Journal of Head Trauma Rehabilitation:
Prevalence and Psychological Correlates of Traumatic Brain Injury in Operation Iraqi Freedom
MacGregor, Andrew J. PhD, MPH; Shaffer, Richard A. PhD, MPH; Dougherty, Amber L. MPH; Galarneau, Michael R. MS; Raman, Rema PhD; Baker, Dewleen G. MD; Lindsay, Suzanne P. MSW, MPH, PhD; Golomb, Beatrice A. MD, PhD; Corson, Karen S. PhD
Naval Health Research Center (Drs MacGregor, Shaffer, and Corson and Mr Galarneau), Science Applications International Corporation (Ms Dougherty), University of California (Drs Raman, Golomb, and Baker), VA San Diego Healthcare System (Dr Baker), and San Diego State University (Dr Lindsay), San Diego, California.
Corresponding Author: Amber L. Dougherty, MPH, Research Epidemiologist, Naval Health Research Center, 140 Sylvester Rd, San Diego, CA 92106 (firstname.lastname@example.org).
This work was supported by the US Navy Bureau of Medicine and Surgery, Washington, DC, under Work Unit No. 60819. The views and opinions expressed herein are those of the authors and do not necessarily reflect the official policy or position of the Department of the Navy, Department of Defense, nor the US Government. This research has been conducted in compliance with all applicable federal regulations governing the protection of human subjects in research (Protocol NHRC.2007.0004).
The authors thank Dr Jerry Larson, Naval Health Research Center, for his contribution in consulting on this project.
Objective: To describe the prevalence and psychological correlates of traumatic brain injury (TBI) among injured male combatants in the Iraq conflict.
Participants: A total of 781 men injured during military combat between September 2004 and February 2005.
Main Outcome Measures: Mental health diagnosis (ICD-9 290–319), particularly posttraumatic stress disorder and mood/anxiety disorders, assigned through November 2006.
Results: 15.8% met criteria for TBI (13.4% mild, 2.4% moderate-severe TBI), 35.0% other head injury, and 49.2% non-head injury. Multivariate logistic regression suggested lower rates of posttraumatic stress disorder and mood/anxiety disorders among those with mild and moderate-severe TBI.
Conclusions: These findings could reflect a problem with differential diagnosis or, conversely, a low rate of self-presentation for symptoms. Further research is needed to elucidate the psychological consequences, clinical implications, and overall impact of TBI among military combat veterans.
TRAUMATIC BRAIN INJURY (TBI) is defined as brain damage secondary to an externally inflicted trauma and is a significant source of morbidity among military personnel.1,2 The incidence of TBI during the current US military conflict in Iraq is elevated compared with previous conflicts and has been referred to as the conflict's signature wound.3 Posttraumatic stress disorder (PTSD), an anxiety disorder triggered by a traumatic event and characterized by symptoms of avoidance, reexperiencing, and hyperarousal, is a potentially important sequela of TBI.4–6
Research on the relation between TBI and PTSD has yielded mixed findings.6 Some have argued that loss of consciousness, a hallmark symptom of TBI, can result in impaired recollection of the event, thus precluding the reexperiencing symptoms required for PTSD diagnosis.7–10 Furthermore, studies examining patients with TBI with self-reported amnesia for the traumatic event found low rates of PTSD.11–13 Severity of TBI may also play a role. In general, research supports the occurrence of PTSD following mild TBI.11,14–18 Other studies identified an inverse relation between TBI severity and PTSD incidence; those with mild TBI were more likely to develop PTSD than those with more severe TBI.7,19,20 At least 2 studies, however, found PTSD to be prevalent following severe TBI.21,22 A recent study by Hoge et al23 found that among combat veterans, those reporting mild TBI were more likely to meet criteria for PTSD than those with other combat injuries. 3
In addition to PTSD, multiple studies have found TBI to be associated with major depression, other anxiety disorders, and bipolar affective disorder, and a recent military study found increased rates of somatic and neuropsychiatric symptoms.24–30 Previous research has been limited by lack of a comparison group and a focus on civilian populations. The experience of TBI in military operations may differ in that the circumstances surrounding the causal event (eg, being involved in direct combat) would likely be considered traumatic as well.
The purpose of this study was to describe the prevalence of TBI among a population of battle-injured male combatants and to characterize the presence of psychological correlates of TBI, particularly PTSD. It was hypothesized that TBI would be associated with higher rates of mental health diagnoses compared with nonhead injuries.
Patients were identified from the US Navy-Marine Corps Combat Trauma Registry Expeditionary Medical Encounter Database (CTR-EMED). The CTR-EMED, a deployment health database maintained by the Naval Health Research Center (NHRC), consists of documented clinical encounters of deployed military personnel.31,32 Eligible personnel for this analysis were 881 Operation Iraqi Freedom (OIF) male combatants who presented to forward deployed medical treatment facilities for battle injury during the 6-month period from September 2004 to February 2005.
A total of 841 (95.5%) eligible personnel had a matching record in the Career History Archival Medical and Personnel System (CHAMPS). A database maintained by NHRC, CHAMPS contains demographic, career, and medical information of all military members on active duty in the US Armed Services since 1973 (see Gunderson et al, 2004, for a detailed description of CHAMPS).3 Medical diagnosis information is in the form of inpatient and outpatient clinical records, with diagnoses assigned by providers and subsequently coded. To ensure accuracy of diagnosis codes, US Military Treatment Facilities are required to routinely audit all medical codes; reports of these audits are provided to the Office of the Assistant Secretary of Defense/Tricare Management Activity on a monthly basis. Ten individuals were excluded because of evidence of military discharge less than 90 days into the follow-up period. A total of 50 individuals were identified as possibly sustaining a TBI, but had no documentation of TBI severity and were thus excluded from the study population.
The final study population consisted of 781 patients. Age ranged from 18 to 54 years (mean = 24.1 ± 5.4 years). The majority (75.9%) of patients were Marines, 19.6% were in the Army, and 4.5% were in other services or unknown. Most patients (84.5%) were of ranks E1–E5 (junior enlisted). Of the 781 injuries, 68.0% were minor, 18.6% were moderate, 9.5% were serious, and 4.0% were severe. The largest proportion of injuries (41.3%) was from improvised explosive devices, followed by other blast injuries (19.1%), and gunshot wounds (17.7%).
Traumatic brain injury was defined using CTR-EMED clinical records after thorough review by CTR-EMED clinical research staff. A narrative field (completed by the provider at the point of injury) describing the injury was evaluated and a diagnostic code based on the International Classification of Diseases, Ninth Revision (ICD-9) was assigned to each. An ICD-9 code in the following ranges was defined as a TBI (n = 124): 800–801.9, 803–804.9, and 850–854.1.2
Injury severity was described using 2 standardized measures of injury classification assigned by CTR-EMED clinical research staff: (1) Abbreviated Injury Scale (AIS) and (2) Injury Severity Score (ISS).34,35 The AIS refers to the severity of a specific injury, ranging from 1 (relatively minor) to 6 (currently untreatable). In the present study, TBIs were categorized as mild (AIS 1–2) and moderate-severe (AIS 3–5). The ISS is an overall measure of injury severity ranging from 0 to 75 and is derived from AIS scores in following 6 body regions: head/neck, face, chest/back, abdomen, extremities, and external.35,36 In the present analysis, ISS was categorized as minor injury (ISS 1–3), moderate injury (ISS 4–8), serious injury (ISS 9–15), and severe injury (ISS 16 or higher).37,38 If available, ICD-9 and severity coding were validated using radiological and surgical reports.
Patients with non-head injuries, the reference group, were defined by the presence of an AIS code indicating an anatomic region other than the head, neck, or face. A separate category, other head injury, was used to prevent potential misclassification of TBI within the reference group and was defined as an injury to the head, neck, or face that did not meet the criteria for TBI.
Three outcomes were considered: (1) diagnosis of any mental health problem, (2) diagnosis of PTSD, and (3) diagnosis of mood/anxiety disorder. Diagnoses in the form of ICD-9 codes were abstracted from CHAMPS. CHAMPS was updated through November 2006; therefore, there were approximately 22–27 months of follow-up time, although some participants were discharged from the military over the course of the follow-up period. Upon military discharge, CHAMPS no longer monitors personnel. Those discharged without a mental health diagnosis were assumed to have not developed the outcome.
A diagnosis of PTSD was indicated by an ICD-9 code 309.81, and any mental health disorder was indicated by an ICD-9 code in the range 290–319, excluding 305.10 (tobacco addiction). PTSD diagnosis must have been made at least 1 month postinjury, as the definition of PTSD requires symptoms to persist for at least 1 month; any diagnosis of PTSD less than 1 month postinjury was treated as a previous mental health diagnosis. Other mental health outcomes of interest included mood disorders (ICD-9 296, 300.4, 301.13, 311) and anxiety disorders (ICD-9 300–300.02, 300.21–300.29, 300.3, 308.3, 308.9, 309.81). Because of a typically high rate of comorbidity, mood and anxiety disorders were combined for analysis. Though not primary outcomes of interest, rates of adjustment disorders (ICD-9 309.0–309.9, excluding 309.81), substance abuse disorders (ICD-9 291, 292.0, 292.1, 292.3–292.9, 303, 304, 305.0, 305.2–305.7, 305.9), and other mental health disorders (any other ICD-9 code between 290 and 319 not previously listed) were also examined.
Other covariates from the CTR-EMED clinical record that were assessed for adjustment purposes include ISS, injury mechanism, age, and military rank. Intelligence, reportedly related to development of PTSD,39 was measured with the Armed Forces Qualification Test (AFQT) score abstracted from CHAMPS.40 The AFQT score is computed from a test taken by all enlisted service members upon entrance into the military. The score is based on test sections addressing mathematics and reading comprehension and is expressed as a percentile. Marital status was also abstracted from CHAMPS. Previous mental health diagnosis has been identified as a risk factor for PTSD development; this was ascertained from CHAMPS.41 Patients with an ICD-9 code between 290 and 319 (excluding 305.1) at any time while in the military since January 1, 2000, and prior to the date of injury were considered to have a previous mental health diagnosis.
All statistical analyses were performed with SAS version 9.1 statistical software (Cary, North Carolina). Prevalence of TBI was calculated for the entire cohort and stratified by injury mechanism. Differences across groups by injury status were tested using chi-square and Fisher exact tests for categorical variables and analysis of variance for continuous variables. Prevalence rates for mental health diagnoses were reported by injury status. Logistic regression modeling was used to relate TBI with subsequent mental health diagnosis; covariates significantly associated with injury status (P < .05) were adjusted for in this regression analysis.
Among all injuries, 50.8% involved a head injury. The prevalence of TBI among the total cohort was 15.8% (13.4% mild, 2.4% moderate-severe). Approximately 84% of moderate-severe TBI (16 of 19) cases were additionally confirmed via radiological and surgical reports at higher levels of care. Demographic and injury-specific variables stratified by injury status (ie, mild TBI, moderate-severe TBI, other head injury, and nonhead injury) are presented in Table 1. Age differed by injury status, though this was only marginally significant (p = .05). Military rank, service, marital status, AFQT score, and rate of previous mental health diagnosis did not differ significantly by injury status. Improvised explosive devices were responsible for a larger percentage of TBI and other head injury when compared with nonhead injury.
Rates of mental health outcome by injury status are shown in Table 2. In the overall cohort, the rates of any mental health outcome, PTSD, and mood/anxiety disorder were 30.3%, 16.5%, and 22.0%, respectively. Median time until any mental health diagnosis was 131 days (range = 1–729 days). Rates of any mental health diagnosis among mild and moderate-severe TBI were 27.6% and 47.4%, respectively. Rates for other mental health disorders (including postconcussion syndrome and other disorders classified as organic to the injury) differed significantly across injury groups; those with moderate-severe TBI had significantly higher rates than those with nonhead and other head injuries. Rates of PTSD, mood/anxiety disorders, and adjustment disorders did not differ significantly across injury groups.
Based on a strong association between injury severity (using overall ISS) and any mental health outcome, with minor injuries showing significantly lower rates compared with all other levels (data not shown), multivariate logistic regression was conducted separately for minor injuries (ISS 1–3) and moderate-severe injuries (ISS ≥ 4). Thus, the minor-injury group contained only mild TBI, and the moderate-severe injury group contained both mild and moderate-severe TBI and was more likely to contain individuals with polytrauma. The minor and moderate-severe injury groups were similar on demographic variables, and the minor injury group was less likely to contain those injured via gunshot wound. Age, injury mechanism, and injury severity were adjusted for in all models. Table 3 shows the results of the logistic regression analysis. Both mild and moderate-severe TBI were associated with lower rates of mental health problems, including PTSD and mood/anxiety disorders. This finding was not present, however, when restricting the analysis to patients with minor injuries overall (ISS 1–3).
To our knowledge, this is one of the first studies from OIF to estimate TBI prevalence and examine subsequent psychological correlates. Among a cohort of male battle-injured veterans, approximately 1 in 6 met the criteria for TBI. Among those with moderate-severe injuries (ISS ≥ 4), TBI was associated with fewer mental health diagnoses when compared with non-head injuries; similar associations were not found among those who suffered minor injuries (ISS 1–3).
Compared with previous military conflicts, the rate of head injury during OIF was significantly higher. In a meta-analysis of military conflicts between 1914 and 1976, the overall prevalence of head and neck injury among casualties was estimated at 16%.42 The increased prevalence of head injury in our combat population may be explained by a greater proportion of blast injuries and a greater survival rate for injured personnel.3 The overall rate of head injury found in this study (50.8%) is consistent with at least 2 studies of OIF casualties. It should be noted that these previous studies assessed head injury, not TBI specifically.32,43 Two recent studies, however, produced conflicting results. Terrio et al30 identified 70.2% of veterans who reported combat injuries met criteria for TBI, and Hoge et al23 found approximately 47% of injured veterans met criteria for TBI; this compared to only 15.8% in the present study. One possible explanation for these discordant results may relate to the different methods of TBI assessment; Terrio et al and Hoge et al relied on primarily self-report measures, whereas the present study measured provider-diagnosed TBI documented in clinical records from the point of injury.
The present study found, when comparing mild and moderate-severe TBI with non-head injuries, lower rates of mental health diagnoses among overall moderately-severely injured (ISS ≥ 4) patients. Results were significant for mood/anxiety disorders and approached significance for PTSD. Other studies using injured, non-TBI reference groups have yielded contradictory results. One study found rates of depression to be higher among those with severe TBI in comparison with injured controls,44 and another study found similar 6-month rates of PTSD among those with mild TBI compared with an injured control group.14 The results depart from other studies of military combat populations that found head injury to be positively associated with psychological outcome.23,45,46 It is imperative to note these previous studies that identified the positive association utilized self-report measures as the primary outcome, whereas the present study utilized diagnoses, which is contingent on self-presenting for care.
There are many possible explanations for lower rates of mental health diagnoses in the TBI group than the nonhead injury group when considering only those with moderate-severe injuries (ISS ≥ 4). This may represent problems with differential diagnosis, as physicians may ascribe mental health concerns to the TBI and not assign a psychological diagnosis. Previous studies have elucidated the symptom overlap between TBI and PTSD,47–49 and other research supports postconcussion symptoms as being similar to mood and anxiety disorders.50 Conversely, diagnosis may be affected by TBI-related deficits in processing and expressing of mental health symptoms, or by an aversion to report; military personnel may view TBI-related symptoms as less stigmatizing than mental health symptoms. In addition, extremity injuries may also play a role in the results of the present study. More than 90% of patients in the nonhead injury–group sustained injuries to the extremities. Although this group generally had less severe injuries overall than the TBI groups, injuries to the extremities may result in more immediate and visible disability, whereas disability due to TBI may take longer to become fully recognized. Alternatively, the findings may support the inverse associations previously found for TBI severity and incidence of PTSD and mood/anxiety disorders.15,51–53 Those with an impaired recollection of the event due to a head injury may not process the memory as completely as those without a head injury, thus not allowing the trauma to be encoded, which may lead to decreased psychological effects. This would not, however, explain the association found with mild TBI. It should also be considered that combat exposure, not measured in the current study, may differ across injury groups. Therefore, the association identified with mental health diagnoses may be a product of other traumatic exposures experienced aside from physical injury; thus, a causal pathway between TBI and mental health outcomes cannot be clearly established. Selective loss to follow-up via military discharge may also play a role. During the first year, those with TBI had a higher rate of loss to follow-up (13%) than non-head injuries (7%), although this difference was not significant. Furthermore, these results should not be interpreted as indicating that those with TBI experience fewer mental health symptoms, but that among this study sample they receive fewer mental health diagnoses.
This study has several limitations. Most studies estimating the prevalence of head injury during previous military conflicts utilized primary injuries only. The present study defined an individual as having a head injury if any of their injuries were to the head, neck, or face; this may have led to a greater divergence in head injury rate compared with previous conflicts. However, because of the high percentage of blast injuries, it is likely that the prevalence of head injury has indeed been higher during OIF compared with previous conflicts. Memory of the event, a potential mediator of the relation between TBI and mental health, was not measured in the present study. TBI (including mild TBI) was defined with AIS scores as opposed to other more widely accepted measures of brain injury severity (eg, Glasgow Coma Scale). Because of the austere environment in which these combat injuries are sustained, Glasgow Coma Scale is often not recorded prior to the administration of life-preserving treatments. As such, AIS is currently the best retrospective measure of TBI severity for this population, but this does not allow for comparison to studies that categorize TBI severity with other measures.
The primary outcome measures were ascertained from an electronic database that tracks, among other things, medical encounters. Most previous studies in the area of TBI and mental health have utilized survey instruments with all participants to ascertain a diagnosis. To receive a mental health diagnosis in this database, a patient would first have to present for care. This likely led to an underestimation of psychological morbidity due to either an aversion to seek treatment or only the most severe cases presenting. An additional consideration was the high rate of loss to follow-up via military discharge due to the nature of the CHAMPS database, and the inability of CHAMPS to track personnel postdischarge. Small sample size may also have affected the results; with only 19 personnel meeting criteria for moderate-severe TBI, it is difficult to identify statistically or clinically significant associations. As a result of potential bias from self-presentation for care, loss to follow-up, and small number of outcomes for those with moderate-severe TBI, results should be interpreted with caution.
The primary strength of the current study is that, to our knowledge, it is one of the first studies from OIF to examine the prevalence of TBI and its relation to later psychological morbidity. In addition, the injury-specific information available from the Navy-Marine Corps CTR-EMED, including injury mechanism and injury severity, has never before been thoroughly documented within a military combat population. Because this information is collected at baseline, issues such as recall bias are avoided. The use and high matching rate of the CHAMPS database allowed for assessment of demographic variables, as well as previous mental health diagnoses.
In conclusion, the present study found that among a cohort of male, injured OIF combatants, more than one-half had a head injury and one in 6 met criteria for TBI; a majority of the TBIs were mild. Compared with non-head injuries, rates of mental health diagnosis, particularly PTSD and mood/anxiety disorder, were lower among those with mild and moderate-severe TBI; this association was confined to those with overall moderate-severe injuries (ISS ≥ 4) and may be a result of issues with differential diagnosis or self-presentation for symptoms. Future studies should further clarify post-TBI psychological outcomes in combat populations and should utilize Department of Veterans Affairs' data to follow the course of TBI postdischarge. Traumatic brain injury is prevalent during the current military conflict in Iraq, and this study takes an important step in better understanding its psychological ramifications.
1. Warden D. Military TBI during the Iraq and Afghanistan wars. J Head Trauma Rehabil. 2006;21(5):398–402.
2. Ommaya AK, Ommaya AK, Dannenberg AL, Salazar AM. Causation, incidence, and costs of traumatic brain injury in the U.S. Military medical system. J Trauma. 1996;40(2):211–217.
3. Okie S. Traumatic brain injury in the war zone. N Engl J Med. 2005;352(20):2043–2047.
4. Friedman M. Post-Traumatic and Acute Stress Disorders: The Latest Assessment and Treatment Strategies. 4th ed. Kansas City, MO: Dean Psych Press Corp. d/b/a Compact Clinicals; 2006.
5. Shalev AY. What is posttraumatic stress disorder? J Clin Psychiatry. 2001;62(suppl 17):4–10.
6. Bryant RA. Posttraumatic stress disorder and mild brain injury: controversies, causes and consequences. J Clin Exp Neuropsychol. 2001;23(6):718–728.
7. Bryant RA. Posttraumatic stress disorder and traumatic brain injury: can they co-exist? Clin Psychol Rev. 2001;21(6):931–948.
8. Mayou R, Bryant B, Duthie R. Psychiatric consequences of road traffic accidents. BMJ. 1993;307:647–651.
9. Price KP. Post-traumatic stress disorder and concussion: are they incompatible? Defense Law J. 1994;43:113–120.
10. Sbordone RJ, Liter JC. Mild traumatic brain injury does not produce post-traumatic stress disorder. Brain Inj. 1995;9:45–52.
11. Gil S, Caspi Y, Zilberman Ben-Ari I, Koren D, Klein E. Does memory of a traumatic event increase the risk for posttraumatic stress disorder in patients with traumatic brain injury? A prospective study. Am J Psychiatry. 2005;62(5):963–969.
12. Klein E, Caspi Y, Gil S. The relation between memory of the traumatic event and PTSD: evidence from studies of traumatic brain injury. Can J Psychiatry. 2003;48(1):28–33.
13. Turnbull SJ, Campbell EA, Swann IJ. Post-traumatic stress disorder symptoms following a head injury: does amnesia for the event influence the development of symptoms? Brain Inj. 2001;15(9):775–785.
14. Bryant RA, Harvey AG. The influence of traumatic brain injury on acute stress disorder and post-traumatic stress disorder following motor vehicle accidents. Brain Inj. 1999;13(1):15–22.
15. Hickling EJ, Gillen R, Blanchard EB, Buckley T, Taylor A. Traumatic brain injury and posttraumatic stress disorder: a preliminary investigation of neuropsychological test results in PTSD secondary to motor vehicle accidents. Brain Inj. 1998;12(4):265–274.
16. Read KM, Kufera JA, Dischinger PC, et al. Life-altering outcomes after lower extremity injury sustained in motor vehicle crashes. J Trauma. 2004;57(4):815–823.
17. Mather FJ, Tate RL, Hannan TJ. Post-traumatic stress disorder in children following road traffic accidents: a comparison of those with and without mild traumatic brain injury. Brain Inj. 2003;17(12):1077–1087.
18. Creamer M, O'Donnell ML, Pattison P. Amnesia, traumatic brain injury, and posttraumatic stress disorder: a methodological inquiry. Behav Res Ther. 2005;43:1383–1389.
19. Bontke CF, Rattok J, Boake C. Do patients with mild brain injury have posttraumatic stress disorder too? J Head Trauma Rehabil. 1996;11:95–102.
20. Glaesser J, Neuner F, Lutgehetmann R, Schmidt R, Elbert T. Posttraumatic stress disorder in patients with traumatic brain injury. BMC Psychiatry. 2004;4:5.
21. Williams WH, Evans JJ, Wilson BA, Needham P. Prevalence of post-traumatic stress disorder symptoms after severe traumatic brain injury in a representative community sample. Brain Inj. 2002;16(8):673–639.
22. Bryant RA, Marosszeky JE, Crooks J, Gurka JA. Posttraumatic stress disorder after severe traumatic brain injury. Am J Psychiatry. 2000;157(4):629–631.
23. Hoge CW, McGurk D, Thomas JL, Cox AL, Engel CC, Castro CA. Mild traumatic brain injury in U.S. soldiers returning from Iraq. N Engl J Med. 2008;358(5):453–463.
24. Van Reekum R, Cohen T, Wong J. Can traumatic brain injury cause psychiatric disorders? J Neuropsychiatry Clin Neurosci. 2000;12(3):316–327.
25. Schwarzbold M, Diaz A, Marins ET, et al. Psychiatric disorder and traumatic brain injury. Neuropsychiatry Dis Treat. 2008;4(4):797–816.
26. Jorge RE, Robinson RG, Moser D, et al. Major depression following traumatic brain injury. Arch Gen Psychiatry. 2004;61:42–50.
27. Kim E, Lauterbach EC, Reeve A, et al. Neuropsychiatric complications of traumatic brain injury: a critical review of the literature (a report by the ANPA Committee on Research). J Neuropsychiatry Clin Neurosci. 2007;159:1315–1321.
28. Fann JR, Katon WJ, Uomoto JM, Esselman PC. Psychiatric disorders and functional disability in outpatients with traumatic brain injuries. Am J Psychiatry. 1995;152:1493–1499.
29. Jorge RE, Robinson RG, Starkstein SE, Arndt SV. Depression and anxiety following traumatic brain injury. J Neuropsychiatry Clin Neurosci. 1993;5:369–374.
30. Terrio H, Brenner LA, Ivins BJ, et al. Traumatic brain injury screening: preliminary findings in a US army brigade combat team. J Head Trauma Rehabil. 2009;24(1):14–23.
31. Galarneau MR, Hancock WC, Konoske P, et al. The Navy-Marine Corps Combat Trauma Registry. Mil Med. 2006;171(8):691–697.
32. Wade AL, Dye JL, Mohrle CR, Galarneau MR. Head, face, and neck injuries during Operation Iraqi Freedom II: results from the U.S. Navy-Marine Corps Combat Trauma Registry. J Trauma. 2007;63(4):836–840.
33. Gunderson E, Garland CF, Miller MR, Gorham ED. Career history archival medical and personnel system. Mil Med
34. Galarneau MR, Woodruff SI, Dye JL, Mohrle CR, Wade AL. Traumatic brain injury during Operation Iraqi Freedom: finding from the United States Navy-Marine Corps Combat Trauma Registry. J Neurosurg. 2008;108(5):950–957.
35. Gennarelli T, Wodzon E. The Abbreviated Injury Scale—2005. Des Plaines, IL: Association for the Advancement of Automotive Medicine.
36. 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.
37. Copes WS, Champion HR, Sacco WJ, Lawnick MM, Keast SL, Bain LW. The Injury Severity Score revisited. J Trauma. 1988;28(1):69–76.
38. Linn S, Linn R, Sheps S, et al. Injury severity scoring and length of stay in hospital of war casualties—demonstration of an association and possible selection bias. Int J Epidemiol. 1993;22(5):905–910.
39. Macklin ML, Metzger LJ, Litz BT, et al. Lower precombat intelligence is a risk factor for posttraumatic stress disorder. J Consult Clin Psychol. 1998;66(2):323–336.
40. US Department of Defense. Test Manual for the Armed Services Vocational Aptitude Battery. North Chicago, IL: US Military Entrance Processing Command; 1984. DOD No. 1340. 12AA.
41. Mason S, Wardrope J, Turpin G, Rowlands A. The psychological burden of injury: an 18 month prospective cohort study. Emerg Med J. 2002;19:400–404.
42. Dobson JE, Newell MJ, Shepherd JP. Trends in maxillofacial injuries in war-time (1914–1986). Br J Oral Maxillofac Surg. 1989;27:441–450.
43. Gondusky JS, Reiter MP. Protecting military convoys in Iraq: an examination of battle injuries sustained by a mechanized battalion during Operation Iraqi Freedom II. Mil Med. 2005;170(6):546–549.
44. Max JE, Koele SL, Smith WL, et al. Psychiatric disorders in children and adolescents after severe traumatic brain injury: a controlled study. J Am Acad Child Adolesc Psychiatry. 1998;37(8):832–840.
45. Vasterling JJ, Constans JI, Hanna-Pladdy B. Head injury as a predictor of psychological outcome in combat veterans. J Trauma Stress. 2000;13(3):441–451.
46. Chemtob CM, Muraoka MY, Wu-Holt P, Fairbank JA, Hamada RS, Keane TM. Head injury and combat-related posttraumatic stress disorder. J Nerv Ment Dis. 1998;186:701–708.
47. Sumpter RE, McMillan TM. Misdiagnosis of post-traumatic stress disorder following severe traumatic brain injury. Br J Psychiatry. 2005;186:423–426.
48. Trudeau DL, Anderson J, Hansen LM, et al. Findings of mild traumatic brain injury in combat veterans with PTSD and a history of blast concussion. J Neuropsychiatry Clin Neurosci. 1998;10(3):308–313.
49. Hiott W, Labbate L. Anxiety disorders associated with traumatic brain injuries. Neurorehabilitation. 2002;17:345–355.
50. Alexander MP. Mild traumatic brain injury: pathophysiology, natural history, and clinical management. Neurology. 1995;45(7):1253–1260.
51. Warden DL, Labbate LA, Salazar AM. Posttraumatic stress disorder in patients with traumatic brain injury and amnesia for the event. J Neuropsychiatry Clin Neurosci. 1997;9:18–22.
52. Van Reekum R, Bolago I, Finlayson MAJ, Garner S, Links PS. Psychiatric disorders after traumatic brain injury. Brain Inj. 1996;10(5):319–327.
53. Alexander MP. Neuropsychiatric correlates of persistent postconcussive syndrome. J Head Trauma Rehabil. 1992;7(2):60–69.
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