have the appropriate training and experience. 
Medical, nursing and other staff caring for people with suspected TBI admitted for observation should all be 
capable of performing the observations recommended in this guideline. The acquisition and maintenance of 
observation and recording skills require dedicated training and this should be available to all relevant staff. 
Specifi c training is required for the observation of infants and young children. 
63
 
   
   
 

3.10 In-hospital support for families/wha¯nau and carers 
Early support can help the injured person’s family/wha¯nau or carer(s) prepare for the effects of head injury. 
This support may reduce the psychological sequelae experienced by the family/wha¯nau or carer(s) and 
result in better long-term outcomes for both the injured person and their family/wha¯nau or carer(s). For the 
family/wha¯nau or carer(s) thrust into a hospital acute care setting, the shock can be overwhelming and cause 
additional tension or stress. It can be a particularly traumatic experience for a child visiting a sibling or parent 
with a head injury. 
Measures to make the experience less daunting should be put in place.7 There should be a protocol for all 
staff to introduce themselves to family/wha¯nau members or carers and briefl y explain what they are doing. In 
addition, a photographic board with the names and titles of personnel in the hospital departments caring for 
people with head injury can be helpful. 
Consumer information sheets detailing the nature of head injury and any investigations likely to be used should 
be available in the Emergency Department.7 Staff should consider how best to share information with children 
and introduce them to the possibility of long-term complex changes in their parents or siblings. Literature 
produced by consumer groups may be helpful. Fact sheets prepared for people and their families with TBI are 
being prepared (see BIANZ www.brain-injury-nz.org or ACC www.acc.co.nz).
The presence of familiar friends and family/wha¯nau at the early stage following admission can be very helpful. 
The person recovering consciousness can easily be confused by unfamiliar faces and the unfamiliar environment 
in which they fi nd themselves. Family/Wha¯nau or carers are often willing to assist with simple tasks, which, as 
well as helping nursing staff, helps friends and family/wha¯nau to take an active role in the recovery process. 
Family/Wha¯nau or carers should be encouraged to talk and make physical contact (eg, holding hands) with the 
injured person, although it is important to ensure family/wha¯nau, carers and friends do not feel that they have 
to spend many hours at the bedside, and to ensure they also have breaks and sleeps from time to time. This 
may be an opportune moment to mention consumer support organisations and introduce their literature. 
Voluntary consumer support groups can speak from experience about the real-life impact that follows head 
injury and can offer support following discharge from hospital. This is particularly important where statutory 
services are lacking. There should be a board or area displaying leafl ets or contact details for consumer support 
organisations, either locally or nationally, to enable family members to gather further information. 
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3.11 Discharge from hospital
recommendations
grade
3
A person with suspected traumatic brain injury may be discharged if:
C
•  the person has a Glasgow Coma Scale score of 15 (or in children, normal consciousness as 
assessed by the paediatric version of the Glasgow Coma Scale) and CT is not indicated
or 
•  head or cervical spine imaging is normal and the person has returned to a Glasgow Coma 
Scale score of 15 (or in children, normal consciousness as assessed by the paediatric 
version of the Glasgow Coma Scale)
and
•  no other factors are present that would warrant a hospital admission 
•  there are appropriate support structures for safe transfer and subsequent care and 
supervision.
People with suspected traumatic brain injury who have been admitted to hospital may be 
C
discharged to the community if:
•  there is resolution of all signifi cant symptoms and signs
•  there are appropriate support structures for their safe transfer and subsequent care and 
supervision.
Infants or children presenting with suspected traumatic brain injury who require imaging of 
C
the head or cervical spine should not be discharged until assessed by a clinician experienced 
in the detection of non-accidental injury.
All personnel involved in the triage and assessment of infants and children with suspected 
C
traumatic brain injury should have training in the detection of non-accidental injury.
All people with any degree of suspected traumatic brain injury who are discharged should 
C
receive verbal advice which:
•  outlines the risk factors in their community setting 
•  explains that some people make a quick recovery, but may later experience complications
•  gives instructions on contacting community services in the event of delayed complications.
People who initially presented with drug or alcohol intoxication and are being discharged 
C
should receive information and advice on alcohol or drug misuse.
People with any degree of suspected traumatic brain injury with no carer at home should 
C
be discharged only when there is negligible risk of late complications, or when suitable 
supervision arrangements have been organised.
People with mild traumatic brain injury may be advised in their discharge information that bed 
B
rest may temporarily help alleviate excessive dizziness, but will not aid recovery.
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
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good practice points
People discharged from hospital after a traumatic brain injury should have had their general 

practitioner notifi ed either before or at the point of discharge, with details of any residual 
impairments and details of the planned follow-up.
People who are discharged after a suspected traumatic brain injury sustained after a self-

harm or suicide attempt should have a risk assessment performed and should be referred as 
appropriate.
This is the opinion of the Guideline Development Team, or feedback from consultation within New Zealand where no evidence is available.
These recommendations have been reproduced from the NICE guideline.7
All people discharged from hospital after a TBI should have had their general practitioner notifi ed either before 
or at the point of discharge, with details of any residual impairments and details of the planned follow-up.
People who are discharged after sustaining a suspected TBI from a self-harm or suicide attempt should have 
a risk assessment performed and should be referred as appropriate (also see Chapter 14, Special issues). 
For more details of management of people after a suicide attempt, see the guideline, The Assessment and 
Management of People at Risk of Suicide available at www.nzgg.org.nz.
3.11.1 Discharge and Glasgow Coma Scale status 
People presenting with suspected TBI should not be discharged to the community until they have achieved a 
Glasgow Coma Scale score of 15. 
3.11.2 Bed rest
People should not be routinely recommended bed rest, but may be advised that if they suffer excessive 
dizziness, bed rest may help. A controlled trial randomised people with mild TBI to bed rest for six days post-
injury or no bed rest. They found that bed rest had no effect on the speed of resolution of symptoms. However, 
there was signifi cantly less dizziness reported by the intervention group, and it was concluded that bed rest may 
have some palliative effect on dizziness in the fi rst two weeks post-injury.94 
3.12 Referral to rehabilitation in the acute phase after traumatic brain injury
The information in this section refers to the rehabilitation issues in the acute phase after TBI. More detailed 
information about identifying clinically signifi cant TBI and rehabilitative needs is provided in Chapter 4, 
Rehabilitation services. Rehabilitation may begin in hospital, be organised to commence following discharge 
from hospital, or begin when the person re-presents with symptoms after discharge. Careful assessment of the 
need for rehabilitation during the acute management of head-injured people should take place during hospital 
care, prior to discharge and if the person has continuing or emergent symptoms of signifi cant brain injury 
following discharge. 
A small number of people will also develop late complications despite normal CT results and an initial 
absence of signs and symptoms. A well designed system of high-quality discharge advice and post-discharge 
observation by a carer is required to ensure that people receive appropriate care as needed, as soon as 
possible. The role of carers at home in the early post-discharge observation of people with TBI is important and 
should be guided by clear and detailed information. There should be clearly defi ned pathways back to hospital 
care for people who show signs of late complications.7,8 For more details of post-discharge follow-up see 
Chapter 8, Management of persistent symptoms and activity limitation following mild traumatic brain injury.
Early rehabilitative intervention in clinically signifi cant TBI improves outcomes.95,96 Therefore, rehabilitation 
66
should start as soon as possible.
 
   
   
 

3.12.1 Assessment for rehabilitation in the acute stage
Once a person with TBI has regained consciousness, it is important to determine what neurological damage 
they might have sustained in order to determine their need for immediate rehabilitative interventions. The 
3
assessment should be done by someone with expertise in assessment of neurological impairment and 
disability, and results and required actions should be documented accurately. The following areas should be 
assessed:
•  motor impairments, such as weakness, altered tone and lack of coordination in the limbs
•  problems with speech and swallowing 
•  sensory impairment, including visual problems such as reduced visual acuity, loss of visual fi eld, gaze 
palsies and hearing loss
•  cognitive impairments, especially of memory, concentration and/or orientation 
• language 
problems, particularly cognitive communication disorder or aphasia
•  reduced control over bowels and bladder 
•  emotional, psychological and neurobehavioural problems.8
With more severely injured people, the fi rst stage of rehabilitation may occur at the acute stage of intensive care 
in hospital, where interventions focus on reducing impairment and secondary complications. As the person 
starts to recover, they may need rehabilitation in a hospital inpatient or community residential environment to 
enable their successful discharge to the community.
If a person with TBI is still in hospital (including intensive care unit) 48 hours following the injury, the advice 
of and a review by a rehabilitation team should be sought as soon as possible. The purpose of this review 
is to determine appropriate referral and interim management to prevent the development of secondary 
complications.8 
3.12.2 Post-acute referral to rehabilitation
Before discharge is considered for people who have had a clinically signifi cant TBI, an assessment of the 
need for immediate inpatient or outpatient rehabilitation must be undertaken. People who require post-acute 
inpatient care should be transferred to a specialist rehabilitation unit as soon as they are medically stable and 
able to participate in rehabilitation.95,96 
Before a person with TBI is discharged following emergency care, there should be an assessment of their 
need for rehabilitation, and referral if necessary. They should be assessed for any residual physical, cognitive, 
emotional or behavioural defi cits which are negatively affecting their functioning and referred to specialist 
follow-up services (hospital based or community) as appropriate.8 
The awareness of the person, their family/wha¯nau and carer(s) of the current problems and how to manage 
them should also be assessed. All people being discharged after a TBI should be given details of who to contact 
if they have any concerns and how to contact them. They should also receive information about any problems 
they are likely to face and how to manage them. A member of the person’s family/wha¯nau, or a friend or carer, 
with the injured person’s consent, should also be given this information.8,97 
3.12.3 Criteria for referral to rehabilitation
People with TBI will need referral to a specialist rehabilitation service which is familiar with the problems of 
people with TBI, if they have: 
• diffi culty with body functions
• diffi culty with activities that they were able to complete prior to the injury 
• diffi culty participating in their usual social roles (pre-injury, or as it would have been had the injury not 
occurred).8
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People should be referred to a service that can assess the nature and severity of diffi culties in these areas 
and includes access to a multidisciplinary team. The service should have the capacity to identify appropriate 
interventions to aid recovery or compensation. 
Ideally, rehabilitation will take place in the person’s usual environment. This does not exclusively mean their 
home environment, but also includes other settings in which their usual social role requires them to function. 
Where this is not practical, rehabilitation is undertaken in an environment conducive to intervention, and 
intervention strategies are generalised (with active support) into the usual environment. See also Chapter 4, 
Rehabilitation services.
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Chapter 4:
Rehabilitation services
4
Overview
•  Over the past 20 years there has been a signifi cant change to the rehabilitation model. Rehabilitation 
services for people with TBI should be based on achieving well-being rather than on a model of defi cit and 
dependency.
•  In order for TBI rehabilitation to be effective, rehabilitation services should:
−  approach people with TBI from a participation perspective
−  have the necessary skills and experience to provide appropriate and context-specifi c assessments and 
interventions for people with TBI.
•  Rehabilitation for people with clinically signifi cant TBI has been shown to be effective in terms of improving 
outcomes for adults and children with TBI, and their carers, and is cost effective.
•  Rehabilitation services must acknowledge that different people require different input at different stages in 
their recovery.
•  There are distinct stages of rehabilitation and each has a different aim in relation to TBI. The four stages are:
1. acute care/neurosurgery
2. residential rehabilitation
3. non-residential rehabilitation
4.  longer-term community support.
•  The transition between the stages of TBI rehabilitation should be seamless, which requires effective 
communication and sharing of information.
•  There is substantial evidence of the effectiveness of community-based rehabilitation.
•  People with TBI may be referred to different types of residential services for rehabilitation. There are specifi c 
criteria for referral to these residential services.
•  Coordination of services and communication between them, both potentially diffi cult, are a very necessary 
part of effective TBI rehabilitation.
•  There is international agreement (both research and expert opinion) on the benefi ts of individual ‘case 
managers’ to support the individual and their family throughout the course of their recovery.
•  Delivery of rehabilitation is most effective when done by a coordinated, multidisciplinary team of people from 
a range of different disciplines, taking an interdisciplinary approach. 
4.1 The 
rehabilitation 
process
Before describing rehabilitation services, it is necessary to be clear about what constitutes best practice 
rehabilitation in the 21st century. In the past 20 years there has been a sustained move away from a defi cit-
based, clinician-dominated rehabilitation model. That model was based on the premise that all that was 
required to deliver good outcomes for people was to identify defi cits caused by the disease process and provide 
interventions that ameliorated those defi cits either through functional recovery or adaptation. This linear 
model of rehabilitation was represented by the International Classifi cation of Impairments, Disabilities and 
Handicaps98 and tended to reinforce existing hospital-dominated structures where hospital services focused on 
impairments, and people with disabilities were left to look after themselves or were considered substantially 
later in the rehabilitation process.
69
 
   
   
 

Modern rehabilitation practice is based around fi ve key points.
1.  The process is non-linear (see Figure 4.1).
2.  There is an early focus on participation. Impairment and activity restriction are assessed and interventions 
planned in the context of the individual’s participation goals.
3.  The person’s strengths and wishes are acknowledged, as well as those of their support team, rather than the 
focus being solely on defi cits.
4.  The majority of the rehabilitation process occurs in a community context and in the absence of health 
professionals. The role of the health care professional is to facilitate, problem-solve, educate and identify, 
and remove barriers to full community integration for the individual. They also have the role of ensuring 
that the person and their support team can take on as much control of the rehabilitation process as they are 
happy and able to handle at that time. This is a continually iterative process.
5.  Rehabilitation is a process that includes four core components:
i.  assessment – to determine the relevant rehabilitation approach
ii.  planning – that involves the development of meaningful and collaboratively determined goals
iii. interventions – that are specifi c, measurable, attainable and time-limited to meet these goals
iv. evaluation – of that intervention, before further iterations of this cycle. 
These points apply to TBI rehabilitation as well as rehabilitation in general. In order to practise effective TBI 
rehabilitation in the current environment, the following approaches are recommended.
1.  Approach people with TBI primarily from a participation perspective, considering issues around their ability 
to: 
− live independently
−  drive or use public transport 
−  return to work or education 
−  participate in leisure and social activities 
− fulfi l family roles and maintain personal, sexual and family relationships. 
 
These restrictions are often shared by family members who may be living under considerable long-term 
strain. 
2.  Have the necessary skills and experience to provide appropriate and context-specifi c assessments and 
interventions for people with TBI that are likely to contribute to enhanced participation and/or quality of 
life. Despite a primary focus on participation, the ICF model acknowledges that intervention at the level of 
pathology and impairment may have substantial benefi ts for the person. Too rigid a focus on participation 
(eg, that issues around pathology and impairment are missed) can have devastating consequences, for 
example failing to make a diagnosis of depression or seizures post-TBI or failure to prevent contractures. 
This means that the rehabilitation team needs to have the necessary skills to undertake assessment and 
management at all levels of health for people following TBI but with an emphasis on the level of participation.
70
 
   
   
 

figure 4.1:
interaction of concepts 
Health condition
(disorder/disease)
4
Body function and 
Activities
Participation
structure (impairment)
(limitation)
(restriction)
Environmental factors
Personal factors
Reproduced from: World Health Organization. Towards a Common Language for Functioning, Disability and 
Health: ICF. Geneva: WHO; 2002.
Rehabilitation for people with clinically signifi cant TBI has been shown to be both effective in terms of improving 
outcomes for adults and children with TBI and their carers, and cost-effective.10,11,99–103
Rehabilitation for people with clinically signifi cant TBI may differ from rehabilitation in general due to the 
infl uence of executive defi cits on the rehabilitation process. Executive defi cits refer to limitations associated 
with primarily frontal lobe damage, which infl uences attention and concentration, initiation and goal direction, 
judgement and perception, learning and memory, speed of information processing and communication and 
other cognitive skills, such as planning and organisation.104,105
Rehabilitation services for individuals after TBI must attend to the following issues for the person with TBI:
•  a compromised ability to set goals, plan and organise and initiate behaviour to achieve these goals, and 
diffi culty inhibiting behaviour incompatible with these goals. The individual with frontal lobe injury may have 
reduced ability to apply strategies or actions fl exibly to new situations and to think clearly under stress. Thus, 
individuals with TBI are more likely to respond to an antecedent approach to intervention. An antecedent 
approach is one that is proactive (ie, identifying potential challenges and barriers for the individual in 
advance rather than relying on consequences and rewards applied after the event, as in some traditional 
approaches to behaviour management)106
•   a compromised view of the individual’s world and evaluation of self, which may ‘take the form of perplexity 
regarding one’s lack of ability, frank unawareness of defi cits, active denial of the effects of the injury or some 
combination of these’107
•  cognitive and physical fatigue, which frequently accompanies the condition.108 Note that the individual may 
be restless, distractable, disorganised or abnormally loquacious. Mood may be exaggerated with ready 
laughter or tears. The individual may be swift to argue, diffi cult to reason with, and may deny fatigue
•  a lack of correspondence between the results of conventional assessment of structured tasks and 
performance in everyday life.
Neurological recovery following TBI can occur over an extended period of many months or years. Fundamental to 
rehabilitation services is the appreciation that different people need different input at different stages in their 
recovery, and that sometimes lifelong support may be required. The carers of people with signifi cant TBI may 
also require support over long periods of time.
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4.2  Stages of rehabilitation 
This section addresses needs for rehabilitation for people at the moderate to severe end of the spectrum of 
injury and those with prolonged unresolved symptoms.
Rehabilitation starts as soon as possible, even in the acute stages of intensive care in hospital. Interventions 
at this stage focus on reducing impairment and preventing secondary complications (pathology), such as 
contractures, malnutrition, pressure sores and pneumonia. As the person starts to recover, intensive residential 
rehabilitation may be required to make the successful transition between a residential environment and home. 
Post-acute residential rehabilitation has traditionally focused on regaining mobility and independence in self-
care to allow the individual to manage safely at home. This needs to be placed in the context of participation 
goals so that discharge to home is not seen as an end in itself but a milestone on a much longer journey. 
Discharge home can occur very early, even following very severe injury. Those involved in the rehabilitation 
process (particularly the person with TBI and their family/wha¯nau and carer(s)) need to be able to consider all 
possible options and choose the most appropriate option for them.
Once back in a home-based setting, people with TBI may need continued input to maximise their ability 
to function in their environment. Interventions focus on enhancing participation, improving quality of life, 
promoting psychological adjustment and minimising carer stress. These stages are illustrated in the ‘stages of 
rehabilitation’ model (see Figure 4.2).
The critical point of the ‘stages of rehabilitation’ model is that people with TBI may need to access different 
services as they progress through the different stages. Their transition between services should be smoothed 
by effective communication and sharing of information between services so that they progress in a seamless 
continuum of care through the different stages. 
figure 4.2:
‘stages of rehabilitation’ model f or people with traumatic brain injury
Acute care/neurosurgery
Ward-based therapy
Residential rehabilitation
Specialist rehabilitation
Non-residential rehabilitation
Outpatients
TBI clinics/out-reach/home-based/
day activity centres/vocational and social
Longer-term community support
Specialist case coordination
Re-assess as required
Maintenance of gains
Residential support
Adapted from: Turner-Stokes L. Head Injury Rehabilitation – How Should it be Provided?: Head Injury 
Rehabilitation – a Parliamentary Select Committee; 2001. 
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There has been considerable debate about whether services should be based in the hospital or the community. 
The answer depends on the mix of clinician skills and environment; these may be able to be delivered best in a 
non-hospital environment and this is certainly the trend in New Zealand for people with TBI requiring residential 
rehabilitation. There is substantial evidence of the effectiveness of community-based rehabilitation.109–112 
The outcome over fi ve to 10 years will be determined by all the different steps being in place. The important 
challenge is to make sure that each person can access the service most appropriate to their needs at the time 
that they need it. 
4
Rehabilitation within the community is supported by a number of New Zealand policies, including the 
Public Health and Disability Act 2000113 that establishes the New Zealand Health Strategy (www.moh.govt.
nz/publications/nzhs) and the New Zealand Disability Strategy (www.odi.govt.nz/nzds/) as guides for health 
care planning and funding. The vision of the New Zealand Disability Strategy is for ‘a society that highly values 
the lives and continually enhances the full participation of disabled people’. It recognises that this will be 
realised when disabled people are integrated into community life and community-based services ensure 
that disabled people (and their families/wha¯nau or carers) are supported. The Code of Health and Disability 
Services Consumers’ Rights114 prescribes that health services are delivered that enhance respect, dignity, and 
independence. In addition, the Injury Prevention, Rehabilitation, and Compensation Act 2001 reinforces ACC’s 
responsibility to provide rehabilitation ‘to the maximal extent practicable’.
Whilst the ‘stages of TBI rehabilitation’ model provides a useful illustration of the need for different services 
at different stages, with seamless continuity of care, the reality is much more complex and three-dimensional 
in practice. People with TBI progress through the different stages at very different rates. Many may not require 
hospitalisation at all and pass straight on to services in the community. A small minority with very severe TBI 
spend many months in hospital. People with TBI may also need to access services at different times as their 
needs change. This may involve re-access to inpatient services or a review of community rehabilitation and 
support needs as appropriate. 
4.3  Organisation of services
Rehabilitation services for people with TBI should be based on achieving well-being and independence rather 
than on a model of defi cit and dependency. Within each stage of rehabilitation, a range of different service 
providers is involved, which must somehow be coordinated, and these services change according to the stage 
of rehabilitation. Figure 4.3 represents community-based rehabilitation, developed around the ICF model of 
functioning.115
figure 4.3:
a model of functionally oriented, communit y-based rehabilitation
  Community services 
  Interdisciplinary rehabilitation team 
  TBI case coordinator 
  Family/wha¯nau/carers 
  Person with TBI 
Reproduced from: Bilbao A, Kennedy C, Chatterji S, et al. The ICF: Applications of the WHO model of functioning, 
disability and health to brain injury rehabilitation. Neurorehabilitation 2003;18(3):239–50.
73
 
   
   
 

There are a number of different services and supports involved in rehabilitation of people with TBI. Because 
TBI rehabilitation is a dynamic process, the involvement of various organisations, services and people may 
change over time. Coordination of the different services, although potentially diffi cult, is a very necessary part of 
effective TBI rehabilitation.
4.3.1 Residential services 
There are different types of residential service to which people with TBI may be referred for rehabilitation (also 
see Section 1.9.2.2, Residential rehabilitation). The fi rst of these is residential rehabilitation, where the person 
both lives and undertakes rehabilitation in these facilities; the second is residential support services, where 
the person needs a sympathetic place to live (such as with a landlord who understands TBI and the chronic 
problems associated with the condition). Each type of residential rehabilitation has a different focus and 
specifi c criteria for referral, although for the rehabilitation environments there will be considerable overlap in 
the services provided. These include:
• hospital 
inpatient 
rehabilitation: 
−  a need for ongoing medical treatment
•  a secure facility replicating as much as possible a typical environment (this could include mental health 
services/drug and alcohol services):
−  a need for 24-hour supervision due to the risk of possible harm to self or others
•  a residential facility replicating a typical environment:
−  a need for 24-hour environmental manipulation that promotes rehabilitation, such as an ordered 
household, ie, support for executive dysfunction issues with managed lighting, noise, visitors and 
communication, support to complete everyday tasks and establish and maintain a routine and supported 
reduction of assistance towards independence 
−  a need for preparation for independent living, including gradual support to take over all the tasks for 
independence 
−  a requirement for services that are not normally available in a typical environment (eg, percutaneous 
endoscopic gastrostomy feeding, wheelchair access, meals prepared, ongoing assistance with everyday 
activities)
• residential 
support:
−  when the person cannot take up rehabilitation until they are in a stable environment or they cannot 
maintain function without a stable environment
−  when the person may be mobile but is cognitively compromised
−  in order for the person to retain normal social roles as far as possible (eg, not being dependent on parents 
in adulthood)
− when supervision (of various levels) is needed.
4.3.2 Coordination and communication
With so many different services and so many people involved, the major challenges of rehabilitation are 
coordination and communication. Service planning and commissioning is required to link health and social 
services’ provision with other statutory and voluntary service providers, including employment, education and 
housing authorities.
74
 
   
   
 

4.3.2.1 Case coordination
recommendations
grade
People with traumatic brain injury who require rehabilitation should have a case coordinator/
B
key worker appointed.
A paediatric case coordinator/key worker should be appointed for children and young people 
B
4
with traumatic brain injury.
The case coordinator/key worker should:
B
•  be focused on the needs of the person with traumatic brain injury and their carer(s)
•  have specialist training 
•  provide continuity and good communication
•  be the key point of contact.
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
good practice point
Any change of case coordinator or ACC case manager should be immediately advised to the 

person with traumatic brain injury and their carer(s).
This is the opinion of the Guideline Development Team, or feedback from consultation within New Zealand where no evidence is available.
Case coordination is a concept with an established history in both adult and paediatric rehabilitation, although 
the label can vary. For example, it can be called key working or case management. Case coordination implies 
a role for a specifi ed individual who takes responsibility for coordinating the assessment, management and 
support activities for a specifi ed client. These terms are used interchangeably here. 
Following consultation on the draft guideline, the Guideline Development Team has suggested that the term 
‘case coordinator’ or ‘key worker’ is generally used in New Zealand to describe the person who undertakes this 
role. The Guideline Development Team acknowledges that this person may be an ACC case manager (or lifetime 
planner), the person’s general practitioner or a member of an established multidisciplinary rehabilitation team, 
depending on the individual circumstances of the client. Ultimately it is a matter of fi nding the right person to 
fulfi l the role of case coordinator in the context of the person’s life at that time. The roles of the case coordinator 
are specifi ed below, following a discussion of some of the relevant literature on effectiveness.
Apart from the obvious logistic need for coordination in multidisciplinary rehabilitation, a controlled study 
showed that participants receiving coordinated care showed greater gains throughout the study period and 
maintained the treatment effect after treatment ended, and that their carers exhibited less distress compared 
with the control group.116 
There is international support from both the research evidence and experts in the rehabilitation fi eld for the 
benefi ts of individual ‘case management’ or an equivalent system to support the individual and their family 
throughout the course of their recovery.8 A 1998 systematic review found that studies of the effectiveness of 
case management show that the clearest demonstration of benefi t is in vocational status, with studies using 
different models of case management showing similar improvements.10 It reported confl icting evidence on other 
effects of case management, such as improvements in disability, living status and family well-being, although 
particular benefi ts were identifi ed in one study where a single case manager administered insurance benefi ts.10
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The systematic review also reported that participants receiving the case management showed signifi cantly more 
improvement, as measured by the Disability Rating Scale (DRS), than the control group, and suggested that pre-
settlement of permanent disability advances for economic assistance helps people with TBI, possibly because it 
helps them to focus on rehabilitation. It concluded that although present evidence is mixed, use of several case 
management models should be continued and evaluated to identify which model is most effective.10 
A more recent study found that case management for people with TBI also improves the rate of unexpected 
outcomes.117 
A quasi-randomised study of case management for people with severe TBI in the UK, published in 1994, was 
unable to show a difference in important endpoints.118 The case-managed group was referred for more services, 
but the particular model of case management did not involve budget-holding so there was no way for the case 
manager to infl uence further the provision of services for people who needed them. 
In New Zealand, the current practice is that people with TBI who require ongoing support have a case manager 
appointed by ACC (provided ACC has been notifi ed of the need for further assistance). The case manager has a 
role in coordination of assessments and management throughout the lifetime of a claim. For people with severe 
and very severe TBI, an ACC lifetime planner may also be appointed. There may be a need, in addition to the ACC 
case manager role, for one of the clinicians involved in the rehabilitation and/or support of the person with TBI, 
to provide a specifi c ‘key worker’ role. This can only be determined on a case-by-case basis with full discussion 
among all the people involved.
The case coordinator should:
•  be focused on the needs of the person with TBI and their carer(s)
•  have specialist training in the role and in the needs of people with TBI and the services provided for them, 
and in the case of paediatric case coordinators, the particular needs of and services for children with TBI 
•  provide continuity and good communication
•  be the key point of contact for the rehabilitation team with ACC and other agencies and family/wha¯nau.
It is important that the person with TBI knows who their case coordinator is and that they, and their carer(s), are 
immediately advised of a change of case coordinator or ACC case manager. 
4.4 Rehabilitation 
teams
recommendations
grade
Common goals of the team should be consumer centred.
C
The assessment and planning of rehabilitation should be by a coordinated, multidisciplinary 
C
team taking an interdisciplinary approach.
Teams should have clear, skilled leadership and effi cient coordination.
C
The case coordinator should be central to deciding which other disciplines need to be 
C
involved in the planning and delivery of rehabilitation.
All health care practitioners working with people following a traumatic brain injury need to 
B
have had specialist training in the application of their disciplines to neurological conditions.
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
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4.4.1 Types of team
The composition of teams of professionals from different disciplines involved in the rehabilitation of a person 
who has had a TBI may be multidisciplinary, interdisciplinary or transdisciplinary.
In multidisciplinary teams, professionals work alongside each other, but not necessarily together. Discipline-
specifi c interventions running in parallel rehabilitation therapy services within hospital settings often adopt a 
discipline-specifi c approach.
4
Interdisciplinary teams are more integrated in approach than multidisciplinary teams. The team members 
plan an integrated rehabilitative programme together and work towards an agreed set of common goals, with 
collaborative interventions and joint sessions of therapy. Most specialist brain injury rehabilitation teams work 
in this way in New Zealand.
In transdisciplinary teams, the boundaries between individual disciplines of team members are relaxed, and 
team members adopt a common problem-solving approach. This approach is often appropriate for community-
based rehabilitation services, where it may not be practical for the full team to meet for every therapy session 
for each individual.
Whichever team approach is taken, the team will require clear, skilled leadership and effi cient coordination 
to provide effective rehabilitation.7 Delivery of rehabilitation is most effective when done by a coordinated, 
multidisciplinary team of people from the different disciplines involved119 taking an interdisciplinary 
approach.120
In New Zealand, most specialist brain injury rehabilitation teams meet and plan together with the person with 
TBI and their family/wha¯nau and carer(s) in the rehabilitation ward. However, teams in the orthopaedic, medical 
and surgical wards often work in isolation and require specifi c measures to support interdisciplinary working.
In general, the common goals towards which the team works should be consumer centred (ie, those that the 
person with TBI and their family/wha¯nau and carer(s) consider to be important and achievable).7 This is an ideal 
and there are situations, such as poor insight or suicidality, where it may not be appropriate. Teams, including 
case coordinators working with people after TBI, should work in partnership with the family.
4.4.2 Community access to multidisciplinary care
Currently in New Zealand, people receiving care in middle-sized or larger centres may have the rehabilitation 
delivery coordinated by a multidisciplinary team. In the community there are also multidisciplinary 
rehabilitation teams operating. People may be receiving help from a variety of agencies all at one time; many 
neuropsychologists, occupational therapists, speech-language therapists and physiotherapists are private 
providers. 
There are also providers operating teams of rehabilitation clinicians in the community. 
General practitioners in some centres may fulfi l the role of medical rehabilitation specialists (at least for mild 
and moderate injuries). There may be specialist workplace assessors, or occupational medicine practitioners, 
and for children and young people there may be Group Special Education and specialist teachers involved. 
There may be little communication or collaboration between the providers of different services, and effort is 
required to ensure effective coordination and communication. 
4.4.3 Team composition and role
The composition of the team – that is, the different disciplines represented on the team – will depend upon the 
needs of the person and the stage of rehabilitation. Assessment and planning and the delivery of rehabilitation 
to people who have had a TBI will require expertise in participation-focused assessment and delivery of 
services. Along with this primary focus, expertise and understanding of the domains of potential impaired 
function, together with knowledge of possible non-neurological complications, will allow a comprehensive, 
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but client-centred, goal-planning approach to rehabilitation. Specifi c areas where expertise in assessment and 
management is required include:
•  the process of social integration for an individual and their family
•  the person’s leisure, vocation and study needs
•  the person’s safety in their home or other environment 
•  the person’s functioning in daily activities
•  sharing of information in an appropriate form, time and environment
•  family and social support
•  motor impairments, such as weakness, altered tone and lack of coordination in the limbs
•  problems with speech and swallowing
• sexuality 
issues
•  sensory impairment, including visual problems such as reduced acuity, loss of visual fi eld and gaze palsies, 
hearing loss and loss of smell and taste
•  cognitive impairments, especially of memory, concentration, insight and/or orientation 
•  cognitive and physical fatigue
•  emotional issues, mood disturbance and other psychological disturbance
• language 
problems, particularly cognitive-communication disorder or aphasia
•  reduced control over bowels and bladder. 
4.4.4 Teams for children and young people
In addition to the disciplines above, rehabilitation teams working in paediatric settings should include the 
injured child’s family/wha¯nau, formal and informal carer(s) and an education representative. Family therapists, 
play therapists and child psychotherapists should be available as needed. A paediatric case coordinator/key 
worker should be appointed who, where necessary, can liaise with mental health services, education and Child, 
Youth and Family Services.
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Chapter 5:
Rehabilitation following clinically signifi cant 
traumatic brain injury – assessment
Overview
5
•  There is a substantial research gap in evaluating the impact of various service confi gurations, service delivery 
methods and specifi c interventions for people with TBI in New Zealand, particularly from the perspective of 
the individual with TBI and their family/wha¯nau.
•  A TBI can result in defi cits that can be classifi ed generally as physical, cognitive, behavioural/emotional 
or communicative. The identifi cation of these defi cits and any consequential impact on functioning is an 
important step towards helping the person with TBI, their family/wha¯nau and carer(s).
•  Diagnostic assessment within rehabilitation services aims to determine where there is a probable injury to 
the brain, and if so, to determine the nature and extent of the injury and the short- and long-term effects of 
the injury.
•  Many of the symptoms of TBI overlap with other conditions; physical, psychological and psychiatric. It 
is important to attribute symptoms correctly to TBI or other medical conditions and to identify and treat 
comorbid conditions in order to develop an effective TBI rehabilitation plan.
•  When TBI is sustained in childhood, neuropsychological and other assessments may need to be repeated 
several times as the child matures to adulthood.
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recommendations
grade
People who have had a traumatic brain injury should be assessed for functional defi cits in 
C
activities of daily living and be assessed for specifi c impairments in: 
•  control over bowels and bladder 
•  speech and swallowing 
• motor 
control
• sensory 
function
•  language production and comprehension
•  cognition and memory
•  behaviour and emotion
•  potential medical and psychiatric comorbidities, which have symptomatic overlap with 
traumatic brain injury.
All people with traumatic brain injury should be considered for referral for a 
C
neuropsychological assessment to evaluate cognitive functioning.
Assessment should include seeking information from family/wha¯nau and carers who knew 
C
the person before their injury and who are caring for the person post-injury.
Staff assessing people with traumatic brain injury should have training and expertise in the 
C
application of their disciplines to people with neurological disorders.
Staff assessing children and young people with traumatic brain injury should have general 
C
paediatric training and specifi c expertise in the application of their disciplines to children with 
neurological disorders.
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
good practice points
An assessment of the Glasgow Coma Scale for the purpose of estimating the severity of 

traumatic brain injury should be made from 30 minutes after the injury.
The primary focus of assessment should be on the person’s participation goals, and an 

assessment of activity limitation and impairments should be made within this context.
A speech-language therapist should lead communicative and dysphagia assessments.

A neuropsychologist should lead a cognitive and behavioural assessment.

Rehabilitation teams should have access to suitable health care practitioners to provide 

consultative services, education and oversight, especially when particular health care 
practitioners are unavailable to be members of a team.
This is the opinion of the Guideline Development Team, or feedback from consultation within New Zealand where no evidence is available.
TBI rehabilitation is a complex process. There is little robust evidence about commonly used interventions. 
Many of the interventions studied have tended to be delivered from a hospital-based, clinician-driven paradigm 
of TBI rehabilitation, which is at odds with the rehabilitation paradigm briefl y described at the beginning of 
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Chapter 4, Rehabilitation services. This chapter is based on Rehabilitation Following Acquired Brain Injury: 
National Clinical Guidelines produced by the Royal College of Physicians and British Society of Rehabilitation 
Medicine, in 2003. It draws heavily on literature around people with stroke.8
In an evidence-based guideline it is necessary to draw together what evidence there is for the effectiveness of 
various interventions. This will not necessarily refl ect the importance of those interventions or the frequency 
with which those interventions are used in everyday practice. There are many textbooks about TBI rehabilitation 
practice that offer a more cohesive, pragmatic, if not necessarily formal evidence-based approach (eg, 
Ponsford’s ‘rehabilitation for everyday adaptive living’ (REAL) guide121 or Rosenthal’s textbook122).
There is a substantial research gap in evaluating the impact of various service confi gurations, service delivery 
methods and specifi c interventions currently offered in New Zealand for people with TBI, particularly from the 
5
perspective of the individual with TBI and their family/wha¯nau. This research could inform future versions of this 
guideline and infl uence improvements in clinical practice to ensure best outcomes are achieved by people with 
TBI and their families/wha¯nau and carers.
This section covers the diagnostic and assessment procedures after the acute phase of TBI for people who have 
been referred to rehabilitation services following a moderate to severe TBI, or people who have been referred for 
specialist assessment with unresolved symptoms following mild TBI. For initial diagnosis and assessment see 
Chapter 2, Pre-hospital assessment, management and referral to hospital.
A TBI can result in defi cits that may generally be classifi ed as physical, cognitive, behavioural/emotional or 
communicative. Identifi cation of these defi cits and any consequential impacts on functioning is an important 
fi rst step towards being able to effectively help the person with the TBI, their carer(s) and family/wha¯nau. 
Assessment should include seeking information from family/wha¯nau and carers who knew the person before 
their injury and who are caring for the person after the injury, as they will be able to add information.8,123 
The diagnostic assessment within rehabilitation services is to determine whether there is a probable injury to 
the brain; and if so, the nature and extent of that injury and the short- and long-term effects that the injury is 
likely to have caused. Once determined, this assessment aids in establishing the needs for immediate and long-
term medical and rehabilitative care. For example, if the person has suffered injuries which mean they are kept 
prone, impairments of balance and motor control may be less apparent.
The diagnosis and assessment of the severity of a brain injury may be complicated by the presence of non-brain 
injuries and brain injury symptoms that are masked by medical problems, particularly in the case of ‘mild’ TBI.69 
The assessment of people with probable TBI should always be performed by people with training and expertise 
in the application of their disciplines to people with neurological disorders.7,8,10 Likewise, the assessment of 
children and young people under the age of 18 with probable TBI should be performed by people with training 
and expertise in the application of their disciplines to children with neurological disorders.7,8,11 
5.1  Non-neurological medical sequelae of traumatic brain injury
Non-neurological medical complications of TBI are common and varied, and include pulmonary, metabolic, 
nutritional, gastrointestinal, musculoskeletal and dermatological problems.69 It is outside the scope of this 
guideline to detail the best practice for the assessment of these medical issues. However, it is important that 
the diagnostic procedures include assessment of potential medical issues,8 and that where they are detected 
the person be referred for the appropriate treatment.
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5.2 Differential 
diagnosis
Many of the symptoms of TBI overlap with other conditions, both physical and psychological/psychiatric, 
including dissociative, motivational and somatoform disorders. For example, a need to check things constantly 
because of memory diffi culties may be misinterpreted as obsessive-compulsive disorder.124 
It is important to attribute symptoms correctly to TBI or other medical conditions, and to identify and treat 
comorbid conditions in order to develop an effective TBI rehabilitation plan. This may require specialist 
diagnosis and identifi cation. Where progress is not as expected, and it is unclear whether a person’s symptoms 
are due to TBI or one of these other disorders, they should be referred for a specialist neuropsychological 
assessment.124 
Also see Chapter 14, Special issues for more details of mental health disorders and other conditions, which may 
or may not be resulting from the TBI.
5.2.1 Differential diagnoses in children and young people
In children and young people, developmental, psychological and psychiatric conditions (including attention 
defi cit hyperactivity disorder [ADHD], foetal alcohol effects, hearing and visual impairments, drug and alcohol 
use in adolescents, developmental disorders, non-TBI-related cognitive diffi culties and emotional problems) 
may have symptomatic overlap with the effects of TBI. Where there is a lack of clarity about the aetiology of the 
symptoms, or where progress is less than expected, a specialist assessment should be made to identify and 
refer for treatment any non-TBI causes of the symptoms. 
5.3 Physical 
assessment
children and young people
There is no adequate evidence in this area specifi cally for children and young people with TBI that can be 
used to guide decision-making. The information and recommendations for adults should be used with 
caution in these groups.
Assessments of the physical functioning of people with TBI should include assessment for the following:
• motor 
defi cits:
− muscle 
weakness and paralysis
−  abnormal muscle tone (spasticity)
− defi cits in joint range of motion
− ataxia/coordination
• sensory 
defi cits:
− visual/hearing loss
•  symptoms, eg, headache, fatigue, pain 
• dysphagia 
• seizures
• functional 
mobility:
−  changing and maintaining body position
−  carrying, moving and handling objects
−  walking and moving (including, but not limited to, crawling, climbing, running, jumping and swimming)
− mobilising 
with the aid of assistive technology.
There is some evidence that a specialist in physical rehabilitation medicine should lead both the physical 
assessment and planning of physical therapy.10 
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5.3.1 Dysphagia assessment
A speech-language therapist should lead both the assessment and planning of dysphagia therapy. It should 
include:
•  a detailed diagnostic assessment to address issues of diagnosis, probable causality and disability 
•  a rehabilitation-focused assessment, which addresses the need for, and the potential to benefi t from, 
rehabilitation.125
5.4 Communicative 
assessment 
Communicative assessments should be performed by a speech-language therapist, in conjunction with others 
in the team.8 Assessments of the communicative functioning of people with TBI should include assessment for 
5
the following:
• language 
defi cits; expression and comprehension
•  cognitive communication disorder
• dysarthria
•  apraxia of speech
• acquired 
dyslexia
• acquired 
dysgraphia.
5.5 Neuropsychological 
assessment
All people with clinically signifi cant TBI should have an assessment of cognitive and behavioural/emotional 
functioning. This will usually be undertaken by a neuropsychologist.8
A neuropsychological assessment includes an interview of the person with TBI and their family/wha¯nau 
and carer(s), plus standard assessment measures, and focuses on assessment defi cits in cognitive and 
behavioural/emotional functioning.
A detailed neuropsychological assessment can contribute to the evaluation of the following: 
•  the likely impact of cognitive impairment on the rehabilitation programme
•  areas of strength on which the person may be able to build during rehabilitation (and the person’s prognosis 
in terms of their ability to function independently in the community or to return to work, study or driving)
•  help to identify the appropriate areas for effective rehabilitation input.8 
The assessment can encompass any or all of the following:
•  a detailed diagnostic assessment to address issues of diagnosis, probable causality and disability 
•  a rehabilitation-focused assessment, which addresses the need for, and the potential to benefi t from, 
rehabilitation 
•  a vocation-focused assessment, which addresses limitations to, and suitability for, specifi c vocational 
pursuits 
•  a permanent functional impairment assessment, which addresses the extent of permanent disability 
associated with the injury 
• a 
behavioural management assessment, which focuses on behaviour analysis and may assist in the 
development of behaviour modifi cation programmes.
5.5.1 Cognitive assessment 
Cognitive assessment identifi es the person’s functional-cognitive abilities through an occupational therapy 
assessment in the home, work, school or community context.
Cognitive assessment requires input from a multidisciplinary rehabilitation team along with family/wha¯nau and 
carers. Face-to-face contact is essential for assessment.
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Assessment of the cognitive functioning of people with TBI should include the following areas:8
•  insight and awareness 
• attention
• memory
•  speed of information processing
• perception 
• complex 
problem-solving 
• self-monitoring
• social 
judgement.
5.5.2 Behavioural/Emotional assessment 
Assessment of the behavioural and emotional functioning of people with TBI should include the following:8 
• emotional 
lability
• poor 
initiation 
• mood 
change 
• adjustment 
problems
•  personality changes, including:
− aggressive outbursts
− disinhibition 
− inappropriate 
sexual behaviour
• poor 
motivation 
•  drug and alcohol misuse
•  mental health disorders, particularly depression, anxiety disorders and psychosis.
Chapter 14 provides more detail on special issues.
5.5.3 Tools for neuropsychological assessment 
children and young people
There is no adequate evidence in this area specifi cally for children and young people with TBI that can be 
used to guide decision-making. The information and recommendations for adults should be used with 
caution in these groups.
caution – absence of evidence
When TBI is sustained in childhood, neuropsychological assessment may need to be repeated several 
times as the child matures to adulthood.
There are two main types of computerised neuropsychological testing.
1.  Those tests designed to detect reduced cognitive functioning compared with a baseline measure, usually 
intended to detect mild TBI sustained by sports players. These tests include CogSport (www.cogsport.com) 
and IMPACT (www.impact.com), also known as concussion screening.
2.  More comprehensive computerised test batteries that are based on standardised neuropsychological testing 
such as Integneuro and Neuromarker.6
Concussion screening has the advantage that it does not require a neuropsychologist, and may be of value for 
the initial assessment of people with mild TBI. When there has been a pre-injury base line measurement, these 
tests, which may be recorded by team doctors in some sports, provide a simple binary indication of ‘yes there 
is/no there is not a change in cognitive function’. They are therefore appropriate for medical practitioners to use 
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as part of an initial assessment of mild TBI. If there are signifi cant abnormalities on such screening assessments 
that do not recover rapidly to normal, referral for assessment by a neuropsychologist is indicated.126 
Computerised neuropsychological testing is not particularly useful for assessment of people with moderate to 
severe TBI. 
Test batteries, based on standardised neuropsychological measures, are intended for use by 
neuropsychologists and other appropriately trained practitioners who are able to interpret the results. These 
tests can be used for all levels of severity of TBI. 
Although there is some recent evidence of the validity and reliability of some of these tests,127,128 there are 
no good trials comparing them with the traditional (non-computerised) forms of testing. A question remains 
about whether the performance measured by computerised tests equates with that measured by the non-
5
computerised tests. There is insuffi cient evidence to recommend them for routine use. The use of computer-
based tests inevitably results in the loss of information gained from observation of the way in which the test 
participant performs a particular task.
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Chapter 6:
Rehabilitation following clinically signifi cant 
traumatic brain injury – intervention 
Overview
•  TBI is a complex process and currently there is little robust evidence about commonly used interventions.
•  A person who has had a TBI may show physical effects of the injury, which may require physical rehabilitation 
for which there is strong evidence for improving functional independence.
•  Recovering mobility is an important goal for people who are immobile following a TBI.
6
•  Both urinary and faecal incontinence are common following severe TBI. This can be distressing, socially 
disruptive and can hinder progress in other areas of rehabilitation.
•  When a person has post-TBI sensory (visual or hearing) disturbance, this may exacerbate disorientation and 
confusion, or impact on higher cognitive function.
•  Pain is frequently under-diagnosed in people with TBI, therefore specially adapted assessment tools or the 
skills of a speech-language therapist and family/wha¯nau and carers may be required to elicit symptoms 
accurately.
•  People may have communication impairments following a TBI and may require speech-language therapy as 
an intervention.
•  The nature of cognitive defi cits resulting from TBI depends, to some extent, on the severity and location of 
the injury. Cognitive defi cits are likely to be more diffi cult in terms of rehabilitation than the physical and 
behavioural effects of TBI, and harder for the family/wha¯nau, carers and employers to recognise, accept and 
accommodate.
• Cognitive 
rehabilitation 
has been shown to be effective, although the effectiveness of specifi c interventions 
is unclear. There is very little evidence for the effectiveness of medications for the cognitive sequelae of TBI.
•  A person who has suffered a TBI may show psychological/behavioural effects from the injury. Behavioural 
rehabilitation attempts to aid the recovery, improve function where possible, and provide strategies to 
minimise the negative impact of the symptoms that persist.
•  Anxiety, depression and other mental health conditions are common after TBI and often increase if not 
identifi ed and treated.
•  People with TBI who have diffi culties in activities of daily living should be assessed and an individual 
treatment programme should be developed and implemented.
• Sleep 
diffi culties and fatigue are both common problems following TBI of all severities.
•  Return to employment or an alternative occupation is a primary goal and a central factor in the restoration of 
the quality of life for people with TBI.
•  There is strong evidence that vocational rehabilitation improves vocational outcomes for people with TBI in 
securing sustainable employment or alternative occupation, and is cost effective.
•  A substantial proportion of people with TBI, particularly at the more severe end of the spectrum, may suffer 
effects on sexuality, such as impaired sexual functioning.
•  There is little evidence on the treatment of sexual dysfunction in people with TBI; most advice for 
rehabilitation focuses on counselling, for which there is no evidence of effectiveness. There is no good 
evidence for any particular medications for the control of sexually inappropriate behaviour.
•  Continuous or intermittent input from a rehabilitation team may be appropriate over long periods of time 
following TBI.
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This chapter is based on Rehabilitation Following Acquired Brain Injury: National Clinical Guidelines produced 
by the Royal College of Physicians and British Society of Rehabilitation Medicine, in 2003. It draws heavily on 
literature around people with stroke.8
As stated in Chapter 5, in an evidence-based guideline it is necessary to draw together what evidence there 
is for the effectiveness of various interventions. This will not necessarily refl ect the importance of those 
interventions or the frequency with which those interventions are used in everyday practice. There are many 
textbooks of TBI rehabilitation practice which offer a more cohesive, pragmatic, if not necessarily formal 
evidence-based approach (eg, Ponsford’s REAL guide121 or Rosenthal’s textbook122).
There remains a substantial research gap in evaluating specifi c interventions currently offered in New Zealand 
for people with TBI, particularly from the perspective of the individual with TBI and their family/wha¯nau.
Throughout this section and this guideline we refer the reader to the MedSafe data for details of the 
contraindications and adverse effects of medications. More information can be found at www.medsafe.govt.nz.
There is a very small literature of robust research evaluating rehabilitation interventions in a TBI population. In 
the following sections, many of the recommendations are extrapolated from fi ndings in populations with other 
brain injuries (particularly stroke) or in mixed populations including some people with TBI.
children and young people
There is no adequate evidence in this area specifi cally for children and young people with TBI that can be 
used to guide decision-making. The information and recommendations for adults should be used with 
caution in these groups.
6.1 Physical 
rehabilitation
recommendations
grade
A physiotherapist or occupational therapist with neurological expertise should coordinate 
C
physical therapy to improve the motor function of people with traumatic brain injury.
Any physical treatment approaches should take account of any associated orthopaedic or 
C
musculoskeletal injuries.
The physical rehabilitation programme should include a written and illustrated plan for other 
C
members of the team, including family/wha¯nau and carers.
A speech-language therapist with dysphagia expertise should coordinate the dysphagia 
C
therapy.
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
good practice point
Any programmes should be adapted to accommodate the person’s normal environment and 

activities as far as possible.
This is the opinion of the Guideline Development Team, or feedback from consultation within New Zealand where no evidence is available.
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A person who has had a TBI may show physical effects of the injury. These effects may include:
•  loss of motor control: both speed and coordination
•  abnormal muscle tone and movements, including spasticity and tremors
•  impaired bladder and bowel control
• seizures
• impairments 
of 
vision, hearing, smell and/or taste
•  impairments in the ability to produce speech
• signifi cant fatigue, both physical and cognitive
•  impaired stamina and endurance.10 
The aim of physical rehabilitation is to aid the recovery of normal functioning as far as possible, and to 
provide compensatory strategies to minimise the negative impact of the symptoms that persist (ie, to increase 
independence through the facilitation of motor control and skills). There is strong evidence that demonstrates 
the effectiveness of this approach in improving functional independence.8 
6
Physiotherapists and occupational therapists, and in the case of children or young people, paediatric 
physiotherapists and occupational therapists, need to be both skilled in the physical management of 
neurological defi cits and experienced in the recognition and handling of associated cognitive and behavioural 
defi cits which may impact on the ability of the injured person to engage and cooperate in therapy sessions, and 
the functional application of motor control (ie, their ability to carry over physical gains into daily activities).8 
Therefore, a physiotherapist or occupational therapist with neurological expertise should coordinate physical 
therapy to improve the motor function for all people with brain injuries.8
Any of the current physical treatment approaches should be practised within a neurological framework 
to improve the injured person’s function, but should also take account of any associated orthopaedic or 
musculoskeletal injuries.8
The physical rehabilitation programme should include a written plan, with illustrations where appropriate, to 
guide other members of the team (including family/wha¯nau and carers) in carrying over motor skills into other 
daily activities.8
It is the opinion of the Guideline Development Team that, where possible, and particularly when the person is 
in the community, any programmes should be adapted to accommodate the person’s normal environment and 
activities, eg, gardening, walking, swimming or doing structured exercises under the supervision and/or with 
the assistance of family/wha¯nau or carers.
In the case of dysphagia, speech-language therapists need to be skilled in the management of dysphagia both 
in providing compensatory strategies that ameliorate the swallowing dysfunction and in physical rehabilitation 
to aid the recovery of normal functioning as far as possible.
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6.1.1 Motor control and function
recommendations
grade
People with traumatic brain injury who are unable to maintain their own sitting balance 
C
should have timely provision of an appropriate wheelchair and suitable supportive seating 
package, with regular review of the seating system as their needs change.
Age-appropriate supportive seating and wheelchairs should be provided for children and 
C
young people.
People with complex postural needs should be referred to a specialist interdisciplinary team 
C
which includes expertise in specialist seating.
People with mobility problems should be considered for appropriate walking or standing aids.
C
Orthoses should be individually fi tted.
C
The following should be considered as an adjunct to conventional therapy: 
B
•  treadmill training with partial bodyweight support 
• strength 
training 
• gait 
re-education 
• exercise 
training.
A carefully monitored and evaluated trial of botulinum toxin A (BTX-A) for the treatment of 
C
focal spasticity in adults with traumatic brain injury may be considered.
A carefully monitored and evaluated trial of BTX-A for the treatment of focal spasticity in 
C
children with traumatic brain injury may be considered, with awareness that a longer-term 
treatment may be necessary before any benefi ts are found.
A trial of intrathecal baclofen for the treatment of severe spasticity in adults or children with 
C
traumatic brain injury may be considered, but should be carefully monitored for possible 
complications, including pump malfunction.
A carefully monitored and evaluated trial of tizanidine may be considered, particularly for 
C
spasticity of the lower extremities.
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
good practice point
Any rehabilitation programme should include a fl exibility routine when there is any spasticity.

This is the opinion of the Guideline Development Team, or feedback from consultation within New Zealand where no evidence is available.
6.1.1.1 Supportive seating and standing
Maintaining an upright posture helps to prevent osteopenia, loss of muscle bulk and normal cardiovascular 
and autonomic responses.8 Aiding sitting and standing will also promote normal postural tone, proprioceptive 
information and maintain range and alignment of joints.8 
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Postural re-training is an important precursor to gait re-education. In the early stages, supportive systems 
help to maintain the trunk and head in a good position and free the upper limbs for functional use. As truncal 
stability improves, systems which encourage more active movement may be introduced to achieve dynamic 
balance in sitting and standing.
People who have had a TBI who are unable to maintain their own sitting balance should have timely provision 
of an appropriate wheelchair and suitable supportive seating package. The potential need for accommodating 
communication devices and regular review to ensure the continued suitability of the seating system as their 
needs change should also be taken into account.8 People who are unable to stand independently should be 
provided with a suitable standing aid if appropriate, and this provision should be continued into the community 
if still required at the time of transfer.8 In the case of children and young people, age-appropriate supportive 
seating and wheelchairs should be provided.
People with complex postural needs should be referred to a specialist interdisciplinary team which includes 
expertise in specialist seating.8
6
6.1.1.2 Aids and orthoses
Orthoses such as ankle-foot orthoses or hand splints may help some people to maintain normal posture and 
stability during function. People with mobility problems should be considered for appropriate walking or 
standing aids to improve stability, which may include ankle-foot orthoses.8 Care must be taken when fi tting 
orthoses to avoid pressure areas, especially where deformity exists or sensation is impaired. If an orthosis is 
supplied it should be individually fi tted.8 
6.1.1.3 Rehabilitation of motor control
Recovering mobility is an important goal for people who are immobile following a TBI, and is a key factor in 
regaining functional independence. In addition to neurological impairments arising directly from the TBI, people 
who have been unconscious or immobile for signifi cant periods lose muscle bulk and cardiovascular fi tness, 
and this must be appropriately addressed in terms of the physical capacity of the individual person. 
When planning a programme to improve motor control and general fi tness, the following should be considered: 
•  treadmill training with partial bodyweight support as an adjunct to conventional therapy 
•  strength training to improve motor control in targeted muscle groups 
•  gait re-education to improve walking ability 
•  exercise training to promote cardiorespiratory fi tness.8
6.1.2 Spasticity
Spasticity is a condition that results when the nervous system has lost control of the coordination between 
the contraction and relaxation of muscles. Spasticity causes muscle stiffening, and fl accidity may also be 
present. Spasticity may be exacerbated by various stimuli (such as a full bladder, pressure areas) which need 
to be managed appropriately. It is the Guideline Development Team’s opinion that a sound fl exibility routine is 
necessary to counteract the effects of spasticity, and should be included in any rehabilitation programme for 
motor control. There should be a team approach to management, with goals set prior to considering any of the 
additional options outlined below.
6.1.2.1 Botulinum toxin A 
A recent systematic review of the effectiveness of botulinum toxin A (BTX-A) for treating focal upper and 
lower limb spasticity found that in most cases BTX-A decreases muscle tone across most conditions, with 
an improvement in range of motion, gait and function.129 However, the improvement does not always reach 
statistical signifi cance, which may be due to both methodological issues and the wide range of conditions 
causing spasticity included in the review.129 
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A randomised controlled trial of the use of BTX-A to treat adults (including people with TBI) presenting with focal 
hypertonia affecting upper or lower limbs found that the intervention group had better scores on many scales 
than the placebo control group, although the goal attainment scale score in both groups was similar at 12 
weeks. It was concluded that selective use of BTX-A can result in improvements in range of movement and focal 
disability in spasticity of the lower limbs.130 
There is therefore a small body of evidence that BTX-A may be effective for the treatment of spasticity in adults 
with TBI, and a carefully monitored and evaluated trial of BTX-A may be considered.129,130
A longitudinal study of BTX-A in children found earlier improvement in less complex motor control tasks (hand 
tapping) and pinch force tasks, but improvement in more complex, forward-reaching tasks occurred much later 
or not at all, and concluded that although BTX-A reduced tone and increased range of movement of the spastic 
upper extremity, the degree of motor improvement is dependent upon the complexity of the task.131 There is 
limited evidence for the effectiveness of BTX-A in children with lower limb spasticity from cerebral palsy.132 Any 
trial of BTX-A in children should therefore be carefully monitored for effectiveness.
For both adults and children, repeated treatments are likely to be required as BTX-A effects generally last no 
longer than two to three months.
See MedSafe data at www.medsafe.govt.nz for contraindications and side effects of BTX-A.
6.1.2.2 Intrathecal baclofen
A meta-analysis of studies on the effectiveness of intrathecal baclofen for severe spasticity found positive 
effect sizes (of between 1.12 and 10.00) for all studies in all diagnostic groups, including TBI.133 The cumulative 
overall success rate of intrathecal baclofen was estimated to be 78.1%, and at an average of 1.8 years after 
implantation; the mean current dosage level was 246 mcg/day (SD:192).
However, a small controlled trial of intrathecal baclofen in children and young people aged between four and 
19 at the start of the trial found that although there was a favourable outcome in all participants, with the 
greatest benefi t being a reduction of lower limb tone and carers noting improved muscle tone, behaviour, sitting 
and general ease of care, signifi cant complications were reported in some of the 12 participants, including 
hypotension (2), bradycardia (2), apnoea (2), sedation (1), mechanical pump complications (10 occasions in 
fi ve years), cerebrospinal fl uid fi stula (1), local infection (3), and meningitis (2). The study lacked the power to 
determine whether the complications noted were due to the intrathecal baclofen.134 
See MedSafe data at www.medsafe.govt.nz for contraindications and side effects of intrathecal baclofen.
6.1.2.3 Tizanidine 
A small randomised controlled trial examining the effectiveness of tizanidine for spasticity due to acquired brain 
injury found that the average lower extremity and spasm scores decreased signifi cantly. The treatment was 
signifi cantly better than placebo in decreasing lower and upper extremity tone. With a reduction in motor tone, 
there was also an increase in motor strength.135 A non-systematic review of the antispastic effect of tizanidine 
in placebo-controlled trials reported that the treatment group showed a reduction in muscle tone scores of 21–
37% compared with 4–9% for the placebo group and that 60–82% showed an improvement in muscle tone.136 
Therefore, there is a small body of evidence that tizanidine may be effective for the treatment of spasticity in 
adults with TBI, particularly for spasticity of the lower extremities, and a carefully monitored and evaluated trial 
of tizanidine may be considered.  
See MedSafe data at www.medsafe.govt.nz for contraindications and side effects of tizanidine.
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6.1.3 Continence
recommendations
grade
People with continence problems should not be discharged from residential care until 
C
continence aids and services have been arranged at home and carer(s) have been adequately 
prepared.
A plan for the rehabilitation of urinary incontinence should include:
C
•  a regular monitoring programme
•  strategies for alerting the carer(s) to the person’s need to pass urine where there are 
communication problems
•  a toileting regimen based on reinforcement in cases of cognitive impairment.
Anticholinergic medication should only be prescribed after demonstration of an overactive 
C
6
bladder.
Intermittent catheterisation should be considered in adults with a postmicturition residual 
C
volume of >150 ml.
Long-term catheters, if necessary, should be used as part of a planned catheter management 
C
programme using an agreed protocol.
The impact of long-term catheters, particularly indwelling urethral catheters, on sexual 
C
function should be considered.
Supra-pubic catheters should be used in preference to long-term urethral catheters.
C
In the case of constipation, an active bowel management regimen should be instituted as 
C
soon as possible, which includes:
• ensuring 
suffi cient fl uid intake 
•  the use of natural laxatives or simple bulk laxatives 
•  exercise and standing, where possible 
•  avoiding medications which slow gut motility
•  maximum privacy and comfort during defecation
•  supported sitting up for defecation at the earliest safe opportunity, and at a regular time 
each day.
Where the rectum is full but no spontaneous evacuation occurs, daily rectal stimulation may 
C
be used.
If the rectum is empty for three days running despite continuing oral intake, the use of an 
C
osmotic laxative or a stimulant should be considered.
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
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good practice points
Bladder and bowel management plans should be developed with the full knowledge and 

support and help of the person’s primary carer.
Intermittent catheterisation should be considered in children with a postmicturition residual 

volume of >10% of bladder capacity.
This is the opinion of the Guideline Development Team, or feedback from consultation within New Zealand where no evidence is available.
children and young people
There is no adequate evidence in this area specifi cally for children and young people with TBI that can be 
used to guide decision-making. The information and recommendations for adults should be used with 
caution in these groups.
Both urinary and faecal incontinence are common following severe TBI, and may occur with less severe injury. 
It is distressing, socially disruptive and a major burden to carers once injured people are discharged home and 
can seriously hinder progress in other areas of rehabilitation. Active continence manage ment and re-training of 
the bladder and bowel, when needed, are therefore critical parts of a rehabilitation programme. 
People with continence problems should not be discharged from residential care until adequate arrangements 
have been made for continence aids and services at home and the carer(s) have been adequately prepared.8
6.1.3.1 Bladder management
People who have continuing post-TBI urinary continence problems should be assessed by a professional trained 
in continence management for people who have a TBI, and where necessary, have access to specialist urologist/
continence management and advice, including further investigation (eg, urodynamics or ano-rectal physiology).8 
The rehabilitation plan should include:
•  a regular monitoring programme, eg, 24-hour voided volume chart and fl uid intake charts 
•  in cases of communication and mobility problems, effective strategies for alerting carers to the person’s 
need to pass urine 
•  in cases of cognitive impairment, an established toileting regimen based on reinforcement.8
Anticholinergic medication should only be prescribed after demonstration of an overactive bladder (eg, by the 
passage of small, frequent volumes on a 24-hour voided volume chart with a postmicturition residual volume of 
<100 ml, or by formal urodynamic investigation).8
6.1.3.2 Catheters
If a person has a postmicturition residual volume of >100 ml, intermittent catheterisation should be considered.8 
In children, an abnormal postmicturition residual volume is >10% of maximal bladder capacity 137 and with 
values above this it would be appropriate to consider a programme of intermittent catheterisation. Long-
term catheters should only be used after full assessment and consideration of less invasive forms of bladder 
management. If necessary they should be used as part of a planned catheter management programme using 
an agreed protocol. The impact on sexual function should be considered, particularly the potential problems 
associated with an indwelling urethral catheter.8 Supra-pubic catheters should be used in preference to long-
term urethral catheters.8
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6.1.3.3 Bowel management
Following TBI, constipation is common due to immobility, use of medications with anticholinergic side effects, 
embarrassment from lack of privacy, and poor fl uid and dietary intake. It may be further exacerbated by other 
coexisting neurological problems such as spinal injury. Constipation may cause discomfort and exacerbate 
spasticity, and it may progress to faecal impaction and overfl ow incontinence if not proactively managed. An 
active bowel management regimen should be instituted to establish the person’s normal pattern as soon as 
possible, with the support and help of the person’s primary carer where appropriate. This should include: 
• ensuring 
suffi cient fl uid intake 
•  the use of natural laxatives such as prunes, kiwifruit or simple bulk laxatives (if fl uid intake is suffi cient) 
•  encouraging exercise and standing, where possible 
•  avoiding medications which slow gut motility, such as codeine and tricyclic antidepressants 
•  careful attention to ensure maximum privacy and comfort during defecation
•  supported sitting up for defecation on a toilet or commode at the earliest safe opportunity, and at a regular 
time each day.8 
6
Daily rectal stimulation (eg, with suppositories or a microenema) may be used where the rectum is full but no 
spontaneous evacuation occurs despite the conditions above.8
If the rectum is empty for three days running, despite continuing oral intake, the use of an osmotic laxative (eg, 
polyethylene glycol) or a stimulant (eg, senna) should be considered.8
6.1.4 Sensory impairment
recommendations
grade
People with visual and/or hearing loss should be assessed and treated by a team with the 
C
appropriate experience or in conjunction with a specialist service.
People with traumatic brain injury with any visual disturbance should be assessed by a team 
A
which includes:
• ophthalmologists
•  orthoptists where there are problems with eye movement/double vision
•  people with expertise in rehabilitation for the visually impaired.
All people presenting post-traumatic brain injury with persistent visual neglect or fi eld defects 
A
should be offered specifi c re training strategies.
All people should be assessed for pain on a regular basis and treated actively in accordance 
B
with their wishes.
Practitioners should be alert to the possibility of pain in people who have diffi culty 
C
communicating, and pay attention to non-verbal signs of pain.
Practitioners and carers should be educated about:
B
•  hypersensitivity and neurogenic pain
•  appropriate handling of the paretic upper limb during transfers.
Pain management protocols should be in place, which include: 
•  handling, support and pain relief appropriate to the individual needs of the injured person
B
•  regular review and adjustment to changing need.
C
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
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children and young people
There is no adequate evidence in this area specifi cally for children and young people with TBI that can be 
used to guide decision-making. The information and recommendations for adults should be used with 
caution in these groups.
When a person has post-TBI sensory disturbance, including partial loss of hearing or vision, this may exacerbate 
disorientation and confusional states or impact on higher cognitive function.8 People with visual and/or 
hearing loss should be assessed and treated by an interdisciplinary team with the appropriate experience or in 
conjunction with another specialist service able to meet their special needs. 
6.1.4.1 Visual disturbance 
Some visual disturbance or loss of vision following a TBI may resolve with time and appropriate rest, but 
this will require expert assessment. Where a person has any visual disturbance, the interdisciplinary team 
involved in the assessment of vision should include ophthalmologists, and orthoptists should also be involved 
where there are problems with eye movement or double vision. People with expertise in rehabilitation for the 
visually impaired should be involved regarding functional use of vision, mobility training and equipment. All 
people presenting post-TBI with persistent visual neglect or fi eld defects should be offered specifi c re-training 
strategies.8
6.1.4.2 Hearing disturbance
In the case of hearing disturbance such as hypersensitivity following a TBI, the interdisciplinary team involved 
in assessment should include audiologists for the assessment of hearing and suitability of hearing aids. Advice 
should be sought from a hearing therapist for hearing-impaired people, with regard to rehabilitation and 
equipment provision.8
6.1.4.3 Pain
Pain is frequently under-diagnosed in TBI and is associated with poor outcomes.8 People with communication 
and cognitive defi cits are often unable to describe their sensory symptoms. Specially adapted assessment 
tools8 or the skills of a speech-language therapist, and family/wha¯nau and carers may be required to elicit 
symptoms accurately.
Painful musculoskeletal sequelae of TBI can include heterotopic ossifi cation, contracture and deformity. 
Shoulder pain is particularly common in upper limb paresis, arising from spasticity in the shoulder girdle 
muscles, malalignment or subluxation due to muscle imbalance or weakness, or secondary damage to soft 
tissues (eg, rotator cuff tears or impingement). 
Neurogenic pain may be associated with local hypersensitivity to touch. Pain may be exacerbated by poor 
handling and the uncontrolled effects of gravity. Successful management depends on an accurate assessment 
and intervention depending on the contributing factors, and preventive measures to support the affected limb 
in all positions. 
All people should be assessed for pain on a regular basis and treated actively in accordance with their wishes.8 
Health care practitioners should be alert to the possibility of pain in people who have diffi culty communicating, 
and should pay particular attention to non-verbal signs of pain.138 Health care practitioners and carers should 
be educated about hypersensitivity and neurogenic pain, and about appropriate handling of the paretic upper 
limb during transfers.8 Protocols should be in place for the management of pain, which include:
•  handling, support and pain relief appropriate to the individual needs of the injured person 
•  review at regular intervals and adjustment in accordance with changing need.8
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6.1.4.4 Neurodevelopmental therapy for children and young people
Neurodevelopmental therapy, originally developed for the treatment of cerebral palsy, is frequently advocated 
by its proponents for people with other forms of neurological impairment, including that resulting from TBI. In 
this therapy, therapeutic handling focuses on facilitating ‘desired’ movements while preventing ‘undesired’ 
movements, which are believed to produce secondary problems that reduce the functional potential of the 
person.
A systematic review of the evidence (which mainly involved children and young people with cerebral palsy) 
for neurodevelopmental therapy found it to be contradictory and inconclusive,139 and there is no evidence to 
support the routine use of neurodevelopmental therapy in children and young people with TBI.
6.1.5 Communication and language rehabilitation
recommendations
grade
A person with traumatic brain injury who has specifi c communication diffi culties should be 
B
6
assessed by a speech-language therapist for suitability for speech-language therapy.
A person with traumatic brain injury who has specifi c communication diffi culties where 
A
achievable goals are identifi ed, should be offered an appropriate treatment programme, with 
monitoring of progress.
A communication rehabilitation programme should: 
•  take into account the person’s premorbid communication style and any cognitive defi cits 
C
•  provide the opportunity to rehearse communication skills in naturalistic situations 
C
•  include the family/wha¯nau and carer(s) in developing strategies for optimum 
C
communication 
B
•  include communication aids where appropriate.
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
good practice points
A communication rehabilitation programme should provide compensatory strategies.

children and young people
Assessment and intervention for communication defi cits in children should be appropriate to 

their age and development.
Assessments and the development of communication rehabilitative strategies for children 

and young people should be done by paediatric speech-language therapists with expertise in 
traumatic brain injury.
This is the opinion of the Guideline Development Team, or feedback from consultation within New Zealand where no evidence is available.
TBI can affect communication in different ways.8 Following a TBI, people may have communication impairments, 
including speech production impairments, which impact on intelligibility and problems with receptive and 
expressive language including reading and writing, and higher-level language skills such as pragmatics and 
more general social interaction. Speech-language therapy intervention should therefore target as necessary: 
•  motor speech production and reduced intelligibility, including disorders of the voice
•  receptive or expressive language skills (including reading and writing) 
•  ‘high level’ abstract language skills and social interaction skills, including social appropriateness.
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6.1.5.1 Interventions and strategies
A person who, post-TBI, has specifi c communication diffi culties should be assessed by a speech-language 
therapist to assess their suitability for intensive or regular speech-language therapy treatment. Where 
achievable goals can be identifi ed, and continuing progress demonstrated, they should be offered an 
appropriate treatment programme, with monitoring of progress.8 The programme should: 
•  take into account the person’s premorbid communication style and any underlying cognitive defi cits 
•  give the opportunity to rehearse communication skills in situations appropriate to the context in which the 
person will live/work/study/socialise after discharge 
•  include the family/wha¯nau and carer(s) in developing strategies for optimum communication within the 
immediate social circle 
•  consider the need for communication aids including gesture drawing, communication charts and 
computerised systems8
•  provide compensatory strategies to manage communication disturbances.
6.1.5.2 Interventions and strategies for children and young people
Assessment and intervention for communication defi cits in children should be appropriate to their age and 
development. Many interventions will be implemented through special education services (see Chapter 12, 
Children and young people and traumatic brain injury). It is important that assessments and the development 
of communicative and rehabilitative strategies be done by people with expertise in the management of children 
with TBI.
6.1.6 Cognitive rehabilitation 
recommendations
grade
Where cognitive impairment is causing management diffi culties or limiting the response to 
C
rehabilitation, specialist advice should be sought.
People with persistent cognitive defi cits following traumatic brain injury should be offered 
B
functionally oriented cognitive rehabilitation.
Cognitive rehabilitation should include:
•  in the acute phase, management in a structured and distraction-free environment and 
A
targeted programmes for those with executive diffi culties 
B
•  attempts to improve attention and information-processing skills 
C
•  teaching compensatory techniques
A
•  the use of external memory aids.
Trial-and-error learning should be avoided in people with memory impairment.
B
A trial of methylphenidate may be considered for adults or children with traumatic brain injury 
C
who have defi cits in the speed of mental processing or attention defi cit hyperactivity disorder 
secondary to traumatic brain injury.
A trial of donepezil hydrochloride may be considered for adults with traumatic brain injury 
C
who have defi cits in memory and sustained attention.
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
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good practice points
Cognitive rehabilitation should include procedural learning information and principles.

Any trial of medication for people with traumatic brain injury should be commenced at low 

doses, with cautious increases in dosage, and be monitored for effectiveness and adverse 
side effects.
Any trial of medication for a person with traumatic brain injury should be preceded by a clear 

explanation to the person with traumatic brain injury and their carer(s), and a caution that 
effects of medications are less predictable in people with traumatic brain injury.
This is the opinion of the Guideline Development Team, or feedback from consultation within New Zealand where no evidence is available.
children and young people
6
There is no adequate evidence in this area specifi cally for children and young people with TBI that can be 
used to guide decision-making. The information and recommendations for adults should be used with 
caution in these groups.
The nature of cognitive defi cits resulting from TBI depends, to some extent, on the severity and location of the 
injury. Cognitive defi cits can include: diffi culties in understanding and/or producing speech; diffi culties with 
attention, memory and the ability to concentrate; diffi culties with initiating and planning daily activities; and 
impairments in other cognitive tasks such as reasoning, judgement, initiation, planning, problem-solving and 
decision-making. Relatively minor impairments in areas such as prioritising and decision-making can have a 
profound effect on functioning. 
Although the physical and behavioural effects of TBI often present signifi cant challenges for rehabilitation, the 
cognitive defi cits may be the most diffi cult for families/wha¯nau, carers and employers to recognise, accept 
and accommodate. This diffi culty may be relatively greater in the case of people with TBI who have few or no 
physical symptoms detectable to the observer, when the people around them may be unable to understand 
why, for example, they cannot remember and follow instructions, or why they sometimes act inappropriately. 
Limitations of the injured person’s insight and awareness of their own diffi culties, in particular, may impact on 
their ability to engage effectively in rehabilitation, and may therefore affect the timing of intervention. 
6.1.6.1 Targets and interventions
The aim of cognitive rehabilitation is both restorative and remedial. Intellectual defi cits may be lessened by 
various repetitive exercises and compensatory or adaptive cognitive rehabilitation, where adaptive devices and 
strategies, together with modifi cation of the environment, are used to try to restore functioning by minimising 
the negative impact of the symptoms that persist. There are four possible strategies involved: 
1.  attempting to restore function
2.  attempting to teach skills to reduce the impact of the defi cits resulting from the TBI
3.  modifying tasks or the environment to aid the performance of tasks
4.  using behavioural approaches such as feedback and reinforcement to support the learning of skills and 
strategies.121 
6.1.6.2 Cognitive management
Where cognitive impairment is found to be causing management diffi culties or limiting the response to 
rehabilitation, specialist advice should be sought.8
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Cognitive rehabilitation has been shown to be effective, although the effectiveness of specifi c interventions 
is unclear.10,100,101,140,141 People with persistent cognitive defi cits following TBI should be offered cognitive 
rehabilitation. This may include:
•  management in a structured and distraction-free environment and targeted programmes for those with 
executive diffi culties (ie, problems with planning, organisation, problem-solving and divided attention), in 
the acute phase142
•  attempts to improve attention and information-processing skills100
•  teaching compensatory techniques to overcome their everyday problems8
•  the use of external memory aids to enhance independence in the presence of memory defi cits143
•  procedural learning information and principles.
Trial-and-error learning should be avoided in people with memory impairment,8 as it tends to reinforce 
unwanted outcomes/behaviours.
6.1.6.3 Specifi c interventions in cognitive rehabilitation
There is good evidence that cognitive rehabilitation is benefi cial for people with TBI and there is no evidence of 
harm. Although one Health Technology Assessment report concluded that the evidence of benefi cial results was 
ambiguous, this report was based on a limited evidence base and only considered particular interventions.140
Another recent robust and comprehensive systematic review concluded that: 
•  functionally oriented cognitive therapy can help adults with TBI to cope with their disabilities and may aid in 
the recovery of cognitive function
•  there is no good evidence that restorative cognitive therapy enhances neuronal recovery or repair or that the 
repetitive cognitive exercises improve functional outcomes
•  there is some evidence that intense, comprehensive-holistic, highly structured programmes that include 
compensatory cognitive therapy can be more effective than more traditional speech, occupational and 
behavioural therapy, although some studies provided confl icting results
•  there is insuffi cient evidence to make specifi c recommendations regarding personal selection criteria for 
specifi c therapies.141
However, the heterogeneous nature of the population of people with TBI, the interventions used in cognitive 
rehabilitation, and the various measures used means that there is little evidence for individual interventions. 
The systematic review above found that there is insuffi cient evidence to draw any conclusions about which 
cognitive rehabilitation programmes are most effective.141 
Many of the complementary and alternative therapies used for TBI primarily, but not exclusively, address 
cognitive defi cits. See Chapter 7, Complementary and alternative medicines.
6.1.6.3.1 Medications for cognitive defi cits
People with TBI may be more sensitive (ie, have a ‘low threshold’) to the effects (positive and negative) of 
medications. Any trial of medication for people with TBI should be commenced at low doses, with careful 
monitoring for both effectiveness and adverse side effects, and cautious increases in dosage. There also needs 
to be a clear explanation to the person with TBI and their carer(s) with a caution that effects of medications are 
less predictable in people with TBI.
There is very little evidence for the effectiveness of medications for the cognitive sequelae of TBI, and input 
from a neuropsychiatrist or other appropriately trained and experienced clinician is advisable before any trial of 
medication.
See MedSafe data (www.medsafe.govt.nz) for contraindications and side effects of medications listed in this 
section.
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6.1.6.3.1.1 Amantadine
Amantadine has been proposed for the treatment of behavioural, motivational and cognitive defi cits in people 
with TBI. However, the small trials in this population have produced confl icting results. The only randomised 
controlled trial in a rehabilitation population (of only 10 people) showed no improvement over placebo.144–146 
A randomised cross-over trial of amantadine versus placebo in 35 hospitalised people with severe TBI showed 
more rapid improvement in the intervention group on primarily cognitive measures, but no difference between 
the two groups by six months.147 There is insuffi cient evidence of the effectiveness of amantadine in people with 
TBI on which to base a recommendation.
6.1.6.3.1.2 Bromocriptine
One small uncontrolled trial of bromocriptine to treat poor motivation in people with TBI was identifi ed. 
Improvements were found in anxiety and depression, and cognitive tests sensitive to motivation or frontal 
lobe involvement were found. However, there were some methodological issues with this study, and there is 
insuffi cient evidence from which to draw conclusions about effectiveness.148 
6
6.1.6.3.1.3 Methylphenidate and amphetamines
A Cochrane review of the effectiveness of methylphenidate and amphetamines used in the acute stage to 
promote recovery from TBI found no evidence of benefi t.149 
A further recent systematic review of methylphenidate treatment of ADHD secondary to TBI in children, 
adolescents and adults found that methylphenidate showed benefi cial effects on hyperactivity and impulsivity 
but smaller effect sizes than observed in primary ADHD, and no robust effect on cognition. A more favourable 
outcome was associated with the initiation of treatment soon after the injury, although this factor was not 
systematically studied, and with trials with relatively long durations. It was concluded that robust trials in this 
population were needed before any recommendation may be made for routine treatment.150 
A small randomised controlled trial of 23 people aged 16 to 64 years with moderate to severe TBI found 
that sub-acute administration of methylphenidate appeared to enhance the rate but not the ultimate 
level of recovery as measured by the DRS and tests of vigilance.151 A further randomised controlled trial of 
methylphenidate used in people with TBI who had been referred specifi cally for assessment and treatment 
of attentional defi cits found that the participants in the treatment arm showed signifi cant improvement in 
the speed of mental processing. It was concluded that methylphenidate may be a useful treatment in TBI for 
symptoms that can be attributed to slowed mental processing.152 
Therefore, there is insuffi cient evidence on which to base any recommendation for routine use of 
methylphenidate and amphetamines in the treatment of people with TBI. However, a trial of methylphenidate 
may be considered where the person has defi cits in speed of mental processing.
6.1.6.3.1.4 Donepezil hydrochloride and other cholinergic agents
A non-systematic review reported that there is some weak evidence that cholinergic agents may be of use 
for the treatment of attention and memory defi cits following a TBI.153 A single uncontrolled trial of three 
acetylcholinesterase inhibitors (donepezil, galantamine and rivastigmine) for the treatment of fatigue, poor 
memory, diminished attention or diminished initiation in people with chronic, stable TBI found that 61% of 
participants had a marked positive response, with almost all responders reporting better vigilance and attention 
leading to better general function. Fifty-fi ve percent of people wanted to continue therapy.154 
One small randomised controlled trial found benefi ts from donepezil hydrochloride on measures of memory 
and sustained attention in people with TBI, benefi ts which may have been sustained after treatment cessation, 
although that is diffi cult to ascertain from this study.155 Several further uncontrolled trials of donepezil in people 
with TBI also reported positive effects on cognition.156–160 
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Thus, although there is insuffi cient evidence on which to base a recommendation for routine treatment with 
cholinergic medication, a trial of donepezil hydrochloride may be considered where the person has defi cits in 
memory and sustained attention. 
6.1.6.4 Cognitive rehabilitation in children and young people
A recent systematic review concluded that there is little evidence for or against cognitive rehabilitation for 
children and young people with TBI.141 In the absence of evidence there is no reason to suspect that the benefi ts 
found for adults would not apply to children when programmes are adapted for this age group. 
Cognitive rehabilitation for children and young people needs to address not only the aim of regaining lost 
functionality, but also the ongoing need to develop more advanced cognitive skills as the child matures. The 
child with TBI will require regular monitoring for the appropriateness and effectiveness of cognitive rehabilitative 
strategies, and the development and implementation of new programmes and compensatory techniques to 
match the needs of the developing child.
Cognitive rehabilitation of children and young people with TBI may be delivered by teams of people from 
neuropsychology, occupational therapy and speech-language therapy, or through educational interventions by 
Group Special Education. See also Chapter 12, Children and young people and traumatic brain injury
Home-based cognitive therapy becomes increasingly appropriate as children reach an age when they would 
usually be expected to become more independent of their families. For example, external memory aids and 
compensatory techniques to assist planning, organisation and problem-solving will help children to become 
more independent of their caregivers.
6.1.6.4.1 Medication for cognitive defi cits in children and young people
6.1.6.4.1.1 Amantadine
Only one case-controlled study of amantadine for the treatment of cognitive impairments in an adolescent 
population (aged 13–18 years) with TBI was identifi ed. The treatment group had a greater improvement 
in functioning than the control group, but the treatment group was more impaired at the start of the trial. 
Subjective improvements were noted in 63% of the treatment group. Nine percent had adverse effects such 
as hallucinations, delusions, increased aggression and nausea/vomiting, which reduced if the dosage was 
decreased or the treatment stopped.161 There is insuffi cient evidence on which to base a recommendation for 
the routine treatment of children with TBI with amantadine.
6.1.6.4.1.2 Stimulants
There is little robust research on the use of stimulant medication in children and young people with TBI. One 
small (n=10) randomised controlled trial of the use of methylphenidate found no signifi cant differences 
between methylphenidate and placebo on measures assessing behaviour, attention, memory and processing 
speed.162 A systematic review of methylphenidate treatment of ADHD secondary to TBI in children, adolescents 
and adults cited above concluded that there is insuffi cient evidence for any recommendation for routine 
treatment.150 This echoes the evidence for use in adults above. There is therefore no evidence on which to base 
a recommendation for the use of methylphenidate or other stimulant medication in this population. However, 
treatment providers may consider a trial of medication, particularly if there is historical evidence of pre-injury 
ADHD symptoms. In that case, target symptoms should be clearly identifi ed before the trial, and effects (both 
benefi ts and adverse effects) should be monitored across more than one setting. The incidence of side effects is 
higher in children with neurological injury, so dosages should start low.
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6.1.7 Psychosocial/Behavioural rehabilitation
recommendations
grade
People with traumatic brain injury should be provided with access to specialist psychological 
C
assessments and interventions to assist in the management of their behavioural diffi culties, 
including substance abuse.
People with severe behavioural problems, especially those with a tendency to wander, should 
C
be referred to specialist behavioural management services.
When there is severe behavioural disturbance, supervision and behavioural management by a 
C
professional trained in behavioural management should be provided.
In the case of people with severe behavioural problems, especially those with a tendency 
C
6
to wander, the interdisciplinary team should develop an integrated approach to manage 
behaviour and refer to specialist behavioural management services when necessary.
Families/Wha¯nau and carers should be given information and ongoing support as required 
C
to help them to understand cognitive and behavioural problems, and guidance on how to 
interact appropriately with the person with traumatic brain injury and how to access services.
Psychotropic medications used to manage agitation and aggression in people who have had 
C
a traumatic brain injury should be carefully selected for their side effect profi les, and the use 
and effectiveness closely monitored.
If no effect is observed within six weeks, the drug should be ‘tailed off’ and another drug 
C
trialled after a suitable wash-out period.
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
good practice points
Treating clinicians should ask about the use of any non-prescription medicines, supplements 

and complementary or alternative medicines.
When necessary, an assessment by a neuropsychiatrist should be made to differentiate 

neurobehavioural diffi culties from symptoms of a functional illness.
A person with traumatic brain injury who may require medication for irritability and aggression 

should be referred to a neuropsychiatrist for treatment.
This is the opinion of the Guideline Development Team, or feedback from consultation within New Zealand where no evidence is available.
children and young people
There is no adequate evidence in this area specifi cally for children and young people with TBI that can be 
used to guide decision-making. The information and recommendations for adults should be used with 
caution in these groups.
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A person who has suffered a TBI may show psychosocial/behavioural effects from the injury. These may 
include outwardly detectable changes in behaviour and personality, such as irritability, agitation, impulsivity, 
disinhibition and verbal and/or physical aggression. There may be changes in mood, with effects such as 
emotional lability, depression, anxiety and suicidality, and sexual diffi culties. Changes in the person’s 
relationships with other people may also occur, with the person being more egocentric and isolated. These 
behavioural changes often cause negative responses from family/wha¯nau, friends and other people, including 
employers, with whom the person with the TBI has contact, and this may impede the person’s recovery. 
Diffi culties in this area of functioning were reported by families as hardest to cope with after TBI. These changes 
can lead to social isolation and people may need access to advocacy, and families/wha¯nau may require ongoing 
support.10 
One longitudinal study of people with TBI found that families may recognise more behavioural changes than 
practitioners. It found that families identifi ed behaviour change in about 80% of the people with TBI, and that 
more behavioural problems were reported by families than by nurses at hospital. Behavioural symptoms also 
appeared to worsen over the three years of the follow-up, with an increase in aggressive behaviour. There was 
no correlation between behaviour change and age or the severity of the injury as measured by post-traumatic 
amnesia.163 
Specifi c issues relating to post-TBI mental health, including treatment, are addressed in Chapter 14, Special 
issues.
6.1.7.1 Targets and interventions
The aim of behavioural rehabilitation is to aid recovery, improve functioning where possible, and provide 
strategies to minimise the negative impact of the symptoms that persist.
6.1.7.1.1 Behaviour management
A variety of unwanted or antisocial behaviours may sometimes develop after brain injury, including verbal 
or physical aggression, sexual disinhibition and attention-seeking behaviour.8 Longitudinal studies suggest 
that planned behavioural modifi cation programmes, consistently applied, are effective in preventing these 
undesired behaviours from becoming established.8
In the case of people with severe behavioural problems, especially those with a tendency to wander, the 
interdisciplinary team should develop an integrated approach to manage behaviour, and referral to specialist 
behavioural management services may be required.7,8 In the event of severe behavioural disturbance, 
appropriate supervision (including one-on-one supervision when required) by a professional trained in 
behavioural management should be provided to ensure the safety of the person and those around them, and to 
provide effective behavioural management.8
If the problems persist or worsen over more than two weeks, or if they give rise to severe concern for safety, and 
cannot be managed in the community, the person should be transferred to a secure residential specialist unit to 
provide a safe environment and specifi c assessment and treatment.8
People with TBI should be provided with access to specialist psychological assessment and interventions to 
assist in the management of their behavioural diffi culties, including substance abuse.8,164,165 Families/Wha¯nau 
and carers should be given specifi c information and ongoing support as required to help them to understand 
the nature of cognitive and behavioural problems, and guidance on how to interact appropriately with the brain-
injured person and how to access services.8
6.1.7.1.2 Training for parents who have traumatic brain injury
There is some evidence that errorless compliance training, a non-coercive intervention for improving child 
compliance, may be an effective intervention for parents with cognitive and behavioural impairments that 
decrease their potential to benefi t from traditional parenting approaches. A small uncontrolled trial of errorless 
104
 
   
   
 

compliance training for parents with TBI of oppositional children (ages two to seven years) found generalised 
and durable increases in child compliance. Improvements were also reported in parent self-esteem.166 
Although the evidence in this area is not robust and insuffi cient on which to base a recommendation for routine 
application for all parents with TBI, consideration should be given to the provision of errorless compliance 
training for people with TBI who are having diffi culties with non-compliant children. 
6.1.7.1.3 Medication for behaviour management
A recent systematic review of pharmacological interventions found that there was insuffi cient evidence to 
determine whether any medications are effective in the treatment of behaviour disorders in people with TBI.167 It 
was reported that there is some weak evidence (based on case studies) that psychostimulants may be effective 
in the treatment of apathy, inattention and slowness, and that high-dose beta-blockers, anticonvulsants and 
antidepressants, particularly selective serotonin reuptake inhibitors (SSRIs), are effective in the treatment of 
agitation and aggression. Some medications, particularly lithium and dopaminergic drugs, can cause adverse 
effects and deterioration. 
6
behaviour management in children and young people
Children and young people may have behavioural sequelae following severe TBI. However, there is little 
evidence specifi cally on behaviour management interventions in children and young people with TBI. 
In New Zealand, this is often managed through Group Special Education and family interventions such 
as parenting initiatives. See Chapter 12, Children and young people and traumatic brain injury for more 
details.
6.1.7.2 Management of emotional and personality issues
Anxiety, depression and other mental health conditions, including substance abuse, are common after TBI and 
often increase if not identifi ed and treated. For more details of management see Chapter 14, Special issues.
Many ‘over-the-counter’ products may cause symptoms of emotional and personality issues, and/or may 
interact with prescribed medications. It is important that the treating health care practitioner asks about the use 
of any supplements and complementary or alternative medicines.
6.1.7.2.1 Irritability, agitation and aggression
In a review of post-TBI irritability, agitation and aggression, it was found that, of people with mild TBI, about 
a third report irritability as a symptom. Thirty percent to 35% of people with mild TBI described irritability one 
year after injury. Furthermore, this was the most commonly reported neurobehavioural symptom. The severity of 
injury did not affect the prevalence of irritability, and while the frequency of most other symptoms decreased or 
stabilised over time, reports of irritability increased between six months and a year after insult. In people who 
had suffered a severe TBI, irritability (as reported by family members) was present in 67% a year post-injury, and 
as prevalent (64%) amongst a separate sample fi ve years post-injury.164 
Acute-onset irritability is probably primarily attributable to organic dysfunction, while late-onset irritability may 
be secondary to a mood disorder arising from poor adjustment to physical and social impairment.164 Symptoms 
of TBI may sometimes be mistaken for mental illness and thus lead to administration of inappropriate and 
ineffectual medications. In some cases, assessment by a neuropsychiatrist can aid in differential diagnosis. 
Also see Chapter 14, Special issues.
Aggression may be exhibited acutely or delayed by some time post-injury and, particularly when manifested 
physically, can distress and endanger carers and practitioners. It may also impact on the rehabilitation of the 
person with TBI, as it may result in exclusion from programmes. Risk assessments should be performed using 
empirically validated, actuarial risk-assessment measures, which are more accurate than clinical judgement 
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alone.168 Family/Wha¯nau and carers should receive support and training in how to manage this behaviour and 
protect their own safety. Also see Chapter 13, Needs of carers.
6.1.7.2.1.1 Pharmacological management of post-traumatic brain injury agitation and aggression in adults
The administration of sedating medication is an appealing option in the management of aggression, as the risks 
imposed by this behaviour are substantially and rapidly reduced. However, while sedation may sometimes be 
appropriate as an emergency measure, it is not acceptable as a long-term solution for the majority of people. In 
most cases, pharmacological restraint will not target the factors underlying irritability and aggression, and it will 
hinder adequate assessment.164 A further drawback is that sedation is not specifi c to suppressing aggressive 
behaviour; all, including appropriate, behaviour will be affected.
Another unwelcome consequence will be to depress further the person’s impaired cognitive functioning, thereby 
hindering new learning (including the acquisition of adaptive behaviours). Finally, people with TBI are very 
sensitive to medication, and undesirable side effects can in themselves prove debilitating. For example, while 
psychostimulants are used in the treatment of distractibility and impulsivity, a potential side effect is increased 
irritability.164 Therefore, it is important that people who may require medication should be discussed with, or 
referred to, a neuropsychiatrist for treatment.
A Cochrane systematic review evaluated the effectiveness of various psychotropic medications used to 
manage agitation and aggression in people who have had a TBI. The conclusion of the reviewers was that while 
numerous drugs have been tried, there is little good evidence to support their effectiveness in this population. 
They suggest that drugs be carefully selected for their side effect profi les, and the use of and effectiveness for 
the individual with TBI be closely monitored. The effects of medication are generally observed within two to six 
weeks from starting medication. It was suggested that if no effect is observed within six weeks, the drug should 
be ‘tailed off’ and another drug trialled after a suitable wash-out period.169
6.2  Optimising performance in daily living tasks 
recommendations
grade
daily living  skills
All daily living tasks should be practised in the most realistic and appropriate environment, 
C
with the opportunity to practise skills outside therapy sessions.
An individual treatment programme aimed at maximising independence in the areas of self-
C
maintenance, productivity and leisure should be developed and implemented.
Family and carers should be involved in establishing the most appropriate routines for 
C
activities of daily living for people with traumatic brain injury, which take account of their 
lifestyles and choices.
All people with traumatic brain injury who have diffi culties in activities of daily living should 
C
be assessed by an occupational therapist, nurse or other health care practitioner with 
expertise in brain injury and experience in this area.
Services should recognise that the provision of ‘care’ for some people with traumatic brain 
C
injury may mean the supervision and practice of community living skills, rather than hands-on 
physical care.
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recommendations
grade
equipment and technology
People with traumatic brain injury who have diffi culties in functioning should be assessed 
C
by people with expertise in this area, to determine whether equipment or adaptations could 
increase their safety or independence.
The need for equipment should be assessed on an individual basis and in the environment in 
C
which it will be used.
The prescription of equipment should take account of any cognitive and behavioural defi cits 
C
and their constraints on the person’s ability, or their carer’s ability, to use the equipment 
safely and appropriately. Where this is in doubt, arrangements should be in place for regular 
6
review.
When an item of equipment has been identifi ed as required for a person with traumatic brain 
C
injury, it should be provided as quickly as possible and before the person is discharged to the 
community.
The person, their family/wha¯nau or carer(s) should be trained in the safe and effective use of 
C
equipment.
The ongoing effectiveness of equipment should be reviewed on a regular basis and in 
C
accordance with the manufacturers’ guidelines.
People and their families/wha¯nau and carers should be given clear written information on 
C
who to contact for repairs, replacement or future help and advice regarding the equipment.
Where necessary, a specialist assessment of each individual’s ability to use a personal 
C
computer should be arranged and the need for adapted hard- and software recorded.
Rehabilitation teams should consider computers and other technology as adaptive sources of 
C
meaningful occupation or as compensatory strategies for people with signifi cant sequelae of 
brain injury.
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
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good practice points
daily living  skills
Carers and family, if willing and acceptable to the person with traumatic brain injury, should 

be trained and supported to help with therapy.
equipment and technology
People with traumatic brain injury should be given information and advice about changes in 

technology and computer use relevant to their needs.
The assessment for, and prescription of, augmentative communication devices should be 

made by suitably accredited clinicians.
Careful consideration should be given to the appropriateness of technology for individuals 

who may be vulnerable, such as people with symptoms of disinhibition or impaired 
judgement. Caution and monitoring of the person’s use of the technology may be necessary in 
some cases.
This is the opinion of the Guideline Development Team, or feedback from consultation within New Zealand where no evidence is available.
6.2.1 Activities of daily living 
children and young people
There is no adequate evidence in this area specifi cally for children and young people with TBI that can be 
used to guide decision-making. The information and recommendations for adults should be used with 
caution in these groups.
People with TBI who have diffi culties in activities of daily living should be assessed by an occupational therapist 
with expertise in brain injury, and an individual treatment programme aimed at maximising independence in 
areas of self-maintenance, productivity and leisure should be developed and implemented.8
The majority of rehabilitation interventions undertaken by the TBI rehabilitation team are aimed at minimising 
impairments and maximising performance in daily living tasks. These tasks include basic self-care and more 
extended activities of daily living (eg, shopping and meal preparation), work and leisure activities. To maximise 
new learning and the relearning of old skills, evidence suggests that activities should be practised in a 
naturalistic and realistic environment. Ideally, this should be the person’s own home and local environment 
with the opportunity to practise skills outside therapy sessions.8 Independence is achieved through practice, 
the learning of adaptive techniques, and the provision of equipment and/or environmental adaptation. Family/
Wha¯nau and carers should be involved in establishing the most appropriate routines for activities of daily living 
which take account of the injured person’s lifestyle and choices,8 and family/wha¯nau and carers should be 
trained and supported to help with this. Services and funders should recognise that the provision of ‘care’ for 
some people with TBI may mean the supervision and practice of community living skills, rather than hands-on 
physical care.8 
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6.2.2 Provision of equipment and adaptations
children and young people
There is no adequate evidence in this area specifi cally for children and young people with TBI that can be 
used to guide decision-making. The information and recommendations for adults should be used with 
caution in these groups.
The provision of equipment or adaptations provides a solution to the individual’s unique needs within their own 
environment. There is strong evidence for the general benefi t and cost effectiveness of equipment provision for 
people who need it, albeit not in the TBI population.8
Every person with TBI who has diffi culties in functioning should be assessed to determine whether equipment 
or adaptations could increase their safety or independence.8 The need for equipment should be assessed on 
an individual basis and in the environment in which it will be used.8 The prescription of equipment should 
6
take account of any cognitive and behavioural defi cits and their constraints on the person’s ability to use the 
equipment safely and appropriately. This also applies to equipment for use solely by the person’s carer(s). 
Where this is in doubt the equipment provider should be responsible for ensuring that arrangements are in 
place for regular review.8
Once an item of equipment has been identifi ed as required for a person with TBI, it should be provided as 
quickly as possible8 and before the person is discharged to the community. The person, their family/wha¯nau 
and/or carer(s) should be thoroughly trained in its safe and effective use. Its ongoing use and relevance should 
be reviewed on a regular basis and in accordance with the manufacturer’s guidelines.8 People should be given 
clear written information on who to contact for repairs, replacement or future help and advice regarding the 
equipment.8
6.2.3 Computers and assistive technology
Personal computers have increasingly become routine household items. As well as providing a useful adjunct 
to therapy in some areas, they offer opportunities for sedentary recreation and social interaction (via e-
mail).8 In some cases the acquisition of computer skills may also provide opportunities for employment. The 
increasing availability of adapted hardware and software can also offer an alternative means of writing for those 
who are no longer able to hand write.8 This can also provide augmented communication and be linked with 
environmental control systems.8
Other new technology, such as cellphones, pagers and personal digital assistants, can also be very useful. One 
large study found that there were signifi cant differences in case closure status and expenditure on vocational 
rehabilitation for people with TBI who were provided with assistive technology compared with those who were 
not, although there were no signifi cant differences in the average earnings of the two groups.170 
Rehabilitation teams should routinely consider computers and other technology as adaptive sources of 
meaningful occupation or as compensatory strategies for people with signifi cant sequelae of brain injury.8
People with TBI should be given information and advice about changes in technology and computer use relevant 
to their needs. Where necessary, a specialist assessment of each individual’s ability to use a personal computer 
should be arranged and the need for adapted hardware and software recorded.8
However, careful consideration of the appropriateness of technology for individuals with TBI is necessary. 
People with symptoms of disinhibition or impaired judgement may be particularly vulnerable to the risks of 
computer technology, such as internet ‘scams’ or predatory behaviour from other users. Caution and monitoring 
of the use of the technology may be necessary in some cases. 
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6.3  Sleep and fatigue 
children and young people
There is no adequate evidence in this area specifi cally for children and young people with TBI that can be 
used to guide decision-making. The information and recommendations for adults should be used with 
caution in these groups.
Sleep diffi culties and fatigue are two very common problems following TBI of all severities. The two problems do 
not necessarily go together, although sleep disturbance can certainly contribute to fatigue. People with TBI and 
health care practitioners recognise two ‘types’ of fatigue:
1.  ‘cognitive fatigue’, where mental effort without physical exertion leads to severe tiredness and an inability to 
proceed 
2.  ‘physical fatigue’, where smaller than expected amounts of physical exertion lead to severe tiredness and an 
inability to proceed.
Fatigue is one of the most frequently reported symptoms following TBI. It often also poses a barrier to return 
to work or other daily activities. There is virtually no good quality evidence relating to its extent, impact and 
effective treatment. The management of fatigue is an important goal of rehabilitation post-injury. It is also 
thought that fatigue may have impact on other symptoms of TBI (eg, headaches, or cognitive and behavioural 
symptoms) which are often reported to be exacerbated when the person is tired. 
Medications sometimes used to help with fatigue following TBI have not undergone investigation in this 
population and should be used cautiously, if at all.
The management of fatigue is sometimes hampered by poor insight, so that while caregivers may recognise the 
impact of the increasing fatigue, this may not be recognised by the person themselves. 
One contributing factor in the development of fatigue may be the development of sleep disorders, including 
diffi culties in both the onset and maintenance of sleep, or changes to the sleep/wake cycle. If these diffi culties 
persist they can then lead to the typical symptoms associated with chronic sleep deprivation. 
Good management of sleep diffi culties can be counter intuitive; for example, a common response to poor sleep 
is to try to stay awake longer during the day, the thought behind this being that the person would be really tired 
by the time they went to bed. However, this may generate an overtired state, with consequent sleep disturbance 
and exacerbated symptoms. Advice from a professional experienced in managing fatigue and/or sleep disorders 
can be useful in establishing a suitable treatment programme. 
6.4 Vocational 
rehabilitation 
recommendations
grade
People with traumatic brain injury should be assessed for the need for vocational 
A
rehabilitation to assist their return to work, or for entering the workforce for those not 
previously employed, and vocational rehabilitation should be provided to those found to
need it.
Standard vocational rehabilitation interventions such as cognitive training and behaviour 
A
modifi cation should be monitored for effectiveness, and supported employment provided for 
those for whom the standard interventions are insuffi ciently effective.
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recommendations
grade
Supported employment should include these fundamental aspects:
B
•  job placement, including:
−  matching job needs to abilities and potential
−  facilitating communication between the person, the employer and carers
− arranging travel/training
−  proactive assessment of the job environment for potential problems by someone with 
expertise in this area
•  job site training and advocacy by the job coach including:
− training
− proactive identifi cation of problems
−  designing solutions in cooperation with the person with traumatic brain injury, carers 
and employers
6
−  ongoing assessment with continuous monitoring of key aspects of the person’s 
performance in work
•  job retention and follow-up by the job coach including:
−  monitoring of progress to anticipate problems and intervene proactively when 
necessary.
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
Return to employment or an alternative occupation is a primary goal and a critical factor in the restoration of 
quality of life for people with TBI. If people with TBI are unable to access, return to or remain in previous or 
alternative employment, there are major economic implications as well as far-reaching consequences for the 
individual and their family/wha¯nau.12 
Not everyone with a TBI will need the same degree of vocational rehabilitation. A systematic review reported 
that 60–85% of people with a mild TBI, 50–60% of people with a moderate TBI, and 20–30% of people with a 
severe TBI were re-employed by one year post-injury,10 so the need for vocational rehabilitation is likely to be 
greater the more severe the injury. Many children with severe TBI will have diffi culty in establishing themselves 
in employment on leaving school171 and may require specialist vocational assessment, advice and support. 
There is also some evidence that women experience more diffi culty with return to work than men.172 
Factors associated with or predictive of return to work include:
• age36,173–175
• sex172 
•  pre-injury level of education45,174–176 
•  pre-injury employment status36 
•  possession of qualifi cations175 
• pre-injury 
occupation177 
•  pre-injury psychiatric history176 
•  pre-injury drug and alcohol use176 
• injury 
severity176,178
•  mechanism of injury including violent mechanism176 and fall59
•  duration of loss of consciousness at time of injury45,174
• post-traumatic 
amnesia5,178 
•  level of disability at discharge174,176,177 
•  Glasgow Outcome Scale at six months179 and at fi ve years post-injury (in people with childhood TBI)180 
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• cognitive 
functioning45,175,178 and specifi c cognitive variables, including verbal memory, verbal fl uency and 
mapped test of planning and strategy173 
•  neuropsychological assessment scores on reading comprehension, immediate and delayed verbal memory, 
level of depression, and dysphasic symptomatology181 
• behavioural 
competence45 
• accurate 
self-awareness 
post-injury182 
•  psychological distress post-injury36,178 
• disability 
post-injury176,183
•  community integration post-injury176
•  social interaction post-injury177
• post-injury 
employment with greater decision-making latitude177 
•  availability of vocational rehabilitation services (vocational guidance and counselling, on-the-job training)184 
•  race (in the USA).185 
6.4.1 Vocational rehabilitation interventions
Those unable to return to paid employment are often not provided with the advice, opportunity and support to 
enable them to fi nd an alternative occupation appropriate to their needs. However, there is consistent strong 
evidence that vocational rehabilitation, such as supported employment, improves vocational outcomes for 
people with TBI in securing sustainable employment or alternative occupations, and is cost-effective.10,186–188 
The return to work of people with TBI who have symptoms that may impact on their employment, whether in 
a previous job or a new one, such as memory problems and planning, may be more durable when any such 
problems are recognised, the appropriate strategies are implemented and the person and their colleagues 
are educated about TBI and its sequelae and impact on employment. Therefore, people with TBI should be 
assessed for the need for vocational rehabilitation to assist their return to work, or for entering the workforce 
for those not previously employed (such as people who sustained a TBI in childhood). Where need is identifi ed, 
the person with TBI should be supported in their employment, or their ability to become employed, which will 
help their ability to participate in employment, and so their ability to earn an income, which will contribute to an 
appropriate quality of life. 
6.4.1.1 Supported employment
Supported employment is only necessary where standard vocational rehabilitation is not suffi cient to achieve 
the desired level of employment for a person with TBI. This may be a short-term transition stage or may be 
long term, especially for people with a severe TBI because regular vocational rehabilitation programmes are 
insuffi cient, and other interventions such as cognitive training and behaviour modifi cation show limited 
success.189
The key feature of supported employment strategies is that they are applied ‘on the job’ in the work 
environment. Supported employment programmes include vocational support (eg, in placement fi nding 
and monitoring, with job coaching, education of employers and colleagues and a plan for progression in the 
workplace that is provided by a specialist vocational rehabilitation provider). 
Training and practice to prepare the person for work may be important, but the job coach always accompanies 
the person to the job site to help them work out on-the-spot solutions to problems as they arise and to facilitate 
communication between them and the employer. Problem-solving on the job is a defi ning principle of supported 
employment. 
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There is strong evidence for the effectiveness of supported employment in improving return to work for 
people with severe TBI.10,186 People with TBI who are not able to return to their previous work or who are 
having diffi culties with their work should receive an assessment of their need for vocational rehabilitation 
and/or supported employment. People with severe TBI should receive an assessment of need for vocational 
rehabilitation and supported employment, even if they have returned to work.12 
A systematic review identifi ed that there are several models of supported employment, including 
apprenticeships, small businesses and work ‘enclaves’. The most common, and the one most appropriate for 
people with TBI, is individual placements, where training and support are provided on an individual basis in 
ordinary work settings. The four fundamental components of supported employment for people with TBI are 
identifi ed below.10
1.  Job placement, including: matching job needs to the person’s abilities and potential; facilitating 
communication between the person with TBI, the employer and carers; arranging travel and/or training; and 
proactive assessment of the job environment for potential problems.
2.  Job site training and advocacy, which dictates an active role for the job coach. The job coach performs 
6
functions usually left to the employer in conventional vocational rehabilitation (such as training), and also 
needs to proactively identify problems and design solutions in cooperation with the person with TBI, carers, 
employers and anyone else involved.
3.  Ongoing assessment with continuous monitoring of key aspects of the person’s performance in work. This is 
usually an intense intervention by the job coach at the beginning of the placement, but is expected to reduce 
as the person successfully adjusts to the work placement.
4.  Job retention and follow-up, where the job coach monitors progress to anticipate problems and intervenes 
proactively when necessary to prevent crises from disrupting the person’s job placement. This may continue 
indefi nitely, but the need is expected to diminish over time. 
6.5 Sexuality
recommendations
grade
The opportunity to discuss issues relating to sexuality should be offered early after signifi cant 
C
traumatic brain injury, to both the person and their partner. This should be initiated by the 
health professionals.
Advice about sexuality should cover both physical aspects (eg, positioning, sensory defi cits, 
C
erectile dysfunction, drugs) and psychological aspects (eg, communication, fears, altered 
roles and sense of attractiveness).
Families/Wha¯nau and carers should be reassured that sexually inappropriate behaviour is not 
C
unusual in people who are in the early stages of recovery from a traumatic brain injury and 
that it should improve with time, and be provided with training in how to avoid inadvertently 
reinforcing the behaviour.
If the sexually inappropriate behaviour is severe, dangerous or persistent, it will need to be 
C
addressed as part of the rehabilitation programme for the person.
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
Sexuality encompasses not only intercourse, but also intimacy, communication and psychological aspects 
including the sense of self-worth, attractiveness and signifi cance of role. Sexual functioning is important and 
desirable for the majority of people, including those who have had a TBI.
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A substantial proportion of people with TBI, particularly at the more severe end of the spectrum, may suffer 
effects on sexuality such as impaired sexual functioning, resulting from both the TBI and medications for 
conditions related to the TBI; and also sexually inappropriate behaviour resulting from behavioural and 
cognitive impairments from the TBI. 
Information, advice and open discussion can be very benefi cial in overcoming sexual problems following TBI, yet 
very few people receive any help. Help needs to be given early and staff need to take the initiative, thus giving 
permission to talk about sex.
6.5.1 Sexual dysfunction
People with TBI may suffer some sexual dysfunction including disorders of desire and an impaired ability 
to achieve or maintain an erection, and an impaired ability to achieve orgasm. This may occur either as a 
consequence of the injury or as a side effect of medication such as antidepressants. It may also occur as a 
psychological result of changed roles within relationships and other issues that may or may not be direct 
consequences of the TBI. 
One study, for example, found that people with TBI, compared with a non-injured control group, reported more 
frequent physiological diffi culties impacting on their sexual energy and drive, and their ability to initiate sex and 
achieve orgasm. The study also found that people with TBI had physical diffi culties impacting on positioning, 
movement and sensation; and body-image diffi culties infl uencing feelings of attractiveness and comfort with 
having a partner view one’s body during sexual activity. 
Men with TBI reported less frequent sexual activity and relationships, and more frequent diffi culties in 
sustaining an erection. Women with TBI reported more frequent diffi culties with arousal, pain, masturbation 
and lubrication. Age at injury and severity of injury were negatively related to reports of sexual diffi culties in 
both men and women with TBI. In men with TBI but without disability, the most sensitive predictor of sexual 
dysfunction was level of depression. For women with TBI, an endocrine disorder and level of depression 
combined was the most sensitive predictor of sexual diffi culties.190 
6.5.1.1 Management of sexual dysfunction
There is very little evidence on the treatment of sexual dysfunction in people with TBI. Most advice for 
rehabilitation focuses on counselling,190,191 but there was no evidence reporting outcomes for counselling 
interventions.
One small uncontrolled study of adults with TBI and SSRI-induced sexual dysfunction reported a trial of the 
addition of mianserin at doses of 7.5–15 mg per day. Improvement in sexual function was reported by 88% 
following this intervention, with 59% reporting that sexual function achieved pre-treatment (with the SSRIs) 
level. Twelve percent did not respond to this intervention and were instead given sildenafi l citrate, which was 
effective.192 Another small uncontrolled trial of an assistive device also reported benefi ts. Thirty men with 
chronic neurological impotence who were offered a trial of vacuum tumescence constriction therapy were 
followed up for an average of 21 months, at which time more than 50% were still actively using the device and 
the average frequency of coitus had increased from 0.3 per week to 1.5 per week (p <0.0001).193 
There is therefore insuffi cient evidence on which to base a recommendation for any routine intervention for 
sexual dysfunction following TBI. 
6.5.2 Sexually inappropriate behaviour
Sexually inappropriate behaviour, also known as hypersexuality, is probably a result of TBI-induced disinhibition 
and can arise in a variety of forms, including frotteurism (eg, rubbing against another person), inappropriate 
touching and sexual comments, exhibitionism, overt sexual aggression and even rape. Surveys show it tends to 
be males who exhibit these behaviours.194
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For example, one review of 477 people admitted to a brain injury hospital in England over fi ve years found 
that 6.5% of them had committed a sexual offence, defi ned as a specifi c event in which the incident resulted 
in a criminal charge, a complaint or intervention. Offences were mainly against staff, but also against family 
members, other people receiving treatment in the hospital and strangers. Nearly 10% of cases included overt 
sexual aggression, and nearly 12% of the incidents were against children. All the incidents were committed by 
males.194 These behaviours can also occur in paediatric populations.195 
Sexually inappropriate behaviour can be emotionally demanding of families/wha¯nau, carers and treatment staff, 
and it may give rise to important legal and management issues and dilemmas. One review of the topic reported 
previously unpublished data showing that 70% of rehabilitation professionals reported that sexual touching 
was a common problem at their facilities, and 20% reported that the use of sexual force by patients was 
common, while 97% claimed that the sexually inappropriate behaviour of such clients had at least a moderate 
impact on the clients’ rehabilitation and community re-entry. Sixty percent of the professionals said they did not 
have adequate training to deal with such behaviour.195 
6
In acute care settings, people with TBI may display themselves in sexually inappropriate ways, masturbate, or 
make inappropriate comments; behaviours which may be best managed by means of the provision of privacy 
and distraction techniques. People with TBI who are in a confused state may make sexual jokes or attempt 
sexual touching of carers or therapists. A clear statement about what is and is not appropriate and removing the 
person’s hand or moving away for a few seconds should be adequate.195 
Family/Wha¯nau members and carers should be reassured that this behaviour is not unusual in people who are 
in the early stages of recovery from a TBI and that it should improve with time, and be provided with training 
in how to avoid inadvertently reinforcing the behaviour.195 However, if the sexually inappropriate behaviour is 
severe, dangerous or persistent, it will need to be addressed as part of the rehabilitation programme for the 
person. The behaviour can be very distressing for family/wha¯nau and carers, who will need support to cope with 
it.196 
There is little evidence of the effectiveness of specifi c interventions, and most research reports individual case 
studies. The following strategies are adapted from a recent review of the topic.195 A neuropsychologist should 
advise which level of approach is suitable for the person with TBI. 
For people with TBI at a basic level of cognitive functioning: 
• establish 
supervision conditions and networks, limiting access to potential victims and avoiding involvement 
in prohibited behaviours (eg, alcohol use) 
•  implement behavioural strategies including role-plays, aversive conditioning or verbal satiation, and 
repetition and reinforcement of desired behaviours
•  clearly differentiate appropriate and inappropriate boundaries and behaviours, and encourage repetition of 
the desired behaviours
•  consider pharmacological interventions
•  incarceration may be necessary in severe cases, and may act as a successful deterrent in some cases.
For people with TBI at an intermediate level of cognitive functioning:
•  provide psychoeducation, including a discussion of interpersonal behaviour and the effect of a brain injury 
on sexuality
• assist 
the individual in understanding the feelings of the recipient(s) of the sexually inappropriate behaviour 
•  the use of videos illustrating the individual’s behaviour and the feelings of others may be useful at this stage
•  encourage consideration of the personal costs of an offence. This is especially important with people who 
have narcissistic and antisocial personality traits
•  foster the practice of broad-based social skills (managing interpersonal contact) in addition to interventions 
specifi cally directed toward the sexually inappropriate behaviour
•  provide a limited discussion about the emotions and thoughts that may increase the risk of an offence.
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For people at a more advanced level of cognitive functioning:
•  establish a relapse prevention plan that includes the relevant antecedents to the sexually inappropriate 
behaviour and identify means of intervening before problematic behaviour occurs
•  challenge those cognitive distortions that allow the individual to minimise or justify sexually inappropriate 
behaviour.
6.5.2.1 Medication for sexually inappropriate behaviour
There is no good evidence for any particular medications for the control of sexually inappropriate behaviour. 
Case studies report successful control of this behaviour with medroxyprogesterone acetate (Depo-Provera).197,198 
However, these studies were uncontrolled and individual cases, and therefore insuffi cient on which to base any 
recommendation.
6.6  Leisure and recreation
recommendations
grade
Traumatic brain injury rehabilitation services should support people with clinically signifi cant 
C
traumatic brain injury in developing alternative leisure and social activities, in liaison with 
local voluntary organisations.
Assessments of all people with traumatic brain injury should include the identifi cation of: 
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•  their level of participation in leisure activities 
•  the barriers or compounding problems which inhibit their engagement in such activities.
People with traumatic brain injury who have diffi culty undertaking leisure activities of their 
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choice should be offered a goal-directed, community-based programme aimed at increasing 
participation in leisure and social activities.
Carers should be given advice on how to maintain their own leisure and social activities while 
C
in a caring role.
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
children and young people
There is no adequate evidence in this area specifi cally for children and young people with TBI that can be 
used to guide decision-making. The information and recommendations for adults should be used with 
caution in these groups.
A return to leisure activities will depend upon both the severity of the TBI and the demands of the leisure activity 
the person wishes to resume. The person will need medical clearance before participating in some activities, 
such as riding, diving and motorbike riding. For details of return to sports and physical activities see Chapter 
14, Special issues. There is a lack of specifi c evidence in this area, and this section is adapted from the UK 
publication Rehabilitation Following Acquired Brain Injury: National Clinical Guidelines.8
Engagement in leisure activities is increasingly recognised as an important determinant of quality of life.199 It is 
consistently highlighted in user surveys, and is now a recognised health domain in the WHO ICF.3 
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People with TBI who do not resume paid employment may have more time to engage in leisure activities. 
However, their ability to engage in these may be inhibited due to: 
•  the cognitive effects of TBI, such as poor executive skills, problem-solving, and decision-making 
•  social and behavioural problems leading to diffi culties in maintaining social relationships 
• environmental 
barriers (such as diffi culty in accessing public buildings and using public transport). 
Targeted problem-solving intervention may be required to help them overcome these diffi culties. 
Community TBI services should guide and support people with clinically signifi cant TBI in developing alternative 
leisure and social activities, in liaison with local voluntary organisations.8,199 Assessments of all people with TBI 
by a rehabilitation professional or team should include the identifi cation of:
•  their level of participation in leisure activities (including indoor and outdoor pursuits) 
•  the barriers or compounding problems which inhibit their engagement in such activities.8
People with TBI who have diffi culty undertaking leisure activities of their choice should be offered a goal-
directed, community-based programme aimed at increasing participation in leisure and social activities.8 Some 
6
targeted programmes for people with disabilities, such as riding or swimming for the disabled, may be helpful.
6.7  Evaluating progress in rehabilitation
The TBI Tools Review for the Development of Guidelines on the Assessment, Management and Rehabilitation of 
Traumatic Brain Injury, 2005, which supports this guideline (see Appendix D for a link to this resource) provides 
an assessment of various tools that may help in evaluating progress in rehabilitation. 
6.8  Discharge from rehabilitation services
Continuous or intermittent input from a rehabilitation team may be appropriate over long periods of time 
following TBI (ie, years) depending on the specifi c goals being addressed. Withdrawal of rehabilitation team 
management may occur appropriately when:
•  the person with TBI wishes to exit from a formal rehabilitation programme
•  no new achievable goals can be identifi ed by the person with TBI and/or their carer(s).
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Chapter 7:
Complementary and alternative medicines
Overview
•  Although many complementary and alternative medicines (CAMs) are advocated for use in people with 
traumatic TBI, there is limited evidence available on their effectiveness.
•  There may be risks of harm or interactions from CAMs. Health practitioners should ask and record what 
people with TBI are using.
• Evidence 
shows 
unacceptable levels of harm from craniosacral therapy in people with TBI.
•  There is no evidence that ginkgo helps cognitive and other impairments following TBI.
There are many therapies and products proposed for use in people with TBI. These are not routine treatments 
and can be grouped under the term ‘complementary and alternative medicine’ or CAM. CAM use in people 
with TBI may be targeted at a particular aspect of functioning (usually cognitive) or at the post-TBI syndrome. 
7
This chapter focuses on the CAMs more commonly advocated for use by people with TBI. The evidence is 
summarised in Table 7.1.
The evidence for CAM is, by nature, ‘emerging’ and this guideline has used a grading system aimed at providing 
plain-language interpretations of the lower levels of evidence that currently exist around CAM. The Guideline 
Development Team has avoided making recommendations in this chapter, so that consumers can weigh the 
evidence presented and in consultation with their advisors reach their own conclusions about whether or not 
they should use a particular treatment for a particular condition. More details of these grades can be found in 
Appendix B and at www.cam.org.nz.
There may be risks of harm or interactions from CAMs. It is important that there is open communication between 
rehabilitation practitioners, CAM practitioners and the person with TBI, their family/wha¯nau and carer(s). It is 
important that the rehabilitation team ask specifi cally about the use of CAMs, including dietary supplements, 
which the person or their carer(s) may not perceive as a ‘therapy’ or ‘medication’.
children and young people
There is no adequate evidence in this area specifi cally for children and young people with TBI that can be 
used to guide decision-making. The information and recommendations for adults should be used with 
caution in these groups.
7.1 Biofeedback
Biofeedback provides feedback of information to the person about some aspect of physical behaviour or 
functioning. Two studies on the use of biofeedback for rehabilitation following TBI were identifi ed. One small 
randomised controlled trial of a standing biofeedback training device for postural training in adults with 
hemiplegia after TBI or stroke found a benefi t from the device.200 A single case study demonstrated benefi ts of 
visual feedback superior to traditional speech therapy for a child with TBI.201 
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7.2 Electroencephalographic 
biofeedback/neurofeedback
Electroencephalographic (EEG) biofeedback, often referred to as neurofeedback, is a test in which electrodes 
are placed on the scalp to measure the electrical activity of the brain. This modifi cation is manifested as 
changes in behaviour or perception.
The literature search found several controlled studies and systematic reviews.202–210 These showed positive 
results in terms of improved outcomes for people with mild to moderate TBI, with both self-reported symptoms 
and independent measures showing improvements in cognitive performance, pain and headache, in some 
cases achieving premorbid functioning in the short term. Studies generally showed an effect after 18 to 20 
sessions of treatment. However, there is not yet enough high-level evidence to identify whether the benefi ts 
observed in these studies are sustained over time. 
7.3 Homoeopathy
Homoeopathy is a system of treating people using very low-dose preparations according to the similia 
principle: ‘like cures like’. In ‘classical’ or individualised homoeopathy, practitioners aim to identify a single 
homoeopathic preparation that matches the person’s general ‘constitution’, including the symptoms for 
which the person is seeking treatment. Owing to differences in elements of people’s constitutions, two people 
with identical conventional diagnoses may receive different homoeopathic prescriptions. It is therefore not 
appropriate to examine the effectiveness of any one remedy applied to all people with TBI.
Only one study of suffi cient quality was found on the use of classical homoeopathy for TBI. This was a 
randomised double-blind placebo controlled trial of 60 adults with mild TBI.211 A total of 18 different remedies 
were used in individualised treatments. The study reported that at the four-month follow-up point, there were 
signifi cant reductions in self-reported symptoms in the treatment group, although there were no improvements 
in standardised cognitive, linguistic or memory tests. The effect or relative benefi t increased with duration from 
injury. Some possible adverse reactions were reported (eg, nausea and dizziness), but the study had insuffi cient 
power to detect whether these were reactions to the treatment.
7.4 Manipulative 
therapies
7.4.1 Craniosacral therapy
Craniosacral therapy is a form of gentle manipulation of the bones of the skull. A systematic review found that 
there is very little research of adequate quality on the use and effectiveness of craniosacral manipulation for 
people with TBI. The one study found that was of moderate quality showed unacceptable levels of harm from 
craniosacral therapy.212 Three out of 55 people in the study showed a ‘very unfavourable response to therapy’, 
including headaches, high blood pressure and spasms. Case series reports cannot defi nitively establish 
a causal relationship between craniosacral therapy and the adverse reactions described. However, these 
documented harmful reactions call into question the safety of craniosacral therapy in this group of people.
7.4.2 Chiropractic
Chiropractic emphasises the ability of the body to heal itself by restoring and maintaining the health of the 
whole person through natural means. Specifi cally, chiropractic aims to restore and maintain joint, muscle and 
nervous system function.
The Guideline Development Team was unable to fi nd any research that met the criteria for review on the use of 
chiropractic in people with TBI.
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7.4.3 Osteopathy
Osteopathy seeks to restore and maintain the health of a person by working on the muscles, joints and other 
structures that make up the neuromusculoskeletal system through gentle manipulative procedures.
The Guideline Development Team was unable to fi nd any research that met the criteria for review on the use of 
osteopathy in people with TBI.
7.5 Herbal 
remedies
7.5.1 Ginkgo
Ginkgo (Ginkgo biloba) extract is one of the most studied complementary medications and one of the most 
commonly recommended complementary medications for people with TBI on internet sites.
Some of the potential benefi ts ascribed to ginkgo include effects on recognition memory, processing speed, 
attention, concentration, mood, tinnitus, sexual dysfunction, nephrotoxicity, glaucoma and claudication. 
Additional potential benefi cial effects, based on analysis of the active constituents, include blockade of cell 
death, antiplatelet activity, free radical scavenging, changes in blood fl ow and protection from anoxia.79,213,214 
A Cochrane review214 and a further review213,214 of ginkgo for cognitive impairment found ginkgo superior to 
7
placebo on a number of measures, but these did not specifi cally review the use of ginkgo in people with TBI. 
A further systematic review79 concluded that ginkgo extract may be valuable for conditions that are commonly 
seen following TBI. There is evidence of effectiveness for treating: tinnitus; impaired cognitive skills including 
memory, concentration, attention and processing speed; and agitation, psychosis and aggression. However, 
the authors caution that there is no good research on the effectiveness of ginkgo extract specifi cally in the TBI 
population, and suggest that research focusing on this area may be warranted. 
Both reviews caution about the side effect profi le of ginkgo extract, as it may have an anticoagulant effect, 
reducing platelet ‘stickiness’. Spontaneous bleeding related to ginkgo extract has been reported. There could 
also be an interaction with other anticoagulant drugs given before surgery.
7.5.2 Ginseng
Most of the research into the effects of ginseng on cognitive skills has focused on either enhancing cognition 
in healthy people or ameliorating the cognitive decline associated with aging and dementia. The Guideline 
Development Team was unable to fi nd any research specifi cally examining the effectiveness of ginseng in 
people with TBI. 
7.5.3 Ashwagandha
The use of ashwagandha, commonly known as withania, is purported to enhance mental functioning, and 
because of this it is sometimes used by people with cognitive impairment post-TBI. It is also claimed to have 
sedative effects, and should not be used concurrently with prescribed sedatives due to the risk of interaction. 
However, there is no data in humans to provide evidence of its effectiveness or harm for people with TBI.
7.5.4 Gotu kola 
Gotu kola (Centella asiatica) is also known as hydrocotyle or Indian pennywort. It is frequently suggested as a 
treatment to enhance mental functioning. However, the research evidence on gotu kola has been on the effect 
it has in promoting the healing of burns and wounds. There is no evidence to support its use to treat impaired 
cognition in people with TBI.
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7.6 Dietary 
supplements
7.6.1 Vitamin B12
Vitamin B  is involved in the regulation of mental function, and supplementation is sometimes suggested 
12
for people with impaired cognition. A Cochrane review215 investigated the effectiveness of Vitamin B  
12
supplementation in improving impaired cognition, but found no evidence to support its use in people with TBI.
7.7 Acupuncture
Acupuncture is a Chinese therapeutic process where needles are used to stimulate points along meridians 
to enhance the healing process. Evidence on the use of acupuncture for post-TBI symptoms is scarce and 
inconsistent.216 Therefore, current evidence does not support the use of acupuncture to treat people with TBI.
7.8 Distant 
healing
A systematic review of distant healing, which includes ‘treatments’ such as prayer, mental healing, therapeutic 
touch and spiritual healing, found that the methodological issues with studies of such interventions prevented 
drawing any fi rm conclusions.217
table 7.1:
summary of the evidence f or complementary and alternative medicine in treating adults with traumatic 
brain injury
intervention
level of evidence*
biofeedback
Evidence with reliability 
There is evidence from a small randomised trial that biofeedback may help 
but open to debate
postural training
eeg biofeedback/neurofeedback
Evidence with reliability 
There is evidence from a systematic review of non-randomised studies that 
but open to debate
neurofeedback may improve symptom scores and measures of memory, pain 
and headache in the short term
homoeopathy
Some evidence but 
There is evidence from one small randomised study that homoeopathy does 
based on studies without 
not improve memory, but may signifi cantly reduce self-reported symptom 
comparable groups
scores
craniosacral therapy 
Some evidence but 
There is evidence from a case series that craniosacral therapy can cause 
based on studies without 
signifi cant problems in some people
comparable groups
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intervention
level of evidence*
chiropractic or osteopathic therapy
No study evidence 
ginkgo
Benefi ts:
Some evidence without a 
•  there is evidence from pathophysiological studies that ginkgo may benefi t 
high degree of reliability 
non-clinical outcomes
•  there is evidence from studies in non-TBI populations of minor 
improvements in cognitive skills
Harms:
Some evidence without a 
•  there is evidence of spontaneous bleeding with ginkgo
high degree of reliability
•  there is evidence for an interaction of ginkgo with warfarin
ginseng, ashwagandha, gotu kol a
No study evidence
vitamin b
No study evidence
7
12
Systematic reviews have not investigated the use of vitamin B  in people with 
12
traumatic brain injury and cognitive impairment
acupuncture
No study evidence
There is poor quality evidence of an effect on the outcomes studied
distant healing
No study evidence
There is poor quality evidence of an effect on the outcomes studied
*  See Appendix B for defi nitions of the levels of evidence.
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Chapter 8:
Management of persistent symptoms
and activity limitations following
mild traumatic brain injury
Overview
•  Symptoms commonly reported following mild TBI include headache, nausea, dizziness, blurred vision, 
confusion, fatigue, poor concentration, memory problems, sleep diffi culties, irritability and noise intolerance.
•  There is some evidence that early, relevant information about common symptoms of mild TBI, emphasising 
high rates of recovery, can positively infl uence the rate of later persistent symptoms.
•  The presence of persistent symptoms following mild TBI necessitates further assessment.
•  A careful assessment of possible alternative causes of symptoms post-mild TBI should also be made to 
ensure correct treatment.
A recent systematic review of published prospective studies of mild TBI shows fairly rapid recovery occurs for 
the great majority of people in the fi rst few hours, to the fi rst month after the injury.67 Many recover within a few 
8
hours. However, these same studies also describe a group of people who fail to recover fully during that time, 
and there is no predictive relationship between the apparent severity of injury (within the overall context of a 
mild TBI) and the persistence of symptoms.
In New Zealand, contracts for mild TBI clinics (sometimes called ‘concussion clinics’) are currently held by 
DHBs and other providers, with their primary role being to attempt to ‘sort out’ the issues for and possible 
management of people with persistent symptoms after mild TBI. These contracts usually include a specialist 
medical assessment, a neuropsychological assessment and a variable number of therapist (usually 
occupational therapy) sessions.
Feedback from clinicians involved with the mild TBI clinics suggests that they do not see exclusively people with 
mild TBI, but also, appropriately, a number of people who have actually suffered a moderate-severe TBI. 
This chapter reviews evidence for the characterisation of people with persistent symptoms following mild TBI 
and effective interventions that improve outcomes for this group, alongside current practice in New Zealand. 
children and young people
There is no adequate evidence in this area specifi cally for children and young people with TBI that can be 
used to guide decision-making. The information and recommendations for adults should be used with 
caution in these groups.
8.1  Symptoms of mild traumatic brain injury
Symptoms commonly reported following mild TBI include headache, nausea, dizziness, blurred vision, 
confusion, fatigue, poor concentration, memory problems, sleep diffi culties, irritability and noise intolerance. 
Defi cits in cognitive functions such as memory, attention and speed of processing are common in the fi rst few 
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days and up to a month after the injury, and the majority of studies report recovery for most within three to 
12 months.67 However, some people will continue to experience clinically signifi cant and disabling symptoms 
beyond a year after the initial injury. 
8.1.1 Symptoms in children and young people
Most studies of outcomes in children and young people post-mild TBI report neither short- nor long-term 
cognitive problems. Headaches, dizziness and fatigue are common in the fi rst week after the injury. One study 
compared younger children (aged between 2.5 and 4.5 years at the time of injury) with mild TBI with a control 
group of children with non-head injuries.218 This study found that 29% of children with mild TBI, compared with 
14% of those in the control group, had been referred to remedial reading, but there were possible confounding 
factors identifi ed. 
The same study found a slight defi cit in visual closure (the ability to fi ll in missing parts of a visual stimulus 
such as a letter missing from a word) in the mild TBI group at six and 12 months post-injury, but this defi cit did 
not relate to reading ability when the children were assessed later.218 Studies reporting behavioural problems 
and academic scores found no difference pre- and post-injury, although two studies suggested there were 
behavioural impairments in injured children regardless of the nature of the injury.67 An injury, even one not 
involving TBI, rather than mild TBI per se was shown to be associated with behavioural issues.
The overall rate of moderate to severe disability, as measured by the Glasgow Outcome Scale, ranged from 0 
to 1%, although one small study reported that 2% of more severely injured children have moderate-severe 
disability at six months post-injury. However, most studies have methodological shortcomings that prevent 
certainty that the outcomes are defi nitely attributable to the mild TBI.67 
8.2  Characterisation of people with persistent symptoms following mild 
traumatic brain injury
The cause of persistent symptoms following an episode of mild TBI is highly controversial. In the past, there 
has been considerable disagreement between two opposing schools of thought about people with persistent 
symptoms. On the one hand, this was thought to be a situation with damage to the brain resulting in 
persistent symptoms, albeit with (usually) normal imaging of the brain, which required time and occasionally 
other interventions for the situation to resolve. The other school of thought characterised the problem as a 
psychological one, with no signifi cant damage to the brain but a problem of pessimistic expectation around 
recovery, catastrophisation, illness behaviour and work intolerance. For a discussion on this, see Ruff (2005).219
A systematic review of the literature in this area concluded that there is a probable organic basis for early 
symptoms (although this doesn’t explain why some people with entirely trivial injuries get the same symptoms) 
but no evidence to support ongoing organic brain ‘damage’ causing persistent symptoms. It was concluded 
that persistent post-concussion syndrome (PCS) after mild TBI, uncomplicated by any focal injury, is biologically 
inseparable from other examples of the post-traumatic syndrome and counsels against use of the term PCS.14 
A further systematic review by the WHO Collaborating Centre Task Force on Mild Traumatic Brain Injury found 
that where symptoms (and associated activity limitation) persist, compensation and/or litigation is a factor, 
but there is little consistent evidence for other predictors. The authors cautioned that the literature was of very 
mixed quality, and that causal inferences were often mistakenly drawn.67 
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8.3  Prevention of persistent symptoms following mild traumatic brain 
injury
recommendation
grade
All people with possible or defi nite mild traumatic brain injury should receive information 
B
about common symptoms and reassurance that recovery over a short period of time (days to a 
few weeks) is highly likely.
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
There is some evidence220,221 that early, relevant information about common symptoms of mild TBI, emphasising 
high rates of recovery, can infl uence the rate of later persistent symptoms. A large randomised controlled trial 
in the UK showed that routine follow-up of a population with predominantly mild TBI resulted in lower rates of 
disabling symptoms at six months.97
8.4  Assessment of people with persistent symptoms after mild traumatic 
brain injury
recommendation
grade
A careful assessment of possible alternative causes of the symptoms post-mild traumatic 
C
8
brain injury should be made to ensure correct treatment, with referral to specialists if 
necessary.
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
good practice points
If a person with a mild traumatic brain injury presents because they have symptoms which 

are causing concern late, or re-presents to health care services after being discharged 
with information, an initial assessment should be performed and the person referred, if 
appropriate.
When a person, particularly a child, with mild traumatic brain injury has symptoms persisting 

beyond a month, a careful reassessment of possible severity should be made.
All people with persisting, clinically signifi cant symptoms of traumatic brain injury after 

four to six weeks should be referred for a specialist assessment, usually including a 
neuropsychological assessment.
An appraisal of the severity and impact of symptoms of traumatic brain injury should be 

made, and:
•  minor problems should be managed symptomatically
•  the person should be offered reassurance and information on symptom management 
strategies.
If there are more severe symptoms, or suspicion that the traumatic brain injury is not ‘mild’, 

the person should be referred for further assessment and rehabilitation, as appropriate.
This is the opinion of the Guideline Development Team, or feedback from consultation within New Zealand where no evidence is available.
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If a person with a mild TBI presents late, or re-presents to health care services after being discharged with 
information because they have symptoms which are causing concern, the initial assessment should follow the 
process outlined in Section 2.5, First assessment – delayed, and the person referred, if appropriate.
As it seems probable that there is a high rate of misidentifi cation of moderate-severe TBI as mild TBI, when 
a person, particularly a child, with mild TBI has symptoms persisting beyond a month, there should be a 
suspicion that the person’s injury may have been more severe than initially thought, and a careful reassessment 
of possible severity should be made.
8.4.1 Assessment for other conditions
Some symptoms consistent with mild TBI may be caused by other conditions. For example, dizziness, tinnitus 
and vertigo can be caused by Meniere’s disease, or by a perilymphatic fi stula, which may also result from head 
trauma.222 Dizziness and vertigo can also be post-traumatic vertigo, which needs to be correctly identifi ed and 
may be amenable to treatment. Cognitive impairments can be caused by both acute and post-traumatic stress 
and other mood and anxiety disorders, which may or may not be connected with the mild TBI. In children and 
young people, ADHD is frequent following a mild TBI, but the evidence shows that it is probably because more 
children with ADHD have TBIs.67 
It is important that a careful assessment of possible alternative causes of the symptoms post-mild TBI is made 
to ensure correct treatment. Referral should be made to specialists, if necessary (eg, an ear, nose and throat 
[ENT] specialist for assessment for unresolved dizziness, tinnitus and vertigo).
8.4.2 Neuropsychological assessment 
All people with clinically signifi cant symptoms of TBI persisting beyond four to six weeks should be referred 
for a specialist assessment including a neuropsychological screening assessment (see Section 5.5, 
Neuropsychological assessment).
8.4.3 Ongoing management
If the assessment shows that the symptoms are probably symptoms resulting from mild TBI, an appraisal of the 
severity and impact of the symptoms should be made. Minor problems such as headache, dizziness and fatigue 
may be managed symptomatically, and the person offered reassurance and information on strategies to manage 
symptoms.
Based on the available evidence, a pragmatic approach to people with persistent symptoms is described in ‘6 
Steps’, (see Appendix D for a link to the resource).
If there are more severe symptoms, or suspicion that the TBI is not ‘mild’, the person should be referred for 
further assessment and possible rehabilitation, as appropriate (see Chapter 5, Rehabilitation following clinically 
signifi cant traumatic brain injury – assessment and Chapter 6, Rehabilitation following clinically signifi cant 
traumatic brain injury – intervention). For the management of symptoms of mental health problems, including 
drug and alcohol problems, see Chapter 14, Special issues
8.5  Return to work or study
Planning for return to work or study depends on a lot of different factors, including the severity of any symptoms 
and/or defi cits, the nature of the work or study, and opportunities for support in the workplace or study 
environment. There is no high quality evidence from published trials to guide management in this area. Some of 
the important issues are covered in one of the supplementary materials accompanying this guideline – 
‘6 Steps’(see Appendix D). Wrightson and Gronwall28 provide some useful information for health providers and 
consumers seeking guidance about return to work and study. (Also see Chapter 14, Special issues.)
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Chapter 9:
Post-discharge follow-up and support
for people with traumatic brain injury 
Overview
•  Some people who have had a mild TBI experience long-term disability following discharge from hospital, 
which may include headaches, dizziness and other persistent symptoms.
•  All people with any degree of severity of head injury and their carers should be made aware of the possibility 
of longer-term symptoms and disabilities from TBI.
•  People who have been discharged following a TBI, and their carers, should be provided with written 
information and verbal instructions on what signs or symptoms require reassessment or the need for further 
information, along with details of who to contact for help.
•  There is good evidence that routine follow-up of people with TBI that is outside the ‘mild’ or ‘trivial’ TBI range 
improves outcomes.
•  Any person who has had a head injury, who may or may not have received medical attention at the time of 
the injury, who later seeks contact with primary care or an Emergency Department with symptoms of TBI 
should be offered an appointment with a professional trained in assessment of the sequelae of TBI.
•  Following TBI, the needs of people and their families/wha¯nau and carers change over time, and for some, 
may increase signifi cantly. Many may require long-term counselling and emotional support.
•  People who have experienced TBI, and their carers, will need a variety of information upon discharge. There is 
9
evidence that the need for information is one of the most commonly unmet needs of parents of children with 
TBI, yet information has been identifi ed as the single most important form of support for families.
•  Information on TBI should be given in simple, easy-to-understand language.
•  People who have had a TBI and are being transferred to rehabilitation services should have a management 
plan prepared, which should detail the care, rehabilitation and support needed, and how it is to be provided.
The post-discharge follow-up and support needs of people who have had a possible or defi nite TBI and their 
families/wha¯nau and carers range from the need for information provided at discharge to long-term support of 
the person with TBI. 
People with any degree of head injury or TBI should only be discharged to their homes if it is certain that there 
is somebody suitable there to supervise them. People with no carers at home should only be discharged if 
suitable supervision arrangements are organised.
children and young people
There is no adequate evidence in this area specifi cally for children and young people with TBI that can be 
used to guide decision-making. The information and recommendations for adults should be used with 
caution in these groups.
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9.1 Follow-up 
recommendations
grade
Anyone with traumatic brain injury and a recorded Glasgow Coma Scale of 13 or less at any 
B
stage after the fi rst 30 minutes OR who received a CT scan of the head as part of their initial 
assessment should be routinely followed up with, as a minimum, a written booklet about 
managing the effects of traumatic brain injury and a phone call in the fi rst week after the 
injury. This follow-up needs to be undertaken by someone trained in identifying and managing 
common problems following traumatic brain injury.
Any person who has had a head injury and later seeks contact with primary care or an 
C
Emergency Department with symptoms of traumatic brain injury should be referred for 
assessment by a professional trained in assessment of the sequelae of brain injury.
Anyone with moderate or severe traumatic brain injury discharged from a residential 
B
rehabilitation setting should be considered for scheduled telephone follow-up contact using 
motivational and problem-solving techniques.
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
9.1.1 Detection of late sequelae 
Some people who have had a mild TBI experience long-term disability following discharge from hospital.4 
Symptoms such as headache, dizziness, memory defi cits, slowness of thought, poor concentration, 
communication problems, inability to work and problems with self-care have been described. These people, if 
the symptoms last for three months or more, are sometimes categorised by the International Classifi cation of 
Diseases (ICD-10) as having post concussion syndrome (PCS). However, there is considerable disagreement 
about the use of this term.14 (See Chapter 8, Management of persistent symptoms and activity limitations 
following mild traumatic brain injury.)
People who have been discharged from an Emergency Department, general practitioner or other community 
service with none of the indications for immediate intervention or likely need for rehabilitation (see Chapter 
4, Rehabilitation services and Chapter 5, Rehabilitation following clinically signifi cant traumatic brain injury 
– assessment), and their carers, should be given information and verbal instructions on what signs or symptoms 
warrant reassessment or need for further information, along with details of who to contact for help (see Section 
9.2, Continuing care and support).
9.1.2 Routine follow-up of people with traumatic brain injury 
There is good evidence that routine follow-up of people with TBI outside the ‘mild’ range improves 
outcomes.97,223 These studies used, as a minimum, a telephone call in the fi rst week, supplemented where 
necessary by face-to-face follow-up and/or intervention. 
A UK study by Wade et al (1998), especially when taken with that group’s earlier (negative) randomised 
controlled study, suggested that people with more signifi cant injuries get most benefi t from routine follow-up.97
In the fi rst UK trial by Wade and colleagues (1997),224 1156 consecutive participants with ‘head injury’ 
presenting to an Emergency Department or admitted to hospital were randomised to receive routine follow-up 
or not to follow up. By six months there was no signifi cant difference between the groups on various measures 
although sub-group analysis suggested people with more severe injuries (post-traumatic amnesia for more than 
one hour) benefi ted more than those with milder injuries.
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In the 1998 trial, 314 randomised people were admitted to hospital with ‘head injury’ and 60% had post 
traumatic amnesia longer than one hour. In the intervention group, all participants were given written 
information on head injury and advice on how to cope with it. This information covered:
•  managing post-concussion symptoms
•  coping with reduced speed of information processing
• likely 
prognosis and recovery times
•  how to reduce the impact of cognitive and emotional stress on post-concussion symptoms and conversely 
the stress associated with post-concussion symptoms
•  coping with post-traumatic stress 
•  advice on graduated return to normal activities. 
Around 25% of the participants could not be contacted by phone. Of the remainder, 10% received a telephone 
follow-up call only, 19% were assessed face to face, 34% were assessed face to face and received additional 
telephone support and 12% were assessed face to face and required further outpatient contact, which included 
a range of services, including neuropsychological assessment. By six months, participants in the trial group 
had signifi cantly better scores for social disability and lower symptom scores on a post-concussion symptom 
checklist. For example, on the Rivermead Post Concussion Questionnaire, 68% of the intervention group versus 
45% of the control participants scored in the lowest two categories, that is reporting with fewer symptoms.
In a randomised controlled trial of 202 adults with mild TBI225 in Australia (Glasgow Coma Scale score 13–15, 
post traumatic amnesia <24 hours, no focal neurological signs, did not have a CT scan) the intervention group 
had a neuropsychological assessment at one week from the injury (but received no feedback about the results) 
and received an information booklet aimed at helping them to cope with the effects of mild TBI. The control 
group received neither the assessment nor the booklet. By three months, the intervention group had lower 
scores on most items on a post-concussion checklist, signifi cantly so for anxiety and sleeping diffi culty. They 
also had lower scores on a ‘global severity’ score. There was no difference between the groups on formal 
9
neuropsychological assessment. There is some uncertainty about whether these benefi ts are simply due to the 
information booklet or whether having a neuropsychological assessment could also have affected the results. A 
high rate of loss to follow-up (38%) means some caution needs to be applied to the fi ndings in general.
In a USA trial of 171 people following moderate and severe TBI discharged from inpatient rehabilitation,223 
intervention group participants received seven scheduled telephone follow-up calls from a ‘care manager’ 
over one year. This person was specifi cally trained in this role and used motivational interviewing principles in 
carrying out goal-setting, reassurance and problem-solving. Eighty-four percent of the calls involved information 
provision and/or counselling alone, with 15% involving specifi c referrals. The control group received no contact 
from the research team. At 12 months follow-up, participants in the intervention group had signifi cantly better 
scores on the primary composite outcome index and on specifi c composites such as functional status and 
quality of well-being. There were no signifi cant differences on vocational status or community integration.
9.1.3 Self-referrals
Any person who has had a head injury, who may or may not have received medical attention at the time of 
injury, and later seeks contact with primary care or an Emergency Department with symptoms of TBI should 
be offered an appointment with a professional trained in assessment of the sequelae of brain injury.8 This 
assessment should follow the process detailed in Section 2.5 First assessment – delayed and should include 
assessment for the prognostic factors to meet ACC’s funding/planning needs.
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9.2  Continuing care and support
recommendations
grade
The aim of long-term services should be to enable and sustain optimal societal participation 
C
for both the person with traumatic brain injury and their family/wha¯nau and carer(s), while 
supporting personal choice and helping them to adjust to the new situation.
Information should be given in both written and verbal formats.
C
Written information should be concise and clear, use simple, easy-to-understand language 
C
and be illustrated with graphics, if appropriate.
People who have had a traumatic brain injury and their carers should receive information 
C
including: 
•  symptoms and signs which may indicate what to do about them and the need for further 
investigation
• reassurance about symptoms and signs which are not unexpected 
•  advice about safety and self-care measures
•  advice on alcohol or drug misuse for people who initially presented with drug or alcohol 
intoxication
•  details of community resources
•  information for carers on the diffi culties of an injury that cannot be detected by those who 
do not know about the injury.
A letter or e-mail detailing the clinical history, examination and any imaging should be sent 
C
to the general practitioners of all people who have attended an Emergency Department with 
a head injury and been discharged. A copy of this letter should be given to the person or their 
carer(s).
All people with any degree of severity of head injury and their carers should be made aware of 
C
the possibility of long-term problems from a traumatic brain injury and of services they could 
contact should they experience long-term problems.
People who have had a traumatic brain injury and are being transferred to rehabilitation 
C
services should have a written management plan (of which they are given a copy) that details: 
• current 
needs
• key 
contacts
• responsible 
services/professionals
•  sources of continued information, support and advice.
Management plans should be agreed jointly between the person, their carer(s) and health and 
C
social care professionals from the services involved in the transition prior to transition and a 
time-frame for review agreed.
Upon transfer or discharge, there should be a written discharge report which includes:
C
•  the results of all recent assessments
•  a summary of progress made and/or reasons for case closure
•  recommendations for future intervention.
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recommendations
grade
Copies of the management plan and the discharge report should be provided to the person 
C
and their family/wha¯nau and carer(s), and to all professionals relevant to the person’s current 
stage of rehabilitation.
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
good practice point
Information about possible long-term effects should be given in a practical and reassuring 

manner, and efforts should be made to alleviate the concerns of people with traumatic brain 
injury and their carers.
This is the opinion of the Guideline Development Team, or feedback from consultation within New Zealand where no evidence is available.
children and young people
There is no adequate evidence in this area specifi cally for children and young people with TBI that can be 
used to guide decision-making. The information and recommendations for adults should be used with 
caution in these groups.
The needs of people who have sustained a TBI, and their families/wha¯nau and carers, change over time and for 
some may increase signifi cantly. Many people who have had a TBI require long-term counselling and emotional 
support to assist understanding and adjustment to altered family roles and circumstances.
Families and carers also report the need for information, practical support, continued education and easy 
9
access to health and social care systems to combat isolation, emotional distress, stress and practical overload. 
Ongoing support is required in the community in order to maximise independence and quality of life for what 
may be, in younger people, the next 50 years or more of their lives.
The aim of long-term services should be to enable and sustain optimal societal participation for both the 
person with TBI and their family/wha¯nau and carer(s), with personal choice, and will involve helping them to 
adjust to the new situation.8,113 Services will need to be delivered in a whole range of settings and, importantly, 
will involve adapting and developing a range of specialised professional skills and attitudes to working with 
people with TBI and their carers. A social/educational model of care is appropriate, and effective services will 
emphasise on collaboration between rehabilitation specialists and people involved in the everyday life of the 
person with TBI.
9.2.1 Information 
People who have been in receipt of medical and rehabilitative care will need a variety of information upon 
discharge, depending upon the severity of their injury, the time since the injury and at what point the 
information is being given. The people who are caring for them at home, after discharge, will also need 
information. There is evidence that the need for information is one of the most commonly unmet needs of 
parents of children with a TBI,226 while information has been identifi ed as the single most important form of 
support for families.11,227 
People who are being discharged early after an injury may require observation at home by their carers. A 
systematic review identifi ed one observational study in which carers were given specifi c, explicit written 
information. The study reported high levels of compliance with written instructions for home observation after 
Emergency Department discharge.228 Compliance was better when the injured person had experienced some 
loss of consciousness, or was younger, and where the observer was the person’s mother.
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One qualitative study examined effective formats for information to be provided to people with acute and 
chronic disorders who regularly attended an outpatient clinic.229 They found that people are frequently likely to 
seek further information following (rather than during) an encounter with their care provider; and that they want 
a permanent record of personal health data and relevant educational information. 
Information needs to be concise, clear and illustrated with graphics, if appropriate. Receiving information of 
this sort favourably affected the participants’ trust in, relationship with and confi dence in their physicians, and 
when, during therapy, they were given printouts of graphic trends depicting their responses to therapy, people 
were more motivated to adhere to their treatment plans and more satisfi ed with their care.229 There is no reason 
why this information should not apply equally to carers as well as people with TBI.
Information should be proactively offered, and it should not be assumed that carers will ask for information they 
require. There is evidence that many carers will not seek information even when needed, particularly for less 
severely injured people.11,230 Results of a UK study stated that information should be provided to all people with 
possible TBI regardless of severity of injury or functional impairment.230 A Cochrane systematic review concluded 
that both verbal and written health information should be given to people and their carers on discharge to 
home.231
The combination of verbal and written health information enables the provision of standardised care 
information to people and their carers, which appears to improve knowledge and satisfaction. Information 
should be given in simple, easy-to-understand language.232,233 
People who have had a possible or defi nite TBI and their carers will need clear information in the following 
categories:
•  symptoms and signs which may indicate a need for further investigation, including what action the person or 
their carer(s) should take if they experience any of these (such as, go to a general practitioner or Emergency 
Department) and an indication of urgency
• reassurance about symptoms and signs which are not unexpected and about which they need have no 
concerns, specifi cally including the expected progress and resolution of the after-effects of the TBI, together 
with details of what to do if the signs and symptoms do not resolve in the expected time-frame
•  advice about safety and self-care measures, including minimising the risk of re-injury and caution with use of 
drugs and alcohol
•  information and advice on alcohol or drug misuse for people who initially presented with drug or alcohol 
intoxication
•  information about community resources
•  information for carers on the diffi culties of an injury that cannot be detected by those who do not know about 
the injury.7
9.2.1.1 Communication with community services 
There is also a need for information to be supplied to the person’s general practitioner about the nature of the 
injury and expected outcomes, so that the general practitioner is prepared if the person or their carer(s) seek 
further help at a later date.7
A communication (letter or e-mail) should be generated for all people who have attended an Emergency 
Department with a head injury, and sent to their general practitioners when they are discharged. This letter 
should include details of the clinical history, examination and any imaging. This letter should be open to the 
person or their carer(s), or a copy should be given to them.7 
9.2.1.2 Advice about long-term problems and support services 
There is no evidence that enables both sensitive and specifi c identifi cation of people who will have longer-term 
sequelae from TBI.7,67 Even a proportion of people with mild TBI may have long-term disabling sequelae.51,234–239 
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Therefore, all people with any degree of severity of head injury and their carers should be made aware of the 
possibility of long-term symptoms and disabilities from a TBI and should be made aware of the existence of 
services that they could contact should they experience long-term problems. Details of support services should 
be included on discharge advice cards. People should also be advised to contact their doctors about these 
problems.8 
Information about possible long-term effects should be given in a practical and reassuring manner, and efforts 
should be made to alleviate the concerns of people with TBI or their carers. This is particularly important for 
people who appear more anxious and who may, for example, attribute unrelated symptoms to the TBI, after the 
TBI sequelae have resolved.
9.2.1.3 Information for people with mild traumatic brain injury on discharge from Emergency Department or 
community services
People with a possible or defi nite TBI who have been assessed in an Emergency Department, by a general 
practitioner, or by another service in the community as having no risk factors indicating immediate need for 
further monitoring or intervention, should receive verbal advice and a written advice card.231 The details of 
the card should be discussed with the person and their carer(s). If necessary (such as for people with literacy 
or language diffi culties, or with visual impairment), other formats (such as pictures, tapes or videos) should 
be used to communicate this information. Communication in languages other than English should also be 
facilitated.7
The risk factors outlined in the information card should be the same as those used in the initial community 
setting to advise people on Emergency Department attendance (see Chapter 4, Rehabilitation services). People 
and carers should also be alerted to the possibility that a few people may make a quick recovery but could go on 
to experience delayed complications. Instructions should be included on contacting community services in the 
event of delayed complications. 
9
The person being discharged will need to have someone who can look after them for the fi rst few days, and 
sometimes longer, after discharge. The information on the card given to the injured person should be explained 
to the carer as well as to the person being discharged.7 When being given the information, people should be 
given the opportunity to ask questions and express concerns, and the practitioner should provide reassurance 
and advice.
9.2.1.4 Information on discharge from hospital to community rehabilitation services
People who have had a TBI and are being transferred to rehabilitation services should have a management 
plan prepared. The person with TBI and their carer(s) should be given information about, and offered contact 
with, the appropriate voluntary services and self-help groups that may be useful to them.8,11,226,229,230,240,241 The 
management plan should detail the care, rehabilitation and support needed, and how it is to be provided.
Transfer to the community should include a written management plan8 outlining:
• current 
needs
• key 
contacts
• responsible 
services/professionals
•  sources of continued information, support and advice.
Management plans should be agreed jointly between the person, their carer(s) and health and social care 
professionals from the services involved in the transition. The management plan should be accepted by all 
parties prior to transition and a time-frame for review agreed (usually three to six months post-discharge), 
although earlier review should be available if requested by the injured person or their carer(s).8 
Upon transfer or discharge, there should be a written discharge report that includes:
•  the results of all recent assessments
•  a summary of progress made and/or reasons for case closure
135
•  recommendations for future intervention.8
 
   
   
 

Copies of both the management plan and the discharge report should be provided to the person and their 
family/wha¯nau and carer(s) where appropriate and to all professionals relevant to the person’s current stage of 
rehabilitation, especially the general practitioner.8 
9.2.1.5 Information for people with traumatic brain injury and their carers on discharge from rehabilitation 
services
People who have had a TBI and are being discharged from rehabilitation services, and their carers, should be 
appropriately prepared for the discharge. They should be given information that details:
•  management of ongoing problems for which further rehabilitation is not appropriate
•  sources of continued information, support and advice.
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Chapter 10:
Ma¯ori and traumatic brain injury
Overview
•  In New Zealand, there are signifi cant ethnic disparities in the prevalence of TBI.
• Ma¯ori have high incidence rates of TBI and evidence suggests that TBI is under-reported in Ma¯ori.
• Ma¯ori are at risk of poorer outcomes following TBI.
• Ma¯ori traditionally have a holistic view of health and this should be considered in rehabilitation of Ma¯ori with 
TBI.
•  An increase in the Ma¯ori health workforce may improve access and improve overall outcomes for Ma¯ori with 
TBI.
•  Communication is increasingly regarded as central to the practice of primary health care, directly and 
indirectly determining the outcome of the interaction. 
• Ma¯ori with TBI have specifi c and unique rehabilitation needs.
recommendations
grade
At the service level
C
•  Practitioners working with Ma¯ori with traumatic brain injury should receive training and 
support in culturally safe practice.
At the individual level
C
•  Rehabilitation of Ma¯ori with traumatic brain injury should include the diagnosis and 
management of traumatic brain injury-related syndromes, including mental illness and 
substance abuse.
10
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
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good practice points
Nationally
•  A national action plan aimed at improving outcomes for Ma¯ori with TBI should be 

developed.
•  Accurate ethnicity data for TBI incidence should be collected.

At the service level
•  Accurate ethnicity data for people with TBI managed by a service should be collected.

•  Where possible, the case coordinator/key worker for Ma¯ori with TBI should be Ma¯ori, or 
where this is not possible, the case coordinator should have support from a Ma¯ori cultural 
advisor.
• Ma¯ori community health workers and other Ma¯ori health workers fl uent in te reo Ma¯ori 
should be considered as part of the rehabilitation team for Ma¯ori with TBI.
•  Neuropsychological and other assessment measures that have been standardised for 
Ma¯ori populations should be used, where possible.
At the individual level

•  Rehabilitation practitioners assessing Ma¯ori with TBI should consider the validity of the 
questions within neuropsychological and other assessment measures that have not been 
standardised for Ma¯ori.
•  All decisions should be made in consultation with the individual with TBI, and if they wish, 
their wha¯nau.
•  Effective methods of delivery of quality information should be employed. Information 
should be provided in appropriate formats, both verbal and written.
• The 
wha¯nau of the person with TBI should be supported during the rehabilitation process.
This is the opinion of the Guideline Development Team, or feedback from consultation within New Zealand where no evidence is available.
This chapter presents information about the epidemiology of TBI and TBI risk factors in Ma¯ori. This chapter 
also includes discussion of potential improvements to service delivery that aim to provide Ma¯ori with more 
appropriate and effective care. Information from the rest of this guideline applies equally to Ma¯ori, and this 
chapter supplements the general guideline with information specifi c to Ma¯ori with TBI. 
10.1 Epidemiology of traumatic brain injury in Ma¯ori
There are signifi cant ethnic disparities in the incidence and prevalence of TBI in the New Zealand population. 
TBI is a major health issue for Ma¯ori, as they have a high incidence rate with relatively poor outcomes. It is 
important to note that any analysis is somewhat limited due to ongoing diffi culties in the accurate collection of 
ethnicity data,242 as well as inaccuracy in the coding of admission and discharge diagnoses of TBI.85 With these 
limitations in mind, it is likely that the incidence of mild TBI (14%) is under-reported in Ma¯ori and that moderate 
or severe TBI is more common (at 21.5%)243 than would be expected on demographic grounds. ACC’s Summary 
Guidelines on Ma¯ori Cultural Competencies for Providers highlights the need for the collection of accurate 
ethnicity data.244 
The major causes of TBI for Ma¯ori are road accidents, sports injuries and assaults.243 The high-risk groups for 
these injuries include children, young adults and older people, with statistics from ACC indicating that males 
aged 15 to 30 years make up the largest group, followed by children under 15 years. 
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Some research shows that ethnic disparities are even more evident amongst children. A retrospective review 
of all children and young people under 15 years of age, who were admitted to Auckland’s Starship Children’s 
Hospital over a 45-month period to October 2001, highlighted that head and thoracic injuries predominated 
and were typically associated with lower limb injuries. Ma¯ori and Pacifi c children represented 74% of all these 
cases.245 
An overview of injuries in New Zealand246 discussed the need for further research aimed at identifying 
modifi able environmental factors and the initiation of preventive action. It is estimated that the risk of injury 
(including TBI) for Ma¯ori is 1.5 to 2.5 times greater than the risk for non-Ma¯ori.
Predominantly anecdotal evidence suggests that Ma¯ori are at risk of poorer outcomes following TBI. One 
study showed that prison populations appeared to have disproportionately high rates of TBI and recurrent 
TBI compared with the general population, with the majority of those in prison with TBI being Ma¯ori.247 Dual 
diagnosis of TBI and substance abuse or TBI and mental illness is also more common in Ma¯ori than non-Ma¯ori.84 
See also Chapter 14, Special issues.
10.1.1 Ma¯ori traumatic brain injury action plan
The disproportion in incidence and outcomes of TBI for Ma¯ori compared with non-Ma¯ori is such that the 
Guideline Development Team considers the development of an action plan, targeted at improving outcomes, 
necessary.
The Guideline Development Team considers that a TBI action plan could be adapted from the Ma¯ori 
Cardiovascular Action Plan.248 The Cardiovascular Action Plan was developed to provide a guide for 
cardiovascular policy development and implementation for health services in New Zealand. Within the Plan, 
several areas for health service action aimed at improving outcomes for Ma¯ori were proposed. For more details, 
see the guideline for The Assessment and Management of Cardiovascular Risk, available at www.nzgg.org.nz. 
An action plan for improving outcomes for Ma¯ori with TBI should focus on the following:
•  policy – Treaty of Waitangi-based policy and decision-making
•  information systems – complete and consistent collection of ethnicity data, service provider funding
•  access, delivery and standards development – TBI rehabilitation health needs assessments, kaupapa Ma¯ori 
10
health services
•  audit, evaluation and quality standards improvement – measurement of key performance indicators to 
monitor service responsiveness to Ma¯ori TBI rehabilitation needs
• Ma¯ori TBI workforce and health service development
• kaupapa 
Ma¯ori research.248
10.2 Health perspective of Ma¯ori
Ma¯ori currently make up 15% of the New Zealand population.33 However, Ma¯ori are not a homogeneous group. 
Although there are many cultural norms and similarities amongst Ma¯ori, it is important to recognise that 
there are also differences. Health care practitioners should ascertain whether the person wishes to receive 
Ma¯ori culture-specifi c service delivery. Simply asking the person directly may not be suffi cient, as people may 
sometimes decline for fear of ‘being a nuisance’ or because they wish to please a non-Ma¯ori practitioner, so the 
option should be offered to the person by a Ma¯ori practitioner or cultural advisor.
Ma¯ori with a head injury and possible TBI, or their carers and wha¯nau, may not be proactive in seeking help 
because they are not aware of the risks. In particular, less serious injuries may be managed within the wha¯nau 
without seeking medical help. To Ma¯ori, the head is tapu and some iwi do not like the head being touched at 
all. For providers there needs to be an awareness and cultural sensitivity, particularly in regards to imaging 
processes and surgical procedures on the head following a head injury so that Ma¯ori with TBI and their wha¯nau 
139
 
   
   
 

can make fully informed decisions. Information explaining head injury and the need for procedures such as CT 
scans, MRI and surgical interventions in a culturally acceptable way should be developed for Ma¯ori in order to 
facilitate the provision of ‘best practice’ care and achieve quality outcomes.
Traditionally, Ma¯ori have a more holistic view of health than the general population. When providing health and 
rehabilitation care and support for Ma¯ori with TBI, it is important to remember that the person and their needs 
are not to be considered in isolation, but in the context of their environment, both physical and social (that is, 
their physical circumstances and their wha¯nau). Under a Ma¯ori culture-specifi c approach, the well-being of the 
wha¯nau should be considered alongside the well-being of the person with TBI. Consultation with Ma¯ori, hapu¯ 
and iwi resources should be sought when assessing the need for any interventions for the person with TBI. All 
decisions, where possible, should be made collectively with the person’s wha¯nau, with permission from the 
person with TBI. 
10.3 Service delivery for Ma¯ori
Ma¯ori have historically had low rates of access to and utilisation of health services and, more specifi cally, 
disability support services.249 Data about the health care sector’s workforce indicates that 5.4% of the regulated 
health care workforce is Ma¯ori, far below the desired level.250 It has been suggested that a contributing factor 
to low service utilisation could be the low proportion of Ma¯ori service providers. To improve access for Ma¯ori to 
services, and to improve overall Ma¯ori TBI outcomes, steps are needed to increase the Ma¯ori health care sector’s 
workforce and strengthen the capacity of Ma¯ori service providers. 
Communication is increasingly regarded as central to the practice of primary health care, directly and indirectly 
determining the outcome of the interaction. International research251 has identifi ed the impact and importance 
of communication between the general practitioner and the person seeking care for that person’s health, and 
the links this communication can have with perceived discrimination.252
However, a qualitative study in New Zealand has shown that when non-Ma¯ori general practitioners talk about 
Ma¯ori health, they often use language that can imply or attribute ‘blame’ on Ma¯ori for their health status, or 
use language that justifi es existing service provision.253 This may negatively impact on the effectiveness of 
interactions between Ma¯ori and their general practitioners. Practitioners working with Ma¯ori with TBI should 
receive training and support in culturally safe practice. Where possible, the case coordinator/key worker for 
Ma¯ori with TBI should be Ma¯ori, and preferably of the same sex as the person with TBI. Where a Ma¯ori case 
coordinator is not possible, the case coordinator should have support from a Ma¯ori cultural advisor.
A study exploring TBI rehabilitation processes and outcomes in Ma¯ori, Pacifi c peoples and European New 
Zealanders in New Zealand showed both similarities and differences,254 and highlighted where TBI rehabilitation 
service delivery needs for Ma¯ori may differ from those of non-Ma¯ori. Suggestions arising from this research were: 
•  to involve and support the family, extended family and/or partners
•  to promote the ‘Whatever It Takes’ model 
•  to endorse and implement cultural practices
•  to recruit more Ma¯ori rehabilitation professionals 
•  to involve rehabilitation staff at a management level
•  to appoint a cultural advisor as part of the rehabilitation team
•  that spending more time with Ma¯ori may be necessary in order to ensure accurate information is provided, 
and to allow them to ask questions (see also Section 9.2.1, Information, on provision of information)
•  that continual clarifi cation of understanding and probing for feedback may also be of benefi t
•  that managed care does not allow for ‘extra’ time in some practices, but this important aspect of culturally 
appropriate services may need to be factored into policy
•  that the provision of culturally, aesthetically appropriate surroundings is important to the level of comfort for 
Ma¯ori, which may include physical, cultural or spiritual aspects of care
140
•  to obtain input from tangata and/or mana whenua.
 
   
   
 

Many of these suggestions will not be able to be implemented immediately. Where these measures are not 
currently achievable, the minimum provision for Ma¯ori with TBI should be the availability of advice and support 
from a Ma¯ori cultural advisor.
10.4 Assessment of Ma¯ori with traumatic brain injury
Neuropsychologists also need to take into account formal education levels and language abilities when 
assessing Ma¯ori with TBI. Most neuropsychological assessment tools have not been standardised for Ma¯ori 
populations and therefore there is uncertainty about the applicability of the measures and the interpretation 
of the results of neuropsychological assessments for Ma¯ori. Neuropsychological measures often have 
culturally determined elements which may be inappropriate for New Zealand; correction for these may improve 
applicability within New Zealand.255 The same issues will apply to some measures used by other disciplines and 
all rehabilitation practitioners assessing Ma¯ori with TBI should consider the validity of assessment tools. 
10.5 Wha¯nau support
The wha¯nau of the person with TBI will also need support. Regular wha¯nau meetings could be considered during 
rehabilitation, and advice on fi nancial issues and support groups should be included in discharge information. 
See also Section 9.2.1, Information, for details of information.
Where wha¯nau members are carers of the person with TBI, and particularly where they are involved in the 
provision of rehabilitation interventions, training and support should be provided (see Chapter 13, Needs of 
carers).
10
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Chapter 11:
Pacifi c peoples and traumatic brain injury
‘I am not an individual,
I am an integral part of the cosmos.
I share divinity with my ancestors, the land, the seas and the skies.
I am not an individual because
I share a tofi  with my family, my village, my nation.
I belong to my family and my family belongs to me.
I belong to my village and my village belongs to me.
I belong to my nation and my nation belongs to me.
This is the essence of my sense of belonging.’
Tui Atua Tupua Tamasese, 1997
Overview 
•  In New Zealand, 5% of ACC’s ‘concussion’ claimants identifi ed as Pacifi c peoples in 2003. It is likely that 
Pacifi c peoples are under-represented in TBI-related claims for a number of reasons.
•  It is important to acknowledge the traditional beliefs and culture of Pacifi c peoples and to be cognisant of 
the stigma that surrounds illness and disability. Cultural diversity between and within Pacifi c cultures should 
also be recognised and acknowledged.
•  Health care practitioners should be aware of the barriers to access for Pacifi c peoples (eg, cost and language) 
and be proactive in offering services. 
•  Currently, there is a lack of high-level evidence to guide recommendations when planning TBI rehabilitation 
for Pacifi c peoples. However, guidance on providing culturally appropriate service and improving outcomes 
11
for Pacifi c peoples is summarised in this chapter.
•  At present, there is a lack of research on outcomes of TBI for Pacifi c peoples in New Zealand.
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recommendations
grade
Socioeconomic circumstances, such as access to transport or a telephone, should be 
C
considered when planning traumatic brain injury rehabilitation.
Language interpreters should be offered regardless of perceived profi ciency in English.
C
There should be a Pacifi c team or at least one Pacifi c health care practitioner available as part 
C
of the multidisciplinary rehabilitation team for Pacifi c peoples with traumatic brain injury.
A Pacifi c cultural advisor and/or matua should be available to traumatic brain injury 
C
rehabilitation staff for consultation.
All information should be produced in Pacifi c languages and in oral form (eg, videos), where 
C
possible.
The need for culturally aesthetically appropriate physical surroundings and environments for 
C
Pacifi c peoples should be taken into account.
Caution should be used with assessment tools that have not been developed or standardised 
C
for Pacifi c peoples. Decisions regarding assessment, rehabilitation and coordination should 
be based on contextual information from a variety of sources and should include Pacifi c input.
Traumatic brain injury assessment and rehabilitation processes for Pacifi c peoples should be 
C
structured so that they involve family, extended family and an interpreter and/or matua, and 
include cultural protocols, where required.
Traumatic brain injury rehabilitation staff should be aware that there is much diversity 
C
between Pacifi c cultures, and that detailed concepts of rehabilitation will also vary between 
and within cultures.
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
good practice points
Traumatic brain injury rehabilitation staff should be aware of traditional Pacifi c beliefs and the 

stigma surrounding illness and disability in order to minimise the potential for giving offence.
Services should be offered to Pacifi c peoples with traumatic brain injury, rather than expecting 

them to initiate contact and ask for it.
This is the opinion of the Guideline Development Team, or feedback from consultation within New Zealand where no evidence is available.
11.1 Pacifi c peoples in New Zealand
The term ‘Pacifi c peoples’ describes the diverse range of people living in New Zealand who have migrated from 
nations of the South Pacifi c, and/or who identify with one or more of the Pacifi c islands because of ancestry 
or heritage. Due to migration, 6.5% of New Zealand’s current total population is of Pacifi c ethnicity.256 New 
Zealand’s 2001 Census reports that almost half, or 115,017 of the Pacifi c population are Samoan, followed 
by Cook Island Ma¯ori (52,569), Tongan (40,716), Niuean (20,148), Fijian (7,041), Tokelauan (6,204) and 
144
 
   
   
 

Tuvaluan (1,965). The majority (60%) of this population were born in New Zealand with about two-thirds of this 
population located in the Auckland region.256 
This section provides a broad overview of issues utilising a pan-Pacifi c approach. However, it is important to 
recognise and acknowledge the cultural diversity between and within Pacifi c cultures. Each nation has its own 
specifi c set of cultural beliefs, customs, values and traditions. The status, authority, tradition, obligations and 
power structures are different for each group.257 Moreover, the level of familiarity a Pacifi c individual has with 
New Zealand culture (aculturation) will determine the extent to which the content of this section applies.
In 2003, 5% of ACC’s ‘concussion’ claimants identifi ed as Pacifi c peoples.258 However, Pacifi c peoples may be 
under-represented in TBI-related claims, given that the Pacifi c population is comparatively younger than the 
general population in New Zealand, and that younger people make the most claims. Faleafa (2004) has also 
concluded that there is a relationship between Pacifi c peoples’ over-representation in certain social indicators 
and characteristics associated with the increased likelihood of sustaining TBI, such as high involvement in 
motor vehicle accidents, assaults, sports-related injuries, higher unemployment, lower educational levels, 
higher crime involvement and lower socioeconomic status.259 
11.2 Perception of health for Pacifi c peoples
Perceptions of health are governed by cultural norms and values. Traditionally, Pacifi c cultures are more 
sociocentric (ie, their orientation is towards the social group) than non-Ma¯ori and non-Pacifi c New Zealanders, 
who tend towards being more individualistic (where orientation is towards the individual).260 There are many 
values common to Pacifi c nations, such as respect, reciprocity, communalism, collective responsibility, 
gerontocracy, humility, love, service and spirituality.261 
Pan-Pacifi c concepts of family encompass the immediate and extended family, as well as the wider community. 
Traditionally, people in need of care through illness, disability or age have been cared for by their families and 
within the extended family structure. Caring for people is seen as the responsibility of the family, as only family, 
it is felt, will provide care with the necessary kindness. While this may be a tremendous support and strength of 
Pacifi c families, it could act as a barrier to obtaining services outside the family.262 
Traditional Pacifi c concepts of health are holistic, where well-being is defi ned by the equilibrium of mind, body, 
spirituality, family and environment. The Fonofale model263 is one example that captures this concept from a 
Samoan perspective, portraying six dimensions of health: 
• familial
11
• spiritual
• physical
• mental 
• other 
(encompassing demographic and situational variables) 
•  cultural (the philosophical drive, attitudes and beliefs of Pacifi c islands’ culture). 
These dimensions are interdependent with the environment, context and time relevant to the individual. As 
with Ma¯ori models of health, the dimensions are considered to be interwoven and interdependent, with altered 
states of wellness occurring when one or more of the dimensions is out of balance.
11.3 Access to and utilisation of health and disability services
Pacifi c peoples have historically had low access and utilisation rates of disability support services in general. 
One contributing factor is thought to be the high degree of stigma attached to disability in Pacifi c cultures, so 
that the presence of disability is shaming for the family and may carry with it a fear of ‘gossip’.262 This has been 
related to traditional spiritual explanations of disability (eg, as a punishment from God or a curse due to a family 
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wrong). Although there is no evidence that this attitude extends to TBI-related disabilities in people who have 
had no pre-existing disability, it is important to acknowledge traditional Pacifi c beliefs and to bear in mind the 
stigma surrounding illness and disability in order to minimise the potential for giving offence.262 
Pacifi c peoples tend to see health care professionals less for many reasons. This includes seeing health care 
professionals for ACC matters. There may a perception amongst Pacifi c employees that they will not be believed 
if they report an injury, especially if it happened at work. Cost can also be a reason for not seeking medical care. 
People may not be able to afford the ACC co-payment that is charged, and may be anxious about paying for the 
prescription of medications. 
Language diffi culties are a further barrier to accessing services. Trying to explain how an injury happened and 
describing their symptoms can be very challenging for a Pacifi c person with limited English. There may be no 
(similar) words in Pacifi c languages to describe certain symptoms, so the health care professional may become 
frustrated at being unable to get a ‘good history’. 
The use of therapies and medicines traditional to their culture may also be preferred by many Pacifi c peoples, 
and lead to non-utilisation of ACC-funded providers and lack of reporting of an injury.
11.4 Rehabilitation planning for Pacifi c peoples with traumatic brain injury
There is a lack of high-level evidence on which to base recommendations when planning TBI rehabilitation for 
Pacifi c peoples. However, the needs of Pacifi c peoples must still be addressed in order to provide a culturally 
appropriate service and endeavour effectively to improve outcomes for Pacifi c peoples. The following guidelines 
have been suggested:
•  Service accessibility: In some situations, asking for help (which can extend to seeking services) for Pacifi c 
peoples is seen as rude because help is usually offered rather than requested.262 Therefore, in order for 
rehabilitation to be effective, the service will need to be offered to people with TBI, rather than expecting 
them to initiate contact and ask for it. Socioeconomic circumstances must also be considered (eg, access to 
transport or a telephone).
•  Communication: Many Pacifi c peoples for whom English is a second language describe the considerable 
disadvantages in not being able to communicate clearly and confi dently, and the consequent reluctance 
to consult outside their own small communities. Shyness resulting from this diffi culty in communicating, 
together with the cultural reluctance to attract attention to one’s self, exacerbates the problem so that it 
becomes a signifi cant barrier to accessing care and services.262 Language interpreters should be offered 
regardless of perceived profi ciency in English.
•  By Pacifi c for Pacifi c: Ideally, there should be a Pacifi c team or at least one Pacifi c health care practitioner 
available as part of the multidisciplinary rehabilitation team. It is also advisable to have a Pacifi c cultural 
advisor and/or matua available to staff for consultation. For mainstream services, establishing partnerships 
and consulting with Pacifi c health providers is essential.
•  Pacifi c-appropriate resources: Much of the health and disability service information, as well as TBI 
rehabilitation-specifi c information, comes in written form. Although it is important for consumers to have 
written information available due to the potential defi cits in memory that can occur following TBI, this is not 
culturally appropriate for Pacifi c peoples with their oral tradition, and may require too high a profi ciency in 
written English.262 All written material should be produced in Pacifi c languages and in oral form (eg, videos) 
where possible. 
•  Holistic approach: The role in rehabilitation of the family, extended family and community should be 
acknowledged and empowered. Individual attitudes and beliefs surrounding TBI and TBI rehabilitation (eg, 
spiritual beliefs) should be identifi ed and incorporated into the rehabilitation plan. Culturally aesthetically 
appropriate physical surroundings and environments are important for level of comfort for Pacifi c peoples 
and should be taken into account.
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•  Caution with assessment tools: There is no formal research investigating the reliability and validity of the 
use of any commonly used standardised tests and tools with Pacifi c peoples. Consequently, an invalid 
assessment may give rise to recommendations for a rehabilitation programme that may have minimal 
effectiveness for a Pacifi c person. Health care practitioners are advised to be cautious with assessment 
tools. For example, neuropsychologists need to take into account formal education levels and language 
abilities when assessing Pacifi c peoples.259 Any decision-making regarding assessment, rehabilitation and 
coordination should be based on contextual information from a variety of sources and should include Pacifi c 
input.
•  Cultural protocol: One of the practicalities of working in an ethical and culturally safe manner with Pacifi c 
peoples is that more time may be needed to ensure accurate and reliable information is gathered.259 
Involving family and extended family, as well as an interpreter and/or matua, and then including cultural 
protocols where required (such as a prayer and/or blessing), may all play a role in the assessment and 
rehabilitation process.
•  Cultural diversity: While commonalities across Pacifi c cultures do exist and can be applied to rehabilitation, 
detailed concepts of rehabilitation will also vary between and within Pacifi c cultures. 
11.5 Research issues
There is a lack of research on outcomes of TBI for Pacifi c peoples in New Zealand. Therefore this chapter is 
largely based on expert opinion, and provides a starting point for health care practitioners working with the 
Pacifi c TBI-rehabilitation community.
Rigorous and culturally appropriate epidemiological and outcomes-focused research investigating TBI in the 
Pacifi c population could inform both the development of evidence-based best practice and resource allocation. 
Any research conducted in New Zealand should routinely specify the ethnic composition of the population 
sample.
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Chapter 12:
Children and young people
and traumatic brain injury
Overview
•  There is a lack of robust evidence on care and support for children and young people with TBI.
•  The impact of TBI on potential development is likely to be greater the younger the person is. The precise 
outcomes of TBI in children are hard to establish because TBI impairments emerge over many years as 
function matures.
•  TBI in early childhood may have lasting effects; more specifi cally, there may be an impact on the child’s 
attainment of developmental milestones.
•  Rehabilitation of children and young people does not differ greatly from rehabilitation of adults, although 
there are some aspects that differ for children, which are summarised in this chapter. 
•  Children who have been admitted to hospital with a TBI should be assessed for functional limitations and 
referred appropriately before discharge.
•  Careful management of the transition from stage to stage (ie, acute care to rehabilitation) is required for 
children and young people who have experienced TBI.
•  Long-term continued monitoring and follow-up of children and young people with TBI is necessary to ensure 
the benefi ts for the individual.
•  Education and training of those working in special education are recommended to minimise any 
misconceptions about TBI in children and young people.
The acute management and rehabilitation of children and young people with TBI is addressed throughout 
this guideline. When management for children differs from that for adults, this is highlighted; otherwise, 
recommendations apply equally to adults and paediatric populations. This chapter addresses aspects of the 
acute care and management which are specifi c to children and young people. Issues for the families and carers 
of children and young people are addressed in Chapter 13, Needs of carers.
12.1 Defi nitions
Defi ning the upper age limit of ‘children and young people’ presents its own diffi culties, as there are various 
approaches taken to the upper limit in the literature. Many studies have taken an inclusive developmental 
12
approach and included young adults in their early 20s because they may, functionally, still be in late 
adolescence and in transition to independent adult life. Others, however, have used arbitrary upper age 
delineators, varying between the ages of 12 and 21 years. 
This guideline has adopted a fl exible and pragmatic approach generally, where it is detailed if the management 
and care differ due to younger age. Generally, this chapter is referring to people under the age of 18 years. 
However, practitioners should use their professional experience to apply this information, and may consider 
some of the information in this chapter appropriate to a physically and emotionally immature young adult, 
providing that it is within the context of their normal social role.
There are differences in the way that rehabilitation may be delivered to children and young people with TBI, 
particularly in the longer term. For example, some cognitive rehabilitation and behavioural management 
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interventions may be delivered under the auspices of special education services (Group Special Education), 
often within school, and this is covered in this chapter. 
There is a lack of robust evidence on many aspects of care and support for children and young people with TBI 
and more research is required. 
12.2 Effects of traumatic brain injury in children and young people 
Following a TBI, there are three classes of sequelae that may be experienced by people of all ages with TBI: 
1. immediate effects
2. longer-term and late-emerging effects
3.  impairments of development as it would have occurred without the injury.
The impact of TBI on potential development is likely to be greater the younger the person is. Childhood and 
adolescence are times of rapid changes physically, cognitively, socially and in capacity, and therefore the 
impact on the pre-injury potential development of a child with TBI may be considerable. Impairments may 
continue to emerge over many years as function matures. 
This impact on potential development makes it particularly diffi cult to establish, from the research base, the 
precise outcomes of TBI for children. It is rare that data suffi cient to predict future development has been 
recorded for children who later have a TBI, prior to their injury. More frequently, performance post-injury is 
compared with inaccurate and incomplete pre-injury data, or post-hoc estimates of pre-injury functioning. 
However, a systematic review reported the following longer-term effects of TBI in children:
•  a predictable pattern of delays and defi cits in language acquisition for children up to the age of three, when 
compared with uninjured children
•  subtle, hidden cognitive defi cits in cases of apparently normal performance in children with focal TBI, where 
the children were using compensatory strategies
•  non-linear changes in growth related to injury variables.11 
There is also good evidence that a TBI in early childhood may have lasting effects. One controlled study in 
Auckland reported that children who had a mild TBI when aged between 2.5 and 4.5 years exhibited impaired 
visual closure (the ability to fi ll in missing parts of a visual stimulus, such as a letter missing from a word) at a 
year after the injury, and that this was related to impaired reading scores at age six years.218 However, although 
these children’s injuries had been classifi ed as ‘mild TBI’, the clinical histories included high proportions of risk 
factors indicative of more serious injury by the criteria being used in this guideline.
In addition, there may be an impact on the child’s attainment of developmental milestones. A child’s disability 
may increase with increasing age, both due to diffi culty with learning and acquiring new skills as a result 
of the brain injury and due to types of brain injury which have their fi rst noticeable consequences at a later 
developmental stage. Development may be delayed or disrupted by a TBI (eg, puberty may be precipitated by a 
TBI)195 and by the loss of socialisation that may occur as a result of the TBI, such as the impact of an extended 
hospitalisation, absence from school and other activities. This loss of socialisation, and other impacts on 
development, may have age-inappropriate impacts on behaviour that persist into adulthood. 
12.3 Rehabilitation of children and young people with traumatic brain injury
Rehabilitation of children and young people with TBI does not fundamentally differ greatly from rehabilitation 
of adults. Most information about rehabilitation strategies and interventions is covered in Chapter 6, 
Rehabilitation following clinically signifi cant traumatic brain injury – intervention. However, there are some 
aspects of rehabilitation that differ for children. One difference in the management of TBI in children is that most 
children with TBI are, or will be, at school, and that many rehabilitative interventions will be implemented within 
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and focused on the demands of the school environment. The child will also have two major environmental 
infl uences: home and school, with different rules and values, which create additional demands on the child. 
An analysis of data for 24,021 children aged 0 to 19 years (77.8% between 1 and 14 years of age) admitted to 
hospital in the USA with at least one head injury found that 63.6% also had other injuries, 16.6% of which were 
severe.264 The level of severity of TBI as assessed by the Glasgow Coma Scale was mild in 67.7%, moderate in 
7.8% and severe in more than 11.5%. When discharged from hospital, 16% of these children and young people 
with TBI had one to three functional limitations – about half of these were limitations in bathing, dressing and 
walking – and 6.2% had four or more limitations (90% in bathing, dressing and walking, 75% in self-feeding, 
cognition and behaviour, 67% in speech, 29% in vision and 16% in hearing). Ninety percent of the children 
with one to three limitations and 37.7% of those with four or more were discharged to home. Despite these 
limitations, referral for physiotherapy (24%), occupational therapy (13%) and speech-language therapy (10%) 
was low. 
It was noted that nearly all of the discharged children were scheduled for a later follow-up hospital visit and 
further referrals for rehabilitative care may have been made at that time. However, rehabilitation should start 
as soon as possible after the injury and be continuous, and the delay in initiating rehabilitation was seen as 
undesirable in terms of the likely possible effects on outcomes for the children and their families.264 
It is important that all children who have been admitted to hospital with a TBI be assessed for functional 
limitations and referred appropriately before discharge.
12.3.1 Transitions
recommendation
grade
The management of transitions for children and young people with traumatic brain injury 
should include:
• case 
coordination
C
•  planning for re-integration starting soon after the acute injury 
C
•  a full assessment of the needs of the young person with traumatic brain injury in an 
C
education environment.
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
12
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good practice points
The management of transitions for children and young people with traumatic brain injury 

should include:
•  coordinated transition plans prepared with the family/wha¯nau and carer(s), the child/
young person with traumatic brain injury, educators, and rehabilitation specialists 
•  information provided to schools about traumatic brain injury and possible long-term 
impairments
• the 
provision of updates and orientation to school peers
•  clear and effective communication 
• the 
provision of training/education on an ongoing basis to all staff involved in the child’s 
education 
•  alternative options for learning 
•  supplementary therapy services 
•  planning for transition to adulthood with formal transition programmes
•  preparation for transitions including: 
−  the student being prepared for new situations, environments, people and challenges
−  staff who will be involved in the child’s education being advised of their strengths, 
problems, needs and appropriate resources and strategies
−  preparation of carers
•  the adaptability and modifi cation of the curriculum to meet the student’s needs
•  monitoring during transitions for support for emergent needs.
This is the opinion of the Guideline Development Team, or feedback from consultation within New Zealand where no evidence is available.
Transitions – such as from acute care to rehabilitation, from inpatient care to home, return to school and from 
school to adult life – can be particularly stressful for children and young people and their carers, and require 
careful management. 
Transitions are likely to require support, particularly if the child or young person has functional limitations 
resulting from the TBI.8 There is little robust evidence about specifi c aspects of transition planning and support 
specifi cally in this population. However, the evidence is consistent that the management of transitions should 
include the following:
• case 
coordination265 
•  planning for re-integration that starts as soon after the acute injury as possible266 
•  a full assessment of the needs of the student265–267 
• coordinated 
transition plans prepared with input from a multidisciplinary team consisting of the family/
wha¯nau and carer(s), the student with TBI, educators, and rehabilitation specialists265–268 
•  at hospital discharge, health professionals should provide schools with information about TBI and possible 
long-term impairments, so that children returning to school receive appropriate support265,266,269 
• the 
provision of updates and orientation to school peers265 
•  clear and effective communication between all parties266,268 
• the 
provision of training/education in the particular needs of the student with TBI to all staff who will be 
involved directly or indirectly in the child’s education266,267 on an ongoing basis, ie, with new staff each year265 
• alternative 
options for learning, such as within the regular classroom, special classes or home instruction,267 
but with home-bound instruction as short as possible265 
•  supplementary and therapy services available in conjunction with class placement267 
•  planning for transition to adulthood that starts no later than age 16 years and preferably at age 14 years267 
with formal transition programmes270 
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•  preparation for transitions including:267 
−  the student being prepared for new situations, environments, people and challenges
−  staff who will be involved directly or indirectly in the child’s education being advised of their strengths, 
problems, needs and appropriate resources and strategies
−  preparation of carers
•  adaptability of the curriculum to meet the student’s needs, including modifi cation, where necessary, of pace, 
tutoring, assignments, materials and environment267 
•  careful and frequent monitoring during transitions for support for emergent needs.265
12.3.2 Provision of rehabilitation 
recommendations
grade
Children with clinically signifi cant traumatic brain injury should receive long-term continued 
C
monitoring and follow-up.
Teachers and other educational staff involved in the teaching and rehabilitation of children 
C
and young people with TBI should receive education tailored to the specifi c needs of the 
school and the particular characteristics of the child with traumatic brain injury about: 
•  typical impairments in memory and learning
•  common problems with behavioural and emotional self-regulation
•  the high risk of academic failure in children with moderate to severe traumatic brain injury
• factors 
infl uencing the rate of recovery
•  the ability of the rehabilitation team to help address learning problems as they arise.
Parents and other carers of children and young people with TBI should be provided with 
C
training in direct intervention and advocacy skills, including how to recognise when to seek 
specialist help and advice.
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
good practice points
The parents and carer(s) of a child with traumatic brain injury should be closely involved in 

the provision of information to educational staff working with the child.
All teachers, particularly special education staff and resource teachers for learning and 

behaviour should be routinely trained to recognise patterns of impairment resulting from 
12
traumatic brain injury and to seek specialist advice, where appropriate.
The need of siblings for support, assessment and education should be considered.

This is the opinion of the Guideline Development Team, or feedback from consultation within New Zealand where no evidence is available.
Rehabilitative interventions will be delivered by paediatric rehabilitation teams, by parents and carers, and by 
special education services, sometimes through the child’s school. 
There is evidence that the benefi cial effects of some interventions may be lost when the intervention is 
discontinued, and that long-term continued monitoring and follow-up is necessary to maintain, reinforce and 
generalise the benefi ts for the individual.271 
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12.3.2.1 Education 
School-based interventions for children and young people with TBI require an understanding of the 
neuropsychological sequelae of TBI.272 However, there is evidence that large proportions of special education 
staff may have misconceptions about TBI and its sequelae that, if not corrected, could negatively impact on the 
success of rehabilitation for the child or young person with TBI, and have adverse effects on their general well-
being. One study testing knowledge of TBI and its sequelae in children in education professionals attending a 
special education conference found that the educationalists had misconceptions about recovery from severe 
TBI, the need for other than purely physical rehabilitation, memory loss, and about common issues such as 
anger, irritability and learning new things.272
A small study of Australian students with brain injury and their parents found similarly that all the parents and 
six of the seven students reported incidents of feeling misunderstood or disliked by teachers and peers.270 Lack 
of awareness of brain injury sequelae resulted in reduced understanding by teachers of the students’ specifi c 
school needs. For example, poor memory and organisation were not recognised by teachers as contributing 
factors to non-completion of work. Many students experienced anguish and humiliation, leading to social 
isolation, low self-esteem, and school avoidance, while all parents reported high levels of stress in relation to 
their children’s schooling.270
One study found that educational psychologists were well aware of the need of younger children with TBI for 
additional support, for longer, than adolescents. The authors looked at whether a now-outdated, but once 
widely held theory was still adhered to: the Kennard Principle: that brain damage sustained in childhood has 
less serious consequences due to the plasticity of the brain, and found that the educational psychologists were 
aware that this was not the case.273 
Although there is no evidence to show that education staff in New Zealand have the same extent of 
misconceptions about TBI in children and young people, the need for education and training of educationalists 
involved with children with TBI is well supported in the literature267,272 and will apply equally well to New 
Zealand. There is evidence that the education of teachers and other educational staff involved in the teaching 
and rehabilitation of children and young people with TBI should address the following areas: 
•  typical impairments in memory and learning
•  common problems with behavioural and emotional self-regulation
•  the high risk of academic failure in children with moderate to severe TBI
• factors 
infl uencing the rate of recovery
•  the ability of the rehabilitation team to help address learning problems as they arise.272
It is also suggested that information be tailored to the specifi c needs of the school and the particular 
characteristics of the child with TBI. The parents and carer(s) of the child should be closely involved in this 
process.
More generally, it is important that all teachers, but particularly special education staff and resource teachers 
for learning and behaviour be aware of the potential for sequelae from TBI, even from mild TBI, for possibly 
extended periods of time. TBI in early childhood may be overlooked until it manifests as behavioural issues in 
later years.
12.3.2.1.1 Educational implications of common consequences of traumatic brain injury in children
This section is adapted with permission from: Ylvisaker M, Todis B, Glang A, et al. Educating students with TBI: 
themes and recommendations. J Head Trauma Rehabil 2001;16(1):76–93.265
12.3.2.1.1.1 Neurological recovery
Often, children experience prolonged and unpredictable improvement, based on several dynamics of 
neurological recovery.
154
 
   
   
 

Implications
•  Educational systems need to be fl exible and programmes highly individualised.
•  Frequent review and modifi cation of the student’s placement and programme may be required, a practice not 
consistent with the tradition of annual review.
12.3.2.1.1.2 Evolving ability profi les
In some cases, the student’s disability increases over time, possibly related to a type of brain injury that has its 
fi rst noticeable consequences at a later developmental stage or to the dynamics of the student’s adjustment. 
Implications
•  Long-term monitoring systems must be implemented, even if the student is not receiving special education 
services. 
•  School staff need to be alert to the possibility that the disability may gradually increase over time, so that 
intervention can be implemented as promptly as possible.
12.3.2.1.1.3 Disability related to vulnerable parts of the brain
Theoretically, any part of the brain can be involved in TBI. However, closed head injury is frequently associated 
with damage to the frontal lobe and anterior and medial temporal lobes, resulting in relatively weak control over 
cognitive processes such as: attention; disorganised thinking and acting; relatively weak planning in relation 
to peers, problem-solving and strategic behaviour; relatively weak learning from consequences; relatively 
weak effortful learning and retrieval; diffi culty holding several thoughts in mind at one time; infl exibility; 
perseveration; inconsistent behaviour and academic performance; concrete thinking and diffi culty generalising; 
relatively weak social perception; and awkward social behaviour.
Implications
•  Impairments may be diffi cult to assess. Many of these impairments are consistent with good performance 
on psychological, neuropsychological and psychoeducational testing. Therefore, necessary services and 
supports may not appear to be justifi ed on testing alone.
•  Disability may be misinterpreted (eg, neurological disinhibition as a psychiatric disorder), with inappropriate 
services a possible consequence.
• Traditional 
teaching 
and behaviour management that emphasise the manipulation of consequences may be 
ineffective.
•  Long-term, contextualised coaching in ‘executive functions’ may be necessary.
Needs related to temporal lobe (including limbic system) injury may include weak learning (new learning) 
relative to the knowledge base acquired before the injury and weak emotional/behavioural regulation.
Implications
•  The student may need much more repetition than would seem necessary.
12
•  The student may need substantial antecedent support for behavioural self-regulation.
Needs related to widespread microscopic damage include relatively slowed processing.
Implications
•  The student may need reduced assignments, evaluation of work based on quality not quantity, and time 
accommodations, particularly in examination settings.
Strengths related to relative sparing of posterior parts of the brain may include the retention of much pre-injury 
knowledge and skills and basic motor and sensory functions.
Implications
•  Assessments must go far beyond testing academic knowledge and skill (acquired before the injury) and 
sensorimotor functions.
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12.3.2.1.1.4 Psychoreactive phenomena
The evolution of emotional consequences after a life-threatening injury is unpredictable but may include 
reactions that profoundly infl uence educational performance. At one stage or another after the injury, some 
children become depressed and withdrawn, others angry and defi ant, and others overtly desirous of pleasing, 
resulting in social vulnerability.
Implications
•  Schools should monitor students’ mental health and social relationships after an injury, and provide 
counselling and support when indicated.
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Chapter 13:
Needs of carers
Overview
•  The effects on the family/wha¯nau and carer(s) of a child with TBI can be considerable.
•  Continuity of support for people with TBI should also include support for their families/wha¯nau and carers. 
Carers should be assessed on an individual basis for their needs for support. Carers should also be provided 
with relevant information and be fully involved in the development of a management plan. Carers should be 
provided with specifi c opportunities for training and emotional support and counselling, where appropriate.
•  There is good support for interventions targeted at increasing social support for families/wha¯nau and carers 
of children and young people, but little outcomes-focused research detailing the effectiveness of specifi c 
interventions.
recommendations
grade
Carers should be individually assessed when assuming the carer role and at regular intervals 
C
thereafter, including for:
• the 
care 
provided
•  the need for support, including respite care
•  the need for training 
•  their stress and mental health issues.
Support should be provided for carers, including:
B
• information 
•  professional and social support 
•  emotional support, including family therapy and relationship/marital counselling, as 
required.
A guide to traumatic brain injury rehabilitation services and resources should be provided to 
C
carers.
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
13
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good practice points
A holistic view should be taken of the person with traumatic brain injury and their carer(s) 

within the context of their wider family/wha¯nau and social networks.
Health care practitioners working with people with traumatic brain injury should be aware of 

who the primary carers are, including both paid, formal carers and unpaid, informal carers 
who are usually family/wha¯nau members.
Family members, including carers, of people with traumatic brain injury should be able to 

maintain their previous social roles as far as possible and it should not be assumed that 
family members will automatically accept the carer role.
Moderating factors of the ability to cope should be used to inform decisions about the 

interventions to provide for carers of people with traumatic brain injury.
Additional support should be provided for carers, including:

• crisis 
support 
•  training and education for the carer role
•  training in behavioural management techniques when the person with traumatic brain 
injury has behavioural and personality changes resulting from the traumatic brain injury
• respite 
care.
This is the opinion of the Guideline Development Team, or feedback from consultation within New Zealand where no evidence is available.
In this section, ‘carers’ refers to people, usually members of the person’s family, who provide care for the person 
with TBI as a result of their relationship with that person, rather than because they are professional caregivers. 
This may include both paid, formal carers and unpaid, informal carers (who are usually family/wha¯nau). Many 
carers do not receive any fi nancial recognition for their input, yet their carer role can have a serious impact on 
their earning ability, as many families suffer considerable loss of income following a family member having a 
TBI.10,11 
13.1 Interventions for people with traumatic brain injury and their families/
wha¯nau and carers 
It is important that a holistic view of the person with TBI and their carer(s), within the context of their wider 
family/wha¯nau and social networks, is taken, as most interventions and support will need to address 
interactions between more than one individual. It should not be assumed that a person will take on the role of 
primary carer simply because of their relationship to the person with TBI. Therefore, it is important for the well-
being of the family of the person with TBI that the family members, including carer(s), be able to maintain their 
previous social roles as far as possible. Practitioners working with people with TBI should be aware who the 
primary carers might be. 
The research in this area is extremely heterogeneous, with little consistency in the outcomes examined, which 
makes comparison of fi ndings particularly diffi cult. Furthermore, there is very little outcomes-focused research 
addressing the effectiveness of interventions for these issues. However, there are considerable effects on the 
families/wha¯nau and carers of people with longer-term sequelae of TBI, which consistently include:
•  loss of or diffi culty in maintaining their normal (pre-injury) social and professional roles71–73,240,241,274–277 
•  a reduction in the family’s social and fi nancial status11,73,276 
•  high levels of health problems, including high stress levels and clinical anxiety and depression in up to two-
158
thirds of carers11,70–72,240,274,278–280
 
   
   
 

 
(These problems are related to the level of unmet need for support,70 being the primary carer,280 and 
cognitive, behavioural, emotional and personality changes in the person with TBI;280,281 while the degree of 
depression is related to the number of adverse events following the injury.278 One study found that the most 
distressing factor for carers was the impact that caregiving had on their personal health and free time)274
•  a reduction in family functioning and an increase in family relationship problems11,73,277,280 
•  an increase in marital breakdown73,277 
•  an increase in loneliness and social isolation for carers73,276 and the person with the TBI.274,276 
Moderating factors for the ability of families and carers of people with TBI to cope with the demands of caring for 
the injured people include:
•  coping style, including fl exibility in adjusting life goals and motivation,275 and the carer’s own satisfaction 
with their ability to cope with the demands240 
•  a positive attitude towards seeking social support282 
•  good pre-injury family functioning11 
•  adaptation by carers, including learning ways to manage particular problems71 
•  the availability of social support. 
Although some of these are intrinsic to the person with TBI and their family/wha¯nau, these factors can be used 
to inform decisions about the interventions to provide for carers of people with TBI. 
There are reports of high levels of burden, distress and health problems for carers of people with TBI. Therefore, 
it is important that continuing support for people with TBI include support for their families/wha¯nau and carers 
upon whom the TBI has also impacted, and who will, in most cases, be providing much of the day-to-day care 
and support for the person with TBI. There is evidence that although friends and wider family/wha¯nau provide 
help and support in the time immediately after the injury, this support usually tails off and the burden of care 
falls more and more on the immediate family as time passes.276 This makes it more diffi cult for the carers to 
maintain their social networks. 
13.1.1 Carer assessment
Carers may have needs themselves resulting from their carer role, and they should be assessed on an individual 
basis for their needs for support, on assuming the carer role and at regular intervals thereafter.70 Carer 
assessment should include assessment of:
•  the care provided
•  the need for support, including respite care
•  the need for training in their carer role
•  their stress and mental health issues.
Carers’ needs for support include:
• the 
provision of adequate information11,73,227,240,241,283 
•  adequate professional and social support73,227,241,278,279 
• the 
provision of emotional support including family/wha¯nau therapy and relationship/marital 
counselling73,196,227 
13
• crisis 
support (eg, for suicidality) 
•  training and education for the carer role, particularly a need for training in behavioural management 
techniques when the person with TBI has behavioural and personality changes resulting from the TBI
• respite 
care.
Siblings of people with TBI can be signifi cantly affected.121 They may become direct carers themselves when 
parents are absent and they may suffer from a lack of attention because of the focus on the person with TBI.
159
 
   
   
 

13.1.2 Information
The provision of information following discharge to the community is discussed in Chapter 9, Post-discharge 
follow-up and support for people with traumatic brain injury. Additional information should include contact 
details for carers’ support groups and other local resources. Information should be provided in both written and 
verbal forms.231 
Families/Wha¯nau and carers also often express a need for a ‘map’ of TBI rehabilitation providers and 
resources.241 A guide to TBI rehabilitation should be provided to carers, which details:
•  the skills, roles and responsibilities of the practitioners involved in rehabilitation, such as clinical 
psychologists, counsellors, psychiatrists, paediatricians, ACC case coordinators and therapists of different 
disciplines
•  who is responsible for the provision of what service
•  who to contact for help
•  entitlements to support.
The case coordinator will be able to help people with TBI and their carers to navigate the system, and should be 
the fi rst point of contact, and this should be emphasised in the guide. 
13.1.3 Social support
Carers should be fully involved in the development of management plans and be involved in decisions about 
ongoing care and support for people with TBI. They should also be assisted to develop the social supports 
necessary for their role. Social supports that have been shown to be effective for carers of people with TBI 
include:73 
• friends 
• family/wha¯nau 
• religion 
•  TBI support groups.
For people without easy access to support groups, such as those not living in the major urban centres, 
telephone support groups have been shown to be effective.284 Carers of people with TBI should be encouraged 
and supported in developing and maintaining social support networks, including friends and wider family/
wha¯nau, and support groups. In New Zealand, there is also the Brain Injury Association Liaison Service, which 
can provide help and support to people with TBI and their families/wha¯nau and carers.
13.1.4 Emotional support and counselling
People with TBI and their families/wha¯nau and carers may need counselling and support in a number of areas. 
Some people may fi nd that the changes in roles when a family/wha¯nau member has a TBI prove diffi cult to 
adapt to and they may benefi t from counselling to assist with their adjustment to the new situation.71
Personality, behavioural and mood changes in the person with TBI can put strain on spousal and parental 
family relationships, and marital and/or family counselling may be necessary.73,277,280 There may also be some 
indirect effects of the TBI for which counselling is helpful. For example, a person with sexual dysfunction caused 
by psychological diffi culties with body image as a result of the primary physical sequelae of a TBI, and their 
partner, may benefi t from relationship counselling and/or counselling on sexuality. 
13.1.5 Empowerment
There is some evidence from a small intervention study that the empowerment of famlies/wha¯nau and carers 
of people with TBI can improve outcomes.285 Factors which were found to lead to better adjustment by carers in 
Hong Kong to a family member having a TBI included: 
•  clear personal expectations
•  a desire to master the situation
160
 
   
   
 

• strong 
motivations
• the 
fl exibility to adjust life goals 
•  an awareness of one’s own powerless state.
Empowerment, defi ned in terms of psychological well-being, self-effi cacy, subjective experience of the 
burdens in caregiving and support systems, was effectively taught through an eight-week community-based 
empowerment programme aimed at these factors. Some improvement in the empowerment of the families was 
reported. Although this was a small study with no control group and, therefore, insuffi cient evidence on which to 
base a recommendation for routine application, staff working with families and carers of people with TBI should 
be mindful of the potential benefi ts of supporting them in a way that is empowering. 
13.1.6 Stress management
A small study of parents caring for children with TBI compared the outcomes for the provision of information 
alone with the provision of information plus coaching in stress management techniques.286 They found that the 
group who received information plus stress management showed a signifi cantly greater reduction in depression 
and anxiety levels. Stress management techniques taught as part of the intervention included:
• self-monitoring
•  progressive muscle relaxation and visualisation
• cognitive 
coping
•  suggestions for social support
•  suggestions for dealing with grief.
Although this was a small study and not strong evidence, parental stress has such a substantial effect on 
outcomes for children with TBI that the Guideline Development Team views it is reasonable to consider some 
form of stress management training for parents and/or siblings who are showing signs of stress, anxiety and/or 
depression. 
13.1.7 Training
All families/wha¯nau and carers need to be provided with specifi c opportunities for training in the residential 
rehabilitation environment and after discharge. The responsibility for residential rehabilitation training should 
be with residential providers, whereas the responsibility for after-discharge training should be that of the funder 
of community rehabilitation services for people with TBI.
Carer support groups in general and specifi c community groups dealing with people and families/wha¯nau with 
TBI are good points of contact and sources of information for families and carers. Practitioners working with 
people with TBI are encouraged to provide contact details (phone numbers and/or web addresses) for such 
groups.
13.1.8 Respite care
Any plan for the long-term rehabilitation of someone in the community after severe TBI needs to include a 
provision for respite care for family/wha¯nau and carers. This need for respite may change over time and need 
periodic re-evaluation.
13
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13.2 Parents/Carers of children and young people with traumatic brain injury
recommendations
grade
Families/Wha¯nau of children with traumatic brain injury need provision of support aimed at 
C
enhancing the following:
• social 
support
•  family relationships and functioning
• stress 
management
•  help with adjusting to the new situation.
There should be an assessment of the individual needs of the family, and interventions 
C
individualised to the family’s needs and comprising some or all of the following should be 
provided as needed: 
•  education and information
•  coping strategies, including problem-solving 
•  specialist marital counselling 
•  specialist family therapy
•  specialist psychotherapy for the primary carer(s)
•  support for building and maintaining social support networks
•  the development of sources of emotional support
• fi nancial advice and support.
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
good practice point
Formal support programmes should be developed and provided for the families/wha¯nau, 

carers and siblings of children with traumatic brain injury.
This is the opinion of the Guideline Development Team, or feedback from consultation within New Zealand where no evidence is available.
Parents and carers of children and young people with TBI may be providing much of the rehabilitative care and 
support. In addition to support in their role, parents and other carers need training in direct intervention and 
advocacy skills, including how to recognise when to seek specialist help and advice.271
Siblings are also inevitably involved as carers and in the delivery of rehabilitation, so their need for support, 
assessment and education should also be considered. 
There was little research evidence on the impacts on a family caring for a child with TBI. Members of the 
Guideline Development Team provided the following best practice advice:
1.  Immediate impacts: emotional
 
The impact of the initial injury is great on all members of a family, particularly when there are severe 
consequences, including the need for hospital (sometimes intensive care unit) care and concerns about 
the immediate survival of the child. Clinicians need to understand these effects on parents and siblings. 
Families/Wha¯nau can respond with perhaps unexpected reactions, such as anger, fear and other emotional 
problems. Appropriate referral to counselling services and support networks may be necessary. Much anxiety 
may revolve around a lack of information about the future of the child, the future of the family/wha¯nau, and 
rehabilitation and education possibilities for children with signifi cant TBI.
2.  Immediate impacts: practical
 
Issues such as who cares for siblings when the mother/father is with the child with TBI, maintenance of work, 
study and other social relationships for parents and siblings and a need to cope with day-to-day activities 
162
 
   
   
 

such as laundry and house cleaning and transport of other children to school need consideration at an early 
stage, with appropriate support provided. Alterations to the home environment may be needed both to better 
facilitate day-to-day activities and to promote safety. Respite care in the short term may be critical for family 
members providing 24-hour supervision for a child with TBI.
3. Long-term impacts
 
These depend on the long-term consequences of the TBI, while the child is growing up and at important 
transitional developmental stages for the child, siblings and parents. There are inevitably continuing 
emotional impacts and continuing anxieties over the rehabilitation and educational needs of the child and 
their future prospects in the community.
 
Within this general framework, research shows that the effects on the family/wha¯nau and carer(s) of a child 
having a TBI can be considerable. Effects on parents have been shown to include:
−  parental injury-related stress287–289 that is often long term290 
−  parental mental health issues287,288 
−  deterioration in family fi nances291,292 
− an increased fi nancial burden on the family, related to the degree of functional impairment288
−  the inability of parents to maintain pre-injury employment demands291,292 
−  deterioration in parents’ marital relationship291 
−  changes in family functioning293 
−  a need for modifi cation of housing or new housing, in the case of children with severe functional 
impairment.291 
Siblings of the injured child are likely to be negatively affected by impaired parental relationships and family 
fi nancial stresses. Siblings may be unaware of the nature of the injured child’s condition and prognosis, which 
may be due to clinical staff and parents attempting to protect them. However, the uncertainty and confusion 
that not knowing can cause may result in siblings becoming particularly anxious.121 
Siblings have been shown to be affected in the following ways:
•  negative impact on behaviour,291 particularly in siblings of children with poorer functional outcomes294 
• depression.294 
People outside the family may also be affected by the sequelae of the TBI. Particularly in the case of more 
severe TBI, or where there are cognitive and/or physical defi cits, the child or young person may not be able to 
return to pre-injury levels of participation and achievement in academic, sporting and social activities. This may 
lead to changes in relationships with their peers.295 
13.2.1 Factors mediating the psychosocial effects on children and young people with 
traumatic brain injury and their families/wha¯nau and carers
There is some evidence that outcomes for a child with TBI and their family are affected by a number of different 
factors. These include factors related to the child and family prior to the injury and factors related to the TBI and 
demands of care.
•  The pre-injury psychosocial adjustment of the child. Children with premorbid psychosocial problems are 
more likely to suffer psychosocial adjustment issues subsequent to the injury.296 
13
•  Pre-injury family functioning. Families with poorer functioning prior to a child’s injury are more likely to have 
a greater degree of dysfunction post-injury.293,297,298 Children and young people with TBI whose families have 
pre-injury dysfunction are also more likely to have psychiatric disorders post-TBI,299,300 and to have poorer 
adaptive functioning.301 
•  The response of the primary carer(s) to the child’s injury. Behavioural outcomes for the injured child over the 
fi rst two years have been shown to be related to the emotional reaction of the primary carer acutely after the 
injury.302 
•  Partner support available to the primary carers. Behavioural outcomes for the injured child over the fi rst 
two years have been shown to be related to whether the primary carer (usually the mother) of the child has 
163
 
   
   
 

a partner, although this association did not persist beyond two years post-injury.302 A good relationship 
between the child’s parents, with consensus on roles and responsibilities is also related to better 
psychosocial outcomes for the child and family, as is the amount of paternal time spent with the injured 
child.303 
•  Family functioning. Children and young people with TBI are more likely to develop novel ADHD and conduct 
disorders if their families are dysfunctional post-injury.304 
•  The degree of functional impairment of the child with TBI. This has been shown to be related to family 
functioning.305 
•  Stress levels. Families of children with TBI where the parents/carers have high stress levels are more likely to 
have poorer psychosocial outcomes.306 One study comparing parents of young people aged 15–24 years with 
and without TBI found that parents of people with TBI experienced higher levels of marital stress, and that 
this was related to global psychological distress levels in the mothers.307 
•  Time since the injury. The proportion of parents/carers with high levels of distress reduces over time as they 
adjust to the new situation. However, a substantial proportion continue to have high levels of stress.288,290 
•  Social support. This has been shown to enhance the coping of families of children with TBI,308 and adequacy 
of social support for carers has been shown to be a signifi cant indicator of family functioning.305 The 
availability of social support has also been shown to impact on the carer’s reaction to functional defi cits 
caused by the TBI. Only among carers with low social support were cognitive dysfunction and personal 
unawareness of defi cit adversely related to life satisfaction. In contrast, these characteristics were unrelated 
to life satisfaction among caregivers with adequate social support.309,310 However, a systematic review 
identifi ed that most unmet needs of carers were related to the provision of emotional support.227 
•  Coping. This has been shown to be improved by the empowerment of carers of people with TBI275 (see 
section 13.1.5, Empowerment); seeking social and spiritual support;303,311 strong family relationships;312 and 
acceptance and the use of humour.313 
From this, it can be inferred that families of children with TBI need provision of support aimed particularly at 
enhancing the following:
• social 
support
• family/wha¯nau relationships and functioning
• stress 
management
•  adjusting to the new situation.
Although there is some research on the provision of such support through various interventions, it is largely 
descriptive and infers probable effectiveness from documented need. There is good support for interventions 
targeted at increasing social support8,10,11,240,276,305,309–311,314,315 but little outcomes-focused research detailing 
the effectiveness of specifi c interventions. One Hong Kong-based pilot study described a family empowerment 
programme which was found to be effective and which targeted each of the four aspects described above.285 
Suggested interventions are generally individualised to the families’ needs70 and comprise some or all of the 
following as required:70,196,241,285,308,316 
•  an assessment of the individual needs of the family/wha¯nau and carer(s)
•  education and information
•  coping strategies including problem-solving 
•  specialist marital counselling 
•  specialist family therapy
•  specialist psychotherapy for the primary carer(s)
•  support for building and maintaining social support networks
•  the development of sources of emotional support
• fi nancial advice and support.
In addition, formal support programmes should be developed and provided for families, carers and siblings as 
164
they deliver much of the rehabilitation, have a high rate of stress as a result, and family/wha¯nau functioning is a 
major factor mediating psychosocial effects on children.
 
   
   
 

Chapter 14:
Special issues
Overview
•  Informed consent, as defi ned by the Health and Disability Commissioner, needs to be considered as a special 
issue in the management of TBI. People who have had a TBI sometimes have cognitive and communicative 
diffi culties, which may limit their capacity to make informed decisions about their treatment.
•  Some people with TBI may not be able to return to driving due to prohibiting conditions, such as seizures or 
cognitive impairments that affect judgement, attention, reaction times and emotional/behavioural control. 
However, many people with milder forms of TBI may be able to return to driving or acquire driving skills 
following appropriate assessment.
•  People presenting with TBI have a high premorbid rate of drug and alcohol misuse, and the highest incidence 
of TBI is among young adult males who also have the highest incidence of substance misuse.
•  People with TBI with a history of drug and/or alcohol misuse show higher mortality rates, poorer 
neuropsychological outcomes and a greater likelihood of repeated injuries and late deterioration following 
TBI.
•  People with TBI who have substance misuse problems require careful assessment and management due 
to the cognitive and emotional problems arising from the TBI. However, there is very little robust research 
examining the effectiveness of interventions for drug and alcohol use for people with TBI.
•  People who have had a TBI frequently experience mental health problems. However, there is considerable 
debate about the extent to which these result from TBI and how these disorders are best addressed in this 
population.
• Depression and anxiety disorders are common following TBI, particularly depression. Psychosis following TBI 
is also well recognised.
•  There is a high rate of mental health disorders in children and young people following TBI.
•  There is some evidence of the infl uence of pre-existing psychological conditions on post-TBI mental health 
in children and young people. ADHD and depressive disorders have been identifi ed as the most common 
mental health disorders following a TBI.
•  In the diagnosis of post-TBI depression, there are key issues to consider, which include assessing the 
severity of depression.
•  A number of depression scales have been developed to quantify depression using a graded method. 
•  Interventions for post-TBI mental health disorders are frequently part of a broad neuropsychological 
rehabilitation programme. However, there is little evidence about specifi c interventions for this population.
•  There is some evidence that multiple TBIs can have cumulative effects, leading to poorer outcomes.
•  The term ‘concussion’ is widely used and this chapter provides some clarity on the defi nition of concussion.
•  Signs and symptoms associated with a suspected TBI are listed in this chapter.
•  There is little evidence, variability in practice and little expert consensus on how repeated TBIs should be 
managed for children. 
•  After controlling for demographics, pre-existing conditions and head injury severity, there is no difference in 
14
outcomes between people with TBI from violent causes and those whose injury is from other causes.
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14.1 Capacity and consent
recommendations
grade
Health care practitioners should make every effort to ascertain injured people’s wishes with 
C
regard to each individual intervention, and where this cannot be determined, to discover what 
their attitude to treatment might have been but for the traumatic brain injury.
A clinical neuropsychologist and/or a speech-language therapist should be consulted with 
C
regard to assessing an individual’s cognitive abilities or enhancing communication.
Where a person lacks, or may lack, capacity, and treatment is considered which appears to be 
C
against their wishes, the advice of a psychiatrist should be sought with regard to determining 
capacity and any possible application of the Mental Health Act 1992.
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
good practice points
Family and carers, particularly the next of kin, should be consulted about the likely wishes of 

the individual in light of their premorbid values and beliefs.
Specialist assistance from a neuropsychologist or neuropsychiatrist should be sought to 

maximise the capacity of the person to consent to treatment.
When the person with traumatic brain injury is Ma¯ori, a Ma¯ori facilitator should also be 

involved in the process of gaining consent.
This is the opinion of the Guideline Development Team, or feedback from consultation within New Zealand where no evidence is available.
Informed consent is a process requiring: effective communication between all concerned; the provision of all 
necessary information about options, risks and benefi ts to the consumer; and the consumer’s freely given and 
competent consent.317 New Zealand legislation governing informed consent is covered by the Code of Health and 
Disability Services Consumers’ Rights,114 and more information can be obtained on the Code and its application 
from the Health and Disability Commissioner’s website at www.hdc.org.nz.
The capacity to consent to treatment requires the injured person to be able to:
1.  understand and retain information about the treatment proposed and any alternative options that may be 
available
2.  weigh up the benefi ts and risks associated with treatment, including any possible consequences of declining 
treatment.
People who have a TBI sometimes have cognitive and communicative diffi culties that limit their capacity 
to make informed decisions about their treatment and to give consent. Alternatively, they may be able to 
understand, but their judgement can be clouded by related symptoms such as depression, especially where 
hopelessness is a prominent feature. 
In the above situations assessment may be complex. The treating health care practitioner is required to provide 
management in the best interests of the person who lacks capacity, but those ‘best interests’ must be carefully 
established,13 as outlined below.
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•  Health care practitioners have a duty of care to make every effort to ascertain injured people’s wishes with 
regard to each individual intervention and, where this cannot be determined, to discover what their attitude 
to treatment might have been but for the TBI. 
•  Family and carers can play an important role in indicating the likely wishes of the individual in light of their 
premorbid values and beliefs, but cannot give consent for them. It is, however, important that family and 
carers be involved, particularly next of kin. 
•  A clinical neuropsychologist and/or occupational therapist and/or speech-language therapist may be helpful 
in assessing the individual’s cognitive abilities or in enhancing communication to ascertain their level of 
capacity for consent and their wishes with regard to treatment.
•  In complex situations where the person with TBI lacks, or may lack, capacity, and treatment is considered 
which appears to be against their wishes, the advice of a psychiatrist should be sought with regard to 
determining capacity and any possible application of the Mental Health Act.318 
The capacity to consent can fl uctuate in people with TBI and efforts should be made, with specialist assistance 
from a neuropsychologist or neuropsychiatrist, to maximise the capacity to consent of the person. When the 
person with TBI is Ma¯ori, a Ma¯ori facilitator should also be involved. Also see Chapter 10, Ma¯ori and traumatic 
brain injury.
14.2 Driving
good practice points
The rehabilitation team should:

•  inform the person and their family/wha¯nau and carer(s) about the law and driving after 
brain injury
•  provide clear guidance for the general practitioner and family, as well as the person, about 
any concerns about driving.
Land Transport New Zealand should undertake discussions with relevant agencies to 

formulate new recommendations regarding people driving following a traumatic brain injury.
This is the opinion of the Guideline Development Team, or feedback from consultation within New Zealand where no evidence is available.
There are a number of reasons why some people with TBI may not be able to return to driving. Prohibiting 
conditions include seizures, visual fi eld defects or cognitive impairments that affect judgement, attention, 
reaction times and emotional/behavioural control. However, many people with milder forms of brain injury 
may be able to return to driving or acquire driving skills following appropriate assessment. Driving is a complex 
activity which requires intact cognitive abilities as well as a certain level of physical ability. Determining when 
someone is unfi t to drive following a TBI can be very diffi cult, especially when such a decision may have very 
signifi cant ramifi cations for the individual, eg, work loss, fi nancial disadvantage.
The rehabilitation team should inform the person and their family/wha¯nau and carer(s) about legal 
requirements regarding fi tness to drive following TBI. They should also provide clear guidance for the general 
practitioner and family, as well as the person, about any concerns regarding driving. They also need to reinforce 
the need for disclosure and assessment in the event that return to driving or, in young people, learning to drive, 
is sought post-injury.8 
14
167
 
   
   
 

14.2.1 New Zealand legislation 
The responsibilities of registered medical practitioners under the Transport Act (Vehicle and Driver Registration 
and Licensing) 1998 are detailed in Medical aspects of fi tness to drive: a guide for medical practitioners (www.
landtransport.govt.nz/licensing/docs/ltsa-medical-aspects.pdf).
New Zealand law requires medical practitioners to: 
•  advise the Director of Land Transport New Zealand (LTNZ), via the Chief Medical 
Advisor’s offi ce, of any individual who poses a danger to public safety by 
continuing to drive when advised not to 
•  consider the guidelines in Medical aspects of fi tness to drive when conducting a 
medical examination to determine whether an individual is fi t to drive. 
14.2.1.1 Specifi c information
‘The medical examination’ is detailed in Medical aspects of fi tness to drive: a guide for medical practitioners 
(page 14). Details specifi c to driving following a TBI are also included (page 44).
Enable New Zealand (phone toll free on 0800-171-981) can provide current information on where to get driving 
assessments in New Zealand.
14.2.1.2 Driving licence revocation procedures
In New Zealand, the guidelines for action to be taken when a medical practitioner considers that a person is 
medically unfi t to drive are summarised as follows: 
•  voluntary surrender of the licence and discontinuation of driving with no questions asked
•  compulsory review by the Director of LTNZ, which may lead to the revocation of any class(es) or all classes of 
licence held, limitations on the use of any class(es) held and the right to have any revocation or limitation 
reviewed by the District Court. 
The general practitioner’s role is to:
•  advise the person with regard to the above options, if necessary in writing 
•  advise the person that a second opinion may be obtained, if required 
•  advise the Director of LTNZ, in the event that the doctor’s advice to cease or limit driving is not accepted by 
the person, that in the opinion of the general practitioner, the person is likely to continue driving. 
For full details see Medical aspects of fi tness to drive: a guide for medical practitioners (pages 9 and 17−20).
14.2.2 Beyond the legislation 
The LTNZ Medical aspects of fi tness to drive: a guide for medical practitioners (page 24) describes two categories 
of people with ‘head injuries’.
1.  ‘Minor’ head injury.
•  'An individual who sustains a minor head injury without loss of consciousness 
or any other complication should not drive for 3 hours'
•  'An individual who sustains a minor head injury but does lose consciousness 
should not drive for 24 hours and should have a medical assessment before 
returning to driving'
•  'An extension of the recommended periods’ is advised with complications, 
specifi ed as ‘loss of good judgement, decreased intellectual capacity, post-
traumatic seizures, visual impairment or loss of motor skills’. Clearance by a 
medical practitioner required before allowed to drive.
168
 
   
   
 

2. ‘Serious or signifi cant’ head injuries
These are defi ned as ‘acute intracerebral haematoma requiring surgery or 
compound depressed fracture or dural tear or with more than 24 hours’ post-
traumatic amnesia’. The LTSA [LTNZ] requires that ‘all cases are fully and properly 
assessed’ prior to ‘any suggestion of a return to driving’. 
•  'Most individuals with severe head injuries, including those with post 
concussion syndrome, should not drive within six months of the event, and a 
return to driving should be subject to a medical practitioner assessment.
The Guideline Development Team considers these categories are insuffi cient to describe the variety of situations 
that exist after TBI. The Guideline Development Team recommends that LTNZ undertake discussions with 
relevant agencies to formulate new recommendations regarding driving following TBI.
14.2.3 Alcohol and other drugs in association with driving
Alcohol and other prescribed, over-the-counter or recreational drugs can signifi cantly impair cognitive 
functioning. Many people with TBI report increased sensitivity, particularly to the effects of alcohol. Therefore, 
a zero-tolerance rule should apply for alcohol and recreational drugs prior to driving for a period equal to twice 
the minimum standdown period for the severity of TBI. The central nervous system and psychotropic effects of 
prescribed or other medications and supplements should be considered when advising about driving for people 
with TBI who require these medications.
14.3 Drug and alcohol use and misuse
recommendations
grade
Any comorbid issues should be identifi ed and addressed in people with traumatic brain injury 
C
and drug and alcohol problems.
Family/Wha¯nau members and other carers need to be educated on how to identify high-risk 
C
situations, and how to identify and respond to warning signs and relapses relating to drug 
and alcohol misuse in people with traumatic brain injury.
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
14
169
 
   
   
 

good practice points
People with traumatic brain injury should be advised that the effects of psychoactive drugs 

and alcohol may be increased, and that they should abstain from use for twice as long as the 
time taken for all symptoms to resolve.
Rehabilitation professionals should refer people with traumatic brain injury and substance 

misuse problems to specialist drug and alcohol services.
Families/Wha¯nau should be involved early to aid in determining drug and alcohol issues in 

people with traumatic brain injury.
Management strategies for drug and alcohol issues in people with traumatic brain injury 

should be developed in collaboration with specialist traumatic brain injury staff. Formal 
systems of collaboration between specialist traumatic brain injury staff and drug and alcohol 
service staff should be developed.
Drug and alcohol service staff working with people with traumatic brain injury should receive 

training in traumatic brain injury sequelae and their effects on drug and alcohol use.
This is the opinion of the Guideline Development Team, or feedback from consultation within New Zealand where no evidence is available.
People presenting with TBI have a high premorbid rate of drug and alcohol misuse. In addition, the highest 
incidence of TBI is among young adult males, who also have the highest incidence of substance misuse. Post-
injury, people with TBI with a history of drug and alcohol misuse have an extremely low rate of employment.319 
Corrigan found that alcohol intoxication was present in one-third to half of people admitted to hospital with 
TBI and that nearly two-thirds of people receiving rehabilitation after TBI may have had a history of substance 
misuse that preceded their injuries.320,321 
There is also a high rate of post-injury drug and alcohol misuse in people who have had a TBI. This rate, 
however, at least for alcohol, appears to be similar to that in the general (non-injured) population.322
People with more severe disability post-TBI have lower alcohol consumption rates. Younger people and people 
with higher blood-alcohol levels on original presentation with TBI are more likely to show an increasing 
consumption of alcohol longer term following the TBI.322 People with TBI also report a reduced tolerance of 
alcohol and drugs. 
In the Guideline Development Team’s opinion, people with TBI should be advised that the effects of 
psychoactive drugs and alcohol may be increased, and that they should abstain from use for double the time 
taken for all symptoms to resolve.
A recent literature review on drug and alcohol use in people with TBI found that rehabilitation professionals 
often lack comprehensive training and skills in the treatment of substance misuse.165 It suggested that 
rehabilitation professionals need to refer people with TBI and substance misuse problems to relevant agencies, 
including treatment outside the rehabilitation facility. It also suggested that they should recommend whether 
inpatient or outpatient intervention is required.165 
The converse may also be true: that drug and alcohol professionals have little understanding of the:
•  way drugs and alcohol are metabolised post-TBI
•  impact of impulse control and overall poor decision-making
• social 
isolation
•  other sequelae of TBI that impact on drug and alcohol consumption (such as the difference between 
170
addiction issues and the management of drug and alcohol issues related to executive dysfunction). 
 
   
   
 

Standard interventions may need modifi cation for people with TBI. However, there is some diffi culty in working 
out the relative effects of TBI and drugs and alcohol. Therefore, the management of drug and alcohol issues 
in people with TBI should be developed in collaboration with specialist TBI staff, along with formal systems of 
collaboration. It is also important to involve families early to aid in determining issues. All staff working with 
people with TBI should receive training in TBI sequelae and their effects on drug and alcohol use. 
14.3.1 The infl uence of pre-injury drug and alcohol use on outcomes
People with TBI with a history of drug and/or alcohol misuse show higher mortality rates, poorer 
neuropsychological outcomes and a greater likelihood of repeat injuries and late deterioration following TBI.320 
This is particularly the case for people with a history of more severe substance misuse problems. 
There is a considerable body of evidence identifying a strong relationship between post-TBI mental health 
problems, such as depression and anxiety, and pre-injury psychiatric history. However, an analysis of the 
research indicates that pre-injury substance use is the signifi cant factor, and when this factor is accounted for, 
other psychiatric conditions are no longer signifi cant as predictors of post-TBI mental health issues (see Section 
14.4, Mental health in adults with traumatic brain injury). Determining pre-injury drug and alcohol use may 
therefore be of use in predicting an increased likelihood of post-injury mental health problems. 
14.3.2 Assessment and diagnosis and interventions for drug and alcohol misuse 
A review of the literature on drug and alcohol use in people with TBI concluded that there should be routine 
quantitative assessment, records review and long-term monitoring to identify and follow up drug and alcohol 
misuse in people with TBI.165 Assessment should use standardised tools and measures to allow for the 
comparison and collection of data.323,324 
It is also important that comorbid issues are identifi ed and addressed to maximise the effectiveness of 
rehabilitation and treatment for drug and alcohol misuse. For example, many women with alcohol misuse issues 
have a history of sexual misuse which will impact on the success of the rehabilitation.325 
People with TBI who have substance misuse problems require special treatment due to the cognitive and 
emotional problems arising from the TBI.326 Although there is research describing the problem of drug 
and alcohol misuse in people with TBI, there is very little robust research examining the effectiveness of 
interventions aimed at this specifi c population. 
Research has identifi ed four ‘types’ of people who have had a recent TBI based on pre-injury alcohol 
consumption, alcohol problems and alcohol dependence. These ‘types’ corresponded to people with a history 
of:
1. alcohol misuse
2. alcohol dependence
3.  alcohol dependence in remission
4.  normal or non-drinkers. 
It is suggested that if health care practitioners match people’s types to specifi c interventions, such as 
educational and motivational interventions, as well as treatment for substance misuse, this may result in more 
effective care.327
A small study of 50 adults, looking at how motivated people with recent TBI are to change their alcohol drinking 
habits and what factors affect their motivation, found that after a TBI, drinkers frequently contemplate changing 
14
their alcohol use, and that a history of alcoholism, higher daily consumption and alcohol being a factor in the 
injury were all associated with greater readiness to change.328 Comparison with a separate medical sample also 
supported a TBI being associated with greater action to change alcohol use. It was concluded that the use of 
motivational interviewing techniques may facilitate change during this period. 
171
 
   
   
 

A comprehensive review of the TBI and substance misuse literature found that people with TBI and a history of 
pre-injury substance misuse are at risk of resuming the substance misuse on discharge to the community.165 
Family/Wha¯nau members and other carers need to be educated on how to identify high-risk situations and how 
to identify and respond to warning signs and relapses in people with TBI. 
14.4   Mental health in adults with traumatic brain injury
recommendations
grade
If a person with TBI has signifi cant neuropsychiatric problems, local mental health teams 
C
should be involved in the development of a management plan, including inpatient 
management, discharge management and follow-up.
Specialist neuropsychiatry support should be available to local mental health teams in the 
C
management of people with complex neuropsychiatric problems following TBI.
If a person with TBI is unwilling to stay in hospital yet needs to do so because it would not be 
C
safe for them to go home, consideration should be given to the need for treatment under the 
Mental Health Act 1992.
Staff should be aware of their duty of care to ensure the safety of people who are putting 
C
themselves or others at risk, including ensuring carer safety and immediately accessible 
assistance and support.
Services for people with traumatic brain injury, including:
C
•  local acute care and rehabilitation services contracted to manage people with traumatic 
brain injury
•  local mental health services 
• ACC 
personnel, 
should collaboratively specify and document policies for dealing with people with traumatic 
brain injury who have mental health issues, whether they pre-date or follow the traumatic 
brain injury.
Where traumatic brain injury is a result of deliberate self-injury, or where people with 
C
traumatic brain injury exhibit suicidality, they should have a psychiatric assessment including 
a risk assessment and consideration of the need for further intervention from the mental 
health team.
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
good practice point
Staff of mental health services should receive training in recognition of the particular issues 

they may encounter in people with traumatic brain injury.
This is the opinion of the Guideline Development Team, or feedback from consultation within New Zealand where no evidence is available.
172
 
   
   
 

People who have had a TBI frequently experience mental health problems, and there is considerable debate 
around the extent to which these result from the TBI and how these disorders are best addressed in this 
population. Post-injury depression and other mood disorders, anxiety disorders, and other mental health 
disorders can negatively impact on the success of rehabilitation and the functioning and quality of life in both 
people with TBI and their carers.329 
Formalised close and collaborative liaison is essential between TBI rehabilitation services and mental health 
services, and mental health staff should receive training in recognition of the particular issues they may 
encounter in people post-TBI. If a person has signifi cant neuropsychiatric problems, local mental health teams 
should be involved in after-care planning.8
Specialist neuropsychiatry support should be available to support local mental health teams in the 
management of people with complex neuropsychiatric problems following TBI.8 
People who have had a severe TBI sometimes lack insight into their diffi culties, so if a person is unwilling to stay 
in hospital yet needs to do so because it would not be safe for them to go home, consideration should be given 
to the need for treatment under the Mental Health Act 1992.8,318 However, even if people cannot be admitted 
under the Mental Health Act, staff should be aware of their duty of care to ensure the safety of people who are 
putting themselves or others at risk. This should include ensuring carer safety and immediately accessible 
assistance and support.
The Guideline Development Team has found that a recurring message from health care practitioners working 
with people with TBI is the diffi culty of adequate cohesion between mental health services, rehabilitation 
services and ACC. This is thought to partly refl ect historical service divisions, different funding streams and 
uncertainty about what services are able and willing to offer.
In the Guideline Development Team’s opinion, local acute care and rehabilitation services contracted to manage 
people with TBI, along with local mental health services, need to work together to specify and document 
policies for dealing with people with TBI who have mental health issues, whether they pre-date or follow the 
TBI. ACC personnel need to be involved in these discussions and ‘sign off’ any local policies so that they can be 
included in existing and future contracts. 
14.4.1 Mood disorders
Depression is particularly common post-TBI. For example, a recent large cross-sectional study found that 42% of 
adult outpatients with TBI referred for assessment at a trauma centre had diagnosable depression.330 An earlier 
study found that about 25% of people with a TBI met diagnostic criteria for a major depressive episode and 
more for a minor depressive episode.331 A large study of World War II veterans compared the lifetime incidence 
of depression for those with and without TBI, and found that the lifetime prevalence of major depression in the 
TBI group was 18.5% compared with 13.4% in those with no TBI (OR 1.54, 95% CI 1.17–2.04). This increase 
in depression was not explained by a history of myocardial infarction, stroke or alcohol misuse, but the risk of 
depression increased with severity of the head injury.332 
Several studies of depression in the non-TBI community have found that depression inhibits cognitive 
functioning, particularly executive functioning, and motivation – a reduction in ‘goal-directed’ behaviour. 
In depressed people with TBI, depression-caused impairments in cognition and motivation will be additive 
to the impairments caused by the TBI, increasing the level of disability and reducing the effectiveness of 
rehabilitation.329 It is therefore important that depression is identifi ed and treated in people with TBI.
14
There is less research on the incidence of mania secondary to TBI. One study of 66 adults with TBI found that 
9% met the criteria for mania at some point during follow-up, a frequency signifi cantly greater than that seen 
in other brain-injured populations such as people who have had a stroke. Mania post-TBI was not found to be 
associated with the severity of the injury, extent of physical or cognitive impairment, level of social functioning, 
or previous family/personal history of psychiatric disorder.333 
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14.4.2 Anxiety
Anxiety disorders are also common following a TBI. One study found that the reported incidence of anxiety 
disorders in people post-TBI was as follows: generalised anxiety disorder 3% to 28%, panic disorders 4% 
to 17%, phobic disorders 1% to 10%, obsessive compulsive disorder 2% to 15% and post-traumatic stress 
disorder (PTSD) 3% to 27%.334 
14.4.3 Psychosis
Psychosis following TBI is well recognised, and has a higher prevalence in the post TBI population than in the 
general population, with an increased risk (RR 0.2–16.3) having been reported in various studies.335 
14.4.4 Post-traumatic stress disorder
Historically, there has been some controversy about the possibility of the coexistence of TBI and PTSD. It was 
argued that the amnesia and loss of consciousness associated with TBI prevented memories of the trauma, 
and thus there would be no memory of trauma to trigger PTSD. However, more recently the research has 
demonstrated that PTSD resulting from the TBI can and does occur in people with TBI.336–338 For example, one 
study of 96 people admitted to a brain injury unit following severe TBI found that, at a six-month follow-up, 
27% had clinical PTSD.339 Another study of 66 people who had suffered a severe TBI found that at an average 
of nearly six years (range 1–26 years) post-injury, 18% had moderate-to-severe symptoms of PTSD which were 
unrelated to the severity of the injury, educational background, premorbid or current measured intelligence 
quotient, or memory impairment.340 
One small study suggested that there may be a relationship between the duration of unconsciousness and the 
development of PTSD. In this study, 46 people who were receiving post-TBI rehabilitation were divided into two 
groups according to whether they had experienced a prolonged period of unconsciousness (>12 hours) at the 
time of injury. It found that 27% of the people who were not unconscious for an extended period, but only 3% 
of those who were unconscious for more than 12 hours as a result of the accident, were diagnosed as having 
current PTSD.341 (See Section 14.4.10.1, Diagnosis and management of post-traumatic stress disorder for people 
with traumatic brain injury.)
14.4.5 Suicidality
TBI sometimes results from self-harm or an attempted suicide. People with TBI may also become suicidal 
following their injury. Where TBI is a result of deliberate self-injury, or where people with TBI exhibit suicidality, 
they should have a psychiatric assessment including a risk assessment and consideration of the need for 
further intervention from the mental health team.8 
For more details of the management of people after a suicide attempt, see the guideline for Assessment and 
Management of People at Risk of Suicide available at www.nzgg.org.nz.
14.4.6 Post-traumatic brain injury mental health disorders in children and young people
It is known that there is a high rate of mental health disorders in children and young people following a TBI. 
One study of children and adolescents (aged 6–15 years), a year post-TBI, found a high rate of novel psychiatric 
disorders, and that 78% of these disorders persisted in 48% of the children studied.342 
Another study found that 19% of children had ADHD post-TBI, and this was novel (ie, secondary to the TBI in 
nearly half).343 
Another study of children and young people (aged 5–22 years) found that 30.4% had one or more psychiatric 
hospitalisations following the TBI prior to admission to rehabilitation.344 A large matched-controls study of 
children aged 14 years or less, three years after they had sustained a mild TBI, found that the incidence of any 
psychiatric illness was 30% in the children who had a mild TBI, signifi cantly higher than the 20% in those with 
no TBI.345 
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One prospective cohort study of children found that PTSD developed in 13% of children with severe TBI that was 
accompanied by traumatic amnesia. Predictors of PTSD included female gender and early post-injury anxiety 
symptoms, which are consistent with predictors of PTSD that develop after non-head-injury trauma.346 Another 
study comparing children with and without TBI who had been involved in vehicle accidents found that, 13 weeks 
after their accidents, 38% of children with TBI and 46% of those without TBI had PTSD.347 
One small prospective cohort study examined the incidence of mania in children hospitalised following TBI. 
They found that 8% developed mania or hypomania, and suggested that the severity of injury, location of 
lesion(s) and family history of major mood disorder may be associated with the development of mania post-TBI 
in children.348 This incidence is similar to that found in adults post-TBI.333 
14.4.7 The infl uence of pre-injury mental health disorders on outcomes
One aspect of the debate is how the effects of a TBI are confounded by a pre-injury history of mental health 
disorders and related personality factors. One concern is that premorbid characteristics and issues may 
be misinterpreted as symptoms resulting from the TBI, and thereby reduce the accuracy of diagnosis. 
More seriously, a mistaken belief that post-injury symptoms are not attributable to the injury could lead to 
misdiagnosis, and under the ACC system in New Zealand, could be a barrier to appropriate and adequate care 
and management. The infl uence of pre-existing substance misuse is addressed in Section 14.3, Drug and 
alcohol use and misuse. This Section addresses the infl uence of mental health conditions other than substance 
misuse.
There is a large body of literature detailing the theoretical infl uence of pre-injury psychological functioning on 
the development of post-TBI psychological disorders.349 However, there are fewer papers testing this theoretical 
approach by actually measuring the relationship. The literature search identifi ed a number of studies examining 
the prevalence of pre-injury mental health issues and comparing outcomes for adult and paediatric TBI survivors 
with and without such history. 
However, it is important to remember that an ‘association’ between pre-injury factors and post-injury outcomes 
is merely an association. Causality in any individual case cannot be inferred from a statistical association, nor 
does a lack of a statistical association mean that in individual cases there is no infl uence on outcomes from 
pre-injury factors. Nonetheless, pre-existent mental health diffi culties may be conceptualised as vulnerability 
factors for post-injury psychological problems.
14.4.8 Post-traumatic brain injury mental health disorders
There is very little research which excludes or separately analyses drug and/or alcohol misuse in the pre-
existing mental health conditions examined. However, when pre-existing drug and alcohol misuse is excluded, 
the evidence is consistent that there is no relationship between pre-existing mental health disorders and those 
occurring after the TBI. 
One paper, reporting on two Australian studies, examined the possible relationship between pre-injury 
morbidity and post-injury outcomes as a function of severity of injury. The study found that in both a matched 
control study of people six years after a severe TBI and a second study of people with a mild TBI, there was no 
effect of pre-injury characteristics on any of the outcomes measured.350 
Another small case-controlled study of people with mild TBI and with or without a pre-injury history of 
depression found no differences on self-reported post-concussive symptoms, Minnesota Multiphasic 
Personality Inventory scales, or neuropsychological measures between the case-matched groups. It was 
14
concluded that health care practitioners need to be cautious in attributing post-concussive symptoms or 
neuropsychological defi cits to a pre-existing affective disorder.351 A further study found that people with 
depression post-TBI had a higher frequency of previous psychiatric disorders than people post-TBI with no 
depression, but that when drug and alcohol misuse was excluded from the analysis, the difference between the 
groups was no longer signifi cant.331 
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14.4.8.1 Post-traumatic brain injury psychosis
A recent systematic review of the literature about psychosis post-TBI has identifi ed considerable methodological 
issues with the previous research and the analyses of the data.335 It was concluded that while there was a 
strong association between pre-existing psychotic disorders and TBI (ie, people with psychotic disorders were 
more likely to have a TBI), there was little, if any evidence of suffi cient quality to support a causal link between 
TBI and psychosis. However, this paper used schizophrenia as a synonym for psychosis, which is incorrect 
– people with post-TBI psychosis may have many psychotic symptoms without presenting clinically as having 
schizophrenia. An addendum to the review described a recently published paper, which the review authors said 
provided ‘weak’ evidence for head injury as a cause of psychosis.335 
Although the body of literature on this topic has some methodological shortcomings, it is largely consistent in 
reporting post-TBI psychosis. Attributing psychosis to a TBI should only be done after much careful discussion 
and investigation of pre-injury signs and symptoms. (See Section 14.4.10.2, Diagnosis and management of 
post-traumatic brain injury psychosis.)
14.4.8.2 Mental health in children and young people with traumatic brain injury
There is a reasonable body of evidence around the infl uence of pre-existing psychological conditions in children 
and young people post-TBI. However, the variation in and the width of the age groups included in the research 
makes it impossible to analyse for specifi c age groups. 
ADHD and depressive disorders have been identifi ed as the most common new mental health diagnoses 
following a TBI.342 One study showed that while pre-injury ADHD is about fi ve times more common (ie, about 
20% of the sample studied) in children and young people who have moderate-severe TBI than those who have 
no TBI, about 19% of children without pre-injury ADHD develop ADHD secondary to the injury.343 Another study 
found that children with mild TBI but no psychiatric history were at higher risk for hyperactivity in the fi rst year 
after injury (incidence 3%; fi rst year relative risk 7.59; 95% CI 2.7–21.6).345 
One study found a clear relationship between TBI and novel mood and anxiety disorders, and that post-
injury stress levels and the severity of the TBI were the most robust predictors of the development of a newly 
diagnosed psychiatric disorder post-TBI.352 Another study comparing outcomes for children with mild or 
moderate-severe TBI and those with orthopaedic injuries reported that the three groups did not differ on pre-
injury depressive symptoms, but parents of children with TBI reported more depressive symptoms at six- and 
12-month follow-ups. It was suggested that TBI increases the risk of depressive symptoms, especially among 
more socially disadvantaged children.353 
Another study found that, in children, psychosocial adjustment deteriorated signifi cantly after a TBI, and that 
post-injury psychosocial impairments are common in children with moderate to severe TBI and are related to 
injury severity.296 The study concluded that in most cases, the problems cannot be attributed exclusively to pre-
injury dysfunction.
A series of studies examining psychiatric outcomes for a cohort of children aged 6–14 years when hospitalised 
for a TBI, found that at three months post-injury, a pre-injury psychiatric condition was a predictive factor for 
a psychiatric disorder. However, this was not the case at either the six-month or one-year follow-up. Constant 
predictors of psychiatric disorder were severity of injury (when classifi ed as mild or severe), socioeconomic 
class, intellectual functioning, behaviour/adaptive function, pre-injury family functioning and family psychiatric 
history. Newly diagnosed psychiatric disorders at the two-year follow-up were again also related to pre-injury 
psychiatric history.299,300,354,355 
The research in this area consistently fi nds an increase in the risk of novel psychiatric disorders, particularly 
ADHD, depression and anxiety disorders, following a TBI, which may be related to the severity of the TBI. A 
proportion of these disorders may be attributable to the infl uence of pre-injury psychiatric history, but there are 
a number of both injury-related and other factors which are equally or more important.
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14.4.9 Diagnosis and management of mental health disorders post-traumatic brain injury
This section is adapted for New Zealand from the recent evidence-based UK Concise Guidance for the Use of 
Anti-depressant Medication in Adults Undergoing Recovery or Rehabilitation Following Acquired Brain Injury
produced in 2005 by the British Society of Rehabilitation Medicine, the British Geriatrics Society and the Royal 
College of Physicians’ Clinical Effectiveness and Evaluation Unit.13 
14.4.9.1 Diagnosis of post-traumatic brain injury depression
good practice points
The main issues to be considered are: 

•  whether the depression is severe enough to affect health or impede recovery 
•  whether the depression is likely to respond better to antidepressant medication or other 
interventions
•  whether the antidepressant medication for the individual is safe and acceptable 
•  how to monitor the effectiveness of treatment
•  how long to continue treatment.
Using an appropriate depression screening tool, for adults or children, should be a part of 

routine practice.
Depression screening tools should not be used as the sole indication for initiation of 

treatment. Diagnosis should always involve clinical judgement by a specialist experienced in 
managing people with TBI.
The person with TBI should be referred to a psychiatrist with expertise in treating people with 

TBI if:
•  the risk of suicide is judged signifi cant
•  the initial treatment is not effective within two months
•  the presentation is complex 
•  pharmacotherapy is indicated and the familiar medication strategies are contraindicated.
This is the opinion of the Guideline Development Team, or feedback from consultation within New Zealand where no evidence is available.
In the diagnosis of post-TBI depression there are some key issues to consider, as outlined below.
1.  Does the person have depression which is severe enough to affect their health or to impede their recovery?13 
It is normal (ie, not clinical depression) to have ‘low’ mood post-TBI, as the person may go through a period 
of grief and adjustment to their new situation, which is not depression. Standardised diagnostic criteria 
should be used in the diagnosis, drawing from the criteria in the fourth edition of the Diagnostic and 
Statistical Manual – Text Revision (DSM-IV-TR).356 The person with TBI with grief and other common (non-
depression) reactions to TBI will need support and treatment if depression is diagnosed.
2.  Is the depression likely to respond to anti-depressant medication or are other interventions more 
appropriate?13
3.  If antidepressant medication is considered likely to be helpful, is it safe and acceptable for that particular 
individual?13
4.  How do you determine if treatment has been effective, and if so, how long do you continue treatment?13
14
Basic history-taking should include a routine general health enquiry with open questions such as ‘How do you 
feel in yourself?’. However, this may not always be suffi cient to identify depression in people with TBI, and it is 
therefore appropriate to employ a screening method as part of routine practice. More detailed assessment is 
then required for those in whom depression is suspected, to identify symptoms of actual depression or lowered 
177
 
   
   
 

mood from the general effects of TBI, and to quantify the severity of mood disturbance prior to considering 
treatment.
The simple ‘Yale question’ (‘Do you often feel sad or depressed?’) has been proposed as providing a good 
screening assessment of depression.357 The advantages of this single question are its apparent simplicity and 
timeliness. However, a dichotomous answer of ‘Yes’ or ‘No’ may in itself be problematic. Firstly, the answer 
requires intact comprehension and at least a reliable ‘yes/no’ response, which may not be present in some 
people following TBI. Secondly, the question, in fact, contains two different components, to which the responses 
may be different. For example, it is not uncommon for people to feel sad about their loss, but not depressed. 
Therefore, there needs to be some comparison with their normal mood state. 
As with all screening tests, a dichotomous response does not provide a sensitive measure against which to 
assess the benefi ts of treatment, particularly in cases where there may have been some partial improvement 
in mood. Also, some people may not report low mood. Some people report emotional blunting and loss of 
enjoyment for everyday activities (anhedonia). People from some cultures may need different phrasing. For 
example, people from a Chinese culture may respond more informatively to a question on whether their energy 
levels are lower than usual.
14.4.9.1.1 Assessing severity
A number of scales have been developed to quantify depression in a more graded manner.
These exist in several different formats which may be chosen to suit the person’s capabilities.
•  Non-verbal rating scales – such as visual analogue scales in different forms. These may be useful where 
verbal communication is limited but visuo-spatial skills are adequate, although facilitation will often be 
required.
•  Questionnaire-based tools – may be completed at interview or by self-report where the individual has 
suffi cient verbal skills.
•  Scales based on observation of behaviour such as crying, withdrawal and apathy may be useful where the 
individual is unable to respond to either non-verbal rating scales or questionnaire-based tools.
Some of the scales require special training and experience to administer; others are more intuitive. Some, 
including the Hospital Anxiety and Depression Scale, and the Beck Depression Inventory (BDI–II), are restricted 
by copyright, and it is necessary to purchase a licence for their use. 
Short forms have been developed for some instruments, such as the Geriatric Depression Scale (GDS-15) 
and the Beck Depression Inventory (BDI FastScreen), but these have been developed in general populations 
rather than for people with TBI, so their usefulness in this context is still uncertain. Preliminary work with the 
BDI–II suggests that a rather different sub-set of the cognitive and affective items may be more appropriate in 
a TBI population in general. However, the BDI–II has been reported to give false positives on measurement of 
somatisation in some people with TBI. 
It is perhaps useful for generalist clinical settings to have available a very simple set of screening tools for quick 
assessment in cases of suspected depression. Of the current freely available tools, a reasonable selection for 
use in general practice and rehabilitation settings for people with TBI might include:
•  the Depression Intensity Scale Circles – a simplifi ed visual analogue scale specifi cally designed for people 
with communication or cognitive diffi culties, but who have adequately preserved visuo-spatial skills
•  Short-Form GDS-15 – a simple questionnaire-based tool for people with adequate verbal and language skills
•  Signs of Depression Screening Scale – a simple tool based on observation of behaviour such as crying, 
withdrawal and apathy, which may be useful where the individual is unable to respond to either of the 
previous tools.
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Tools for use with children and young people could include:
•  the Child Depression Inventory (CDI)
•  the Reynolds Child Depression Scale
• the 
BDI.
Depression scales may be useful for screening, for determining the extent of low mood and in monitoring 
responses to intervention. However, tools do not provide a diagnosis, merely an indication, and may be 
insuffi cient, particularly in the TBI population. They should not be used as the sole indication for initiation of 
treatment, and diagnosis should always involve clinical judgement by a specialist experienced in people with 
TBI. 
There is no one tool which may be applied universally, but it is appropriate for rehabilitation teams to familiarise 
themselves with a chosen selection, so that they reach a shared understanding of the meaning of a particular 
score. Further to this, more detailed assessment may be undertaken through interview and/or observation. 
Figure 14.1 presents a proposed schema for screening and assessment of depression at different levels, and 
the extent of clinical expertise which may be required.
14
179
 
   
   
 

figure 14.1:
assessment of depression in traumatic brain injury
Which people?
Administered  
level i:
by
screening at each clinical review
Yale question
Medical staff or 
All
‘ Do you often feel sad or depressed?’
other member of the 
Or ask nursing staff/carers/ family
multidisciplinary 
‘Do you think he/she feels sad or depressed?’ or 
team (MDT)
’Is their mood different from the normal state?’
level ii:
simple assessment of severit y
Visual analogue scales, eg,
•  Depression Intensity Scale Circles
•  Numeric Graphic Rating Scale
Any person with TBI 
Verbal scales, eg,
in whom depression 
•  Geriatric Depression Scale – Short Form
is suspected or for 
(GDS-15)
Members of the MDT
whom treatment is 
• Hospital 
Anxiety 
and Depression Scale 
being considered
(HADS)*
•  Beck Depression Inventory FastScreen
(BDI–IIFast)*
Behavioural scales
•  Signs of Depression Screening Scale
• Stroke 
Aphasic 
Depression 
Scale
level iii:
more complex assessment by 
People with TBI with 
structured interview (requires 
Clinical psychologist 
complex presentation 
training)
or MDT member with 
or in whom the  
•  Present State Examination to complete
appropriate training
diagnosis is in doubt 
DSM-IV-TR
(see Level 1)
•  Or based on standard assessment tool, eg, 
BDI–II*
Severe/Resistant 
level iv:
Psychiatrist or 
depression or
f ormal psychiatric assessment
neuropsychiatrist
suicide risk

Use of the HADS and the BDI scales is restricted by copyright.
It is necessary to purchase a licence to use these tools.
Adapted from the UK’s Concise Guidance for the Use of Anti-depressant Medication.13 
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14.4.9.1.2 Continued monitoring
Screening and assessment of depression carries no benefi t if it is not followed with appropriate treatment, 
planning and continued monitoring to ensure response. Whatever the assessment process used, it must be 
timely and practical to allow for repetition on subsequent occasions for comparison.
The person with TBI should be referred to a psychiatrist with expertise in treating people with TBI if:
•  the risk of suicide is judged signifi cant
•  the initial treatment is not effective within two months
•  the presentation is complex 
•  pharmacotherapy is indicated and contraindicated. 
14.4.10 Interventions for mental health disorders in people with traumatic brain injury
Interventions for post-TBI mental health disorders are frequently part of a broad neuropsychological 
rehabilitation programme. There is very little evidence about specifi c interventions for this population. It is 
known that mental health disorders negatively impact on the success of rehabilitation, and that early diagnosis 
and treatment of psychiatric disturbances can improve rehabilitation outcomes.323,329,352,358 An interdisciplinary, 
‘multi-pronged’ approach is necessary, with participation of the person with TBI, family members and health 
care practitioners and therapists.323 
14.4.10.1 Diagnosis and management of post-traumatic stress disorder for people with traumatic brain inury 
good practice point
Assessment for differential diagnosis should consider the overlap in symptoms between mild 

traumatic brain injury and post-traumatic stress disorder. If there is doubt, the person should 
be referred for a specialist neuropsychological assessment.
This is the opinion of the Guideline Development Team, or feedback from consultation within New Zealand where no evidence is available.
PTSD is an anxiety disorder. The DSM-IV-TR lists the following criteria for diagnosis: 
1.  exposure to or witnessing of an event that is threatening to one’s well-being
2.  symptoms of re-experiencing, such as intrusive memories, nightmares, a sense of reliving the trauma, or 
psychological and physiological distress when reminded of the trauma
3.  avoidance of thoughts, feelings  or reminders of the trauma, and inability to recall parts of the trauma, 
withdrawal, and emotional numbing
4.  arousal, as manifested in sleep disturbance, irritability, diffi culty concentrating, hypervigilence or heightened 
startle response.356
PTSD is frequently comorbid with other mental health problems, and is associated with impairment in social 
and occupational functioning.359 PTSD may be overlooked in people with TBI due to symptomatic overlap, 
particularly in someone who presents with mood or behavioural diffi culties. As there is also some overlap in 
symptoms between mild TBI and PTSD,360,361 it is important that assessment for differential diagnosis be done 
with this in mind, and if there is doubt the person may need to be referred for a specialist neuropsychological 
assessment.
People often experience a range of PTSD symptoms following trauma, but the majority of these reactions will 
remit in the following months to one year.359 Cognitive-behavioural therapy is widely used for the treatment of 
14
PTSD and may be of particular value to people with cognitive disability.359,362 
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14.4.10.2 Diagnosis and management of post-traumatic brain injury psychosis 
good practice point
People who have possible psychotic symptoms post-traumatic brain injury should be referred 

to a psychiatrist with expertise and experience in the management of people with traumatic 
brain injury.
This is the opinion of the Guideline Development Team, or feedback from consultation within New Zealand where no evidence is available.
The DSM-IV-TR includes a diagnostic category – psychotic disorder due to traumatic brain injury (PDTBI) – the 
criteria for which are: 
1.  the presence of hallucinations or delusions
2.  evidence that the psychosis is a direct consequence of TBI
3. the psychosis is not better accounted for by another mental disorder
4. the psychosis does not occur exclusively during a state of delirium.356
There may be some differences, compared with the non-TBI population, in presentation with post-TBI 
psychosis. One study found that only 14% of people with post-TBI psychosis experienced negative symptoms of 
schizophrenia (such as apathy and withdrawal) whereas between 25% and 84% of people with schizophrenia 
but no TBI had such symptoms.363 
The diagnosis and management of post-TBI psychosis and psychotic symptoms require specialist assessment 
and management. People who, post-TBI, have possible psychotic symptoms should be referred to a psychiatrist 
with expertise and experience in the management of people with TBI. 
14.4.10.3 Pharmacotherapy
recommendation
grade
There should be careful consideration of the sensitivity of people with traumatic brain injury 
C
to psychotropic medication before trial use. The use of psychotropic medication should be 
avoided where possible, and used with caution where indicated.
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
good practice points
In any trial of psychotropic medication, the ‘start low and go slow’ approach should be 

adopted.
Medications that have an adverse effect on central nervous system functioning, particularly 

antipsychotics such as barbiturates, benzodiazepines, phenytoin and haloperidol, should be 
avoided.
Serum drug levels should be monitored as necessary.

The risks, benefi ts and harms should be discussed with the injured person and their carer(s), 

and it should be explained that response to medication after traumatic brain injury is less 
predictable than in standard practice.
This is the opinion of the Guideline Development Team, or feedback from consultation within New Zealand where no evidence is available.
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There are very few well constructed trials of medication for mental health disorders in the TBI population. A 
Cochrane review evaluating pharmacological treatments of psychosis, depression, anxiety and agitation in 
neurological conditions concluded that few suffi ciently rigorous trials had been conducted. There was also 
no evidence to support any particular pharmacological approach to treatment in people with neurological 
conditions, including TBI.364
The Guideline Development Team endorses a proposed management approach for pharmacotherapy for post-
TBI psychiatric conditions, with observation of the following rules:
•  people with TBI are frequently very sensitive to, and may have an unpredictable response to, psychotropic 
medications, so there should be careful consideration before trial use. In any trial of a medication, the ‘start 
low and go slow’ approach should be adopted
•  as a general rule, the use of psychotropic medication should be avoided where possible, and used with 
caution where indicated
•  avoid, if possible, medications that have an adverse effect on central nervous system functioning, 
particularly antipsychotics such as barbiturates, benzodiazepines, phenytoin and haloperidol
•  monitor serum drug levels as necessary 
•  always discuss the risks, benefi ts and harms with the injured person and their carer(s), and explain that 
response to medication after TBI is less predictable than in standard practice.323,324
14.4.10.3.1 Pharmacotherapy for post-traumatic brain injury depression
recommendations
grade
A specifi c selective serotonin reuptake inhibitor should be the fi rst choice for treatment of 
C
post-traumatic brain injury depression unless the anticholinergic effects of a tricyclic are 
considered desirable.
The person with traumatic brain injury should be kept under direct clinical monitoring while 
C
the drug dose is increased to an effective dose to ensure that the drug is tolerated and 
producing the required improvement in mood.
People with traumatic brain injury should be asked about any over-the-counter remedies, 
C
herbs or supplements they are taking to check for potential interactions and adverse effects.
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
good practice point
If selective serotonin reuptake inhibitors have been trialled and are not effective, or have 

produced unwanted side effects or drug interactions, the person should be referred for review 
to a psychiatrist with expertise in treating people with traumatic brain injury.
This is the opinion of the Guideline Development Team, or feedback from consultation within New Zealand where no evidence is available.
The UK guideline for the use of antidepressant medication in people with acquired brain injury13 found that a 
systematic literature search was unable to identify any formal research on which to base recommendations. 
Therefore, the UK guideline used the criteria from the British Royal College of Physicians: The Psychological Care 
14
of Medical Patients: A Practical Guide365 from which the following text is adapted.
The aetiology of post-TBI depression is often multifactorial. It is important to understand the reasons why it 
occurs in order to determine the circumstances in which antidepressants may or may not help (see Figure 14.2). 
183
 
   
   
 

Antidepressants may be helpful for depression and possibly other mood disorders, such as emotional lability, 
but are unlikely to be helpful where clinical features of the TBI itself mimic depression.
figure 14.2:
reasons f or depression f ollowing traumatic brain injury
Reasons why depression may occur following traumatic brain injury
•  An emotional response to the sudden onset of disability and its associated life changes which may 
include physical, fi nancial, vocational, and/or relationship losses.
•  A direct result of the brain injury leading to altered biochemical balance within the brain and 
resulting change in the background level of mood.
• A 
preceding 
vulnerability to depression.
Reasons why symptoms which mimic depression may occur following traumatic 
brain injury
•  Other emotional disorders associated with brain injury, such as apathy or emotional lability, may 
give the appearance of depression, even in the absence of a depressive disorder.
•  Somatic symptoms which characterise depression in the normal population may occur as a result 
of hospitalisation or from the brain injury itself. This may lead to over-estimation of the degree of 
depression on standard tests. These symptoms may include:
–  loss of energy, appetite and libido
–  altered sleeping habits
–  poor concentration and inability to make decisions.
•  Abnormal physical expression of emotional status may give the appearance of depression, eg:
–  disorders of facial expression 
– fl at speech patterns
–  general physical slowness.
Adapted from: British Royal College of Physicians: The Psychological Care of Medical Patients: A Practical 
Guide.365
SSRIs have generally replaced tricyclic antidepressants as the drugs of fi rst choice in depression because 
of their better side effect profi le. This may be particularly important in people with TBI who may have poor 
tolerance of side effects such as sedation. A specifi c SSRI, such as citalopram or sertraline, represents a 
reasonable fi rst choice of agent unless the anticholinergic effects of a tricyclic agent are positively desirable (for 
example sedation or suppression of hyper-salivation or if the tricyclic is also treating other post-TBI disorders, 
such as headache).
Six SSRIs are currently available – fl uoxetine, fl uvoxamine, paroxetine, sertraline, citalopram and escitalopram. 
There are important pharmacokinetic differences between them, notably in their ability to inhibit hepatic 
cytochrome P450 iso-enzymes, which are responsible for the metabolism of many drugs. In vitro studies 
suggest that citalopram and sertraline are least likely to inhibit these iso-enzymes and therefore least likely 
to cause interactions with other drugs. A survey of rehabilitation consultants and geriatricians in the UK has 
demonstrated these two agents to be the most common fi rst choice for the management of depression following 
acquired brain injury at the current time. However, both fl uvoxamine and sertraline have limited availability in 
New Zealand, and are not currently subsidised by PHARMAC. 
Escitalopram is a newer agent, which appears also to be highly selective with minimal inhibition of cytochrome 
P450 iso-enzymes. Trials suggest that it is at least as effective as citalopram in the management of severe 
depression, but it has yet to be evaluated in people with TBI (www.biopsychiatry.com/escitalopram.html).
184
 
   
   
 

Other more recently introduced antidepressants include venlafaxine, mirtazapine and reboxetine. These have 
different pharmacological properties and are claimed to have greater specifi city, equivalent or better effi cacy 
and fewer side effects than the earlier classes of antidepressants.365 As yet, however, they have not been 
tested for people with TBI, and may also be signifi cantly more expensive as they are not currently subsidised 
by PHARMAC. At present they should be used as second line drugs when SSRIs have not been effective or have 
produced unwanted side effects or drug interactions. If this is the case, the person should be referred for review 
to a psychiatrist with expertise in treating people with TBI. 
The person with TBI should be kept under direct clinical monitoring whilst the drug dose is increased to an 
effective dose to ensure that it is tolerated and producing the required improvement in mood. Some people 
in the community may already be taking complementary and alternative medicines and supplements, such as 
St John’s Wort, which may sometimes interact with prescribed medications causing serotonin syndrome and 
hypomania. It is important that people be asked about any over-the-counter remedies, herbs or supplements 
they are taking.
14.4.10.3.2 Psychotherapeutic approaches
recommendation
grade
Cognitive-behaviour therapy tailored for any cognitive impairment should be used for people 
C
with post-traumatic brain injury, depression and anxiety.
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
good practice points
Cognitive-behaviour therapy should be adapted and administered for people with traumatic 

brain injury by clinical psychologists familiar with traumatic brain injury as well as cognitive-
behaviour therapy.
Simple problem-solving measures should be used to address factors contributing to low mood 

or anxiety.
This is the opinion of the Guideline Development Team, or feedback from consultation within New Zealand where no evidence is available.
There are a number of psychotherapeutic approaches commonly used for psychological conditions such 
as mood and anxiety disorders.365 However, there is very little evidence from trials specifi cally in the TBI 
population.
Psychotherapeutic interventions are widely considered to be potentially helpful for people who have the 
cognitive and communicative abilities to engage successfully (see following sections). However, at the current 
time, these programmes are rarely available within general medical settings, and tend to be a longer-term 
intervention. 
14.4.10.3.2.1 Cognitive-behavioural therapy 
Cognitive-behavioural therapy focuses on changing an individual’s dysfunctional thoughts (cognitive patterns) 
in order to change their behaviour and emotional state. For children and adolescents in the general population 
(ie, non-TBI), cognitive-behavioural therapy is currently the treatment with the best evidential support for 
14
anxiety and depressive disorders.366,367 In adults in the general population (ie, non-TBI), there is good evidence 
to support cognitive-behavioural therapy for people with mild to moderate depression or anxiety disorders.368 
However, the Guideline Development Team was unable to identify any well constructed trials of cognitive-
behavioural therapy in the TBI population. The one recent randomised controlled trial of cognitive-behavioural 
therapy in people with post-stroke depression found no improvement in the group receiving the therapy for any 
185
of the outcomes measured.369
 
   
   
 

There is caution expressed by some authors that cognitive-behavioural therapy may not be appropriate or would 
need to be tailored for people with some types of cognitive impairment.13,329 However, some research suggests 
that it may be of particular value to people with cognitive disability when suitably adapted.359,362 Psychologists 
familiar with TBI, as well as cognitive-behavioural therapy, should administer the cognitive-behavioural therapy, 
with modifi cations as appropriate. 
14.4.10.3.2.2 Behavioural therapy
In behavioural therapy, the person is encouraged to increase activity levels, particularly pleasant events and 
activities, which are assumed to be rewarding and to lead to improved mood. The Guideline Development 
Team was unable to identify any robust research showing the effectiveness of behavioural therapy in treatment 
of depression for people with TBI, although it has been demonstrated as effective in other populations.370 
However, there is some evidence that behavioural approaches may be ineffective in depression post-TBI. 
Furthermore, some people with TBI may have the normal responses to reward disrupted by the brain damage.329 
14.4.10.3.2.3 Life review therapy
Life review therapy is a form of psychotherapy in which people are aided to review their lives and place their 
conditions in the context of their lives, and has been suggested as benefi cial for people with depression 
following TBI. Although there is no evidence for life review therapy use in the TBI population, a small 
randomised controlled trial in people who were depressed following a stroke found that after only three 
sessions, the intervention group showed signifi cant improvements in depression and life satisfaction scores 
compared with the control group.371 
14.4.10.3.2.4 Practical help/problem-solving
Simple problem-solving measures to address environmental or other factors which contribute to low mood or 
anxiety (such as missing home and family, or worries about life outside hospital) may be benefi cial.13 
14.5 Repeated traumatic brain injury and traumatic brain injury in sports
Repeated TBI is where a person has suffered a TBI whether diagnosed and treated or not, on more than one 
occasion. There is some evidence that multiple TBIs can have cumulative effects, leading to poorer outcomes.
A USA review of sports-related recurrent brain injuries concluded that people who have had at least one 
previous TBI have an increased risk for subsequent TBI.49 Where mild TBIs occur over an extended period of 
months or years, they can sometimes result in cumulative neurological and cognitive defi cits, but where the 
repeated mild TBIs occur within a period of hours, days or weeks, the outcomes may (rarely) be ‘catastrophic or 
fatal’.
One study of college athletes compared the effects of a concussion in those who had experienced three 
previous concussions with the effects in matched controls with no previous TBI.50 They found that when tested 
two days post-injury, athletes with multiple concussions scored signifi cantly lower on memory testing than 
athletes with a single concussion. Athletes with multiple concussions were 7.7 times more likely to demonstrate 
a major drop in memory performance than athletes with no previous concussions. 
Repeated or multiple TBIs are of particular concern in sports, where players may be at greater risk of a 
repeated head injury. ‘Second-impact syndrome’ (SIS) occurs when an athlete sustains a second TBI before 
the symptoms from the fi rst TBI have resolved. The person’s status may rapidly worsen, and coma and death 
may eventually result. Although SIS may not be as common as some have proposed,372 the identifi cation of the 
initial concussion, which may have been only mild, and appropriate immediate and longer-term management, 
including return to play, is essential.
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Owing to the lack of robust evidence on which to base recommendations for the management of sporting 
injuries, the Second International Conference on Concussion in Sport in Prague in 2004 produced a ‘Summary 
and agreement statement’,373 from which this section is adapted.
14.5.1 Concussion or traumatic brain injury?
The term ‘concussion’ is widely used, particularly in sports, to refer to the full range of severity of injury, from 
‘injury to the head without TBI’ through to ‘severe TBI’. For example, READ codes use the term ‘concussion’ even 
when there are extended periods of loss of consciousness. While the Guideline Development Team does not 
believe it is possible to stop the use of the term ‘concussion’ because it is used so widely, it is important to have 
some clarity about the term to ensure that people who have suffered ‘concussion’ receive appropriate care. 
For the purposes of this guideline, the defi nition of the term concussion as given in the ‘Prague guidelines’ (see 
Section 14.5.1.1, Defi nition of concussion)373 is being adopted.
14.5.1.1 Defi nition of concussion
Sports concussion is defi ned as a complex pathophysiological process affecting the brain, induced by traumatic 
biomechanical forces. Several common features that incorporate clinical, pathologic and biomechanical injury 
constructs may be used in defi ning the nature of a concussive head injury. These include:
•  concussion may be caused by a direct blow to the head, face, neck or elsewhere on the body with an 
‘impulsive’ force transmitted to the head
•  concussion typically results in the rapid onset of short-lived impairment of neurological function that 
resolves spontaneously
•  concussion may result in neuropathological changes but the acute clinical symptoms largely refl ect a 
functional disturbance rather than structural injury
•  concussion results in a graded set of clinical syndromes that may or may not involve loss of consciousness. 
Resolution of the clinical and cognitive symptoms typically follows a sequential course
•  concussion is typically associated with grossly normal structural neuroimaging studies
•  in some cases, post-concussion symptoms may be prolonged or persistent.
Therefore, it can be seen that there is some overlap between the labels of ‘concussion’ and ‘injury to the head 
but no TBI’, and ‘mild TBI’.
Concussion can be further described as ‘simple’ and ‘complex’ concussion. In ‘simple’ concussion, symptoms 
resolve progressively over seven to 10 days after the injury, and no intervention is necessary other than limiting 
play/training while symptomatic. ‘Complex’ concussion, on the other hand, gives rise to persistent symptoms 
and symptom recurrence with exertion and more severe symptoms indicative of TBI, such as seizures, loss 
of consciousness and prolonged cognitive impairment. Complex concussion may also result from multiple 
concussions over time, or where repeated concussions occur with progressively less impact force.373 People 
suffering complex concussion should always be referred for specialist assessment and management.
14
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14.5.2 Immediate management of and return to play after sporting injuries 
recommendations
grade
If there is any one of the following, traumatic brain injury should be suspected and 
C
appropriate management instituted:
•  loss of/impaired consciousness
• any 
seizure
• amnesia:
−  unaware of period, opposition, score of game
−  unaware of time, date, place
• headache
• nausea/vomiting
•  unsteadiness/loss of balance and/or poor coordination
• dizziness
•  feeling stunned or ‘dazed’
•  seeing stars or fl ashing lights
•  ringing in the ears
• double vision
•  vacant stare/glassy eyed
• slurred 
speech
•  inappropriate playing behaviour – for example, running in the wrong direction
•  appreciably decreased playing ability
•  confusion, such as being slow to answer questions or follow directions
• easily 
distracted, poor concentration
•  other symptoms, such as sleepiness, sleep disturbance and a subjective feeling of 
slowness and fatigue in the setting of an impact 
•  displaying unusual or inappropriate emotions, such as laughing or crying
• personality 
changes.
When a player shows any symptoms or signs of a concussion:
C
•  the player should not be allowed to return to play in the current game or practice
•  the player should not be left alone and should be regularly monitored for deterioration
•  the player should be medically evaluated after the injury
•  return to play must follow a medically supervised stepwise process
•  a player should never return to play while symptomatic.
Return to play after a concussion should follow a stepwise process, proceeding to the next 
C
level only if asymptomatic. If any symptoms occur after concussion, the person should revert 
to the previous asymptomatic level and try to progress again after 24 hours.
1.  No activity. When asymptomatic, proceed to level 2.
2.  Light aerobic exercise.
3. Sport-specifi c training.
4.  Non-contact training drills.
5.  Full contact training after medical clearance.
6. Game play.
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
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Taking a detailed clinical history is essential. The health care practitioner should bear in mind that:
•  many athletes will not recognise all the concussions that they may have suffered in the past
•  there should be specifi c questions about previous symptoms of a concussion, not just the perceived number 
of past concussions
• the 
recall of concussion injuries by team-mates or coaches has been shown to be unreliable
•  there is an increased risk of subsequent concussion injuries after a fi rst concussion is documented
•  questioning should also request information about all previous head or neck injuries
•  when there are faciomaxillary injuries, concussive injuries may be missed unless specifi cally assessed.373
If any one of the following symptoms or problems is present, a TBI should be suspected, and appropriate 
management instituted. A player does not need to have lost consciousness to suffer a TBI.
1. Cognitive features:
−  unaware of period, opposition, score of game
− confusion
−  amnesia (memory loss)
−  loss of consciousness
−  unaware of time, date, place.
2. Typical symptoms:
− headache
− dizziness
− nausea
−  unsteadiness/loss of balance
−  feeling stunned or ‘dazed’
−  seeing stars or fl ashing lights
−  ringing in the ears
− double vision
−  other symptoms, such as sleepiness, sleep disturbance and a subjective feeling of slowness and fatigue 
in the setting of an impact may indicate that a concussion has occurred or has not resolved.
3. Physical signs:
−  loss of or impaired consciousness
−  poor coordination or balance
−  concussive convulsion/impact seizure
−  gait unsteadiness/loss of balance
−  slow to answer questions or follow directions
−  easily distracted, poor concentration
−  displaying unusual or inappropriate emotions, such as laughing or crying
− nausea/vomiting
−  vacant stare/glassy eyed
− slurred speech
− personality changes
−  inappropriate playing behaviour – for example, running in the wrong direction
−  appreciably decreased playing ability.
Neuropsychological testing is particularly important in evaluation and should be used as and where 
appropriate, with baseline testing where possible. 
14
The consensus of the Second International Conference on Concussion in Sport on immediate treatment was that 
when a player shows any symptoms or signs of a concussion:
•  the player should not be allowed to return to play in the current game or practice
•  the player should not be left alone
189
 
   
   
 

•  regular monitoring for deterioration is essential
•  the player should be medically evaluated after the injury
•  return to play must follow a medically supervised stepwise process
•  a player should never return to play while symptomatic. ‘When in doubt, sit them out!’373
14.5.2.1 Return to play 
Return to play after a concussion should follow a stepwise process (see Figure 14.3).
1.  No activity, complete rest. Once asymptomatic, proceed to level 2.
2.  Light aerobic exercise such as walking or stationary cycling.
3. Sport-specifi c training – for example, skating in hockey, running in soccer.
4.  Non-contact training drills.
5.  Full contact training after medical clearance.
6. Game play.
With this stepwise progression, the athlete should proceed to the next level if asymptomatic at the current level. 
If any symptoms occur after concussion, the person should revert to the previous asymptomatic level and try to 
progress again after 24 hours.
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figure 14.3:
algorithm: safe steps to return to pl ay af ter a possible traumatic brain injury
Any recurrence 
1. Complete rest until 
Yes
or emergence of 
asymptomatic
symptoms?
2. Light aerobic exercise
Note: This algorithm refers to return to 
No resistance training
play for sports. ‘Complete rest’ means 
No
avoidance of sporting activity. Normal 
light exercise should be taken, unless 
Yes
advised otherwise by a specialist.
Any recurrence 
or emergence of 
3. Sport-specifi c training
symptoms?
Yes
No
Any recurrence 
4. Non-contact training drills
or emergence of 
symptoms?
No
5. Full contact training after 
medical clearance
Yes
Any recurrence 
or emergence of 
Yes
symptoms?
No
Any recurrence 
6. Game play
No
or emergence of 
symptoms?
14
Adapted from the British Royal College of Physicians: The Psychological Care of Medical Patients: A Practical 
Guide.365
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14.5.3 Repeated traumatic brain injury in children
good practice points
Children and adolescents should not resume sports or training until all of the physical 

symptoms of concussion have fully resolved, following the ‘return-to-play’ guide.
Return to school should be carefully managed following concussion, with the child monitored 

for recurring or emergent symptoms.
This is the opinion of the Guideline Development Team, or feedback from consultation within New Zealand where no evidence is available.
Most of the evidence on repeated TBI comes from the literature on sports injuries, presumably because sports 
are activities where people are more at risk of injuries than in other pastimes. This literature usually focuses on 
adolescents and young adults. However, there is a lack of research on repeated TBIs specifi cally in children.374 A 
child who is symptomatic following a head injury may have sustained a far greater impact force compared with 
an adult with the same post-concussive symptoms. There may also be persistent effects on school performance 
and behaviour long after the clinical symptoms and measurable neuropsychological impairments have resolved. 
A recent review of the topic reported that there is little evidence (no evidence-based guidelines), variability in 
practice and little expert consensus on how repeated TBIs should be managed in children. It was concluded that 
people over 15 years of age can be managed conservatively following adult guidelines, with an awareness that 
TBI symptoms may take longer to resolve than in adults. It is critical that children and adolescents not resume 
sports or training until all of the physical symptoms have fully resolved, following the guide in Section 14.5.2.1, 
Return to play.374 
Return to school should be carefully managed, with the child monitored for recurring or emergent symptoms 
(also see Chapter 12, Children and young people and traumatic brain injury).
14.6 Violence and traumatic brain injury 
recommendation
grade
All personnel involved in the triage and assessment of people with head injuries/traumatic 
C
brain injury should have training in the detection of violence and non-accidental injury.
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
People with violence-related injuries often present rehabilitation challenges. After controlling for demographics, 
pre-existing conditions and head injury severity, there is no difference in outcomes between people with TBI 
from violent causes and those whose injury is from other causes.375 However, people with TBI resulting from a 
violent injury are more likely to be young, male, members of minority groups and single, and to be premorbid 
drug and/or alcohol misusers than other people with TBI. Post-injury, this group reports less community 
integration and more headaches, confusion and sensory and attention disturbances than people whose TBI 
results from non-violence-related causes.375–378 
One study of women who presented at two Emergency Departments in Auckland with injuries found that 260 
(9%) were identifi ed as victims of assault.379 Assault-related injuries most commonly involved the head (OR 
12.8; 95% CI 9.33–17.68). Women who presented with assault-related injuries and had known assailants were 
most likely to have been injured by a partner or former partner, and more likely than women with unintentional 
injuries to be younger and of Ma¯ori or Pacifi c islands origin. They were also more likely to be discharged from the 
Emergency Department without referral for follow-up treatment, and were more likely to leave the Department 
without completing treatment. 
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14.6.1 Non-accidental injury in children 
A signifi cant proportion of head injuries in children are non-accidental and these may result in a different 
pattern of morbidity from that seen in adults.7 One study, for example, of children admitted to hospital with non-
accidental head injury found that 68% of these children were neurologically abnormal at an average follow-up of 
59 months.43 There was a wide range of abnormalities and outcomes including speech and language diffi culties 
(including autistic spectrum disorder) in 64%, cranial nerve abnormalities in 20%, and visual defi cits and 
epilepsy compounding learning diffi culties in 25%. It was concluded that these children require the support of a 
multidisciplinary team in the community. 
14.6.2 Management of traumatic brain injury from non-accidental causes
The management of violence and assault issues are outside the scope of this guideline. However, all personnel 
involved in the triage and assessment of people with head injuries should have training in the detection of non-
accidental injury.7,8 
Rehabilitation is often hindered or rendered impossible when the person with TBI is threatened with further 
violence. Staff assessing people with TBI should include assessment for violent cause of injury or exposure to 
violence, and where it is identifi ed, refer as appropriate.
For more information see Family Violence Intervention Guidelines: Child and Partner Abuse (www.nzgg.org.nz).
Also see Chapter 5, Rehabilitation following clinically signifi cant traumatic brain injury – Assessment, on 
assessment. 
14
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Chapter 15:
Implementation
The aim of this guideline is to improve outcomes for people in New Zealand who have a TBI. To achieve this goal 
the promotion and dissemination strategy for this TBI guideline can be implemented on four levels:
1.  increasing knowledge, making practitioners aware of the guideline (education infl uence)
2.  changing attitudes, such that practitioners agree with and accept recommendations as a better standard of 
care (personal factors)
3.  changing behaviour, such that practitioners change their clinical practice to conform with the guideline
4.  changing outcomes by improving health and quality of care for consumers.
There is an imperfect evidence base to support decisions about which guideline dissemination and 
implementation strategies are likely to be effi cient under different circumstances.380 The principal fi ndings of a 
2004 systematic review show that the following approaches have had some effect:
•  dissemination of the guideline information
•  reminders of the most effective treatments 
• educational 
outreach
•  educational material, audit and feedback.380
15.1 Implementation activities
15.1.1 Increasing knowledge
Dissemination
•  The full guideline and supporting documents will be published.
•  Electronic formats of the guideline and supporting documents, such as pro forma discharge letters, would be 
useful as they can be easily downloaded and utilised.
•  Summaries of the guideline should be developed for specifi c groups.
•  Guideline recommendations could be summarised in relevant publications.
•  Consumer information that is developed might be offered in Pacifi c languages in written and oral forms (eg, 
tapes and videos).
•  The guideline will be presented at relevant conferences by members of the Guideline Development Team and 
other experts.
•  General practitioner peer review groups offer an ideal forum for the introduction and discussion of the 
guideline. Local Guideline Development Team members could be involved in these meetings.
Targeted resources
In order to facilitate the dissemination of information to the appropriate groups and individuals, tailored 
information about the TBI guideline recommendations could be developed for a variety of audiences, including:
•  the health care practitioners who fi rst assess and treat people with TBI (particularly accident and emergency 
service personnel and primary care practitioners)
•  rehabilitation service personnel
•  those working with children and young people in settings such as paediatric wards, children’s rehabilitation 
facilities and Emergency Departments
•  consumers and their families, wha¯nau and carers.
15
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15.1.2 Changing attitudes
ACC, DHBs and related agencies should initiate discussions to consider:
•  how TBI services should be structured, ie, centralised TBI specialist unit(s) versus distributed services
•  how to meet the recommendations for the skill set within multidisciplinary assessment teams for people
with TBI
•  a plan for maximising the coordination of trauma services
•  how to develop an alerting call system, with appropriate protocols
•  how to develop family/local supports and coordination for people with TBI
•  how to develop a Ma¯ori TBI action plan
•  how to develop the case coordinator/key worker role
•  how to set up and collect evaluation data 
•  how to set up and collect the recommended performance indicators 
•  how to develop educational outreach programmes aimed at reinforcing the main guideline messages to a 
variety of audiences such as general practitioners, emergency services, rehabilitation providers and DHBs
•  how to encourage collaboration between education services, ACC, DHB mental health services, disability 
support services, Work and Income New Zealand, housing services and other organisations to assess 
whether services provided by these agencies meet the guideline recommendations.
ACC could also discuss the driving rules for people who have had a brain injury with Land Transport
New Zealand.
15.1.3 Changing behaviour
Collaboration
At a local level, regional ACC offi ces and local DHBs could:
•  review the ways local acute care and rehabilitation services contracted to manage people with TBI, plus local 
mental health services, work together to specify and document policies for dealing with people with TBI who 
have mental health issues (whether they pre-date or follow the TBI)
•  initiate collaboration between agencies (eg, adult education schemes, employment schemes, charities) to 
obtain adapted hard- and software and training to enable people with TBI to develop appropriate computer 
skills.   
Services for Ma¯ori
ACC and DHBs should consider developing a TBI action plan for Ma¯ori that will address ways of:
•  increasing the Ma¯ori health care workforce in TBI through recruitment and retention programmes
•  liaising with local Ma¯ori providers. Scholarships and other support could be developed to encourage the 
Ma¯ori health care workforce into the TBI fi eld
•  seeking input from local Ma¯ori providers, tangata or mana whenua to assist with service delivery for Ma¯ori 
with TBI.
Services for children and young people
•  ACC could consider the development of the case coordinator/key worker role.
•  An action plan for the management of TBI rehabilitation for children and young people should be developed.
Carers
Appropriate agencies should implement processes for:
•  the assessment of carers’ needs
•  the allocation of respite care
•  the assessment of support needs of carers of those with TBI (including fi nancial support).
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Access to services
As a result of the Current Practice Review5 and discussions on the guideline, it appears that there is a need to 
ensure that people who have had a TBI are able, when appropriate, to access the following services easily:
•  specialist rehabilitation units for:
–  children and young people
– adults
•  imaging services, particularly in rural areas
•  specialist clinics for managing persistent symptoms
•  training for carers
•  age-appropriate residential support.
15.1.4 Changing outcomes
Model discharge letters, posters for Emergency Departments and other tools should be developed to provide 
ongoing reminders for staff of the guideline’s best practice recommendations.
In order to assess whether the guideline has been operationalised throughout New Zealand and whether 
there have been corresponding improvements in care and outcomes for people with TBI, evaluation of the 
implementation activities should be undertaken. This evaluation should occur before the guideline is due to be 
revised.
Evaluation at the programme level depends on a number of factors, including funder requirements, provider 
goals and service structure. There are several key questions for a programme-level evaluation:
1.  Are the overall results of the programme consistent with the expectations of:
–  the service’s consumers (individuals, families/wha¯nau and carers)?
– the providers?
– the funders?
2.  Was the programme carried out as specifi ed in the guideline?
3. How do the results of this programme compare with those of similar programmes (or similar clients in a 
different type of programme) both locally and overseas?
4.  Do the results justify the costs (for consumers, providers, funders)?
5.  Can we improve our service to better meet the needs of consumers and funders? How?
6.  Can we improve the effi ciency with which we provide the service without compromising results?
7.  What is the service’s case-mix?
8.  What are the benefi ts or limitations of the programme for enhancing interdependence?
Some programmes may have poor evaluation results because people with severe TBI generally have poorer 
outcomes than other individuals, whatever the rehabilitation. So the outcomes of a programme with a relatively 
large percentage of people with severe TBI are likely to be generally poorer than those for a programme dealing 
mainly with individuals with mild or moderate TBI, independent of programme content or quality.
There are some additional questions to be considered:
•  How does the service measure resource use? This will vary with the type of service, eg, length of stay, hours 
of contact time, numbers of visits in the community.
•  How does the service measure consumer and funder satisfaction?
•  How does the service measure programme implementation?
•  How does the service control outcome measures for factors that affect outcomes, eg, premorbid status, drug 
abuse, other medical/surgical or psychiatric conditions, family/wha¯nau circumstances? As a minimum, this 
information needs to be collected (see Section 8.4, Assessment of people with persistent symptoms after 
mild traumatic brain injury), although it is acknowledged that gathering such information can be diffi cult.
15
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15.2 Performance indicators
Owing to the complexity and scope of the guideline, a comprehensive set of performance indicators for this 
guideline could be developed at a later date. 
In the interim, the NICE guideline7 has identifi ed the following performance indicators relating to the criteria 
used to order imaging of the head. 
To audit adherence to these NICE criteria, prospective data collection on all people with suspected TBI assessed 
in Emergency Departments should be undertaken. 
For each of these people, data on a variety of risk factors should be collected. The following broad categories of 
risk factor should be addressed: 
•  loss of consciousness since injury 
•  Glasgow Coma Scale scores since injury 
• age 
•  mechanism of injury 
•  signs of open or depressed skull fracture 
•  signs of basal skull fracture 
•  results of imaging 
•  post traumatic seizure 
•  focal neurological defi cit 
• vomiting 
• amnesia 
(retrograde and anterograde) 
• coagulopathy 
• headache 
•  drug or alcohol intoxication 
•  irritability or altered behaviour 
•  paraesthesia in the extremities 
•  neck pain or tenderness. 
Collecting this data will highlight areas where people seem to be receiving imaging for inappropriate criteria, or 
conversely are not being imaged despite meeting the criteria laid out in this guideline.
15.3   Potential impact of the guideline 
The Guideline Development Team expects an evolutionary, rather than revolutionary, response in service 
delivery for TBI following the publication of this guideline. Given the lack of existing New Zealand incidence 
and outcome data, it would be unreasonable to expect major changes in a short time period. Rather it is hoped 
that this guideline will provide an overall framework within which to consider service provision for people with 
TBI and their families, and a basis for the development of policy, contracts for services, audit, research and 
initiatives led by community groups.
In some specifi c areas, particularly in the criteria for diagnosis and classifi cation of injury severity and the 
assessment processes for people with suspected TBI, implementation of the guideline recommendations will 
lead to better practice and less variation around New Zealand.
The Guideline Development Team hopes that the implementation of this guideline and subsequent 
development of TBI services in New Zealand will lead to the following situation:
Nationally
1. Defi nitions of TBI (and ‘not TBI’), along with severity grading for defi nite TBI, will be applied consistently.
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2.  People with possible TBI will be assessed in a consistent fashion using adequate tools by people trained in 
those assessments.
3.  All people with suspected or confi rmed TBI will receive information in a form that they can understand 
about common symptoms and likely outcomes, emphasising rapid and full recovery for the great majority of 
people with TBI at the less severe end of the spectrum.
4.  Over time in New Zealand, the development of a limited number of highly specialised facilities for adult 
severe TBI rehabilitation providing outreach services will complement the current residential and community 
rehabilitation services operating around the country.
5.  A range of options for caregiver relief will be available to families and carers.
6.  Children with severe TBI will continue to have access to follow-up from highly specialised rehabilitation 
services.
7.  TBI research will be developed (see Appendix A).
At a service level
1.  All people assessing and/or managing children and young people with possible or defi nite TBI will 
understand the particular issues that make the assessment and management of TBI in children and young 
people different from that in adults. In general the following statements, unless qualifi ed, apply equally to 
children, young people and adults.
2.  People at risk of acute complications from TBI will have appropriate investigations instituted in a timely 
fashion. Conversely, people at low risk of acute complications will not undergo unnecessary investigation.
3.  All people with moderate and severe TBI and those people with mild TBI meeting the criteria for, or actually 
having, a CT scan in the acute phase will have some form of follow-up organised, with the details of that 
follow-up being developed by local services and funders.
4.  People with persistent symptoms following mild TBI who have signifi cant activity limitation or participation 
restriction after four to six weeks will be considered for referral to a specialist clinic staffed by profesionals 
experienced in the management of this situation and with the ability to perform neuropsychological 
assessments. Such clinics will be available and have the capacity to see clients in a timely fashion following 
referral.
5.  People with TBI requiring admission to hospital will be managed by staff trained in the observation and 
management of people with TBI.
6.  People at signifi cant risk of acute complications of TBI who are not in a tertiary referral centre will have their 
case discussed with a member of the neurosurgical team at the tertiary referral centre with regard to whether 
transfer to that centre is appropriate.
7.  People with severe TBI requiring intensive care management will be managed according to best practice 
guidelines for that situation (not covered in this guideline).
8.  Rehabilitation for people following clinically signifi cant TBI will start as early as possible and rehabilitation 
services will work closely with acute care teams.
9.  Rehabilitation services for people with clinically signifi cant TBI will include, or have access to, staff skilled 
in the management of the full range of issues that arise for this client group. These services will operate 
with a client-centred approach and include a designated ‘case coordinator/key worker’ as described in this 
guideline.
10. Residential rehabilitation services for people with clinically signifi cant TBI will be skilled in the management 
of such clients and acknowledge the special and challenging nature of this work.
11. Community rehabilitation services will provide contextualised rehabilitation to deliver meaningful outcomes 
for people with TBI.
12. Vocational rehabilitation services will provide a full range of services, including job coaches where 
appropriate. Funders will acknowledge the need for substantial workplace support over extended periods of 
15
time for people with clinically signifi cant TBI returning to the workforce.
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13. There will be a clear strategy at both national and service levels for upskilling and accrediting TBI specialist 
rehabilitation staff.
14. The needs of families and carers of people with TBI will be a high priority of rehabilitation services and 
funders over the continuum of those people’s period of activity limitation and participation restriction and, if 
necessary, for the whole of their lives.
15. Rehabilitation services will fully meet the needs of people with TBI from particular groups within our society, 
including Ma¯ori, Pacifi c peoples and people from other ethnic minorities, people with alcohol and drug 
dependence problems and people with mental health disorders.
16. Liaison between different health services will be improved to ensure that the needs of clients with TBI and 
other health problems (particularly alcohol and drug abuse and/or mental health disorders) are met.
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Appendices
A. 
Objectives for future research on traumatic brain injury in New Zealand
B. Guideline 
grading 
systems
C. 
Glasgow Coma Scale (adult and paediatric versions)
D. Additional 
resources and supporting documents
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202
 
   
   
 

Appendix A
Objectives for future research on traumatic 
brain injury in New Zealand
In the process of developing this guideline, the Guideline Development Team identifi ed a number of research 
gaps where there was insuffi cient research. For future guideline updates the Guideline Development Team 
recommends that the following research areas be considered. These are necessarily broad. The order does not 
refl ect a priority ranking.
1.  Quantifying the incidence of TBI in New Zealand (ie, new cases)
 
Currently there is insuffi cient information to establish the incidence of TBI in New Zealand, particularly at the 
mild end of the spectrum, ie, being able to distinguish between cases that are initially ‘suspected TBI’ but 
don’t meet the criteria for ‘defi nite TBI’ as described in this guideline. Within this problem, there are sub-
problems around populations at high risk on the basis of age, gender, ethnicity, geography and comorbidities 
(such as mental health disorders, drug and alcohol misuse). The proportions of people with severe, moderate 
and mild TBI need to be accurately established for effi cient service delivery.
2.  Burden of TBI in New Zealand
 
What is the impact of TBI for individuals (and their families and carers) with TBI of different severity and 
demographic and other characteristics in New Zealand? This will require comprehensive case ascertainment 
and follow-up over long enough periods to measure important outcomes. One question that needs to be 
specifi cally addressed is whether outcomes are as bad as those measured in the 2000 Thornhill study4 (rates 
of disablement of around 45% at one year even for people with mild TBI).
3.  The effectiveness of specifi c interventions for people with TBI
 
There are very many of these that are not adequately tested. The systematic design of appropriate studies 
and testing of interventions would be of international signifi cance.
4.  The effectiveness, timing and content of assessments for people with TBI
 One 
specifi c issue is around assessments of people with mild TBI. Is a policy of early, simple assessment (eg, 
using computerised cognitive screening assessments) followed, where necessary, by more comprehensive 
assessment, more effi cient and/or more effective, than the current policy of delayed, moderately 
comprehensive assessment using mild TBI clinics?
5.  The experience of TBI for people and their carers
 
There is remarkably little known about how people cope with the effects of TBI. The same applies to carers. 
Qualitative research could help to clarify some of these issues and make a difference to the way services are 
delivered.
6.  Children and young people with TBI
 
It is clear from the TBI guideline that there are many areas where there is simply no information specifi c to 
children and young people with TBI. This absence of good information applies to all of the points above and 
specifi c research in this group needs to be considered.
7.  Appropriate tools and measures for use with people with TBI in New Zealand
 
Although there may need to be specifi c work on the psychometric properties of some tools, utility needs 
considerable attention. Which tools, when and for what purpose?
8.  Measurement of performance of TBI services in New Zealand
 
The ability to identify services that are delivering good outcomes and those that are struggling should allow 
for a process of quality improvement over time. This would allow a move away from reliance on measures of 
process as a proxy for performance.
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Appendix B
Guideline grading systems
1. 
Evidence and recommendation grading system (excluding 
complementary and alternative medicine)
Studies were graded using a two-tier system that is detailed in the Handbook for the Preparation of Explicit 
Evidence-Based Clinical Practice Guidelines, published in November 2001 by NZGG.370 This system has been 
adapted from other grading systems currently in use, in particular the SIGN system.81
The searches for this guideline concentrated on fi nding high grade evidence to answer the identifi ed clinical 
questions, such as systematic reviews, randomised controlled trials and, where these were not available, 
observational studies such as well designed cohort and case control studies. Only these types of study design 
were graded. Where these types of study were not available, less rigorous study designs such as cross-sectional 
studies and case studies were considered but were not formally graded.
The two-tier system follows this process.
1.  Critical appraisal of individual relevant studies (identifi ed from the searching) and assigning of a level of 
evidence for the fi rst section of the GATEFRAME checklist that is incorporated into the evidence tables. A 
random sample of appraisals in the guideline were performed independently by two assessors and the 
results compared.
2.  Joint consensus by the Guideline Development Team on the issues of volume, consistency, clinical relevance 
and applicability of the body of evidence in the evidence table (fi lling out the NZGG Considered Judgement 
form for each clinical question) and the development of graded recommendations that attempt to answer the 
clinical questions posed.
Levels of evidence
There are three levels of evidence that can be assigned to the Validity section of the GATEFRAME (Section 1):
+  strong study where all or most of the validity criteria are met
~  fair study where not all the validity criteria are met, but the results of the study are not likely to be infl uenced 
by bias
x  weak study where very few of the validity criteria are met and there is a high risk of bias.
Developing recommendations
Recommendations were formulated by joint meetings of the multidisciplinary Guideline Development Team. The 
group considered the entire body of evidence (summarised in the evidence tables) and fi lled out Considered 
Judgement forms for each clinical question that was identifi ed as being relevant to the guideline (see www.nzgg.
org.nz). The following aspects were discussed: volume of evidence, applicability to the New Zealand setting, 
consistency and clinical impact, with the aim of achieving consensus. Consensus was sought and achieved over 
the wording of the recommendation and grading. In this guideline, where a recommendation is based on the 
clinical experience of members of the Guideline Development Team, this is referred to as a good practice point.
205
 
   
   
 

Grading of recommendations
The NZGG grades of recommendation are as follows:
recommendations
grade
The recommendation is supported by good evidence (where there are a number of studies 
A
that are valid, consistent, applicable and clinically relevant).
The recommendation is supported by fair evidence (based on studies that are valid, but 
B
there are some concerns about the volume, consistency, applicability and clinical relevance 
of the evidence that may cause some uncertainty but are not likely to be overturned by other 
evidence).
The recommendation is supported by international expert opinion.
C
Grades indicate the strength of the supporting evidence, rather than the importance of the recommendations – refer to Appendix B for grading details.
good practice point
Where no evidence is available, best practice recommendations are made based on the 

experience of the Guideline Development Team, or feedback from consultation within
New Zealand.
This is the opinion of the Guideline Development Team, or feedback from consultation within New Zealand where no evidence is available.
2. 
Complementary and alternative medicines grading system
A grading system has been developed by NZGG to assess both study design and quality for complementary and 
alternative medicines (CAMs). This is described in Table 1. This system is compatible with the other grading 
systems used by NZGG and also maps to other international systems (see Table 2). 
Due to the emerging nature of the evidence for CAMs, many studies are non-randomised or uncontrolled. Often 
no Level 1 or Level 2 evidence is available. Sometimes Level 1 or Level 2 studies cannot be carried out because 
it would involve a safety risk for participants. Sometimes it would be too diffi cult to carry out a Level 1 or Level 2 
study large enough to measure rare effects. In these instances evidence is based on lower level studies. 
Lower level evidence is subdivided into Level 3 and Level 4. This serves to illustrate a progression that may 
occur when investigating CAMs from Level 4 through Level 3 and Level 2 to Level 1 evidence. 
Although possible harms and adverse events are important aspects of any CAM, they are frequently only 
reported from lower level studies. Higher level evidence is not often available for the reasons stated above. 
A range of expert opinion also exists. In other grading systems, this is usually included in a fi fth level. This level 
of evidence has not been reviewed for the CAM chapter in this guideline. Note also that the numbers are omitted 
from the level of evidence in the chapter, and that only the words are used.
206
 
   
   
 

table 1: levels of evidence used in the tbi guideline
level of evidence
where the evidence comes from
1 Evidence with a  Studies that use well tested methods to make comparisons in a fair way and 
high degree of 
where the results leave very little room for uncertainty.
reliability 
Trial design: usually Level 1 studies are systematic reviews or large, high-
quality randomised controlled studies.
2 Evidence with  Studies that use well tested methods to make comparisons in a fair way but 
reliability but open 
where the results leave room for uncertainty (for example, due to the size of 
to debate
the study, losses to follow-up or the method used for selecting groups for 
comparison).
Trial design: usually Level 2 studies are systematic reviews without consistent 
fi ndings, small randomised controlled trials, randomised controlled trials in 
which large numbers of participants are lost to follow-up, or cohort studies.
3 Some evidence  Studies where the results are doubtful because the study design does not 
without a high 
guarantee that fair comparisons can be made.
degree of reliability
Trial design: usually Level 3 studies are systematic reviews of case-control 
studies or individual case-control studies.
4 Some evidence  Studies where there is a high probability that results are due to chance 
but based on 
(for example because there is no comparison group or because the groups 
studies without 
compared were different at the outset of the study).
comparable groups
Trial design: usually cohort or case-control studies where the groups were not 
really comparable, or case-series studies.
table 2: systems f or grading the qualit y of individual studies
nzgg* 
nzgg/
sign‡
grade§
usptf**
oxf ord 
nhmrc
ccs 2000
cam
gate†
cebm††
2000‡‡
consensus§§
Level 1
Good / +
++
High
Good
Level 1 
Level I
Level I
abc
Level 2
Fair / ~
+
Moderate
Fair
Level 2 
Level II
Level II
abc
Levels 3 
Poor / –

Low (very 
Poor
Level 3 
Level III 
Level III, IV and V
and 4
low)
ab, and 4
(1, 2, 3) 
and IV
*  New Zealand Guidelines Group
**  US Preventable Services Task Force
†  Graphic Appraisal Tool for Epidemiology
††  Oxford Centre for Evidence-based Medicine
‡  Scottish Intercollegiate Guidelines Network
‡‡ National Health and Medical Research Council 2000
§  Grading of Recommendations Assessment
§§ Canadian Cardiovascular Society 2000 Consensus
Development and Evaluation
207
 
   
   
 

There are methods for considering the evidence from multiple studies that address a specifi c question, 
incorporating trial designs and for weighing competing factors in forming a recommendation. For more 
information on study design and for guidance on balancing the benefi ts and harms of an intervention the reader 
is referred to the following websites:
• www.nzgg.org.nz 
• www.health.auckland.ac.nz/population-health/epidemiology-biostats/epiq/
• www.cebm.net/levels_of_evidence.asp
• www.ahrq.gov/clinic/ajpmsuppl/harris3.htm#table7
• www.gradeworkinggroup.org/links.htm
• www.sign.ac.uk/methodology/index.html
• http://gacguidelines.ca/article.pl?sid=03/01/29/1642226&mode=thread
208
 
   
   
 

Appendix C
Glasgow Coma Scale
Adults
The Glasgow Coma Scale is scored between 3 and 15, 3 being the worst and 15 the best. 
It is composed of three parameters: Best Eye Response, Best Verbal Response and Best Motor Response. The 
defi nition of these parameters is given below.
best eye response (4) 
best verbal response (5) 
best motor response (6)
1. No eye opening
1. No verbal response
1. No motor response
2.  Eye opening to pain
2. Incomprehensible sounds
2.  Extension to pain
3.  Eye opening to verbal 
3. Inappropriate words
3.  Flexion to pain
command
4. Confused
4. Withdrawal from pain
4.  Eyes open spontaneously
5. Orientated
5. Localising pain
6. Obeys commands
Paediatric version
The paediatric version of the Glasgow Coma Scale is scored between 3 and 15, 3 being the worst and 15 the 
best. It is composed of three parameters: Best Eye Response, Best Verbal Response or Best Grimace Response, 
and Best Motor Response. The defi nition of these parameters is given below. 
best eye response 
best verbal 
best grimace 
best motor 
(4) 
response (5) 
response (5) 
response (6) 
1. No eye opening
1. No vocal response
A ‘grimace’ alternative 
1. No motor response 
2.  Eye opening to pain
2. Occasionally 
to verbal responses 
to pain
3.  Eye opening to verbal 
whimpers and/or 
should be used in those 
2. Abnormal extension 
command
moans
infants or children 
to pain (decerebrate)
4. Eyes open 
3. Cries inappropriately
who are pre-verbal or 
3. Abnormal fl exion to 
spontaneously
4.  Less than usual 
intubated.
pain (decorticate)
ability and/or 
4. Withdrawal to painful 
1. No response to pain
spontaneous
stimuli
2. Mild grimace to pain
irritable cry
5. Localises to painful 
3. Vigorous grimace to 
5. Alert, babbles, coos, 
stimuli or withdraws 
pain
words or sentences to 
to touch
4. Less than usual 
usual ability
6. Obeys commands 
spontaneous ability 
or performs normal 
Communication with 
or only responds to 
spontaneous 
the infant’s or child’s 
touch stimuli
movements
caregivers is required to 
5. Spontaneous normal 
establish the best usual 
facial/oro-motor 
verbal response
activity
209
Note: This appendix is included in the full guideline and online at www.nzgg.org. It may be reproduced for 
clinical use. 
 
   
   
 

210
 
   
   
 

Appendix D
Additional resources and
supporting documents
A list of additional resources and supporting documents available for downloading at www.nzgg.org.nz:
•  TBI Tools Review for the Development of Guidelines on the Assessment, Management and Rehabilitation of 
Traumatic Brain Injury, 2005
•  Supplement to the Tools Review (above): The Use of Neuropsychological Tests in the Assessment and 
Rehabilitation of Traumatic Brain Injury in Aoteoroa/New Zealand
•  Traumatic Brain Injury in New Zealand: Current Practice Review. A Report for the Accident Compensation 
Corporation, Medical Research Institute of New Zealand, 2004.
• Medical 
Radiation
• ‘6 
Steps’.
211
 
   
   
 

212
 
   
   
 

Glossary*
Aphasia 
Partial or total loss of the ability to articulate ideas or comprehend spoken or written 
language, resulting from damage to the brain.
Apnoea  
Temporary absence or cessation of breathing.
Arrhythmia 
An irregularity in the rhythm of the heartbeat.
Aspiration 
Food or fl uid entering the trachea and/or lungs.
Ataxia 
Loss of the ability to coordinate muscular movement.
Biofeedback 
The technique of using monitoring devices to furnish information regarding an autonomic 
bodily function, such as heart rate or blood pressure, in an attempt to gain some voluntary 
control over that function. 
Bradycardia 
Slowness of the heart rate, usually fewer than 60 beats per minute in an adult human.
Chiropractic 
A system of therapy in which disease is considered the result of abnormal function of the 
nervous system. The method of treatment usually involves manipulation of the spinal column 
and other body structures.
Claudication 
Pain in the legs due to restriction in blood fl ow or sometimes nerve compression (‘spinal 
claudication’).
Clavicles 
Either of two slender bones in humans that extend from the manubrium of the sternum to the 
acromion of the scapula. Also called collarbone.
Coagulopathy  
A defect in the blood-clotting mechanism.
Cognition 
A term encompassing all the ‘thinking’ modalities of the brain, including alertness, 
registration of new ideas, memory, problem-solving.
Cognitive 
Of, characterised by, involving, or relating to cognition.
Concussion 
A term that is widely used, particularly in sports, to refer to the full range of severity of 
injury, from ‘injury to the head without TBI’ through to ‘severe TBI’. For the purposes of this 
guideline, the defi nition of the term concussion is as given in the ‘Prague guidelines’.141
 
 
The Prague defi nition of concussion is as follows: 
 
 
Sports concussion is defi ned as a complex pathophysiological process affecting the brain, 
induced by traumatic biomechanical forces. Several common features that incorporate 
clinical, pathological and biomechanical injury constructs that may be utilised in defi ning the 
nature of a concussive head injury include: 
1.  concussion may be caused by a direct blow to the head, face, neck or elsewhere on the 
body with an ‘impulsive’ force transmitted to the head
2.  concussion typically results in the rapid onset of short-lived impairment of neurological 
function that resolves spontaneously
3.  concussion may result in neuropathological changes but the acute clinical symptoms 
largely refl ect a functional disturbance rather than structural injury
4.  concussion results in a graded set of clinical syndromes that may or may not involve loss 
of consciousness. Resolution of the clinical and cognitive symptoms typically follows a 
sequential course
213
5.  concussion is typically associated with grossly normal structural neuroimaging studies .

For methodology terms, go to the glossary at www.nzgg.org.nz
 
   
   
 

Consumer 
Where the term ‘consumer’ is used in this guideline, it denotes people receiving or needing 
health care and rehabilitation services. This includes people who have suffered a TBI and 
their families/wha¯nau and informal carers.
Contractures 
An abnormal, often permanent shortening, as of muscle or scar tissue, that results in 
distortion or deformity, especially of a joint of the body.
Contusion 
An injury in which the skin is not broken; a bruise.
Cranial 
Of or relating to the skull or cranium.
Craniocerebral 
Of or relating to both the cranium and the cerebrum.
Craniosacral 
Of or associated with both the cranium and the sacrum.
Dementia 
Deterioration of intellectual faculties, such as memory, concentration and judgement, 
resulting from an organic disease or a disorder of the brain.
Dissociative 
To remove from association; separate.
Dural tear 
A tear in the dura – the external lining covering the brain.
Dysarthria 
Diffi culty in articulating words, caused by impairment of the muscles used in speech.
Dysgraphia 
Impairment of the ability to write, usually caused by brain dysfunction or disease.
Dyslexia 
A learning disorder marked by impairment of the ability to recognise and comprehend written 
words.
Dysphagia 
Diffi culty in swallowing.
Electroencephalograph
An instrument that measures electrical potentials on the scalp and generates a record of the 
electrical activity of the brain. Also called encephalograph.
Emotional lability  Diffi culty with control of emotions and emotional responses (such as crying).
Endocrine disorders
Disorders which involve the over-production or under-production of hormone substances 
from an endocrine gland. Examples include diabetes, hypothyroidism, hyperthyroidism, 
hyperparathyroidism, Cushing’s syndrome and acromegaly.
Epilepsy 
Any of various neurological disorders characterised by sudden recurring attacks of motor, 
sensory or psychic malfunction with or without loss of consciousness or convulsive seizures.
Extracerebral 
Located outside the cerebral hemispheres and inside the skull.
Extradural haematoma
A localised collection of blood, usually clotted, located outside the dura mater but inside the 
skull.
Focal neurological signs
Neurological signs (such as weakness or double vision) that suggest abnormal function in 
one part of the brain.
Gait   
A particular way or manner of moving on foot.
Gaze palsies 
When one or both eyes does not move normally under voluntary control.
Gerontocracy 
A governing group of elders.
214
 
   
   
 

Glaucoma 
Any of a group of eye diseases characterised by abnormally high intraocular fl uid pressure, 
damaged optic disc, hardening of the eyeball, and partial to complete loss of vision.
Haematoma 
A localised collection of blood, usually clotted, in an organ, space or tissue, due to a break in 
the wall of a blood vessel.
Haemotympanum  A collection of blood in the middle ear space. May occur secondary to severe barotitis media, 
basal skull fracture or ear trauma.
Hapu¯  
Groups of wha¯nau with common ancestral links; sub-tribe.
Heterotopic ossifi cation
The development of bony substances in normally soft structures.
Holistic 
Emphasising the importance of the whole and the interdependence of its parts. 
Hydrocephalus 
Excess fl uid and/or pressure within the ventricular system of the brain.
Hypercarbia 
Also called hypercapnia. An excess of carbon dioxide in the blood.
Hypertonia 
Pathologically increased tone in muscles.
Hypoglycaemia 
An abnormally low level of glucose in the blood.
Hypomania 
A mild state of mania, especially as a phase of a manic-depressive cycle.
Hypotension 
Abnormally low blood pressure.
Hypoxaemia 
Reduced oxygen in the blood.
Hypoxia 
Reduced oxygen in the body tissues.
Intracerebral 
Occurring or situated within the brain.
Intracranial 
A wound or injury occurring within the cranium.
Intrathecal baclofen
A drug administered into the cerebrospinal fl uid bathing the spinal cord and brain. It is used 
in the treatment of spasticity, especially that due to spinal cord damage.
Iwi  
A social and political unit made up of several hapu sharing common descent; Ma¯ori tribe or 
nation.
Mana whenua 
People of authority. Mana – authority. Whenua – people.
Meniere’s disease  A name applied to recurrent vertigo accompanied by ringing in the ears (tinnitus) and 
deafness. A dysfunction of the semi-circular canals (endolymphatic sac) in the inner ear.
Meningism 
The symptoms and signs of meningeal irritation associated with acute febrile illness or 
dehydration without actual infection of the meninges.
Morbidity 
Illness; disease.
Myocardial infarction
A term used to describe irreversible injury to heart muscle.
Nephrotoxicity 
The quality or state of being toxic to kidney cells.
Neuron 
Nerve cell. 
Neuropsychiatrist A medical specialist for disorders with both neurological and psychiatric features.
215
 
   
   
 

Neuropsychologist
 A psychologist who specialises in ailments of the mind and mental processes caused by 
diseases of the nervous system.
Orthopaedic 
The branch of medicine that deals with the prevention or correction of injuries or disorders of 
the skeletal system and associated muscles, joints and ligaments.
Orthoptist 
One skilled in the investigation, diagnosis and treatment of defects of binocular vision and 
abnormalities of eye movement.
Osteopathy 
A system of medicine based on the theory that disturbances in the musculoskeletal 
system affect other bodily parts, causing many disorders that can be corrected by 
various manipulative techniques in conjunction with conventional medical, surgical, 
pharmacological, and other therapeutic procedures.
Orthosis 
Device or aid to prevent, correct or control deformities.
Otorrhoea 
A discharge from the ear, especially a purulent one.
Pacifi c peoples 
The diverse range of people living in New Zealand who have migrated from nations of the 
South Pacifi c, and/or who identify with one or more of the Pacifi c islands because of ancestry 
or heritage.
Paresis 
Slight or partial paralysis. 
Pathology 
The scientifi c study of the nature of disease and its causes, processes, development and 
consequences.
Perilymphatic fi stula
 A tear or defect of the thin membranes bewteen the air fi lled middle ear and the fl uid fi lled 
inner ear.
Periorbital 
Situated around the orbit or eye socket.
Post-traumatic amnesia
 Loss of memory after trauma.
Premorbid 
Preceding the occurrence of disease.
Proprioceptive 
A sensory receptor, found chiefl y in muscles, tendons, joints and the inner ear, that detects 
the motion or position of the body or a limb by responding to stimuli arising within the 
organism.
Psychosis 
A severe mental disorder, with or without organic damage, characterised by derangement 
of personality and loss of contact with reality and causing deterioration of normal social 
functioning. 
Psychosocial 
Involving aspects of social and psychological behaviour.
READ codes 
Diagnostic codes used by primary care providers on ACC claim forms.
Retrograde amnesia
 Loss of memory before the trauma/event.
Risk factor 
An aspect of personal behaviour or lifestyle, an environmental exposure, or an inherited 
characteristic that is associated with an increased risk of a person developing a disease.
216
 
   
   
 

Schizophrenia 
Any of a group of psychotic disorders usually characterised by withdrawal from reality,  
illogical patterns of thinking, delusions and hallucinations, and accompanied in varying 
degrees by other emotional, behavioural or intellectual disturbances. Schizophrenia is 
associated with dopamine imbalances in the brain and defects of the frontal lobe and is 
caused by genetic, other biological and psychosocial factors.
Seizure 
A sudden attack, spasm or convulsion, as in epilepsy or another disorder.
Somatosensory evoked potentials
A series of waves that refl ect sequential activation of neural structures along the 
somatosensory pathways following electrical stimulation of peripheral nerves. 
Spasticity 
A condition in which certain muscles are continuously contracted. This contraction causes 
stiffness or tightness of the muscles and may interfere with movement, speech and manner 
of walking.
Stroke 
Sudden decrease in or loss of consciousness, sensation and movement caused by rupture 
or obstruction (as by a blood clot) of a blood vessel of the brain. Stroke is characterised by 
rapidly developing symptoms and signs of a focal brain lesion, with symptoms lasting for 
more than 24 hours or leading to death, with no apparent cause other than of vascular origin. 
Subdural haematoma
Bleeding into the space between the dura and the brain itself.
Tapu  
In Ma¯ori tradition, something that is tapu is considered inviolable or sacrosanct due to its 
sacredness. Things or places which are tapu must be left alone, and may not be approached 
or interfered with. In some cases, they should not even be spoken of.
Tinnitus 
A sound in one ear or both ears, such as buzzing, ringing or whistling, occurring without an 
external stimulus and usually caused by a specifi c condition, such as an ear infection, the 
use of certain drugs, a blocked auditory tube or canal or a head injury.
Vertigo 
An illusory sensation of movement or spinning.
Wha¯nau 
Extended family: relationships that descend from a common ancestor.
217
 
   
   
 

218
 
   
   
 

References
1. 
Accident Compensation Corporation and National Health Committee. Traumatic Brain Injury Rehabilitation 
Guidelines. Wellington: 1998. 
2. 
Accident Compensation Corporation. Clinical Guidelines: Acute Management of Traumatic Brain Injury 
(TBI). Wellington: 2001. 
3. 
World Health Organization. Towards a Common Language for Functioning, Disability and Health: ICF
Geneva: 2002.
4. 
Thornhill S, Teasdale G, Murray G, et al. Disability in young people and adults one year after head injury: 
prospective cohort study. BMJ 2000;320:1631–5. [+]
5. McNaughton 
H. 
Traumatic Brain Injury Rehabilitation in New Zealand: Current Practice Review. Wellington: 
Medical Research Institute of New Zealand; 2004.
6. 
Siegert R, Levack W. TBI Tools Review for the Development of Guidelines on the Assessment, Management 
and Rehabilitation of Traumatic Brain Injury. Wellington: Rehabilitation Teaching and Research Unit, 
Wellington School of Medicine; and Health Sciences, University of Otago; 2005. 
7. 
National Collaborating Centre for Acute Care. Head Injury: Triage, Assessment, Investigation and Early 
Management of Head Injury in Infants, Children And Adults. London: National Institute for Clinical 
Excellence (NICE), 2003.
8. 
Royal College of Physicians, British Society of Rehabilitation Medicine. Rehabilitation Following Acquired 
Brain Injury: National Clinical Guidelines. London: 2003.
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traumatic brain injury. J Head Trauma Rehabil 2003;18(5):387–97. [~/x]
376.  Esselman PC, Dikmen SS, Bell K, et al. Access to inpatient rehabilitation after violence-related traumatic 
brain injury. Arch Phys Med Rehabil 2004;85(9):1445–9. [~]
377.  Gerhart KA, Mellick DC, Weintraub AH. Violence-related traumatic brain injury: a population-based study. 
Trauma 2003;55(6):1045–53. [~/x]
378.  Hanks RA, Wood DL, Millis S, et al. Violent traumatic brain injury: Occurrence, patient characteristics, 
and risk factors from the Traumatic Brain Injury Model Systems project. Arch Phys Med Rehabil 
2003;84(2):249–54.
379.  Fanslow JL, Norton RN, Spinola CG. Indicators of assault-related injuries among women presenting to the 
emergency department. Ann Emerg Med 1998;32(3 Pt 1):341–8. [~/+]
380.  Grimshaw J, Thomas R, MacLennan G, et al. Effectiveness and effi ciency of guideline dissemination and 
implementation strategies. Health Technol Assess 2004;8(6):iii–iv, 1–72. 
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GOV-039784 - Document 4


About the guideline
Thousands of New Zealanders experience traumatic brain injury (TBI) each year. The purpose of the guideline 
is to support informed decision-making by all practitioners working with people who have TBI, their families/
wha¯nau and carers. The guideline does not specifi cally address non traumatic categories of brain injury, such 
as those resulting from poisoning and anoxia, or stroke and other cardiovascular events. The guideline also 
excludes pre- and peri-natal brain damage resulting from prenatal and birth-related events. 
Many aspects of both adult and paediatric rehabilitation following clinically signifi cant TBI lack a robust 
evidence base. Therefore, much of the evidential support for the recommendations in the guideline is 
necessarily drawn from less robust research study designs, or from closely related areas such as the stroke 
literature.
The term ‘head trauma’ or ‘head injury’ is used to mean the original injury. A head injury does not always cause 
an injury to the brain, and the terms ‘head’ and ‘brain’ are used to distinguish between the original injury to the 
head and consequent injury to the brain respectively. 
Following recent international practice, the Guideline Development Team uses, where possible, clinically 
signifi cant TBI or symptomatic TBI to refer to TBI with a need for intervention or other care or support, 
irrespective of the initial severity of injury. Although classifi cation of the initial severity of TBI is useful in the 
prediction of some short- and long-term outcomes, the relationship between initial severity of injury and 
medium- and long-term outcomes has been questioned. 
This guideline was developed by an independent multidisciplinary team of practitioners and consumers under 
the auspices of the New Zealand Guidelines Group (NZGG) and was funded by ACC. 
The Guideline Development Team included: Harry McNaughton (Chair), Michael Ardagh, Andrew Beattie, Vijaya 
Dharan, Margaret Dudley, Chris Dyson, Monique Niumata-Faleafa, Greg Finucane, Kate Hall, Matire Harwood, 
Brenda Kenworthy, Peter Larking, Brigette Larkins, Janet Leathem, William Levack, Joan Limmer, Kelly Lynch, 
Martin MacFarlane, John Mayhew, Jenny McClure, Siobhan Molloy, Harley Pope, Sharon Reilly, Elizabeth 
Rowland, Bernadette Ryan, Richard Siegert, Peter Stormer, Wendy Browne and Denise Udy. 
These summaries have been developed from the TBI guideline entitled Traumatic Brain Injury: Diagnosis, Acute 
Management and Rehabilitation ACC2404. They are intended for use by all practitioners and address the pre-
hospital assessment, the in-hospital acute phase, and the rehabilitation phase of TBI care.
There is limited evidence to guide management in children and young people with TBI. The information and 
recommendations for adults with TBI should be used with caution in these groups. 
For a full discussion of TBI management, it is strongly recommended that you refer to the full guideline, 
Traumatic Brain Injury: Diagnosis, Acute Management and Rehabilitation ACC2404. This is available for 
download from www.acc.co.nz or www.nzgg.org.nz. A printed copy is available from 0800 THINKSAFE
(0800 844 657) or the ACC Injury Prevention Unit: Phone (04) 918 7700. Email: [email address] or
[email address]. 
1

2

,
t
men
Pre-hospital Assessment,
s
s
e
s
s
Management and Referral
 and referral
t
al a
t
i
osp
gemen
key messages
pre-h
mana
• Always treat the greatest threat to life and avoid further harm.
• A falling or persistently reduced Glasgow Coma Scale (GCS) score and amnesia are associated with an
increased risk of intracranial complications.
• Do NOT assume that signs and symptoms of a person’s injury are due to intoxication from alcohol or
drugs.
• Initiate referral to the Emergency Department if there are signs and symptoms that are risk factors for
acute intracranial complications of TBI.
• People who do not require further medical assessment must be provided with written information about 
when to seek medical help.
• Coordinated trauma systems reduce mortality in serious injury, including serious neurotrauma.
3

Contents
Defi nition .........................................................................................................................................................4
Pre-hospital acute assessment .........................................................................................................................5
Treat the greatest threat to life and avoid further harm ................................................................................ 5
Assessment of need for medical attention .........................................................................................................6
Assessing risk indicators for acute complications ........................................................................................ 6
Referral to the Emergency Department ..............................................................................................................8
Initiate referral to the Emergency Department if there are signs and symptoms that are risk factors
for acute intracranial complications of TBI ................................................................................................... 8
Delayed fi rst assessment (>24 hours after the injury) ................................................................................... 8
Criteria for classifying the severity of traumatic brain injury .............................................................................9
Glasgow Coma Scale .......................................................................................................................................10
Adults ....................................................................................................................................................... 10
Paediatric version ..................................................................................................................................... 10
Defi nition
Traumatic brain injury (TBI) is an acute brain injury arising from mechanical energy to the head from external 
physical forces. Criteria for clinical identifi cation include one or more of the following:
• confusion or disorientation
• loss of consciousness
• post-traumatic 
amnesia
• other neurological abnormalities (eg, focal neurological signs, seizure and/or intracranial lesion).
aims of pre-hospital assessment
1. To establish whether trauma to the head has occurred.
2. To estimate the severity of any injury to the brain.
3. To identify hypotension and/or hypoxia (which, untreated, can magnify TBI effects).
4. To identify risk factors for acute complications of TBI which may require intervention, especially 
intracranial bleeding.
5. To identify other injuries that may require urgent management.
4

,
t
men
s
s
e
Pre-hospital acute assessment
s
s
 and referral
t
al a
t
i
Treat the greatest threat to life and avoid further harm.
osp
gemen
Full cervical spine immobilisation should be attempted, unless there is: 
• no alteration of consciousness, and
pre-h
mana
• no neck pain/tenderness, and
• no focal neurological defi cit, and
• no major distracting injury.
Assess for signs and symptoms that are risk factors for acute intracranial complications of TBI. Initiate referral to 
the Emergency Department if these are detected.
Do NOT assume that signs and symptoms of a person’s injury are due to intoxication from alcohol or drugs, even 
when intoxication is suspected.
Promptly transport people with suspected TBI directly to a centre where TBI is managed in its entirety or to a 
centre that can stabilise their condition prior to a transfer to a centre where TBI is managed in its entirety.
Paramedics should be trained in the use of the Glasgow Coma Scale (GCS) and in the detection of non-
accidental injury.
5

Assessment of need for medical attention
Focus on detecting acute complications of TBI, particularly intracranial bleeding. Various assessment tools and 
factors can be used as risk indicators for acute complications of TBI.
Assessing risk indicators for acute complications
tools/
factors
recommendations/comments
gl asgow coma 
Use the GCS to assess people with a head injury.
scale (gcs)
The risk of intracranial complications and consequent need for surgery increases as 
the GCS declines.
Urgent investigation and/or referral is indicated if there is a fall of ≥2 points in the 
GCS, as this may represent the development of intracranial bleeding. 
level of 
Record any loss of, or alteration in, consciousness.
consciousness
Altered consciousness after TBI is associated with an increased risk of developing an 
intracranial complication.
Check blood glucose levels in all people with altered consciousness, as altered 
consciousness may have many causes.
post-traumatic 
Assess and record post-traumatic amnesia in all people with suspected TBI, where 
amnesia
possible.  
Commence assessment for amnesia prospectively (ie, before it has resolved), to 
increase accuracy.
Select and use one of the available validated post-traumatic amnesia measurement 
tools (eg, Modifi ed Oxford Post Traumatic Amnesia Scale [MOPTAS], Westmead Post 
Traumatic Amnesia Scale, Galveston Orientation and Amnesia Test [GOAT]).
Although post-traumatic amnesia is associated with an increased risk of intracranial 
complications, evidence on the precise relationship between post-traumatic amnesia 
and intracranial complications is inconsistent. 
neurological 
Assess and record neurological signs in people with suspected TBI. 
signs
Post-traumatic neurological signs (eg, focal neurological defi cit, seizure) are strongly 
associated with the risk of an intracranial complication. 
bleeding 
Consider the possibility of a bleeding disorder or anticoagulant medication use when 
disorders 
assessing people with suspected TBI, as these may contribute to an increased risk of 
and use of 
intracranial complications. 
anticoagul ants
Check whether alternative or complementary therapies with an anticoagulant effect 
have been taken.
6

,
t
men
s
s
tools/
e
s
factors
recommendations/comments
s
 and referral
t
al a
skull fracture
Undertake clinical assessment of signs of skull fracture, including signs of basal 
t
i
skull fracture (CSF fl uid leak, periorbital haematoma, depressed or open skull injury, 
osp
penetrating injury).
gemen
The risk of intracranial complications is higher in people with a diagnosed skull 
pre-h
mana
fracture.
Routine use of skull X-rays is not recommended as a decision-making tool. 
seizure
Seizure ALONE is rarely a sign of an intracranial haematoma. However, alteration 
in consciousness from a seizure (or drugs used to stop the seizure) cannot be 
differentiated from that caused by an intracranial bleeding complication of TBI. Unless 
recovery is prompt and complete, referral for a CT scan is necessary to exclude such a 
complication.
mechanism of 
High-risk factors for clinically signifi cant TBI after head injury include:
injury
• a pedestrian struck by a motor vehicle
• an 
occupant 
ejected 
from a motor vehicle
• a fall from a height of >1 metre or >5 stairs (less in infants and children).
age
Increasing age (>65 years) is associated with an increased risk of intracranial 
complications and a poorer prognosis following TBI. 
Young infants (<12 months) are also at increased risk of intracranial complications.
drug or 
Although alcohol and drug intoxication can reduce the GCS, it is safer to assume that 
alcohol 
such signs are due to TBI or a complication of TBI rather than intoxication, and proceed 
consumption
accordingly. 
headache
Avoid strong analgesia for headache, if possible, until a full assessment has been 
made in the Emergency Department. 
Analgesics may have a sedative effect and can mask symptoms of complications of 
TBI.
vomiting
Consider any vomiting to be a risk factor for intracranial complications. 
There is debate about the number of vomiting episodes required to identify a high risk 
of intracranial complications.
irritabilit y 
Irritability and altered behaviour may be important signs of deterioration following TBI 
and altered 
in young children.
behaviour
history 
Record any previous neurosurgical intervention, especially if there has been 
of cranial 
cranial neurosurgery in the 6 weeks prior to injury, or if there is a shunt in place for 
neurosurgical 
hydrocephalus.
interventions
7

Referral to the Emergency Department
Initiate referral to the Emergency Department if there are signs and 
symptoms that are risk factors for acute intracranial complications of TBI.
Use emergency services transport to transfer to the Emergency Department if there is:
• any deterioration in the injured person’s condition
• impaired consciousness (GCS <15)
• any focal neurological defi cit since the injury
• any suspicion of a skull fracture or penetrating head injury 
• any seizure since the injury
• a high-energy head injury 
• suspected neck injury.
Consider using a competent adult to transport to the Emergency Department for review (if specifi c indicators for 
emergency services transport are absent) when there is: 
• any loss of consciousness as a result of the injury, unless trivial, apparently resolved and alternative
observation is available
• amnesia for events before or after the injury 
• persistent headache since the injury
• irritability or altered behaviour, particularly in infants and young children
• any vomiting since the injury
• a history of bleeding or clotting disorder
• current anticoagulant therapy
• current drug or alcohol intoxication
• any previous cranial neurosurgery 
• suspicion of non-accidental injury
• age 
≥65 years or ≤1 year 
• concern about the cause of any symptoms by the person undertaking the assessment.
If there are no indications for Emergency Department review, advise people to seek further assessment from a 
general practitioner (GP) or Accident and Medical Clinic if there are:
• adverse social factors (eg, no supervision at home)
• continuing concerns by the injured person or their carer about the diagnosis.
People with no indications for Emergency Department review or further medical assessment can go home with 
written information about when to seek medical help. 
Delayed fi rst assessment (>24 hours after the injury)
It is important to:
• document the episode of external force to the head and any symptoms at the time (eg, loss of 
consciousness, amnesia)
• document the current symptoms and their duration, including pre- and post-event amnesia
• explain that some or all of the symptoms may be related to the injury
• consider the need for acute referral to hospital, specialist referral and/or further investigation.
8

,
t
men
s
s
e
Criteria for classifying the severity of 
s
s
 and referral
traumatic brain injury
t
al a
t
i
osp
gemen
gl asgow coma scale 
duration of post-
severit y of injury
score
traumatic amnesia
pre-h
mana
Mild
13–15
<24 hours
Moderate
9–12
1–6 days
Severe
3–8
7 days or more
If there is a discrepancy between the severity level for the GCS score and post-traumatic amnesia, it is 
appropriate to use the more severe category (eg, GCS score of 14 but post-traumatic amnesia for 2 days = 
moderate TBI). 
Refer: Teasdale G, et al. Acta Neurochir (Wien) 1979; 28:13–16; Carroll LJ, et al. J Rehabil Med 2004(43 Suppl):113–25.
9

Glasgow Coma Scale
Adults
The GCS is scored between 3 and 15, 3 being the worst and 15 the best. 
It is composed of 3 parameters: Best Eye Response, Best Verbal Response and Best Motor Response. The 
defi nitions of these parameters are given below.
best eye response (4) 
best verbal response (5) 
best motor response (6)
1. No eye opening
1. No verbal response
1. No motor response
2. Eye opening to pain
2. Incomprehensible sounds
2. Extension to pain
3. Eye opening to verbal 
3. Inappropriate words
3. Flexion to pain
command
4. Confused
4. Withdrawal from pain
4. Eyes open spontaneously
5. Orientated
5. Localising pain
6. Obeys commands
Paediatric version
The paediatric version of the GCS is scored between 3 and 15, 3 being the worst and 15 the best. It is composed 
of 3 parameters: Best Eye Response, Best Verbal Response or Best Grimace Response, and Best Motor 
Response. The defi nitions of these parameters are given below. 
best eye response 
best verbal 
best grimace 
best motor 
(4) 
response (5) 
response (5) 
response (6) 
1. No eye opening
1. No vocal response
A ‘grimace’ alternative 
1. No motor response to
2. Eye opening to pain
2. Occasionally
to verbal responses 
pain
3. Eye opening to verbal 
whimpers and/or
should be used in those 
2. Abnormal extension
command
moans
infants or children 
to pain (decerebrate)
4. Eyes open
3. Cries inappropriately
who are pre-verbal or 
3. Abnormal fl exion to
spontaneously
4. Less than usual 
intubated.
pain (decorticate)
ability and/or
4. Withdrawal to painful 
1. No response to pain
spontaneous
stimuli
2. Mild grimace to pain
irritable cry
5. Localises to painful 
3. Vigorous grimace to
5. Alert, babbles, coos,
stimuli or withdraws 
pain
words or sentences to
to touch
4. Less than usual 
usual ability
6. Obeys commands
spontaneous ability 
or performs normal 
Communication with 
or only responds to
spontaneous 
the infant’s or child’s 
touch stimuli
movements
caregivers is required to 
5. Spontaneous normal
establish the best usual 
facial/oro-motor
verbal response
activity
Note: This appendix is included in the full guideline and online at www.nzgg.org. It may be reproduced for 
10
clinical use. 

Acute phase of care
key messages
• The Emergency Department assessment and management of people with suspected TBI should focus on
preventing and treating hypotension and hypoxia, obtaining early imaging and attending to co-existing
injuries.
• CT scanning of the head is the primary investigation of choice for the detection of clinically signifi cant
acute complications of TBI.
• The sensitivity of skull X-rays is too low to be the primary investigation.
• Avoid giving strong systemic analgesia until a full assessment has been done.
• Test for blood alcohol levels in all people with suspected TBI and GCS <15 and/or where alcohol 
intoxication is suspected.
• Consider the possibility of non-accidental injury in all children with TBI.
• Avoid corticosteroids in people with acute TBI of any severity.
• Do not discharge people presenting with suspected TBI until GCS is 15.
• Early rehabilitative intervention in clinically signifi cant TBI improves outcomes.
e of care
s
ha
e p
t
cu
a
11

Contents
Emergency Department assessment ...............................................................................................................13
Primary investigation: CT scanning ............................................................................................................ 13
Non-accidental injury in children ............................................................................................................... 16
Neurosurgical care .................................................................................................................................... 16
Use of corticosteroids ............................................................................................................................... 16
Transfer to tertiary care setting .................................................................................................................. 16
Indications for hospital admission ............................................................................................................ 17
12

Emergency Department assessment
The Emergency Department assessment of people with suspected TBI should focus on:
• the management or avoidance of hypotension and hypoxia
• early imaging (rather than admission and observation)
• attention to co-existing injuries and other concerns.
Collect data about the following to aid decision-making:
• age
• mechanism of injury
• vomiting since the injury
• presence of headache and/or seizures since the injury
• presence of anterograde amnesia (impaired memory for events after the injury)
• presence of retrograde amnesia (impaired memory before the injury) of greater than 30 minutes 
• GCS (on presentation and two hours after injury)
• evidence of suspected or open skull fracture
• signs of basal skull fracture
• evidence of trauma above the clavicles
• evidence of drug or alcohol intoxication.
e of care
s
All people with suspected TBI need triage assessment on arrival.
ha
• If high risk on triage for clinically signifi cant TBI, assessment within 10 minutes by an experienced health
e p
care practitioner is required.
t
• If GCS <8, involve anaesthetist/emergency physician/critical care physician to provide appropriate airway 
cu
a
management and assist with resuscitation.
• If low risk on triage for clinically signifi cant TBI, reassessment within one hour by a doctor with appropriate
experience is required.
Establish the need for CT imaging of the head (see ‘Primary investigation: CT scanning below).
Test for blood alcohol levels in all people with suspected TBI and GCS <15 and/or where alcohol intoxication is 
suspected.
• There is considerable similarity in the signs of alcohol intoxication and TBI (GCS is unreliable in alcohol-
intoxicated people).
• Do NOT attribute signs of possible TBI to alcohol intoxication alone when assessing people with suspected
TBI.
Do NOT administer strong systemic analgesia until fully assessed. 
Primary investigation: CT scanning
CT scanning of the head is the primary investigation of choice for the detection of clinically signifi cant acute 
complications of TBI. 
The sensitivity of skull X-rays is too low to be the primary investigation in infants, children and adults.
Request an immediate CT scan for adults who have sustained a head injury with ANY of the following risk 
factors:
• any deterioration in condition
• GCS <13 when assessed, irrespective of time elapsed since the injury
13

• GCS of 13 or 14 two hours after the injury 
• suspected open or depressed skull fracture
• any sign of basal skull fracture
• post-traumatic 
seizure
• focal neurological defi cit
• more than one episode of vomiting
• amnesia for >30 minutes for events before the injury.
Request an immediate CT scan for adults who have sustained a head injury with some loss of consciousness or 
amnesia since the injury and ANY of these risk factors:
• age 
≥65 years 
• coagulopathy 
(history 
of 
bleeding, clotting disorder, current treatment with warfarin)
• high-risk mechanism of injury (a pedestrian struck by a motor vehicle, an occupant ejected from a motor
vehicle, or a fall from a height of >1 metre or >5 stairs).
The decision to CT scan should be applied regardless of the infl uence of intoxication.
In some situations (eg, rural centres with limited access to CT), observation for 24 hours rather than CT scan is a 
reasonable option. 
Discuss the appropriateness of observation with the relevant neurosurgical centre. 
People with the following factors MUST be referred for CT scan:
• any deterioration in condition
• GCS <13 at time of assessment irrespective of time elapsed since the injury or GCS of 13 to 14 two hours after
injury
• any sign of basal skull fracture
• focal neurological defi cit.
It is particularly important to balance the benefi ts and harms of CT scanning in infants and children. Consult a 
specialist with experience in managing TBI if there is doubt on whether a CT scan is required.
children aged 0 to 16 years
Imaging should be considered if ANY of the following factors are present (refer to algorithm):
• post-injury adverse events or signs, including focal neurological defi cits and seizures (except 
immediate)
• a paediatric GCS of ≤13, particularly an initial or ‘fi eld’ (pre-hospital) GCS of ≤13, or any decrease in GCS 
• skull 
fracture, either obvious or suspected on the basis of clinical signs
• injury resulting from a fall from 1 metre or 5 stairs, or less in the case of younger children
• non-accidental cause of injury
• lethargy or irritability on examination.
infants aged 2 years or younger
For this group, there are additional risk factors for TBI supporting CT scanning, including:
• soft tissue injury such as swelling or haematoma
• occipital or temporal/parietal location of injury.
14

diagnostic management and selection f or imaging of children and young people aged <17 years 
History of trauma to head
• Injury resulting from a fall 
CT scan§
Any
Scan +ve or GCS 
from one metre or fi ve
13–14
stairs or more*
• Non-accidental cause of 
injury 
Admit to 
hospital and/or 
Post injury
neurosurgical 
• Any 
deterioration
consult
• Any seizure, except 
immediate
• Examination:†
− initial GCS score ≤13
Scan –ve and 
− GCS score that 
GCS = 15
decreases at any time
− obvious or suspected
skull fracture
− lethargy or irritability
− any focal neurological 
No
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defi cits
s
ha
None
e p
t
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Any non-surgical 
a
Observe and reassess
indicators for 
at two hours
GCS = 15?
Yes
paediatric 
Yes
Note: Any deterioration 
consult or 
– refer for scan immediately
admission?
Paediatric 
No
consult and/or 
admit to hospital 
Discharge with information to 
Recommended minimum 
home observation‡
observation period = four hours
* In younger children, falls from lesser heights may have a high risk of intracranial complications.
†  Use paediatric version of GCS.
‡  Children and young people with a head injury should only be discharged home if they have a responsible
adult who can observe them for any deterioration.
§
CT scanning of infants and children can be diffi cult and may require anaesthesia and pose a signifi cant
radiation risk. If uncertain about benefi ts of CT scan versus risks of scan, seek specialist advice (Emergency 
Department specialist, intensive care unit specialist, neurosurgeon, paediatrician) before scanning.
GCS = Glasgow Coma Scale
15

Consider repeating the CT scan:
• if the initial scan shows an abnormality and there is clinical deterioration
• to check that an original small lesion has not progressed (next day)
• to check that an initial small lesion has resolved spontaneously (in a week or two).
Non-accidental injury in children
Consider the possibility of non-accidental injury in all children with TBI.
A full work-up for suspected non-accidental injury includes:
• skull X-rays as part of a skeletal survey
• ophthalmoscopic examination for retinal haemorrhage
• examination for pallor, anaemia, tense fontanelle
• additional investigations (CT, MRI).
Neurosurgical care
Consult a neurosurgeon if the person has:
• deteriorating status, especially a fall in GCS of ≥2, development of pupil dilatation or other new neurological 
defi cit
• severe 
TBI 
(GCS 
≤8), especially if unconscious from the time of injury
• severe neurological defi cit following TBI
• surgically 
signifi cant lesion on imaging.
Use of cortocosteroids
There is strong evidence to avoid corticosteroids in the management of people with acute TBI of any severity. 
Corticosteroids are associated with an increase in mortality in people with acute TBI. 
Transfer to tertiary care setting
• Resuscitation and stabilisation of the injured person should be completed before transfer.
• Do not transport a persistently hypotensive person until stabilised.
• Intubate and ventilate all people with GCS ≤8 requiring transfer to tertiary care.
• People with suspected TBI should be accompanied by an experienced doctor and an adequately trained
assistant.
• The transfer team should have a means of communication with their base hospital and the tertiary care
facility during the transfer.
 Indications for immediate intubation and ventilation in people with TBI include ANY of the following: 
• coma 
(GCS 
≤8)
• loss of protective laryngeal refl exes
• ventilatory 
insuffi ciency:
– hypoxaemia (PaO  <65 mm Hg on air or <95 mm Hg on oxygen)
2
– hypercarbia (PaCO  >45 mm Hg)
2
• spontaneous 
hyperventilation causing PaCO  <30 mm Hg
2
• respiratory 
arrhythmia.
Indications for intubation and ventilation in people with TBI before transfer include ANY of the following: 
• signifi cant deterioration in level of consciousness
16

• bilateral fractured mandible
• copious bleeding into the mouth
• seizures.
Fully inform carers, family/wha¯nau about the transfer and provide them with as much access to the injured 
person during transfer as is practical.
Indications for hospital admission
Admit to hospital if there are ANY of the following:
• a deteriorating GCS 
• clinically 
signifi cant abnormalities on imaging
• GCS <15 after imaging
• criteria for CT scanning are met but CT scanning is not possible
• focal or abnormal neurological signs 
• early post-traumatic seizure
• skull 
fracture
• high-risk mechanism of injury
• continuing signs of concern to the clinician (eg, vomiting, severe headaches, amnesia)
• other reasons for clinician concern, including drug or alcohol intoxication, other injuries, shock, suspected
non-accidental injury, signs of meningeal irritation, cerebrospinal fl uid leak, where a scalp laceration overlies 
e of care
a fracture, or the person’s age
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• when there is no responsible family/wha¯nau member, caregiver or close friend under whose care the person
ha
could be discharged
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t
• ‘mild’ head injuries with symptoms such as headache, photophobia, nausea and vomiting, or amnesia
cu
requiring management.
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17

in-hospital observation
Minimum neurological observations should include ALL the following:
• GCS
• pupil size and reactivity
• limb 
movements
• respiratory 
rate
• heart 
rate
• blood 
pressure
• temperature.
Perform and record observations at least every 15 minutes until GCS is 15 on two consecutive occasions.
For people with an initial GCS of 15, or who have returned to a GCS of 15 on two consecutive observations, 
the minimum frequency of observations following the initial assessment should be: 
• half-hourly for the fi rst two hours, then
• one-hourly for four hours, then
• two-hourly 
thereafter.
If a person with a GCS of 15 deteriorates at any time after the initial two-hour period, revert to observations 
every 15 minutes or more frequently if necessary and follow the original frequency schedule. 
An urgent reappraisal should be done by the supervising doctor if any of the following signs of neurological 
deterioration occur:
• development of agitation or abnormal behaviour
• a sustained (≥30 minutes) drop of one point in GCS
• any drop of >two points in GCS
• development of severe/increasing headache or persisting vomiting
• new or evolving neurological symptoms or signs.
Consider an immediate CT scan if any of the above signs of neurological deterioration occur. 
Consider further CT or MRI scanning if original CT scan was normal but GCS is <15 after 24 hours of 
observation. 
Assess for post-traumatic amnesia and focal neurological signs at regular intervals.
Provide in-hospital support for families/wha¯nau (and carers).
18

discharge from hospital
Do not discharge people presenting with suspected TBI until GCS is 15.
People with suspected TBI may be discharged if:
• GCS is 15 and a CT scan is not indicated
OR
• head or cervical spine imaging is normal and GCS has returned to 15
AND
• there is resolution of all signifi cant symptoms and signs
• no other factors are present that would warrant a hospital admission
• there are appropriate support structures for safe transfer and subsequent care and supervision.
Do not discharge infants or children with suspected TBI who require imaging of the head or cervical spine 
until assessed by a clinician experienced in the detection of non-accidental injury.
Ensure all people with any degree of suspected TBI receive verbal advice on discharge which:
• outlines the risk factors that may indicate complications 
• explains that some people make a quick recovery, but may later experience complications
• gives instructions on contacting community services in the event of delayed complications.
Ensure that people who initially presented with drug or alcohol intoxication and are being discharged 
e of care
receive appropriate information and advice.
s
ha
If there is no carer at home, discharge people with any degree of suspected TBI only when there is 
e p
negligible risk of late complications, or when suitable supervision arrangements have been made.
t
cu
Do not routinely recommend bed rest as there is no evidence that bed rest aids recovery. Advise people 
a
with excessive dizziness that bed rest may help alleviate their symptoms temporarily. 
People discharged from hospital after TBI should have had their GP notifi ed either before or at the point of 
discharge, with details of any residual impairments and details of the planned follow-up.
People who are discharged after suspected TBI sustained after a self-harm or suicide attempt should be 
referred for psychiatric assessment including a risk assessment. 
19

referral to  rehabilitation
Rehabilitation should start as soon as possible. 
Early rehabilitative intervention in clinically signifi cant TBI improves outcomes.
The following areas should be assessed once consciousness has been regained:
• motor impairments, such as weakness, altered tone and lack of coordination in the limbs
• problems with speech and swallowing
• sensory impairment, including visual problems, such as reduced visual acuity, loss of visual fi eld, gaze
palsies and hearing loss
• cognitive impairments, especially of memory, concentration and/or orientation
• language problems, particularly cognitive communication disorder or aphasia
• reduced control over bowels and bladder
• emotional, psychological and neurobehavioural problems.
Assess the need for rehabilitation before discharging people with TBI. 
Refer to a specialist rehabilitation service if people with TBI have: 
• diffi culty with body functions
• diffi culty with activities that they were able to complete prior to the injury 
• diffi culty participating in their usual social roles.
20

Rehabilitation: services, assessment
and interventions
key messages
• Effective coordination, communication and information sharing between rehabilitation services is 
essential to ensure a seamless transition between the stages of TBI rehabilitation.
• People with TBI should be assessed for functional defi cits in Activities of Daily Living (ADL) and for
specifi c impairments in physical, cognitive, behavioural/emotional and communicative functioning.
• Assessment should include seeking information about pre-TBI functioning from family and wha¯nau, and
take into account the person’s participation goals.
• For children with TBI, neuropsychological and other assessments may need to be repeated several times 
as they mature to adulthood.
• Comorbid conditions, especially those with symptomatic overlap with TBI, should be identifi ed and
treated, if necessary.
• Physical rehabilitation should aim to improve functional independence.
• Return to gainful employment or an alternative occupation is often an important goal in adults with TBI
and may be a central factor in the restoration of quality of life.
s
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 and in
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21

Contents
Rehabilitation services ...................................................................................................................................23
Rehabilitation assessment .............................................................................................................................24
Differential diagnosis ................................................................................................................................ 24
Physical assessment ................................................................................................................................. 25
Communicative assessment ...................................................................................................................... 25
Neuropsychological assessment ............................................................................................................... 26
Rehabilitation Interventions ...........................................................................................................................27
Physical rehabilitation .............................................................................................................................. 27
Communication and language rehabilitation ............................................................................................. 29
Cognitive rehabilitation ............................................................................................................................. 29
Psychosocial/Behavioural rehabilitation ................................................................................................... 31
Optimising Performance in daily living tasks ............................................................................................. 31
Sleep and fatigue ...................................................................................................................................... 32
Vocational rehabilitation ........................................................................................................................... 32
Sexuality ................................................................................................................................................... 33
Leisure and recreation .............................................................................................................................. 33
Discharge from rehabilitation services ....................................................................................................... 34
22

Rehabilitation services
Rehabilitation services for people with TBI should:
• be based on achieving well-being rather than on a model of defi cit and dependency
• approach people with TBI from a participation perspective
• have the necessary skills and experience to provide appropriate and context-specifi c assessments and
interventions
• acknowledge that different people require different input at different stages in their recovery.
There are four distinct stages of rehabilitation.
1. Acute care/neurosurgery
2. Residential rehabilitation
3. Non-residential rehabilitation
4. Longer-term community support
Not all people with TBI will require each of these stages (see full guideline for more information).
Effective coordination of services, communication and information sharing is essential to ensure a 
seamless transition between the stages of TBI rehabilitation.
There is international agreement on the benefi ts of individual ‘case coordinators’ or ‘key workers’ to support the 
individual and their family/wha¯nau throughout the course of their recovery.
Delivery of rehabilitation is most effective when done by a coordinated, multidisciplinary team of people from a 
range of disciplines.
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23

Rehabilitation assessment
A TBI can result in physical, cognitive, behavioural/emotional or communicative defi cits. 
Assessment by rehabilitation services should:
• determine whether there is a probable TBI
• ascertain the nature and extent of the TBI
• identify the resulting defi cits and their possible impact on functioning
• consider whether there are potential medical and psychiatric comorbidities which have symptomatic overlap
with the TBI.
Assess for functional defi cits in ADL and for specifi c impairments in: 
• control over bowels and bladder
• speech and swallowing
• motor 
control
• sensory 
function
• language production and comprehension
• cognition, especially memory
• behaviour and emotion.
Consider referring all people with TBI for a neuropsychological assessment to evaluate cognitive 
functioning.
For children with TBI, neuropsychological and other assessments may need to be repeated several times as 
they mature to adulthood.
Seek information about pre-TBI functioning from family/wha¯nau and carers.
Take into consideration the person’s participation goals when assessing activity limitation and 
impairments.  
Assessment of the severity of TBI may be complicated by:
• the presence of non-brain injuries 
• TBI symptoms that are masked by medical problems.
It is important to assess for potential medical complications of TBI and to refer for appropriate treatment. 
Differential diagnosis
It is important to attribute symptoms correctly to TBI or other medical conditions, and to identify and treat 
comorbid conditions.
Many of the symptoms of TBI overlap with other conditions (both physical and psychological/psychiatric). 
24

In children and young people, various developmental, psychological and psychiatric conditions may have 
symptomatic overlap with the effects of TBI. These conditions include:
• Attention 
Defi cit Hyperactivity Disorder (ADHD)
• foetal alcohol effects
• hearing and visual impairments
• drug and alcohol use in adolescents
• developmental 
disorders
• non-TBI-related cognitive diffi culties and emotional problems.
Request specialist assessment where there is a lack of clarity about the aetiology of the symptoms, or where 
progress is poorer than expected. 
Physical assessment
Assessment of the physical functioning of people with TBI should include checking for the following:
• motor defi cits
– muscle 
weakness and paralysis
– abnormal muscle tone (spasticity)
– defi cits in joint range of motion
– ataxia/incoordination
• sensory defi cits
– visual/hearing loss
• physical symptoms
– eg, headache, fatigue, pain
• dysphagia
• seizures
• impaired functional mobility
– changing and maintaining body position
– carrying, moving and handling objects
– walking and moving (including, but not limited to, crawling, climbing, running, jumping and swimming)
– mobilising 
with the aid of assistive technology.
Dysphagia assessment
A speech-language therapist should lead both the assessment and planning of dysphagia therapy. This should 
s
n
include:
io
• a detailed diagnostic assessment, to address issues of diagnosis, aetiology and functional impairment 
es,
t
ic
en
• a rehabilitation-focused assessment, which addresses the need for, and the potential to benefi t from,
v
v
r
rehabilitation.
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Communicative assessment
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 and in
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Communicative assessments should be performed by a speech-language therapist, in conjunction with 
s
others in the team. 
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rehabili
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s
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Assessments of the communicative functioning of people with TBI should include assessments for:
• language 
defi cits – expression and comprehension
• cognitive communication disorders
25

• dysarthria
• apraxia of speech
• acquired 
dyslexia
• acquired 
dysgraphia.
Neuropsychological assessment
All people with clinically signifi cant TBI should have a neuropsychological assessment of cognitive and 
behavioural/emotional functioning by a neuropsychologist.
Assessment includes an interview with the person with TBI and their family/wha¯nau and carers, plus standard 
assessment measures.
A detailed neuropsychological assessment can: 
• contribute to the evaluation of the likely impact of cognitive impairment on the rehabilitation programme
• contribute to the evaluation of areas of strength on which the person may be able to build during
rehabilitation, and the person’s prognosis in terms of their ability to function independently in the
community or to return to work or study
• help to identify the appropriate areas for effective rehabilitation input.
The assessment can encompass any or all of the following:
• a detailed diagnostic assessment 
• a rehabilitation-focused assessment 
• a 
vocation-focused 
assessment
• a permanent functional impairment assessment 
• a behavioural management assessment.
When TBI is sustained in childhood, neuropsychological assessment may need to be repeated several times as 
the child matures to adulthood.
Cognitive assessment 
Cognitive assessment requires input from a multidisciplinary rehabilitation team along with family/wha¯nau and 
carers. 
Cognitive assessment identifi es the person’s functional cognitive abilities through an occupational therapy 
assessment in the home, work, school or community context. Face-to-face contact is essential for assessment.
Assessment of the cognitive functioning of people with TBI should include the following areas:
• insight and awareness 
• attention
• memory
• speed of information processing
• perception
• complex 
problem-solving
• self-monitoring
• social 
judgement.
26

Behavioural/Emotional assessment 
Assessment of the behavioural and emotional functioning of people with TBI should include assessment for:
• emotional 
lability
• poor 
initiation
• mood 
change
• adjustment 
problems
• personality changes, including:
– aggressive outbursts
– disinhibition
– inappropriate 
sexual behaviour
• poor 
motivation.
It is also important to consider the possibility of drug and alcohol misuse and mental health disorders
particularly depression, anxiety disorders and psychosis.
Rehabilitation interventions
Currently, there is little robust evidence about commonly used interventions. Many of the following 
recommendations are extrapolated from fi ndings in populations with other brain injuries (particularly stroke) or 
in mixed populations including some people with TBI. 
Physical rehabilitation
The aims of physical rehabilitation are to:
• aid the recovery of normal functioning as far as possible
• provide compensatory strategies to minimise the negative impact of the symptoms that persist
• increase independence through the facilitation of motor control and skills.
There is strong evidence of the effectiveness of physical rehabilitation in improving functional independence. 
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A physiotherapist or occupational therapist with neurological expertise should coordinate the physical 
v
v
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e
therapy to improve the motor function of people with TBI.
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t
Physical treatment approaches should take account of any associated orthopaedic or musculoskeletal 
n: s
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injuries.
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The physical rehabilitation programme should include an illustrated written plan for other members of the 
team, including family/wha¯nau and carers.
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A speech-language therapist with dysphagia expertise should coordinate the dysphagia therapy.
es
rehabili
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Any programme should be adapted to accommodate the person’s normal environment and activities as far 
s
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as possible.
27

Motor control and function, and spasticity
Recovering mobility is an important goal for people who are immobile following TBI.
Provide age-appropriate supportive seating and wheelchairs for people with TBI who are unable to maintain 
their own sitting balance.
Refer people with complex postural needs to a specialist interdisciplinary team with expertise in specialist 
seating.
Consider walking or standing aids for people with mobility problems. 
Orthoses should be individually fi tted.
Consider the following when planning a programme to improve motor control and general fi tness: 
• treadmill training with partial bodyweight support 
• strength 
training
• gait 
re-education
• exercise 
training.
Any rehabilitation programme should include a fl exibility routine when there is any spasticity.
Consider a carefully monitored trial of:
• botulinum toxin A (BTX-A) or tizanidine for treatment of problematic focal spasticity
• intrathecal baclofen for treatment of severe spasticity unresponsive to other treatments.
Continence
Urinary and faecal incontinence are common following severe TBI, and can be distressing, socially disruptive 
and hinder progress in other areas of rehabilitation.
Bladder and bowel management plans should be developed with the full knowledge and support of the 
person’s primary carer.
Do not discharge people with continence problems from residential care until continence aids and services have 
been arranged at home and the carer has been adequately prepared.
urinary incontinence
Rehabilitation of urinary incontinence should include:
• a regular monitoring programme
• strategies for alerting carers to the person’s need to pass urine where there are communication
problems
• a toileting regimen based on reinforcement in cases of cognitive impairment.
Anticholinergic medication should only be prescribed after demonstration of an overactive bladder (eg, on a 
24-hour urine collection or by urodynamic investigation) and a postmicturition residual volume of <100 ml.
Consider intermittent catheterisation in adults with a postmicturition residual volume of >150 ml and in 
children with a postmicturition residual volume of >10% of bladder capacity.
If long-term catheters are necessary, they should be used as part of a planned catheter management 
programme using an agreed protocol, and after consideration of the impact on sexual function.
Supra-pubic catheters are preferred over long-term urethral catheters.
28

constipation
For the management of constipation, institute an active bowel management regimen which includes:
• suffi cient fl uid intake
• natural or simple bulk laxatives 
• exercise and standing (if possible)
• avoiding medications which slow gut motility
• maximum privacy and comfort during defecation
• supported sitting up for defecation at the earliest safe opportunity, and at a regular time each day.
Where the rectum is full but no spontaneous evacuation occurs, daily rectal stimulation may be used.
If the rectum is empty for three days consecutively despite continuing oral intake, consider the use of an 
osmotic laxative or a stimulant.
Sensory impairment
Sensory impairment after TBI, including partial loss of hearing or vision, may exacerbate disorientation and 
confusional states or impact on higher cognitive function.
People with visual and/or hearing loss should be assessed and treated by a team with appropriate 
experience or in conjunction with a specialist service.
All people presenting post TBI with persistent visual neglect or fi eld defects should be offered specifi c 
retraining strategies.
Pain is frequently under-diagnosed in people with TBI, especially those with communication diffi culties.
All people should be assessed for pain on a regular basis and treated actively in accordance with their 
wishes.
s
Specially adapted assessment tools or the skills of a speech-language therapist, and family/wha¯nau and 
n
carers may be required to elicit pain symptoms accurately.
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People with TBI, health care practitioners and carers should be educated about:
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• hypersensitivity and neurogenic pain
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• appropriate handling of the paretic upper limb during transfers.
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Pain management protocols should be implemented, and encompass: 
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• handling, support and pain relief appropriate to the individual needs of the person with TBI
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• regular review and adjustment according to changing need.
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Communication and language rehabilitation
People with specifi c communication diffi culties following TBI should be assessed by a speech-language 
therapist for suitability for speech-language therapy. 
Where achievable goals are identifi ed, an appropriate communication rehabilitation programme should be 
offered, with monitoring of progress.
A communication rehabilitation programme should: 
• take into account the person’s premorbid communication style and any cognitive defi cits
• provide opportunities to rehearse communication skills in natural situations 
• include 
family/wha¯nau and carers in developing strategies for optimum communication
• include communication aids where appropriate
• provide compensatory strategies to manage communication diffi culties.
Assessment and intervention for communication defi cits in children should be appropriate to age and 
development, and performed by paediatric speech-language therapists with expertise in TBI.
Cognitive rehabilitation
Cognitive rehabilitation, in general, has been shown to be effective, although the effectiveness of specifi c 
interventions is unclear.
Where cognitive impairment is causing management diffi culties or limiting response to rehabilitation, 
specialist advice should be sought.
Cognitive defi cits are likely to be more diffi cult for the family/wha¯nau, carers and employers to recognise, 
accept and accommodate, than the physical effects of TBI.
People with persistent cognitive defi cits following TBI should be offered functionally oriented cognitive 
rehabilitation.
Cognitive rehabilitation should include:
• in the acute phase, management in a structured and distraction-free environment, and targeted
programmes for those with executive diffi culties (ie, problems with planning, organisation, problem-
solving and divided attention)
• efforts to improve attention and information-processing skills 
• teaching compensatory techniques
• use of external memory aids
• procedural learning information and principles.
Avoid trial-and-error learning in people with memory impairment.
There is very little evidence for the effectiveness of medications for the cognitive sequelae of TBI.
30

Consider a trial of methylphenidate for adults or children with TBI who have defi cits in speed of mental 
processing, or ADHD secondary to TBI.
Consider a trial of donepezil hydrochloride for adults with TBI who have defi cits in memory and attention.
Any trial of medication for people with TBI should be:
• commenced at low doses, with cautious increases in dose
• carefully monitored for effectiveness and adverse side effects 
• preceded by a clear explanation to the person with TBI and their carers (including a caution that the
effects of medications are less predictable in people with TBI).
Psychosocial/Behavioural rehabilitation
Refer people with severe behavioural problems after TBI to specialist behavioural management services. 
Provide information and ongoing support to families/wha¯nau and carers to help them:
• understand cognitive and behavioural problems
• interact 
appropriately with the people with TBI
• know how to access services.
Psychotropic medications used to manage agitation and aggression in people with TBI should be carefully 
selected for their side effect profi le, and closely monitored. If no effect is observed within six weeks the 
drug should be ‘tailed off’ and another drug trialled after a suitable wash-out period.
Ask about the use of any non-prescription medicines, supplements and complementary or alternative 
medicine.
Consider referral to a neuropsychiatrist to:
• differentiate 
neurobehavioural diffi culties from symptoms of functional illness
• treat people who may require medication for irritability and aggression.
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Optimising performance in daily living tasks
daily living  skills
All people with TBI who have diffi culties in ADL should be assessed by an occupational therapist, 
physiotherapist, nurse or other health care practitioner with expertise in TBI and experience in assessment 
of ADL.
An individual rehabilitation programme aimed at maximising independence in areas of self-maintenance, 
productivity and leisure should be developed and implemented.
People with TBI should be given the opportunity to practise daily living skills outside therapy sessions. All 
daily living tasks should be practised in the most realistic and appropriate environments.
Family/Wha¯nau and carers should be involved in establishing the most appropriate routines for ADL for 
people with TBI. 
Services should recognise that the provision of ‘care’ for some people with TBI may mean the supervision 
and practice of community living skills, rather than the provision of ‘hands-on’ physical care.
Carers and family/wha¯nau should be trained and supported to help with rehabilitation, if willing and if 
acceptable to the person with TBI.
equipment and technology
People with TBI who have diffi culties in functioning should be assessed to determine whether equipment 
or adaptations could increase their safety and/or independence.
Prescription of equipment should take account of any cognitive and behavioural defi cits and their 
constraints on the person’s ability, or their carer’s ability, to use the equipment safely and appropriately. 
When an item of equipment has been identifi ed as required for a person with TBI, it should be provided as 
quickly as possible and before the person is discharged to the community.
People with TBI and their families/wha¯nau or carers should be trained in the safe and effective use of 
equipment, and clear written information should be given on whom to contact for repairs or replacement, 
or for future help and advice regarding the equipment.
The ongoing effectiveness of equipment should be reviewed on a regular basis and in accordance with the 
manufacturers’ guidelines.
Rehabilitation teams should consider the use of computers and other technology as an adaptive source of 
meaningful occupation or as compensatory strategies for people with signifi cant sequelae of TBI.
Where necessary, a specialist assessment of each individual’s ability to use a personal computer and the 
need for adapted hardware and software should be arranged.
People with TBI should be given information about changes in technology relevant to their needs.
Assessments for, and prescriptions of, augmentative communication devices should be made by suitably 
accredited clinicians.
Careful consideration of the appropriateness of technology for individuals who may be vulnerable, such as 
people with symptoms of disinhibition or impaired judgement, is required. 
32

Sleep and fatigue
Sleep diffi culties and fatigue are very common following TBI of all severities.
Advice from a professional experienced in managing fatigue and/or sleep disorders can be useful in 
establishing a suitable rehabilitation programme.
Vocational rehabilitation
Return to previous employment or an alternative occupation is often an important goal in adults with TBI and 
may be a central factor in the restoration of quality of life. 
Assess the need for vocational rehabilitation to assist return or entry to the workforce, and provide 
vocational rehabilitation if needed. 
There is strong evidence that vocational rehabilitation improves vocational outcomes for people with TBI, and is 
cost effective.
Monitor the effectiveness of standard vocational rehabilitation interventions, such as cognitive training and 
behaviour modifi cation.
Provide supported employment for those for whom standard interventions are inadequate. Table 1 below 
provides examples of how support can be provided in various areas.
Table 1: examples of vocational support f or people with tbi
job pl acement
• Match job needs to abilities and potential
• Facilitate communication between the person, the employer
and carers
• Arrange travel and training
• Assess the job environment for potential problems
job site training and advocacy by 
• Provide 
appropriate job site training
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• Proactively identify problems
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• Design solutions in cooperation with the person with TBI,
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• Ensure ongoing assessment with continuous monitoring of 
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• Monitor progress to anticipate problems, and intervene
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proactively when necessary
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Sexuality
A substantial proportion of people with TBI experience sexual dysfunction.
Health professionals should initiate discussion relating to sexual dysfunction early after signifi cant TBI, to 
both the person and their partner.
Advice about sexuality should cover:
• physical aspects (eg, positioning, sensory defi cits, erectile dysfunction)
• psychological aspects (eg, communication, fears, altered roles and sense of attractiveness).
Reassure family, wha¯nau and carers that sexually inappropriate behaviour is not unusual in people who are 
in the early stages of recovery from TBI and should improve with time. 
Provide family, wha¯nau and carers with training in how to avoid inadvertently reinforcing inappropriate 
sexual behaviour.
Leisure and recreation
Rehabilitation services should support people with clinically signifi cant TBI in developing alternative leisure and 
social activities, in liaison with local voluntary organisations.
It is important to identify: 
• levels of participation in leisure activities 
• barriers or contributing factors which inhibit return to leisure, sports and social activities.
A goal-directed, community-based programme aimed at increasing participation in leisure and social 
activities should be offered to people with TBI who have diffi culty undertaking the leisure activities of their 
choice.
Provide carers with advice on how to maintain their own leisure and social activities while in a caring role.
Discharge from rehabilitation services
Continuous or intermittent input from a rehabilitation team may be appropriate for long periods of time 
following TBI.
Discharge may be appropriate when:
• there is a wish to exit from a formal rehabilitation programme
• no new achievable goals can be identifi ed.
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36






Receive, Log and Allocate Review Application v31.0
GOV-039784 Document 5
Application
6.0
Allocate the Review  to a Review Specialist
Linked Process
Complete Background Review
5.0
Check for Privacy Act request
Application
4.0
Acknowledge the Review 
levy
-
-
-
3.0
Log review application  decision on a claim
3.1
Log review application  decision
3.2
Log review application  vehicle registration decision
riggers & Inputs
T

1.0
Send review application to Resolution Services
2.0
Check the Review Application
ACC Staff Member
Resolution Coordinator
Review Specialist
Resolution Coordinator
Review Specialist
ACC > Customer Insights and Comms > Manage Customer Reviews and Disputes > Manage Customer Reviews  > Receive, Log and Allocate Review Application
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Receive, Log and Allocate Review Application v31.0
Summary
Objective
To record and acknowledge the receipt of the review application to the applicant, acknowledge the receipt of the review application 
and to allocate it to a Review Specialist so that the ACC decision can be reviewed.
Background
Customers or their representatives can seek an independent review of a decision ACC has made. The review application must be in 
writing and received within 3 months of the decision.
Owner
out of 
Expert
out of scope
Procedure
1.0 Send review application to Resolution Services
ACC Staff Member
Forward the application for review to [email address] within 24 hours of receipt.
NOTE What constitutes a review application?
A application for review must be:
1) in writing (e.g. via letter, email, e-text or ACC33)
2) identify the decision or decisions in respect of which it is made (e.g. by stating the date or subject)
If there is uncertainty as to what the client is reviewing (or whether it is in fact a valid review application) it is important 
to clarify with the client/advocate in the first instance (and confirm the decision they are challenging) - and then for-
ward it to [email address] inbox . This will mitigate the risk of the review becoming deemed.
2.0 Check the Review Application
Resolution Coordinator, Review Specialist
Open the accreviewapplication.co.nz inbox and review each unread email to determine if a new review application has been 
received.
NOTE What if the email is not an application review for review?
• If the email has information about an existing review, forward the email to the allocated Review Specialist.
• If the email relates to a decision about claim, file it in Eos, and send to the Decision Maker for action and copy in the
Decision Maker's Team Manager to ensure the correspondence is addressed.
• If the email relates to a decision about a levy, in Juno_CRM, create an interaction on the customer's account and
attach the email to the interaction.
• If the email is from an Accredited Employer (AEP) or Third Party Administrator (TPA) acknowledging the receipt of a
review application then file the email into the AEP/TPA folder in Outlook, and file away in Eos.
• If the email is about a complaint, then forward the email to [email address].
NOTE What if it is review that needs to be reopened as a result of a settled appeal or court decision?
The original review will be closed so a new review cog needs to be generated in Eos. There will be no new 'review 
application' per se, so the original review application will be need to be used as the ACC33 to 're-log' it. There should 
be the ‘settlement’ letter from Legal Services to the client, and the client’s acceptance of the settlement, and preferably 
the District Court confirmation that the appeal has been withdrawn.
NOTE What if the review is about a fatal claim on behalf of the estate?
If the application concerns a fatal claim on behalf of the estate, an additional process needs to be carried out before a 
review can be made/proceed. Note that the review relates to a fatal claim on behalf of the estate in the allocation task.
NOTE What is a fatal claim on behalf of the estate?
These claims include:
1. Cover issues concerning the deceased.
2. Entitlements that the claimant was eligible for before death such as permanent injury compensation or treatment.
3. Entitlements, such as the funeral grant, that explicitly state the estate is the recipient.
Claims where a party is requesting entitlements for themselves, such as spousal grant or childcare, are not fatal 
claims on behalf of the estate.
Ensure the information in the review application is legible and complete.
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NOTE What if there is an issue with the application?
If the review application form is:
• Illegible: return the application to the sender with a note highlighting which part cannot be read.
• Unsigned: Carry on with the process. Unsigned application are acceptable.
• Unclear on what decision the client wants to review (eg the dates do not match or there is no decision noted in the
correspondence): Contact the customer and clarify the decision that they are wanting to review. If the applicant cannot
be contacted, or does not respond to a request for further information within 48 hours, consider whether the corres-
pondence meets the requirements for a review application.
• Unclear that the customer wants to apply for a review: Contact the customer and clarify their intention. If they do not
want a formal review, contact the decision maker so they can work on the applicant’s request. If the applicant cannot
be contacted, or does not respond to a request for further information within 48 hours, continue with this process.
NOTE What if the customer/representative is submitting an application which they had previously withdrawn?
Refer to Managing Withdrawn and then Re-submitted Review Applications Policy.
Managing Withdrawn and then Re-submitted Review Applications Policy
Establish who submitted the review application to understand how to proceed as some applications cannot be considered.
NOTE What types of applications cannot be considered?
• Review applications from employers about work related personal injury entitlements cannot be considered. In these
cases, lodge the application and instruct the allocated review specialist to speak with the application about the matter
being jurisdictional.
• Review applications received from registered health professionals about a patient's cover and/or support cannot be
considered. In these cases - lodge the application, and instruct the allocated review specialist to contact the client di-
rectly to ask whether it was their intention to go down the review channel and that they authorise the provider to lodge
the review on their behalf.
Ensure that the claim or ACC number is correct.
NOTE What if the claim or ACC number is incorrect?
• If the application requires a claim number, in Eos search for the client through the party record. If this is unsuc-
cessful, contact the client or client’s representative and ask them to provide the correct number.
• If the application requires an account number, in Juno_PolicyCenter search for the business customer.
Determine whether application is for a claim with an active Accredited Employer (AEP) or Third Party Administrator (TPA).
NOTE What if the application is for a claim with an active AEP or TPA?
Then forward the review application to the correct AEP or TPA and request they acknowledge that they have received 
the application. Generate a general task on the relevant claim as a reminder to await an acknowledgement from the 
AE and follow up at two day intervals. This process ends.
NOTE Contact details for Accredited Employers or Third Party Administrators can be found under the relevant em-
ployer in the following lists:
Participating Accredited Employers (Non-work claims only)
Accredited employers list (for work-related claims only)
Ensure there is a current Authority to Act (ATA) on the claim or account if required.
NOTE What if there is no current ATA?
• If the review is a decision about a claim then send the customer/representative the ACC5937 to complete and re-
quest it is returned to [email address].
• If the review is about a levy decision then send the customer/representative the ACC1766 to complete and request it
is returned to [email address].
ACC5937 Authority to act - Client
ACC1766 Giving Access Levy Information
Check whether there is a Review Provider listed as a claim participant. If there is a Review provider listed and no active review 
– remove the Review provider as a claim participant.
Ensure there is only one decision per review application.
NOTE What if there is a levy decision which covers multiple years?
Log the application. Only one application is required in this circumstance.
NOTE What if there are multiple decisions contained within one decision letter?
Where multiple decisions are made within one decision letter, and the outcome of one decision is related to the out-
come of the other decision, log one review application with a secondary review cog.
NOTE What if the decision letter has only one decision, but the review application seeks two different outcomes?
Proceed to log one application for review.
Ensure any documents supporting the review application are for the customer’s review.
ACC > Customer Insights and Comms > Manage Customer Reviews and Disputes > Manage Customer Reviews  > Receive, Log and Allocate Review Application
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NOTE What if the supporting documents are not for the customer’s review?
Contact the external party who sent the application immediately, let them know their error, and destroy the information.
Ensure the application is not a duplicate of another review application.
NOTE What if the application is a duplicate?
• If the application relates to a claim, locate the claim in Eos, and upload the application and update the description to
say ‘duplicate review application’. If the review application has any differences to the initial application - send a gen-
eral task to the RS to draw their attention to the newly submitted application that you consider a duplicate.
• If the application is for a business customer, in Juno_CRM, upload the application and create a new interaction to
say ‘duplicate review application’.
Ensure that the Care Indicator has been updated within the previous four months if required.
NOTE What if the Care Indicator has not been updated in the previous four months?
Contact the decision maker (DM) and their Team Leader (TL) using the Client Care Indicator Template to update the 
Care Indicator.
Email Template - update Client Care Indicator
Care indicated clients
Add a colour category or tick to the email once it has been actioned.
3.0 Log review application - decision on a claim
Resolution Coordinator
In Eos, start the [Review Process] workflow through the [PRC REV: Receive & Log Review] task.
NOTE What information needs to be included?
• lodgement date (date ACC received the application)
• name of applicant
• decision category (in the decision letter)
• code description
• disputed decision date
• business unit responsible or where the decision was made.
Review Codes.docx
Create PRC REV task
Close the task after the above information has been populated to generate the next task in the COG.
Upload the review application, Authority to Act (if applicable) and any other supporting documentation and use the correct 
naming conventions.
Naming Conventions.JPG
NOTE What needs to happen to the documents so that they can be uploaded correctly?
• If an application form (ACC33) was received by email, convert the email message to a PDF file, and attach this to the
front of the application. This will be the official date stamp.
• If an application was received by post and has no date stamp, use the Adobe Pro watermark feature to add a water-
mark.
• If an ATA document is attached and combined with a review application, these will need to be uploaded separately.
Use Adobe Pro to add a Watermark
Convert to PDF, combine, split, and email to Eos
Update any relevant customer and/or advocate information.
NOTE What information needs to be added?
If an ATA is included with the application, add an advocate/representative as a participant to the claim.
If an email address was included with the application, ensure this is correctly recorded at the party record.
Go to step 4.0
Manage Participants (Eos Online Help)
ACC > Customer Insights and Comms > Manage Customer Reviews and Disputes > Manage Customer Reviews  > Receive, Log and Allocate Review Application
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3.1 Log review application - levy decision
Resolution Coordinator
In the Levy Spreadsheet, \\ACCfiles\Data\Public\Resolution Services Folder\8. Hub Folders\8.3 Wellington\Levy Review 
Spreadsheet, start the Review Process workflow.
NOTE What information needs to be included?
• Review Specialist name
• ACC number
• Review number
• Review issue
• Date of ACC decision
• Date review application received
In the I:Drive, set up the customer folder in \\ACCfiles\Data\Public\Resolution Services Folder\8. Hub Folders\8.3 Wellington
\Levy Reviews
NOTE What should be stored in the folder?
• The type of application i.e. Classification Units, CPX. Multiple CU.
• A sub folder with the Review number, Customer name, ACC number
• The application for review
In Juno_CRM, add a flag to the customer's account. The comment in the flag is 'active review'.
Create a Flag
In Juno_CRM, create an interaction and upload the application, ACC1766 Giving access to your ACC Information (if appli-
cable), and any other supporting documentation.
3.2 Log review application - vehicle registration decision
Resolution Coordinator
In the Levy Spreadsheet, start the Review Process workflow.
NOTE What information needs to be included?
• Review Specialist name
• Vehicle registration number
• Review number
• Review issue
• Date of the decision
• Date review application received
In the I:Drive, set up the customer folder in \\ACCfiles\Data\Public\Resolution Services Folder\8. Hub Folders\8.3 Wellington
\Levy Reviews
NOTE What should be stored in the folder?
• The type of application i.e. vehicle registration decision.
• A sub folder with the Review number, Customer name, Vehicle registration number.
• The application for review and a copy of the letter from the NZTA.
4.0 Acknowledge the Review Application
Resolution Coordinator
Check that the application has been received within the three-month timeframe.
NOTE What if the application was received outside the three-month timeframe?
Generate the Acknowledgement of a review application letter (REV18) to the applicant and select the option that ex-
plains that a review specialist will be in contact to discuss the reasons the review application was late.
NOTE What if it is not clear that the review was lodged within the three-month timeframe?
• Allocate the review application to the selected Review Specialist and notify them in the allocation task that is has not
been established whether the application is late.
• Also advise the Review Specialist that they will need to update and send the Acknowledgement of a review appli-
cation letter (REV18) once they have established if the application is late or not.
Generate the REV18 Acknowledgement of a review application letter to the applicant, and if in Eos leave the document as 
incomplete.
REV18 - Acknowledge Review
REV50 - Acknowledge review application - Levy (Business)
NOTE What if the review is reopened review as a result of a settled appeal or court decision?
Tailor the Rev18 'Acknowledge of review application' to state something similar to:
"Further to the settlement agreement of XX date - we have now reopened the review and allocated the following 
review number: "
Check to see whether there is an interested party to the review.
ACC > Customer Insights and Comms > Manage Customer Reviews and Disputes > Manage Customer Reviews  > Receive, Log and Allocate Review Application
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NOTE Who are interested parties?
• Employers are interested parties where the client (employee) has put in a review to challenge the decline of cover for
a work related PICBA and WRGPDI.
• Clients are interested parties where the employer has lodged a work injury dispute review.
NOTE What if there is an interested party?
Generate REV021 Acknowledgement to Interested Party to notify the interested party of the application.
REV21 Acknowledge review to interested party
5.0 Check for Privacy Act request
Resolution Coordinator
Read through the information submitted and identify whether the client has requested a full copy file.
In Eos, complete a 'Complete Request for Copy of Clients Information' task if a full copy file was requested.
NOTE What should be recorded on the 'Complete Request for Copy of Clients Information' task?
Record 'Privacy Act Request received via (email/ACC33/client letter) on (insert date).
6.0 Allocate the Review Application to a Review Specialist
Resolution Coordinator
In the Resolution Coordinator Calculator tool, enter details.
Review Allocation Calculator
NOTE What details should be entered?
• Customer Name
•The review number that has been generated from Eos, or the Levy Spreadsheet
•The date the review was received
•Whether this is a privacy act request
•Whether the review was lodged outside the three-month time frame
•Whether the customer has a representative/advocate and a current Authority to Act on file (or is being requested)
•Any interested parties – such as an employer
Copy the information generated in the calculator tool and paste into the PRC REV: Complete Admin Review task if the review 
is about a decision on a claim in Eos.
NOTE What if the review is about a levy decision?
Copy the information generated in the calculator tool and paste into an email, along with the review application email 
and supporting documents and send to the allocated Review Specialist.
The process ends.
Mark the task as a high priority, change the target date of the task to ‘todays date’ and transfer to the allocator's work queue 
who will allocate the work out to the Review Specialist.
PROCESS
Complete Background Review
Review Specialist

ACC > Customer Insights and Comms > Manage Customer Reviews and Disputes > Manage Customer Reviews  > Receive, Log and Allocate Review Application
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Complete Background Review v32.0
GOV-039784 Document 6
Linked Process
Conduct Initial Customer Contact
5.0
Assess potential resolution options
Linked Process
Refer to Legal Services for external counsel
4.0
Clarify information used to make substantive decision
Linked Process
Seek Internal Guidance
ACC
3.0
Read the  decision information
2.0
Notify the decision maker of the review application
claim
levy
-
-
-
1.0
Read the review application  decision
1.1
Read the review application  decision
1.2
Read the review application  vehicle registration decision
Linked Process
Receive, Log and Allocate Review Application
Resolution Coordinator
Review Specialist
UNASSIGNED
ACC > Customer Insights and Comms > Manage Customer Reviews and Disputes > Manage Customer Reviews  > Complete Background Review
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Complete Background Review v32.0
Summary
Objective
The objective of this process is to understand the ACC decision and the reason for the review application so that the Review Spe-
cialist is prepared to contact the customer to discuss and have a first attempt to resolve the matter.
Owner
out of 
Expert
out of scope
Procedure
PROCESS
Receive, Log and Allocate Review Application
Resolution Coordinator

1.0 Read the review application - claim decision
Review Specialist
Timeframes for Reviews Policy
In Eos, open and read the information in the PRC REV: Complete Admin Review task.
Read the information the customer has provided in and with the review application.
NOTE What if you believe the Review Cog has been generated incorrectly?
• Confirm with the customer/representative that it was not their intention to lodge a review application or that the appli-
cation is a duplicate of an already lodged review.
• Create a contact in Eos stating the Cog was generated in error and then email a Resolution Services Manager with a
request to cancel the Review Cog.
• Provide feedback to the relevant Resolution Manager on the reasons for the cancellation.
NOTE What if you believe the review to be deemed?
A review is considered to be 'deemed' if ACC has failed to arrange a hearing date within 90 days from the date the 
application was received.
If you believe the review is deemed - go to 'Implement Resolution Outcome' and follow the instruction provided to 
operationalise the deemed decision.
PROCESS Implement Resolution Outcomes
NOTE What if the applicant is an employer disputing an work related personal injury entitlement decision of an em-
ployee?
In these cases contact the employer and explain that a Reviewer has no jurisdiction to hear this type of matter, and 
while they are welcome to proceed it is unlikely to achieve outcome they are seeking.
It may be useful to inform the employer what they can review in this situation (i.e. that the accident occurred in their 
workplace (work injury dispute)).
Seek to obtain a withdrawal. If unsuccessful, proceed to referring arranging a Case Conference.
NOTE What if the applicant is a registered health professional lodging a review against a patient cover and/or sup-
port?
In these cases - contact the client directly to ask whether it was their intention to go have a review application sub-
mitted and that they authorise the provider to lodge the review on their behalf.
If the client's intent was to lodge a review, establish whether they would like the provider to continue acting on their 
behalf and obtain an ATA.
If the client does not want to proceed with the review, contact the provider and talk to them about the need for consent 
and your conversation with the client. Obtain a written withdrawal.
NOTE What if the review is about a fatal claim on behalf of the estate?
If the application concerns a fatal claim on behalf of the estate, contact the applicant via email, stating that for the 
application to proceed to review hearing stage the applicant must provide evidence they are either the executor of the 
estate as outlined in the will or have letters of administration.
If they already have evidence of one of the above, proceed with the review as per usual. If they do not have evidence 
of one of the above, letters of administration will need to be obtained before proceeding to review.
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NOTE What if the applicant does not have proof that they can act on behalf of the estate?
Letters of administration will need to be obtained before proceeding to a review hearing. The applicant can do this by 
engaging with a law firm and ACC has the discretion of reimbursing costs up to $1320 if the applicant is successful in 
obtaining the letters of administration, or the Court did not grant legal standing, but you (Review Specialist) believe the 
representative acted reasonably in applying for legal standing to represent the deceased.
In exceptional circumstances, where the representative is not in a financial position to pay, you (Review Specialist) 
may pay the $1320 upfront.
Once the letters of administration are received, proceed with the review as per usual.
Check that the review application was lodged within the three month timeframe.
NOTE What if the review application was lodged outside of the three month timeframe?
Go to Accept or Decline Late Review Application.
PROCESS Accept or Decline Late Review Application
If the review was lodged by a representative, check to see if the outstanding Authority to Act form has been returned. If an ATA 
is not outstanding or required, then continue with the process.
NOTE What if the outstanding Authority to Act form has not been returned?
Follow up with the representative to remind them the ATA is outstanding.
1.1 Read the review application - levy decision
Review Specialist
Timeframes for Reviews Policy
In Outlook, open and read the email and attachments sent by the Resolution Coordinator.
Read the information the customer has provided with the review application.
In Juno_BillingCenter, check if the account is overdue.
NOTE What if the account is overdue?
Email [email address] and ask a hold be placed on the account as a review is underway.
1.2 Read the review application - vehicle registration decision
Review Specialist
Timeframes for Reviews Policy
In Outlook, open and read the email and attachments sent by the Resolution Coordinator.
Read the information the customer has provided to determine the point of contention.
NOTE What if the point of contention is about an incorrect classification?
Contact the business incentives group through the [email address] email with a request to investigate the classification.
The business incentives group will investigate and if required instruct the NZTA to correct the error. On confirmation 
that this has occurred, go to Fulfil Resolution Obligations.
PROCESS Implement Resolution Outcomes
2.0 Notify the decision maker of the review application
Review Specialist
• If the review is about a decision on a claim, identify the allocated decision maker and notify them that an application for 
review has been received.
• If the review is about a levy decision, refer to the 'Business Customer Triage Process' document for direction.
NOTE What if the claim sits within Assisted Recovery or sitting in 'NGCM - Actioned Cases'?
No initial contact or notification is required.
NOTE What if the claim sits with Supported or Partnered Recovery but is not currently assigned to an individual?
If not assigned to an individual then send a 'NGCM General task' to either the 'Supported Recovery' or 'Partnered 
Recovery' queue indicating that a review has been lodged against a decision on file.
NOTE What if the claim is sitting unassigned within a cover team (Cover or Treatment Injury Teams)?
If a cover decision has been issued and closed, the claim should be sitting in either the Dunedin Service Centre Ac-
tioned Cases queue OR the TIC Actioned Cases queue.
Although unassigned, a standard 'general task' (not a 'NGCM-General task') must be sent to the individual who made 
the decision to notify them that a review has been lodged against the decision on file.
NOTE What if the review is about a decision on a claim or a decision about a vehicle registration levy and the deci-
sion maker cannot be identified?
Continue with the process.
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Check whether a Technical Accounting Specialist has provided advice on the disputed decision and if yes, notify them that a 
review application has been received.
Complete in Eos, and send, to the customer, representative, or interested party the REV18, and REV21 (if applicable) that was
generated by the Resolution Coordinator. Send via email if a verified email address exists, or by post if no verified email ad-
dress exists.
3.0 Read the ACC decision information
Review Specialist
If the review application is about a decision on a claim, in Eos, open and read the information that ACC used to make the deci-
sion.
If the review is about a Levy decision, in Juno, read the information used to make the decision.
4.0 Clarify information used to make substantive decision
Review Specialist
Check that you understand the reasons the substantive decision was made.
If the reasons are unclear, refer the decision for expert advice.
NOTE What teams are available to provide advice or guidance?
• Technical Services
• Clinical Services
• Legal Services
• Technical Accounting Services
• Weekly Compensation Team
• Levy Classifications
• Privacy
NOTE What if advice or guidance is needed from Clinical Services?
To obtain instruction on how to seek the required clinical advice/guidance refer to Clinical Referral Instructions.
Clinical Referral Instructions
Reference Guide for Review Specialists when deciding whether to refer a task to Technical Accounting Specialist (TAS)
NOTE What if advice is needed from Levy Classifications?
Email the query to [email address]. The subject line should read 'Resolution Services Query'. The email 
should include:
• Review number
• Customer/representative name (if applicable)
• ACC number
• What the query is about.
If Levy Classification have not responded after 4 working days, contact them again.
NOTE What if advice is required about a privacy issue?
Send an email to [email address] with the following information:
For Resolution Services to complete
Resolution Specialist/Review Specialist:
Customer name:
Claim number:
Relevant ministerial, government services or review identifier:
Date complaint/review received:
Factual summary and timeline
Please include relevant privacy history including previous privacy advice.
Privacy advice required:
Privacy Team to complete
Privacy Advisor:
Privacy advice:
Any other comments/considerations:
If the review application is about a decision on a claim, in Eos, open and complete the PRC REV: Complete an Admin Review 
task and complete the following sections:
• Claimant's reason for lodging the review
• ACC's reason for the original decision
• Legislative basis / case law.
If the review application is about a levy decision, open the Administrative Review form and complete the following sections:
• Claimant's reason for lodging the review
• ACC's reason for the original decision
• Legislative basis / case law.
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Levy Admin Review
Consider whether the review should be referred to Legal Services for legal representation.
PROCESS
Seek Internal Guidance
UNASSIGNED

PROCESS
Refer to Legal Services for external counsel
Review Specialist

5.0 Assess potential resolution options
Review Specialist
Decide whether additional advice is required.
NOTE What type of advice might be useful?
• Comments from Medical or Psychology Advisors
• Advice from the Clinical Advice Panel
• Additional information from the customer/representative
• Additional information from the treating specialist
• A Medical Case Review
• Comments from a radiologist
• Comments from Technical Services
• Comments from Technical Accounting Services
NOTE What if advice or guidance is needed from Clinical Services?
To obtain instruction on how to seek the required clinical advice/guidance refer to Clinical Referral Instructions.
Clinical Referral Instructions
NOTE Can you access specialist advice from the Clinical Advisory Panel (CAP)?
Principal Clinical Advisors have made themselves available once a week (generally a Thursday afternoon) to provide 
advice to Review Specialist over the phone about review cases.
If you would like to speak with a member of CAP, contact your Senior Review Specialist who will triage the requests 
and organise the next available appointment through the Resolution Coordinator team
NOTE Should permission be sought from the client prior to seeking further external clinical comments or notes?
Yes - you must have a conversation with the client/ATA on what you are wanting to do and why (eg releasing and 
seeking medical information with a view of reconsidering ACC's position on the matter at review). This is to ensure 
there is no objection. Once you have obtained a verbal permission make a note in your Eos contact reflecting the 
conversation.
When a client has an active review, a Review Specialist can request medical notes and clinical specialist reports including 
Medical Case Reviews. Review Specialists can request these directly from the Clinic, DHB or Specialist.
NOTE When should the Review Specialist request that the medical case review is completed by a Recovery Team 
Member, Cover Assessor, or Treatment and Support Assessor?
The Review Specialist should request the notes or reports unless it was required before the decision was issued and 
was not requested. For example, clinical advice recommended obtaining a report before issuing a decision but the 
decision maker proceeded with the decision without it.
Some specialty reports such as External Clinical Advice reports for treatment injury claims, Medical Case Reviews for 
Work Related Gradual Process Claims, or Permanent Injury Compensation assessments should be requested by the 
decision making units because they have special referral processes.
Create Document Group
Identify potential resolution options to discuss with the customer/representative.
Resolution Agreement Scenarios.pdf
NOTE What are the resolution options?
• Overturning an incorrect ACC decision
• Upholding a correct ACC decision, and seeking resolution through settlement
• Upholding a correct ACC decision, and choosing to progress through ADR or case conference
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NOTE What pre-work is required prior to offering resolution agreement?
Complete a risk analysis to ensure the potential resolution agreement is robust. Consider:
• what the customer has asked for
• the ACC regulations or contracted costs for what they have asked for
• the possible outcome at review, versus the customer experience
• whether the customer has shown a pattern of seeking monetary resolution without a reasonable basis
• whether the issue has been previously disputed
• whether the customer has a tendency to resort to legal proceedings or complaints to resolve disputes where no
reasonable basis exists
• that the potential resolution agreement is not detrimental to a customer's entitlements
• any ongoing impact for levy years not part of the original decision.
Once completed consult with a Senior Resolution Specialist to ensure the rational for offering a resolution agreement 
is robust.
NOTE What if a potential settlement is over $2,000 in value?
Email a Resolution Manager or Senior Review Specialist to seek prior approval.
If the review application is about a decision on a claim, in Eos, add potential resolution options to the PRV REV: Complete an 
Admin Review task under additional information.
If the review application is about a Levy decision, in the administrative review form, add potential resolution options.
PROCESS
Conduct Initial Customer Contact
Review Specialist

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Conduct Initial Customer Contact v20.0
GOV-039784 Document 7
Attend
Linked Process
Prepare and  Case Conference (CC)
Attend
Alternative
Linked Process
Prepare and  an  Dispute Resolution (ADR)
Task
Linked Process
Create Bulk Print and Send CIR 
6.0
Discuss and agree on the documents relevant to the review
Linked Process
Prepare and Lead an Internal Resolution Consultation (IRC)
Linked Process
Implement Resolution Outcomes
5.0
Discuss resolution options with custom er/representative
4.0
Re-evaluate potential resolution options
3.0
Seek new/relevant supporting information
ACC
2.0
Explain the  decision
alidate customer
1.0
V understanding of decision
Linked Process
Complete Background Review
Review Specialist
ACC > Customer Insights and Comms > Manage Customer Reviews and Disputes > Manage Customer Reviews  > Conduct Initial Customer Contact
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Conduct Initial Customer Contact v20.0
Summary
Objective
The objective of this process is to discuss the review application with the customer, or their representative, check their understanding 
of the review matter, and of ACC’s decision so that we can begin to resolve the matter or continue towards a review hearing.
Background
After completing the background review the customer/representative must be contacted by phone to discuss the review application, 
any new information and the process moving forward.
Owner
out of 
Expert
out of scope
Procedure
PROCESS
Complete Background Review
Review Specialist

1.0 Validate customer understanding of decision
Review Specialist
If intending to call a representative, check if there is a current Authority to Act (ATA).
NOTE What if there is no current ATA on file?
By phone, contact the representative and request the form is returned.
NOTE What if the ATA is never returned?
No details can be discussed with the representative. Contact the customer to discuss the case if possible. If the cus-
tomer refuses to engage and they do not return the ATA form, proceed to Prepare and Attend Case Conference.
PROCESS Prepare and Attend Case Conference (CC)
By phone, contact the customer/representative within 7 days of the receipt of the review application (best practice is within 48 
hours).
NOTE What if the customer or representative is managed in Te Ara Tika, on a communication plan, or will have their 
review managed by External Counsel?
We must respond to customers or representatives in line with their communication restrictions where possible. The 
complexity of their case, gathering of relevant information, timeliness of external counsel, and the volume/nature of the 
communication may mean that it is appropriate to contact the customer or representative and acknowledge the review 
application after the 7 day timeframe.
Use the appropriate authorisation process to confirm you are speaking to the right person.
NOTE What is the authorisation policy for decisions on claims?
Read the Advocates and Holders of Authority Policy to Act policy.
PROCESS Advocates and holders of authority to act Policy
Advocate Communications Policy
When to use an Interpreter Policy
NOTE What if a translator is required to speak with the client?
Use ACC's policy to obtain guidance on engaging with an interpreter.
NOTE What is the authorisation process for levy decisions?
Follow the Perform Authorisation Check - Business Customer process
PROCESS Perform Authorisation Check - Business Customer
NOTE What if you need to update an authorised business customer?
Follow Add or Update Business Customer Authorised Party.
PROCESS Add or Update Business Customer Authorised Party
Confirm ACC has the correct customer/representatives contact details. Include both the telephone number and email address.
NOTE What if the email address has not been verified?
If the email address has been added to Eos but not yet verified - ask the applicant to check their emails and return the 
verification as soon as possible.
If the email address has NOT been added to Eos, follow the steps outlined in the 'Update Client's Party Record' policy.
PROCESS Update Client Party Records
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Tell the customer/representative:
• the reason for the call
• what will be discussed during the phone call
• the review process, including the focus for ACC on seeking resolution
• the role of the Review Specialist.
Ask the customer/representative, in their own words, to explain:
• their understanding of the disputed decision
• why they believe ACC decision is incorrect
• what they are hoping to achieve through the review process.
NOTE What is the expected outcome of the conversation?
The outcome of this conversation is to understand the customer's point of contention or grievance, and help the 
Review Specialist determine whether conciliation or a resolution offer may be appropriate, or whether ACC may need 
to complete further investigation.
2.0 Explain the ACC decision
Review Specialist
Explain why ACC made its decision. This may include an explanation of the legislation and/or medical reports that were used 
to make the decision.
3.0 Seek new/relevant supporting information
Review Specialist
Discuss any information that was received after the decision date and included with the written application for review.
Ask the customer/representative if they have any new information that was not included in the written application to support the 
review application.
NOTE What if the customer/representative has new information?
• Then ask the customer/representative to explain what the new information is and how they believe it is relevant.
• If possible, ask them to send the information via email directly to the Review Specialist and advise they will be con-
tacted again once the information has been considered.
4.0 Re-evaluate potential resolution options
Review Specialist
If new information has been provided by the client/representative, check if further advice is needed to identify or re-evaluate 
potential resolution options to discuss with the customer/representative.
NOTE What type of advice would be useful?
• Comments from Medical or Psychology Advisors
• Advice from the Clinical Advice Panel
• Additional information from the customer/representative
• Additional information from the treating specialist
• A Medical Case Review
• Comments from a radiologist
• Comments from Technical Services
• Comments from Technical Accounting Services
• Advice from Levy Classification
NOTE What if advice or guidance is needed from Clinical Services?
To obtain instruction on how to seek the required clinical advice/guidance Refer to Clinical Referral Instructions
Clinical Referral Instructions
Reference Guide for Review Specialists when deciding whether to refer a task to Technical Accounting Specialist (TAS)
NOTE Should permission be sought from the client prior to seeking further external clinical comments or notes?
Yes - you must have a conversation with the client/ATA on what you are wanting to do and why (e.g. releasing and 
seeking medical information with a view of reconsidering ACC position on the matter at review). This is to ensure there 
is no objection. Once you have obtained a verbal permission make a note in your Eos contact reflecting the conver-
sation.
NOTE Who's role is it to conduct further investigation when required?
When a client has an active review, a Review Specialist can request medical notes and clinical specialist reports in-
cluding/not limited to Medical Case Reviews. Review Specialists can request these directly from the Clinic, DHB or 
Specialist unless a collaborative approach or specific input is required from a Recovery team member or Specialist 
Cover assessor.
Check that the potential resolution options identified in the background review are still relevant.
NOTE What if the potential resolution option has changed from the background review?
In Eos, update the PRC REV: Complete Admin Review 'Additional information' box.
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NOTE What if the matter at review relates to an Individual Rehabilitation Plan (IRP)?
First and foremost consider a conversation with the decision maker about whether the IRP should be updated in line 
with the client's requests. If the relationship is strained it might be more useful to attend Conciliation (under the Alter-
native Dispute Resolution process) with the decision maker. Please note there must be a sound reason for proceeding 
straight to review as these can often be resolved.
5.0 Discuss resolution options with customer/representative
Review Specialist
Discuss with the customer the possible pathway and proceed as appropriate:
• on a resolution option, or
• a withdrawal and review closure (based on your explanation of the decision), or
• whether to proceed to an internal resolution consultation.
Add a contact in Eos, or interaction in Juno_CRM, as appropriate, to record the main points from the conversation.
Proceed to Step 6.0, if the above pathways (listed under 'a') are agreed to be unsuitable.
PROCESS
Implement Resolution Outcomes
Review Specialist

PROCESS
Prepare and Lead an Internal Resolution Consultation (IRC)
Review Specialist

6.0 Discuss and agree on the documents relevant to the review
Review Specialist
Identify and agree the relevant documents with the customer/representative.
NOTE What if the client wants the full file?
Explain to the client that ACC has made a move to providing relevant document as a preference to the full file. This 
ensures the reviewer doesn't receive large amounts of information that has no relevance to the disputed decision. If 
the client has any doubts about the correct information being provided then the Case Conference serves as an oppor-
tunity for this to be discussed and corrected if necessary.
If the client still wants the full file - then relevant documents must be correctly selected. Note in the initial customer 
contact on Eos the clients request for the full file.
NOTE What if the client or representative does not give consent to provide any documents to the Independent Re-
viewer?
You should contact the advocate/client to discuss the consent issues and what documents are considered relevant to 
the review. This process also applies where an issue about consent to disclose information is received later on during 
the management of a review.
If:
a. The advocate/client consents to release of all relevant information then this consent should be noted on file in Eos.
b. The advocate/client are happy to release some degree of relevant information, however dispute remains regarding
the extent of this, then you should engage with their Senior Review Specialist or Resolution Manager in the first in-
stance.
If we are not able to resolve the issue of relevant information and you believe it is relevant to the issue at review, you 
should engage with the Privacy team using their email template.
c. The advocate/client refuse to release any information, you should engage with the Privacy team using their email
template and ask whether ACC should either:
i. send an ACC6239 to Reviewer Services with no relevant information attached, asking the Reviewer to make direc-
tions on documents to be provided; or
ii. whether ACC considers that it is either not desirable or not practicable to obtain authorisation from the individual
concerned and an exception applies whereby we can send relevant information to Reviewer Services without advo-
cate/client consent, effectively as per usual process.
Relevant Document Guidelines
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NOTE What if an employer is an interested party?
• Firstly, we should check if the employer is interested in attending the review or requires a copy of relevant docu-
ments. If they aren’t interested in being involved in the review, then you do not need to send the employer any docu-
ments.
• If the employer does want a copy of the documents as an interested party, the most straight-forward way to tackle
any issues with files is to contact the customer, explain that the employer is entitled to information about ACC’s deci-
sion. Discuss the relevant documents with the customer and ask if the customer is happy for us to send a full copy of
these documents to the employer.
• If the customer is not happy for the full file to go, we should discuss with the employer what information they require.
If they are happy with the ACC45 and ACC33 Review Application, these can be easily sent by email with some infor-
mation about the customer redacted. If there is other information that the employer believes that they require, redac-
tions must be made in line with the redaction process.
• If we can’t contact the customer to discuss the review documents or the customer is not wanting any information to
be provided to the employer, follow the instructions as if the employer is the applicant.
NOTE What if the employer is the applicant?
• The easiest way to tackle any issues with files is to contact the customer, explain that the employer is entitled to
information about ACC’s decision. Discuss the relevant documents with the customer and ask if the customer is happy
for us to send a full copy of these documents to the employer and reviewer. It is important that there is discussion with
the customer about the information contained in their file and if possible, a copy of the file should be sent to customer
to check before releasing to the employer. If the customer provides permission for ACC to do this, then information will
not need to be redacted.
• If the customer is not happy for us to send the full unredacted documents, then we will need to follow the process for
collating information for an employer file and organise information that is not relevant to the review be redacted. Ideal-
ly, we will send the file to the customer to check they are happy with it before releasing it to the employer.
• The customer may advise ACC that they do not want any of their information to go to the employer or Reviewer. In
these situations, we would advise the customer that the employer and Reviewer are entitled to receive certain infor-
mation about the claim (such as information relating to the accident itself and causal link between the accident and the
personal injury) because it has been lodged as a work-related personal injury. We can reassure the customer that per-
sonal information not relating to whether the injury occurred at work will be removed from the file and still give them
the opportunity to review the information before proceeding.
• If we are unable to contact the customer to discuss the provision of documents, we must still provide relevant docu-
ments to the employer and Reviewer with careful redaction. We must give the customer adequate opportunity to
communicate with ACC by making multiple attempts to contact them including sending them a letter if possible.
Discuss with the customer/representative the methods of delivery for the relevant documents. Then go to 'Create Bulk Print 
and Send CIR task' to arrange the preparation and release of these documents.
NOTE What are the delivery options?
• Electronic documents:
- By email (ACC's preferred method)
- By USB
- By CD
• Paper documents:
- By courier to home address - read client the ACC6181
- By courier to rural delivery address (requires pre alert) - read client the ACC6181
- By courier to local ACC branch
ACC6181 Receiving personal information by courier
Proceed to one of the following processes:
• Prepare for Alternative Dispute Resolution (ADR)
• Prepare and Attend Case Conference as agreed with the customer/representative.
PROCESS
Create Bulk Print and Send CIR Task
Review Specialist

PROCESS
Prepare and Attend an Alternative Dispute Resolution (ADR)
Review Specialist

PROCESS
Prepare and Attend Case Conference (CC)
Review Specialist

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Prepare and Attend an Alternative Dispute Resolution 
(ADR) v40.0

GOV-039784 Document 8
Attend
ADR
Linked Process
Prepare and  Review Hearing (RH)
5.0
Action the  outcome agreement
ADR
3.0
Complete  paperwork
4.0
Prepare and attend ADR session
ADR
2.0
Select an  provider
Attend
ADR
Linked Process
Prepare and  Case Conference (CC)
1.0
Identify stakeholders to invite to the 
Linked Process
Conduct Initial Customer Contact
eam Member
eam Member
Review Specialist
Recovery T
Review Specialist
External Provider
Recovery T
Review Specialist
ACC > Customer Insights and Comms > Manage Customer Reviews and Disputes > Manage Customer Reviews  > Prepare and Attend an Alternative Dispute Resolution (ADR)
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Prepare and Attend an Alternative Dispute Resolution 
(ADR) v40.0

Summary
Objective
To provide guidance on when and how to set up an external Alternative Dispute Resolution (ADR) meeting with an independent 
mediator or conciliator for Review Specialists and Recovery Team Members.
Background
An Alternative Dispute Resolution can occur either before or after a case conference, as well as when other issues arise during the 
management of a claim.
Owner
out of 
Expert
out of scope
Procedure
PROCESS
Conduct Initial Customer Contact
Review Specialist

PROCESS
Prepare and Attend Case Conference (CC)
Review Specialist

1.0 Identify stakeholders to invite to the ADR
Recovery Team Member, Review Specialist
Identify all relevant stakeholders who may be able to provide insight or technical advice on the decision at the ADR.
NOTE Who could be relevant stakeholders?
ACC staff who had input into the decision or may assist with resolving issues. This may include:
• Case owner or decision maker
• Legal Services
• Clinical Services
• Technical Services
• Technical Accounting Services
• Weekly Compensation Team
• External medical practitioner
• Vocational Providers
• Allied health providers
• Levy Classification
Working with Resolution Services
Invite potential stakeholders to ADR.
NOTE What if a member of the Levy Classification Team need to attend the ADR?
Email [email address] to request a colleague attend the ADR. The subject of the email should read 
'Resolution Services Attendance Request'. The email should include:
• Review number (if applicable)
• Customer/representative name (if applicable)
• ACC number
• Date and time of the ADR
• Outline a request for attendance at the IRC
10 working days’ notice is required for Levy staff members to attend the ADR.
2.0 Select an ADR provider
Recovery Team Member, Review Specialist
Select an ADR provider.
NOTE Which external ADR provider should be selected?
ACC has two providers of external Alternative Dispute Resolution. Independent Complaints and Review Authority 
(ICRA) uses evaluative mediation and FairWay uses conciliation. Both services are similar and provide the client with 
an opportunity to feel heard and explore alternative resolutions with an external expert.
We should offer client choice for ADR provider where appropriate. If the client already has a live review, then the same 
provider should be used for ADR.
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NOTE What if the ADR relates to a review and a Case Conference has not yet been booked?
In these cases, we can complete an ACC8026 form and book ADR using ICRA or FairWay's booking system.
NOTE What if the ADR relates to a review and a Case Conference has already been booked?
If a review provider has already been engaged, then we can suggest at the Case Conference that ADR is a suitable 
option and work through the appointed review provider to organise a date and time for ADR. Alternatively, we can 
email the review provider requesting ADR be organised.
NOTE What if the customer/representative has requested a face to face ADR meeting?
Firstly, explore the reasons for their preference.
If the client insists on a face to face conciliation AND wants an ACC staff member to attend - talk with your Manager 
about who might be most appropriate to attend.
Arrange Face to Face to Client Meeting
NOTE What if the client requires travel assistance to attend the face to face meeting?
Any costs associated with attending a conciliation can be agreed and reimbursed as part of the conciliation agree-
ment.
If the client requires payment prior to attending the meeting ask for confirmation of the amount (e.g. copy of held 
flights and costs) and arrange a payment to the client via the Resolution Coordinator. This will be paid under a Rev14 
coding.
Prior approval travel policy
If the review is about a decision on a claim, in Eos, add the ADR provider as a party to the client's claim.
NOTE What if you can't locate ICRA or FairWay as a provider in Eos?
When searching for the provider, change the role to “Other Agent” and the party type to “Civil Agent” and then search 
for the provider name (ICRA or FairWay).
Book the conciliation meeting.
NOTE How do you book the meeting with ICRA?
Use the ICRA online booking tool by following the link and entering the password ADRMed2805.
ICRA can provide ADR with one week’s notice. As CIR require up to 18 days to prep and release, if you want to have 
a conciliation or mediation booked sooner, you can send a bundle of relevant documents and a completed ACC8026 
to them directly at [email address].
ICRA request that you password protect the file by using the same password for their online booking system -
ADRMed2805
If a case conference is already scheduled, continue through to a case conference and advise the reviewer in the case 
conference that the parties agree to ADR.
NOTE How do you book the meeting with FairWay?
Use the FairWay online booking tool by following the link.
FairWay can provide ADR with one week’s notice. As CIR require up to 18 days to prep and release, if you want to 
have a conciliation or mediation booked sooner, you can send a bundle of relevant documents and a completed 
ACC8026 to them directly using the booking tool.
If a case conference is already scheduled, continue through to a case conference and advise the reviewer in the case 
conference that the parties agree to ADR.
Upload the ADR Invitation to Eos as VCF011 and note the description as ‘ADR booking confirmation’.
3.0 Complete ADR paperwork
Recovery Team Member, Review Specialist
Complete the necessary paper work to engage the chosen provider.
NOTE What paperwork needs to be completed if the conciliation is being held before a case conference or without 
the need for a case conference?
If the issue/review is about a decision on a claim, in Eos, complete all sections of the ACC8026 Alternative Dispute 
Resolution and leave it as incomplete in Eos or;
If the review/issue is about a levy decision, complete all sections of the ACC8026 Alternative Dispute Resolution form.
ACC8026 Alternative Dispute Resolution Coversheet
Send the chosen provider the relevant documents needed to hold the conciliation.
NOTE What if the relevant documents/full file have already been checked by CIR?
If the file has already been prepared by CIR or the ADR is more than 4 weeks away, send the [PRC REV: Send 
submissions to all parties] task to CIR to dispatch relevant documents to the necessary parties.
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NOTE What if the file has not yet been prepared by CIR or the ADR is not related to a review?
For FairWay, as CIR require up to 18 days to prep and release, if you want to have a conciliation or mediation booked 
sooner, you can send a bundle of relevant documents and a completed ACC8026 to them directly using the booking 
tool.
For ICRA, you can send a bundle of relevant documents and a completed ACC8026 to them directly by email using 
[email address].
ICRA request that you password protect the file by using the same password for their online booking system -
ADRMed2805
4.0 Prepare and attend ADR session
External Provider, Recovery Team Member, Review Specialist
Check that the agreed relevant documents are on hand for the session.
Re-evaluate potential resolution options as an outcome of the ADR.
NOTE If the ADR relates to a review, what are the potential resolution options?
1) If the original decision appears correct, then potential options include a resolution agreement, a withdrawal, or pro-
ceeding to a case conference.
2) If the original decision appears incorrect, then the potential option is to overturn the original decision or further
investigation (this may be in the form of further medical comment etc.)
Await phone contact from the ADR conciliator for a 1:1 conversation to discuss the desired outcome at conciliation, and the 
matter at review in anticipation for the pending meeting.
Prepare any internal stakeholders who will be attending the ADR to represent ACC.
Attend and participate in the ADR session.
NOTE What can you expect at the ADR session?
The provider will facilitate the hearing and may ask for:
• ACC to explain the decision
• The customer/representative to outline their points of contention
• Clarification on matters under contention
• Discussion about potential resolution options
The provider will then confirm the resolution outcome agreement if an agreement is made.
NOTE What will you need to prepare for the conciliation meeting?
• A clear understanding of ACC’s position, why ACC made the decision, and the relevant regulations/legislation.
• An explanation of what information the client would need to provide in order for ACC to change the decision in their
favour
• A willingness to listen to the client and try to understand their perspective
• An openness to different resolution possibilities
Note: There is no requirement to come to an agreement on the day. You can also pause the conciliation at any time to 
get advice or support.
If the ADR relates to a review, approve costs within the Review Specialists Delegation (in line with the review regulations) 
when called upon by the conciliator.
NOTE What if the conciliator requests costs outside of the review regulations?
Any amounts outside of the review regulations must be considered by a Senior Review Specialist or Manager and will 
likely be associated with travel to attend the conciliation.
Delegations Framework
NOTE What if the conciliator or customer requests costs and there is no live review?
Conciliation costs can be agreed to in line with the Review Cost regulations.
5.0 Action the ADR outcome agreement
Recovery Team Member, Review Specialist
Sign the 'ADR outcome agreement' document and return to the provider.
Upload the signed conciliation agreement to the claim in Eos.
Action the ADR conciliation agreement by creating a General Task (marked high priority) and send to either the Supported or 
Partnered Recovery queue.
NOTE What if the conciliation agreement does not relate to a review?
The Recovery Team Member will continue to manage the claim as normal and complete any agreed actions.
NOTE What if the ADR relates to a review and there was an agreement to withdraw a review or overturn an incorrect 
decision?
Go to Implement Resolution Outcomes.
PROCESS Implement Resolution Outcomes
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NOTE What if the ADR relates to a review and no resolution was reached or the agreed actions will take the review 
past 60 days from the date the review was lodged?
Book a case conference using the Prepare and Attend Case Conference process.
PROCESS Prepare and Attend Case Conference (CC)
NOTE What if the ADR relates to a review and the signed conciliation agreement requires ACC to take action?
If the review is not withdrawn, you will continue to manage the review as normal and will ensure that the agreed ac-
tions are completed (see also 'what if the agreed actions will take the review past 60 days from lodgement date').
If the review will be closed, the Review Specialist must keep a task open in their name and monitor the case to ensure 
that agreed actions are completed, until they are confident that the frontline staff member will complete the agreed ac-
tions.
PROCESS
Prepare and Attend Review Hearing (RH)
Review Specialist

ACC > Customer Insights and Comms > Manage Customer Reviews and Disputes > Manage Customer Reviews  > Prepare and Attend an Alternative Dispute Resolution (ADR)
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Review decisions Policy v3.0
GOV-039784 Document 9
Summary
Objective
This policy applies to all decisions made by Independent Reviewers after 1 April 2002, including all those made under the Code of 
ACC Claimants’ Rights.
We must comply with the Code of ACC Claimants’ rights and the AC Act 2001 when managing review decisions. .
Owner
out of scope
Expert
out of scope
Policy
1.0 Rules
We must carry out all the reviewer’s decisions made under the Code of ACC Claimants’ rights or the Accident Compensation 
Act 2001. This includes following any directions and relevant timeframes.
Any consideration of an appeal is made by the Manager Litigation. The Review Advisory Panel can advise on any cases that 
may need to be considered for appeal, or feedback for the review providers or internal ACC staff. You can engage the Review 
Advisory Panel by emailing [email address].
The review provisions in the AC Act 2001, Part 5 apply to all decisions made under the Code of ACC Claimants’ Rights. The 
client may use the review process to challenge decisions made by our Customer Resolution team under the Code of ACC Clai-
mants’ Rights but neither ACC nor the client can appeal a Code of ACC Claimants’ Rights decision after it is considered at 
review.
ACC > Customer Insights and Comms > Manage Customer Reviews and Disputes > Operational Policies > Issues > Disputes > Reviews > Review decisions Policy
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Assess and Arrange Neuropsychological Assessment v39.0
Document 10
Outputs
8.0
Create and send referral documents
9.0
Receive and review Assessment Report
7.0
Create purchase order
6.0
Confirm availability of provider
4.0
Request assessment referral
5.0
Review task
3.0
Contact client or family to discuss assessment
2.0
Determine need for assessment
riggers & Inputs
T

1.0
Receive assessment request
Assistant
Administrator
Assistant
Assessor
Cover 
Recovery 
Recovery Coordinator
Recovery Partner
Recovery 
Recovery 
Recovery Coordinator
Recovery Partner
ACC > Claims Management > Manage Claims > Manage Treatment Interventions / Supports > Assess and Arrange Neuropsychological Assessment
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Assess and Arrange Neuropsychological Assessment v39.0
Summary
Objective
To assess and arrange Neuropsychological assessment requests to support a client’s covered injury.
These requests are managed directly by Recovery Team Members.
Background
The neuropsychological assessment service aims to:
• confirm the existence of traumatic brain injury (TBI) and determine how the client is affected by the TBI
• confirm whether the client’s symptoms have been caused by the injury or if there may be other possible causes
• provide recommendations for intervention, if appropriate.
Assessments look at the client’s cognitive, behavioural, emotional, social and vocational functioning.
Owner
out of 
Expert
out of 
Procedure
1.0 Receive assessment request
Cover Assessor, Recovery Assistant, Recovery Coordinator, Recovery Partner
Assess the request for a Neuropsychological Assessment, refer to Neuropsychological Assessment Overview Service Page for 
more information on the assessment.
Neuropsychological Assessment Overview Service Page
Neuropsychological assessment overview
https://go.promapp.com/accnz/Process/8ce3affe-069f-4f1b-9ebe-414fd618a897?force=False
Service Schedule for Neuropsychological Assessment Services
NOTE What if the request involves a change or update in the client's diagnosis or covered injury?
Refer to the process below.
PROCESS Assess Cover for an Additional Injury or Change in Diagnosis
2.0 Determine need for assessment
Cover Assessor, Recovery Assistant, Recovery Coordinator, Recovery Partner
Confirm the client's eligibility for the assessment.
NOTE What is the eligibility criteria for a Neuropsychological assessment?
A client is eligible for a neuropsychological assessment when they’ve suffered a covered personal physical injury for 
which they have entitlement. See the AC Act 2001, Section 67 for more information.
AC Act 2001, Section 67
https://legislation.govt.nz/act/public/2001/0049/latest/DLM100999.html?search=ad_act__accident+compensation_2001__6
NOTE What do you need to consider when the entitlement request is received and deemed cover exists?
Refer to the Deemed Cover and Entitlements Policy for considerations to determine client entitlement eligibility while 
in deemed cover period.
Deemed Cover and Entitlements Policy
NOTE What if further guidance is needed to determine if an assessment is needed?
Refer to Seek Internal Guidance.
PROCESS Seek Internal Guidance
Approve or decline the request. Refer to NG Principles Decision Making.
NG Principles Decision Making
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3.0 Contact client or family to discuss assessment
Cover Assessor, Recovery Assistant, Recovery Coordinator, Recovery Partner
Contact the client to discuss the need for a Neuropsychological Assessment.
Confirm you are speaking with the right person by asking ACC's identity check questions. If this is not the client, ensure the re-
questor has an Authority to Act on file.
Identity Check Policy
NOTE What if the client requests the Recovery Team Member to discuss the treatment request with another person?
Go to Obtain Authority to Act (ATA).
PROCESS Obtain Authority to Act (ATA)
Explain the purpose of the assessment, and what their rights and responsibilities are.
Client Legislative Rights and Responsibilities Policy
NOTE What if the client has a preferred provider?
If the client has a preference, load the provider and their vendor as a participant. Ensure the vendor and provider are 
contracted for this service by using the Geographic Location search. This enables Recovery Administration to validate 
the email and then email the purchase order directly from Eos if required.
• The Recovery Team Member must ensure all known participants are loaded on the file and then removed when no
longer relevant. For information on how to manage participants, refer to Manage Participants (Eos Online Help).
Manage Participants (Eos Online Help)
Client choice of providers Policy
Check the client has provided consent to collect and share information.
View Client Consent
NOTE What if the client has not provided consent?
Go to Obtain Client Authority to Collect Information.
PROCESS Obtain Client Authority to Collect Information
In Salesforce, record the details of the discussion with the client as a contact.
NOTE What do you have to do to document your decision?
Refer to Issue Recovery Decision process.
PROCESS Issue Recovery Decision
NOTE What if the request is declined?
Generate the SPD999 decision letter and create an NGCM - Send Letter task.
Identify Claims for Rapidly Deteriorating Clients
Add the Neuropsychological Assessment action as an agreed intervention to the Recovery Plan.
NOTE How do you update the Recovery Plan?
Go to Create or Update Recovery Plan.
PROCESS Create or Update Recovery Plan
Contact the client's GP or relevant specialist (if necessary) to request relevant medical information needed to assess the 
assessment request, refer to the process below.
NOTE How do you request medical records?
Refer to Request Clinical Records.
PROCESS Request Clinical Records
4.0 Request assessment referral
Cover Assessor, Recovery Assistant, Recovery Coordinator, Recovery Partner
In Eos, create a referral-specific document group and name it 'Neuropsychological Assessment'. Refer to the system steps 
below for further guidance.
Manage document groups
NOTE What documents need to be included?
• A recent medical certificate
• ACC6300 or ACC6300D Authority to Collect medical and other Records. NOTE: If verbal consent
was provided note this is in the task eform for Recovery Admin
• Any clinical advisor comments
• Relevant clinical notes
• Any relevant reports, ie medical, psychological, counselling reports
• Relevant pre-injury GP/mental health notes for a period of 2 years predating the head injury up to
present should be accessed and included with the neuropsychology assessment referral.
Refer to the Neuropsychological assessment referral page below for more information
PROCESS Neuropsychological Assessment Referrals Service Page
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NOTE What if you don't have the information to complete the referral?
Request the information needed.
PROCESS Request Clinical Records
Perform privacy checks on documents.
Privacy Check Before Disclosing Information Policy
NOTE What do you need to check?
Check documents:
• are relevant to the referral
• do not contain any third party information
• do not contain any other information that needs to be withheld.
For details on what checks you need to complete before sending documents out, refer to NG SUPPORTING INFOR-
MATION Inbound and Outbound Document Checks.
NG SUPPORTING INFORMATION Inbound and Outbound Document Checks
NOTE What if you find information that needs to be redacted?
Send an email to Recovery Administration ([email address]) and include the document to be redacted plus 
your redaction instructions, before adding the document to the document group.
NGCM - Redact information from PDF documents
Add the documents to the group.
NOTE What if there are documents from other claims that are relevant to the assessment?
When a request for a referral is required and the supporting documents are on another claim, it is important to transfer 
the documents to the relevant claim. This will ensure the right documents support the recovery decisions for each 
claim.
To transfer documents from one claim to another:
• Create a bulk print of all documents on the other relevant claim and complete mandatory fields and description
• Open PDF document from email link
• File the PDF away to the relevant claim
• Repeat these steps if there is relevant documents on multiple relevant claims
The PDF should also be renamed something short but relevant, and identify which claim number the information came 
from, so it is included/printed in further referrals or copy files eg. Medical records and reports from claim: 
100XXXXXXXX
Do not create a bulk print on one claim and then move it to another claim, renaming it and using it in a referral for 
advice as it will not appear in any file copy subsequently used.
Manage document groups
At Recovery Plan level, select Add Activity and select NGCM - Manage Referral task.
Creating Manage Referral Tasks - System Steps
NOTE What information do you need to include in the task/e-form?
Refer to the ‘Manage Referral Task Templates document’
Manage Referral Task Templates
NOTE What if you need to seek vendor availability?
Within the task, note if applicable:
• Availability for telehealth or preference for face sessions, or openness to both
• How far can the client travel
• Provider gender preference
• Additional provider skills, specialties or experiences? (EDMR/CBT, paediatrics, experience with prisoners)
Advise in task if you require Admin to advise of positive Vendor responses, prior to sending referral to next best avail-
able Vendor.
NOTE What are the NP104 Standard questions to be included?
a. Provide a summary of injury and medical history as well as all other personal history of relevance
b. Fully assess cognitive and psychological/affective functioning, incorporating named measures of performance and
symptom validity
c. Provide a detailed, balanced clinical opinion on causation of any cognitive or psychological symptoms/difficulties
identified, including discussion of injury versus non-injury factors
d. Provide your opinion on whether or not there is/are any residual cognitive or other difficulty/ies related to the index
event and the functional impact/s of those difficulties
e. Provide your recommendations for any additional assessment/s required
f. Provide your recommendations for ongoing input required and the appropriate avenues for accessing this
g. Please comment if the PPPR Act needs to be considered in regard to welfare and/or property
NOTE How do you refer a task to Recovery Administration?
Refer to Referring Tasks to Recovery Administration - Principles for further information and guidance.
Contracted Suppliers Tool
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Contracted Suppliers Search Tool
Referring Tasks to Recovery Administration - Principles
NOTE What do you do if Mental Injury Claim Information needs to be sent with a referral from a Physical Injury 
Claim?
In Eos, manually transfer the Referral Task generated to the Recovery Administration department with the Sensitive 
Claims Administrator Role.
If Complex Mental Injury reports need to be sent with the referral and there is an open claim, the Recovery Partner 
can be contacted directly to arrange this. If there is not an open claim, you will need to send a task through to the Part-
nered Recovery queue for allocation to a Recovery Partner who can help.
NOTE What if your client has a Care Plan indicator?
Refer to the page 'Consideration for Disclosure of Care Plan Indicators' to determine if disclosure is necessary and 
what information needs to be disclosed.
Considerations for Disclosure of Care Plan Indicators
NOTE What if the request is urgent and needs to be completed that day?
• Call Recovery Administration
• Give the Recovery Administrator who answers the call the claim number
• The Recovery Administrator will open the claim in Eos and find the task on the claim
• Transfer the task into the Recovery Administrator's name. This will move it to their personal Eos queue and stop it
from being reallocated by Salesforce.
NOTE What if the request is required in the future?
If the request is required in the future, set a reminder task for the future date when the service will be required. When 
the reminder task comes up send a task to Recovery Administration to continue with the process. Consider the con-
tract timeframes and SLAs as specified in the service page
NOTE What are the SLAs?
The referral tasks route to the Recovery Administration team with an SLA of 24 hours.
5.0 Review task
Recovery Administrator
Following the task assignment in Salesforce, navigate to Eos and select 'Do Task' from your task queue.
Review the tasks to ensure it has the required information to complete the referral form
NOTE What if you receive a task for a Care Plan Indicator client?
Refer to the page 'Considerations for Disclosure of Care Plan Indicators' to determine what you need to do with the 
information received.
Considerations for Disclosure of Care Plan Indicators
NOTE What if you don't have all the information you need
If required information is missing from the task, or you need guidance on working within the Administration Team, refer 
to the link below
Principles of Working in the Administration Team
6.0 Confirm availability of provider
Recovery Administrator
Identify and select the vendor as specified in the task.
NOTE What if no vendor is specified in the task?
Refer to Client Admin - Finding Providers System Steps
Client Admin - Finding Providers System Steps
Contracted Suppliers Tool
Add the vendor as a participant on the claim.
Add a participant
7.0 Create purchase order
Recovery Administrator
In Eos, generate a purchase order for the specified referral. Refer to the document below to confirm what information is 
needed for the purchase order.
Creating purchase orders using general + QE
Purchase Order - Handy Hints on how to create and edit POs
Purchase Order Details - Neuropsychological Assessment.docx
Manage Participants (Eos Online Help)
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Approve the purchase order.
NOTE What if the purchase order requires a higher delegation?
Save the purchase order. Create and send a Request Authorisation task to a Recovery Leader for a purchase order 
approval.
Refer to the link below.
Request Authorisation for a Purchase Order - System Steps
8.0 Create and send referral documents
Recovery Administrator
Create the referral for a Neuropsychological assessment documents: ACC110 referral to the Vendor and the NPS01 Referral to 
the client.
Populate the ACC110 with information noted on the referral task and include the NP104 standard questions. Ensure you have 
checked that all the relevant information within the task has been captured.
Admin Template - ACC110 Neuropsychological Assessment Referral - vendor
Admin Template - NPS01 Neuropsychological assessment - Client
Complete the document (to convert the document into a non-editable pdf).
Link the referral document to the document group already created.
Perform privacy checks using Inbound and Outbound Document Checks.
NG SUPPORTING INFORMATION Inbound and Outbound Document Checks
NOTE What if the document group contains an old e-form?
Convert the e-form to PDF so it can be emailed by Eos.
Refer to the System Steps link below for further information and guidance on how to convert an e-form to PDF.
Convert an Internal Referral e-form to a PDF document.
NOTE What if the referral contains sensitive personal information?
If the referral contains unnecessary sensitive personal information, refer to NG PRINCIPLES Working in the Adminis-
tration Team, for information and guidance on redactions, password protecting documents and sending passwords to 
providers.
Principles of Working in the Administration Team
Sending docs to providers.docx
Create an email to the provider using the Requests and referrals template, attach the referral and document group and select 
the most appropriate email address (commonly listed under General Purchasing).
NGCM - FINAL Emailing from Eos using a Template - System Steps
Send the referral to the provider.
NOTE What if the provider requires the documents to be sent via courier?
Go to Prepare and Send Client Information by Courier process.
PROCESS Prepare and Send Client Information by Courier
Check the client's preferred communication channel (SMS, email, etc), and if the client has a safe contact (if this has not been 
included in the referral task).
View a safe contact (Eos Online Help)
Send the NPS01 Neuropsychological Assessment referral letter to the client.
NOTE How do you send a notification to a client?
Refer to the system steps below.
Create a Notification - System Steps
In Salesforce, close the assigned referral task.
9.0 Receive and review Assessment Report
Recovery Assistant, Recovery Coordinator, Recovery Partner
Review the Neuropsychological Assessment report (NP104).
NOTE What should you be checking in the report?
Check the following:
• All sections of the report are completed
• Injury, client and Provider details are correct
• Diagnoses (if relevant) are clearly stated
• An explanation for the development of the symptoms and the causal link to the injury event
• There are clear, logical and practical treatment recommendations.
ACC > Claims Management > Manage Claims > Manage Treatment Interventions / Supports > Assess and Arrange Neuropsychological Assessment
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NOTE What if the client fails to attend and/or participate in the Neuropsychological Assessment?
If the client fails to attend or take part in the assessment, you should find out why.
In some cases you may need to decline or stop entitlements/supports.
PROCESS Manage Non-Compliance
Determine the next steps based on the recommendations in the report.
NOTE When should you seek internal clinical guidance?
If the following criteria are met, consider following the assessor's advice without seeking internal clinical comment:
1) The client has cover for a moderate or severe traumatic brain injury (TBI), and
2) The neuropsychological assessor is not recommending any additional covered injury, and
3) You do not have any concerns regarding the report's conclusions or recommendations.
If the following criteria are met, consider seeking internal clinical advice from a Psychology Advisor via the hotline:
1) You are unsure regarding aspects of the conclusions or recommendations of the neuropsychological assessment
report, or
2) The neuropsychological assessor has raised concerns regarding risk, issues or client vulnerability.
If the following criteria are met, consider seeking internal clinical advice from a Psychology Advisor via written guid-
ance:
1) The client has a suspected or covered mild traumatic brain injury (concussion) sustained more than six months ago,
and
2) The neuropsychological assessor has concluded that the client has injury-related cognitive impairment, or
3) The neuropsychological assessor has suggested that the client may be entitled to cover for an additional condition
(e.g. a mental injury).
Go to the Seek Internal Guidance process, if clinical guidance is required.
PROCESS Seek Internal Guidance
NOTE What if you're considering suspending entitlement(s)?
In cases of Complex Mental Injury/Traumatic Brain Injury consider obtaining Psychology Advisor and/or Medical Ad-
visor guidance before suspending entitlements. Refer to the ‘Seek Internal Guidance’ process for details on how to do 
this.
PROCESS Seek Internal Guidance
ACC > Claims Management > Manage Claims > Manage Treatment Interventions / Supports > Assess and Arrange Neuropsychological Assessment
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