Subjective impact of traumatic brain injury on long-term outcome at a minimum of 10 years after trauma– first results of a survey on 368 patients from a single academic trauma center in Germany
© Andruszkow et al.; licensee BioMed Central Ltd. 2013
Received: 9 August 2013
Accepted: 7 October 2013
Published: 10 October 2013
Traumatic Brain Injury (TBI) may lead to significant impairments in personal, social and professional life. However, knowledge of the influence on long-term outcome after TBI is sparse. We therefore aimed to investigate the subjective effects of TBI on long-term outcome at a minimum of 10 years after trauma in one of the largest study populations in Germany.
The current investigation represents a retrospective cohort study at a level I trauma center including physical examination or standardized questionnaires of patients with mild, moderate or severe isolated TBI with a minimum follow-up of 10 years. We investigated the subjective physical, psychological and social outcome evaluating the Glasgow Outcome Scale, short-form 12, and social as well as vocational living circumstances.
368 patients aged 0 to 88 years were included. Patients with severe TBI were younger compared to patients with moderate or mild TBI (p < 0.05). Patients with severe TBI lived more often as single after the trauma impact. A significantly worse outcome was associated with higher severity of TBI resulting in an increased incidence of mental disability. A professional decline was analyzed in case of severe TBI resulting in significant loss of salary.
The severity of TBI significantly influenced the subjective social and living conditions. Subjective mental and physical outcome as well as professional life depended on the severity of TBI 10 years after the injury.
Traumatic Brain Injury (TBI) is worldwide known as a major public health concern potentially resulting in death or neurological impairment [1, 2]. The incidence of TBI is about 300 per 100,000 inhabitants  with almost 50% related to traffic accidents in the Western civilization .
Due to increasing clinical experience and improved treatment algorithms, overall mortality decreased during the last thirty years in traumatized patients . Thus, research also focused on long-term outcome after major trauma including TBI. However, despite this increasing interest in research on long-term outcome following trauma in general, patients with TBI were frequently omitted from study populations due to the known impact on mortality . Furthermore, many long-term outcome studies including patients with TBI exhibit potential limitations. First, research emphasizing on multiple trauma patients might not estimate the complexity of the impact of TBI as the presence of multiple injuries influences morbidity and long-term perceptions [5, 7]. The same limitation might be observed in studies emphasizing TBI without excluding other severe injuries resulting in compromised comparisons between isolated and multiple traumatized patients of different injury severity [6, 8]. In conclusion, only limited information on long term recovery and morbidity more than 10 years after isolated TBI are available [3, 9–11]. Furthermore, these reports commonly focused only on the impact of mild TBI [3, 9], moderate or severe TBI  or special subgroups  limiting general assumptions. Consequently, more comprehensive long-term outcome studies after isolated TBI are required in order to document potential prognosis and to prepare life plans for survivors, families and clinicians . In the presented study we aimed to verify medical, social as well as vocational long-term outcome results after mild, moderate and severe TBI in one of the largest long-term outcome study populations after isolated TBI in Europe.
The study was approved by the institutional ethical review board of the Hannover Medical School, Hannover, Germany, in 2010 (IRB No. 6221). Written informed consent was obtained from all adult participants. In case of children (aged <18 years), parental permission and child assent were used for participation. One or both parents accompanied the questioning and re-examination.
The investigation was designed as a retrospective cohort study at a level I trauma center. The assessment and re-examination of the included patients was performed between December 1st 2009 and October 31st 2011.
Patients were analyzed by our databank and included in the study if the following criteria were fulfilled: Only traumatized patients who have sustained TBI (GCS 3 - 15 points) were included. Minimum follow-up was at least 10 years after trauma. Patients aged 0 to 88 years were included.
In order to focus on the impact of isolated TBI we excluded patients who had sustained any additional injury defined by an Abbreviated Injury Scale (AIS) (version 2005)  larger 2. Because patients might have sustained additional injuries until follow-up due to the long time period we excluded patients who sustained any repeated trauma until follow-up with an AIS score larger than two points and any repeated TBI. Physical or mental handicap previous to TBI which was documented in the patients’ charts led to exclusion as well. Physical or mental handicap was defined as disability of loss of function including inability to communicate or to perform mobility, preventing from participation in any activities of daily living.
Contacting of patients and examination
Patients were recruited according to an established recruitment process : Apriori, patients’ residences were gathered from the charts. If patients had moved, up to three different registration offices were contacted by mail in order to determine the current address. Afterwards, the patients were contacted by mail in a letter describing the purposes of the present study and asked to make an appointment. The patients were contacted via mail and subsequently by phone up to three times. If none of these attempts was successful or three appointments were missed, patients were documented as “not available” to follow-up.
Patients with mild TBI were interviewed over the telephone while patients with moderate and severe TBI were re-examined by an experienced orthopaedic trauma surgeon. For re-examination a self-administered patient questionnaire and a standardized physical examination were used, which have been previously described . The following measures and outcome parameters were raised by this study:
Traumatic brain injury
TBI was classified based on the initial Glasgow Coma Scale (GCS) . All patients were grouped into the three commonly used TBI severity groups: mild (GCS 13 – 15) with absence of a neurological deficit, moderate (GCS 9 – 12) and severe (GCS 3 – 8) [3, 16, 17].
Demographic data, injury severity and social living conditions
Demographic and clinical data were extracted from the patients’ charts including patients’ age and gender. In addition to the GCS classification of the TBI severity, we intended to provide further information of the injury severity. Therefore, we used the Injury Severity Score (ISS) and New Injury Severity Score (NISS) for patients with moderate and severe TBI [12, 18]. Both scores represent the injury severity of TBI according to the AIS score and are highly associated with physical outcome and mortality [12, 18]. As a diversification, the NISS has been evaluated to be more precise referring to the injury severity of TBI [12, 18].
Glasgow outcome scale
Persistent vegetative state: Patient exhibits no obvious cortical function.
Severe Disability: (Conscious but disabled). Patient depends upon others for daily support due to mental or physical disability or both
Moderate Disability: (Disabled but independent). Patient is independent as far as daily life is concerned. The disabilities found include varying degrees of dysphasia, hemiparesis, or ataxia, as well as intellectual and memory deficits and personality changes.
Good Recovery: Resumption of normal activities even though there may be minor neurological or psychological deficits.
Short form 12 (SF-12)
Furthermore, the post-trauma quality of life was observed. Therefore, the short form 12 (SF-12) was used for patient assessment as a modified version of the SF-36 in German language . It implies Physical Component Summary Scale (PCS) and Mental Component Summary Scale (MCS) . For children, school work was interpreted as professional work because daily school work can be interpreted safely as daily mandatory activation.
Social living condition
Regarding the social living conditions, marital status as well as housing situation were analyzed during follow-up by the previously mentioned questionnaire. Housing situation focused on rent accommodation and potential confinement in bed as well as the subjective estimate to perform common housework. The item “fewer friends” intends to verify if a subjectively reported decline of social contacts with close persons that the patient perceives as friendships could be analyzed . All social aspects are presenting subjective associations towards the impact of TBI.
Vocational living condition
Professional decline refers to a subjective estimation of professional descent due to trauma sequelae either with or without professional retraining. The incidence of professional retraining was noted additionally.
Unemployed patients were defined as patients who were not able to work in their pretrauma job because of injury sequelae or were dismissed because of sick leave times when they were generally able to work.
Salary decrease intends to verify if a significant loss of regular salary could be evaluated due to the impact of TBI.
In general, children were excluded from the vocational analysis.
All vocational aspects are presenting subjective associations towards the impact of TBI.
The data were analyzed using the Statistical Package for the Social Sciences (SPSS; version 20; IBM Inc., Somers, NY, USA). Incidences are presented with counts or percentages while continuous values are presented as mean ± standard deviation (SD). Differences between the groups were evaluated with analysis of variance (ANOVA) for continuous data, while Pearson’s χ2-test was used for categorical values. A two sided p-value < 0.05 was considered to be significant.
The detailed flow chart of patients’ recruitment is illustrated in Figure 1: Overall 2,602 patients were analyzed to be potential candidates to participate in the study. 465 patients (17.9%) died before follow-up visit. In addition, 1,443 patients (55.5%) were not available or did not react to the invitations due to unknown reasons. 326 patients (12.5%) refused to participate the study. Finally, a total of 368 patients (14.1%) was successfully enrolled for this study and completely re-examined either by telephone or by physical examination.
Demographic data and social living conditions
Demographic and social data of 368 individuals after TBI
Number of patients
Age at time of injury (years)
Mean ± standard deviation
23.7 ± 16.6
29.0 ± 20.9
22.5 ± 16.4
Range (minimum - maximum)
1.0 - 66.0
1.0 - 76.0
1.0 - 60.0
Age at time of reexamination (years)
Mean ± standard deviation
44.2 ± 16.9
43.4 ± 20.08
26.5 ± 16.5
Range (minimum - maximum)
12.0 - 87.0
11.0 - 87.0
12.0 - 76.0
Time to reexamination (years)
Mean ± standard deviation
20.3 ± 6.5
14.2 ± 4.1
14.0 ± 3.9
Number of patients <18 years
Gender distribution (♂: ♀)
Injury Severity (ISS)
14.8 ± 7.5
21.4 ± 7.1
New Injury Severity (NISS)
24.3 ± 12.3
36.3 ± 14.8
Marital status at follow-up
- Married or cohabitant
Housing situation before TBI
- in rented accommodation
Housing situation at follow-up
- in rented accommodation
- confinement in bed
Evaluating the living conditions, patients with severe TBI lived significantly more often as singles and divorced individuals after trauma impact (Table 1). With regard to the circle of friends, severe TBI led to a significant loss of friendships after trauma (mild TBI: 9.2%, moderate TBI: 11.3%, severe TBI: 31.4%; p < 0.001).
According to the housing situation, no differences referring to the rent accommodation was elucidated between the TBI groups. However, continuous confinement in bed was strongly associated to severe TBI (Table 1).
Outcome measurement according to the injury severity of TBI
5.0 ± 0.0
4.9 ± 0.4
4.3 ± 0.8
43.8 ± 5.3
42.5 ± 5.2
42.9 ± 6.3
55.0 ± 10.8
54.3 ± 9.1
52.2 ± 8.9
Vocational living condition
Vocational situation according to the injury severity of TBI
The current paper presents first results of one of the largest long-term outcome studies after isolated TBI in Europe. With the intention to verify medical, social as well as vocational long-term deficits following TBI in survivors our results can be summarized as follows:
Patients with severe TBI were significantly younger and more often of male gender than those with moderate or mild TBI. The analysis of living conditions revealed more individuals living alone in the severe TBI population after trauma compared to the other TBI groups. A significantly worse outcome according to the GOS as well as a higher incidence of mental disabilities was found after severe TBI. Patients with severe TBI were more often confined to bed than patients after moderate or mild TBI. Severe TBI significantly impacts vocational situation due to an occupational decline resulting in loss of regular income. Moderate and severe TBI were not associated with increased unemployment or professional retraining compared to patients with mild TBI.
Outcome after TBI has been investigated in different settings [3, 9–11, 16, 17]. However, knowledge of the influence of isolated TBI on long-term outcome remains sparse due to several reasons. First, the studies varied considerably according to the definition of “long-term” with a posttraumatic observation period between 5 and 15 years [9, 16, 17]. Furthermore, some studies focused either only on the impact of mild TBI [3, 9] or on the combination of moderate and severe TBI [10, 16], whereas others verified outcome results only in multiple traumatized patients [5, 7]. Third, due to the high mortality after severe TBI even 10 years after trauma  and the reduced probability of severe isolated head injuries after high energy trauma [4, 22], included study populations used to be relatively small.
In the presented study we were obviously faced with the same problem: Almost 50% of the overall study population had to be excluded initially mainly because of in-hospital mortality or the presence of major concomitant injuries. The inclusion rate of 14.1% in our study is in line with current literature. For instance, Cameron et al. analyzed the 10-year outcome after TBI excluding not explicitly further injuries . Identifying an overall potential population of 21,032 patients based upon a Canadian state registry, finally 1,290 took part in the re-examination (6.1%) . In addition, Andersson and colleagues analyzed 198 patients evaluated from a main population of 1,719 patients with mild TBI (11.5%) .
According to the demonstrated demographic results, patients suffering severe TBI were significantly younger and more often of male gender compared to those with moderate or mild TBI. This over-representation of young and male trauma victims has been elucidated in isolated TBI as well as in multiple trauma patients previously [6, 8, 10]. One explanation for the increased incidence of severe injuries in these patients might be argued by the relatively high frequency of traffic accidents  as especially young male patients are known to be involved in high energy trauma . In this context, road traffic accidents have been found responsible for up to 80% of TBI patients .
The living situation after isolated TBI is suspected to be a critical factor for quality of life and daily living activities. Living alone may be a sign of social isolation, but it may also reflect independence [10, 16]. Nevertheless, it seems unlikely to expect that patients surviving severe TBI would be more capable of independent living than those with minor head injuries . In this context, we found more “singles” and divorced individuals after severe TBI compared to moderate or mild TBI. Therefore, the prevalence of living alone presumably reflects social isolation. This suggestion has been also considered by Colantonio et al., who found individuals living alone in up to 60% after moderate to severe TBI . In addition, even after isolated mild TBI an increased incidence of separated relationships has been found: Moreover, the measured incidence of 7% divorced patients meets the presented results (8.3%) . However, as children were also included in the present study, many participants could still be living with their parents. This may be an indicator of more supportive environment but also could indicate compromised independence [8, 10]. The latter aspect is strongly supported by the measured incidence of patients who were confined to bed due to TBI sequelae and those stating an inability to manage common homework in the presented study.
Focusing on long-term outcome measurements, the presented data indicates that survivors of severe TBI had significant impairments: These patients achieved significantly reduced GOS-scores accompanied with increased incidence of mental disability. These findings are congruent with the current literature. Colantonio et al. compared mental tests of patients after moderate to severe TBI with normative expected results revealing increased mental disabilities after moderate and severe TBI . In addition, Jacobsson et al. demonstrated reduced quality of life and impairment after moderate to severe TBI compared with a normative reference sample . Interestingly, in the present study we did not find a significant difference in the quality of life measured by SF-12 between the different TBI groups despite the reported increased impairments measured by GOS. This is in contrast to other studies and might be based on the fact, that we aimed to compare the three severities of TBI rather than matching one of them to a normalized population as other studies did [10, 16]. In this context, a profound influence or diminished quality of life due to mild TBI 10 years after injury is debatable in the current literature: Accordingly, Sadowski-Cron et al. revealed persisting complaints such as headache, concentration deficits and somatic complaints . Furthermore, Zumstein et al. were able to verify mild TBI impacting life quality 10 years after trauma considerably due to posttraumatic somatic syndromes . These complaints have been demonstrated to result in reduced SF-12 scores compared to normative population .
Unemployment is known as a significant problem following TBI [3, 10]. According to the presented results, severe TBI resulted in a significant occupational decline followed by loss of salary. Interestingly, the demonstrated comparable unemployment status between the different TBI groups has not been found in the current literature: Grauwmeijer et al. revealed that patients after moderate and severe TBI with impaired cognitive functioning at hospital discharge were at high risk of long-term unemployment three years later . These findings were supported by the long-term follow-up study of Jacobsson et al., whose patients with moderate to severe TBI had increasing unemployment rates compared to mild TBI . However, these studies evaluated unemployment rates up to 44% after severe TBI which seems considerably higher compared to the presented rate of approximately 13%. Comparability to the presented results could be limited due to increased disability rates measured by GOS: The authors found up to 80% of patients with severe TBI had a GOS less than 4 points meaning that 80% were severely disabled [16, 23] while permanent disability in the presented study was revealed only in 5.6%. Furthermore, it might be assumed that significant reasons for these diverse results are found in the different health care and social systems , which make an international comparison and a prediction of the long-term vocational impact of different TBI severities difficult.
The presented study has several limitations. Due to the follow-up period of at least 10 years, many critical events might have occurred in a persons’ life potentially affecting outcome. Although the participating patients have been asked for life-changing events between the TBI and follow-up, this aspect has to be considered as a potential limitation when interpreting the results. Especially pre-existing psychological and behavioural problems might be missed by this study, because none of the traumatized patients was assessed by specific psychological scores on admission when treated for TBI. We excluded patients with mental handicaps previous to TBI, but minor psychological problems were potentially missed by this study. As these problems might interfere with the presented outcome results, this aspect should be taken into account when interpreting the presented results.
Another major limitation is to be mentioned by including pediatric trauma patients to the study population. Pediatric TBI is known to have a better physical outcome compared to adult patients due to the plasticity of the immature brain [11, 17, 25–31]. Although this aspect is not proven in the literature without remaining criticism [11, 17, 25–31], this study could have been biased considerably. However, we demonstrated the contingent of children between the TBI groups as statistical comparable reducing the bias effect. Nevertheless, results should be interpreted carefully due to this limiting factor.
Furthermore, the length of follow-up and data collection at a single center and its retrospective design might be a limitation and it is likely that the presented findings cannot reflect the advances made in acute care as well as rehabilitation during the last decades. Additionally, one might be aware of a potential selection bias due to the large number of excluded patients which is a known limiting aspect of long-term outcome studies discussed previously.
According to the presented results, patients after severe TBI are confronted with social living, vocational and outcome restrictions. Knowledge of these impairments might regulate further life plans of TBI relatives in order to create more supportive living environments minimizing social isolation. Furthermore, occupational rehabilitation or financial insurance support might be aspects that could limit the financial burden following the occupational decline after severe TBI. In addition, due to the revealed disability after severe TBI the considerable status of physical and mental rehabilitation could be expected emphasizing on the need of social and vocational reintegration.
The authors thank Dr. Nicola-Alexander Sittaro, MD, for supervising the study in the early phase.
This study is part of the doctoral thesis of Mrs. Julia Urner, Trauma Department, Hannover Medical School, Hannover, Germany, and Mrs. Ezin Deniz, Trauma Department, Hannover Medical School, Hannover, Germany.
Author disclosure statement
Industrial support was provided by Hannover Life Re-Insurance, Hannover, Germany. Dr. Nicola-Alexander Sittaro, MD, and Dr. Ralf Lohse, PhD, Hannover Life Re-Insurance, Hannover, Germany, gave advice. No direct or indirect financial support or other assets were transferred to the authors for this study. The authors state that there are no competing interests.
- Flaada JT, Leibson CL, Mandrekar JN, Diehl N, Perkins PK, Brown AW, Malec JF: Relative risk of mortality after traumatic brain injury: a population-based study of the role of age and injury severity. J Neurotrauma. 2007, 24: 435-445. 10.1089/neu.2006.0119.View ArticlePubMedGoogle Scholar
- Lippert-Gruner M, Maegele M, Haverkamp H, Klug N, Wedekind C: Health-related quality of life during the first year after severe brain trauma with and without polytrauma. Brain Inj. 2007, 21: 451-455. 10.1080/02699050701343961.View ArticlePubMedGoogle Scholar
- Zumstein MA, Moser M, Mottini M, Ott SR, Sadowski-Cron C, Radanov BP, Zimmermann H, Exadaktylos A: Long-term outcome in patients with mild traumatic brain injury: a prospective observational study. J Trauma. 2011, 71: 120-127. 10.1097/TA.0b013e3181f2d670.View ArticlePubMedGoogle Scholar
- Majdan M, Mauritz W, Wilbacher I, Janciak I, Brazinova A, Rusnak M, Leitgeb J: Traumatic brain injuries caused by traffic accidents in five European countries: outcome and public health consequences. Eur J Publ Health. 2013, 23: 682-687. 10.1093/eurpub/cks074.View ArticleGoogle Scholar
- Zeckey C, Hildebrand F, Pape HC, Mommsen P, Panzica M, Zelle BA, Sittaro NA, Lohse R, Krettek C, Probst C: Head injury in polytrauma-is there an effect on outcome more than 10 years after the injury?. Brain Inj. 2011, 25: 551-559. 10.3109/02699052.2011.568036.View ArticlePubMedGoogle Scholar
- Cameron CM, Purdie DM, Kliewer EV, McClure RJ: Ten-year outcomes following traumatic brain injury: a population-based cohort. Brain Inj. 2008, 22: 437-449. 10.1080/02699050802060621.View ArticlePubMedGoogle Scholar
- Gross T, Schuepp M, Attenberger C, Pargger H, Amsler F: Outcome in polytraumatized patients with and without brain injury. Acta Anaesthesiol Scand. 2012, 56: 1163-1174. 10.1111/j.1399-6576.2012.02724.x.View ArticlePubMedGoogle Scholar
- Sadowski-Cron C, Schneider J, Senn P, Radanov BP, Ballinari P, Zimmermann H: Patients with mild traumatic brain injury: immediate and long-term outcome compared to intra-cranial injuries on CT scan. Brain Inj. 2006, 20: 1131-1137. 10.1080/02699050600832569.View ArticlePubMedGoogle Scholar
- Andersson EE, Bedics BK, Falkmer T: Mild traumatic brain injuries: a 10-year follow-up. J Rehabil Med. 2011, 43: 323-329. 10.2340/16501977-0666.View ArticlePubMedGoogle Scholar
- Colantonio A, Ratcliff G, Chase S, Kelsey S, Escobar M, Vernich L: Long-term outcomes after moderate to severe traumatic brain injury. Disabil Rehabil. 2004, 26: 253-261. 10.1080/09638280310001639722.View ArticlePubMedGoogle Scholar
- Anderson V, Godfrey C, Rosenfeld JV, Catroppa C: Predictors of cognitive function and recovery 10 years after traumatic brain injury in young children. Pediatrics. 2012, 129: e254-e261. 10.1542/peds.2011-0311.View ArticlePubMedGoogle Scholar
- Baker SP, O’Neill B, Haddon W, Long WB: The injury severity score: a method for describing patients with multiple injuries and evaluating emergency care. J Trauma. 1974, 14: 187-196. 10.1097/00005373-197403000-00001.View ArticlePubMedGoogle Scholar
- Pape HC, Zelle B, Lohse R, Stalp M, Hildebrand F, Krettek C, Panzica M, Duhme V, Sittaro NA: Evaluation and outcome of patients after polytrauma–can patients be recruited for long-term follow-up?. Injury. 2006, 37: 1197-1203. 10.1016/j.injury.2006.07.032.View ArticlePubMedGoogle Scholar
- Probst C, Zelle B, Panzica M, Lohse R, Sitarro NA, Krettek C, Pape HC: Clinical re-examination 10 or more years after polytrauma: is there a gender related difference?. J Trauma. 2010, 68: 706-711. 10.1097/TA.0b013e3181a8b21c.View ArticlePubMedGoogle Scholar
- Teasdale G, Jennett B: Assessment of coma and impaired consciousness. A practical scale. Lancet. 1974, 2: 81-84.View ArticlePubMedGoogle Scholar
- Jacobsson LJ, Westerberg M, Lexell J: Health-related quality-of-life and life satisfaction 6-15 years after traumatic brain injuries in northern Sweden. Brain Inj. 2010, 24: 1075-1086. 10.3109/02699052.2010.494590.View ArticlePubMedGoogle Scholar
- Anderson V, Catroppa C, Morse S, Haritou F, Rosenfeld JV: Intellectual outcome from preschool traumatic brain injury: a 5-year prospective, longitudinal study. Pediatrics. 2009, 124: e1064-e1071. 10.1542/peds.2009-0365.View ArticlePubMedGoogle Scholar
- Lavoie A, Moore L, LeSage N, Liberman M, Sampalis JS: The new injury severity score: a more accurate predictor of in-hospital mortality than the injury severity score. J Trauma. 2004, 56: 1312-1320. 10.1097/01.TA.0000075342.36072.EF.View ArticlePubMedGoogle Scholar
- Jennett B, Bond M: Assessment of outcome after severe brain damage. Lancet. 1975, 1: 480-484.View ArticlePubMedGoogle Scholar
- Bullinger M: German translation and psychometric testing of the SF-36 Health Survey: preliminary results from the IQOLA Project. International Quality of Life Assessment. Soc Sci Med. 1995, 41: 1359-1366. 10.1016/0277-9536(95)00115-N.View ArticlePubMedGoogle Scholar
- Ware J, Kosinski M, Keller SD: A 12-Item Short-Form Health Survey: construction of scales and preliminary tests of reliability and validity. Med Care. 1996, 34: 220-233. 10.1097/00005650-199603000-00003.View ArticlePubMedGoogle Scholar
- Santiago LA, Oh BC, Dash PK, Holcomb JB, Wade CE: A clinical comparison of penetrating and blunt traumatic brain injuries. Brain Inj. 2012, 26: 107-125. 10.3109/02699052.2011.635363.View ArticlePubMedGoogle Scholar
- Grauwmeijer E, Heijenbrok-Kal MH, Haitsma IK, Ribbers GM: A prospective study on employment outcome 3 years after moderate to severe traumatic brain injury. Arch Phys Med Rehabil. 2012, 93: 993-999. 10.1016/j.apmr.2012.01.018.View ArticlePubMedGoogle Scholar
- Schonberger M, Ponsford J, Olver J, Ponsford M, Wirtz M: Prediction of functional and employment outcome 1 year after traumatic brain injury: a structural equation modelling approach. J Neurol Neurosurg Psychiatr. 2011, 82: 936-941. 10.1136/jnnp.2010.210021.View ArticlePubMedGoogle Scholar
- Anderson V, Brown S, Newitt H: What contributes to quality of life in adult survivors of childhood traumatic brain injury?. J Neurotrauma. 2010, 27: 863-870. 10.1089/neu.2009.1169.View ArticlePubMedGoogle Scholar
- Anderson V, Catroppa C, Morse S, Haritou F, Rosenfeld J: Functional plasticity or vulnerability after early brain injury?. Pediatrics. 2005, 116: 1374-1382. 10.1542/peds.2004-1728.View ArticlePubMedGoogle Scholar
- Anderson VA, Catroppa C, Haritou F, Morse S, Pentland L, Rosenfeld J, Stargatt R: Predictors of acute child and family outcome following traumatic brain injury in children. Pediatr Neurosurg. 2001, 34: 138-148. 10.1159/000056009.View ArticlePubMedGoogle Scholar
- Catroppa C, Anderson VA, Morse SA, Haritou F, Rosenfeld JV: Outcome and predictors of functional recovery 5 years following pediatric traumatic brain injury (TBI). J Pediatr Psychol. 2008, 33: 707-718. 10.1093/jpepsy/jsn006.View ArticlePubMedGoogle Scholar
- Catroppa C, Godfrey C, Rosenfeld JV, Hearps SJ, Anderson V: Functional recovery 10 years following pediatric traumatic brain injury: Outcomes and predictors. J Neurotrauma. 2012, 29: 2539-2547. 10.1089/neu.2012.2403.View ArticlePubMedGoogle Scholar
- Crowe L, Babl F, Anderson V, Catroppa C: The epidemiology of paediatric head injuries: data from a referral centre in Victoria, Australia. J Paediatr Child Health. 2009, 45: 346-350. 10.1111/j.1440-1754.2009.01499.x.View ArticlePubMedGoogle Scholar
- Crowe LM, Catroppa C, Babl FE, Anderson V: Intellectual, behavioral, and social outcomes of accidental traumatic brain injury in early childhood. Pediatrics. 2012, 129: e262-e268. 10.1542/peds.2011-0438.View ArticlePubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.