Skip to main content
HHS Author Manuscripts logoLink to HHS Author Manuscripts
. Author manuscript; available in PMC: 2022 May 20.
Published in final edited form as: J Neurotrauma. 2021 Aug 17;38(23):3235–3247. doi: 10.1089/neu.2021.0062

Epidemiology of Chronic Effects of Traumatic Brain Injury

Juliet Haarbauer-Krupa 1,*, Mary Jo Pugh 2,3, Eric M Prager 4, Nicole Harmon 4, Jessica Wolfe 4, Kristine Yaffe 5,6,7
PMCID: PMC9122127  NIHMSID: NIHMS1806978  PMID: 33947273

Abstract

Although many patients diagnosed with traumatic brain injury (TBI), particularly mild TBI, recover from their symptoms within a few weeks, a small but meaningful subset experience symptoms that persist for months or years after injury and significantly impact quality of life for the person and their family. Factors associated with an increased likelihood of negative TBI outcomes include not only characteristics of the injury and injury mechanism, but also the person’s age, pre-injury status, comorbid conditions, environment, and propensity for resilience. In this article, as part of the Brain Trauma Blueprint: TBI State of the Science framework, we examine the epidemiology of long-term outcomes of TBI, including incidence, prevalence, and risk factors. We identify the need for increased longitudinal, global, standardized, and validated assessments on incidence, recovery, and treatments, as well as standardized assessments of the influence of genetics, race, ethnicity, sex, and environment on TBI outcomes. By identifying how epidemiological factors contribute to TBI outcomes in different groups of persons and potentially impact differential disease progression, we can guide investigators and clinicians toward more-precise patient diagnosis, along with tailored management, and improve clinical trial designs, data evaluation, and patient selection criteria.

Keywords: clinical trial designs, epidemiology, patient selection criteria, traumatic brain injury

Introduction

Traumatic brain injury (TBI) is a global public health concern and one of the leading causes of death and disability, with an estimated 64–74 million persons sustaining a TBI each year.1 TBI is traditionally identified as mild, moderate, or severe at the time of injury by a measure called the Glasgow Coma Scale (GCS). Although most of the literature on the outcomes and long-term effects of TBI focus on moderate-to-severe cases, mild TBI (mTBI) has the highest rate of emergency department (ED) visits. Notably, “mTBI,” “concussion,” and “minor head injury” are often used interchangeably, but in this report we use mTBI.26 Internationally, the majority of TBIs (75–90% of reported cases as assessed by the GCS) tend to be mild.7,8 Globally, total cases are likely underestimated, given that many mTBIs go undetected, untreated, and unrecorded because of the lack of a national TBI registry that could be used to obtain comprehensive data on TBI. Although the lifetime prevalence of mTBI is difficult to assess, a global incidence rate is estimated at 100–749 cases per 100,000 persons,914 or ~55.9 million persons.1 In the United States, an estimated 2.87 million TBI-related ED visits (~2.5 million TBI ED visits with ~1% being for mTBI, 288,000 TBI-related hospitalizations, and 56,000 TBI-related deaths) were reported in 201415; ~43% of these will experience long-term disabilities.16,17

TBIs are attributed to several mechanisms of injury, including falls, motor vehicle or other types of road injuries, sports-related injuries, and interpersonal physical violence or violence by other means (e.g., blast injury). These injury mechanisms vary by geographical region, socioeconomic factors, age, and sex. Indeed, stratifying by geographical region can illuminate clear differences in injury type and overall burden of disease.18 For example, incidence of TBI—of all severities—is highest in the United States and Canada, but Southeast Asian and Western Pacific regions experience the greatest overall burden of disease.1 Low- and middle-income countries experience nearly 3 times more TBI cases proportionally than high-income countries; this is attributed to a higher prevalence of risk factors for TBI causes (e.g., motor vehicle crashes) and differences in health systems for patients to seek medical care and address associated health effects. With respect to age, TBI shows a bimodal distribution with the highest incidence in the youngest and oldest age groups.15 These age groups are likely more susceptible to TBI because of increased risk for various causes of injury, such as falls in children under the age of 4 (839 per 100,000) and falls in the elderly over the age of 75 (599 per 100,000), as well as motor vehicle crashes in adults ages 15–24 (236 per 100,000).15

Mild TBI makes up 10–15% of all sports-related injuries across the age span19; ~283,000 children seek care each year at an ED because of sports-related TBI, with the highest rates among males and children between 10 and 17 years of age.20 Although injuries from non-sports activities occur across children’s life spans, sports-related injuries increase around age 6 and peak during the teenage years, a time when children are engaging more frequently in organized sports.21 Males account for a significantly greater proportion of all TBIs than females, with annual incidence rates being 388 per 100,000 males versus 195 per 100,000 females at all ages.12,22 Whereas males have a higher incidence of concussion in some contact sports such as football,20 females have a higher rate in sex-comparable sports such as soccer.23

Incidence of TBI is higher in the military compared to the civilian population.24 This is attributable, in part, to the physically demanding and potentially dangerous operational and training activities and the associated risk for blast exposures from improvised explosive devices, suicide bombers, land mines, mortar rounds, and rocket-propelled grenades.25 Incidence is higher for those in the Army compared to the Navy, Marines, or Air Force and more so for those on active duty than those who are not on active duty. From 2000 through the third quarter of 2019, >413,000 U.S. military personnel worldwide were diagnosed with a TBI; ~83% of cases were considered mild, 10% moderate, and 1% penetrating or severe.26 Similar to civilian populations, females in the military experience TBI at a lower rate, but report more neurobehavioral symptoms after mTBI than their male counterparts,2733 likely, in part, because they often experience TBI secondary to interpersonal violence or military sexual trauma, but also because they are more likely to be screened for TBI than males.34,35

Despite the many epidemiological studies focused on measuring the prevalence of TBI, the true prevalence of TBI is still unknown among populations for which access to care may be limited (e.g., underserved or rural populations) or for which reporting of TBI may be viewed as detrimental to career aspirations (e.g., military, athletics). In addition, the statistics/incidence rates described above indicate the acute effects of exposure to a TBI; 80–85% of those who sustain an mTBI fully recover within 3 months.36 What remains less understood is the incidence, prevalence, and risk factors for the chronic effects of TBI. In the following sections, we summarize the current literature regarding the epidemiology of chronic TBI within key populations and describe how the long-term sequelae of TBI both present with overlapping symptoms and are associated with increased comorbidity with other diseases. We then provide considerations for designing studies that more fully account for the long-term consequences of TBI.

Variables That Impact Traumatic Brain Injury and Outcomes

TBI is increasingly described as a chronic health condition, given that evidence indicates that the health effects of TBI can persist over time, particularly for persons who experience moderate-to-severe TBI.37,38 Many persons with mTBI recover within a short time frame, but recent studies indicate that the effects of a mTBI in children and adults can persist for a year or longer.3942 These findings indicate the need for improved follow-up and management pertinent to the age of the patient.43,44

Although discussing all of the factors that affect TBI recovery is beyond the scope of this article, we highlight a few critical sociodemographic categories that are especially meaningful across the life span. Injury-related, personal, and environmental variables can have a strong impact on an individual course of recovery in children.45 Indeed, reports have shown that pre-injury functioning, family factors such as parenting styles, and intellectual ability can predict outcome,46,47 highlighting the importance of these variables in reducing the impact of a pediatric TBI. For example, one study explored health inequities experienced by children with chronic health conditions, including TBIs of all severities, and how the inequities affect long-term mortality and chronic symptoms.48 The researchers identified serious racial and ethnic health and healthcare inequities in these children. In addition, a 2006 review noted that black children experience more TBI-related hospitalizations and have a higher TBI-related mortality rate than children who are white.49 These findings suggest that general health disparities experienced by minority children may increase the likelihood that those with a TBI will experience condition-related health disparities.

Consistent with this concept, children who have private health insurance show lower mortality rates after TBI than those with public insurance or those who are un-insured; further, there is a higher TBI prevalence in states with greater levels of private insurance, suggesting inadequate recognition of TBI among children with less access to care.50 Disparities also exist across the spectrum of care for adults with TBI, partially attributable to the heterogeneity of available resources. In rural versus urban settings in the United States, TBI (in most cases severe TBI, though it is not clearly reported) is associated with higher mortality rates.51 This could be a product of reduced access to pre-hospital care, trauma centers, neurosurgical interventions, or rehabilitative services. However, people with a TBI who live in rural areas report equivalent satisfaction with their quality of life despite having potentially lower levels of medical resources and reduced social participation.52

Recent studies on adults with mTBI seeking care in EDs revealed several issues related to their care and outcomes: 1) pre-injury factors such as mental health diagnosis, medical history of other health conditions and comorbidities, and previous TBIs are associated with persistent symptoms after mTBI53,54; 2) lingering functional impairments influence emotional health after mTBI55 and can contribute to other injury-related difficulties that affect a patient’s lifestyle at 1 year post-injury55,56; and 3) these factors can compound and influence other socioeconomic factors, such as employment and insurance, but also necessitate the need for medical follow-up.57

Sex must also be considered when describing the impact and outcomes of TBI. Females comprise approximately half of all TBI-related ED visits, 41% of TBI-related hospitalizations, and 27% of TBI-related deaths.58,59 However, these may be underestimates given that a brain injury may go unreported or undetected, especially when the injury is mild. Indeed, although there are no national prevalence estimates for TBI as a result of intimate partner violence, studies in shelters or EDs show that 30–74% of women who experience intimate partner violence have a history of TBI, highlighting the importance and frequency of this occurrence. When women do go to the ED, healthcare providers might not recognize that the symptoms experienced by victims of interpersonal violence could be the result of a TBI.60 In addition to specific types of violence contributing to TBI, hormonal factors may impact recovery outcomes in females. Although the research is still in its infancy and pre-clinical and clinical studies are necessary to determine the underlying neuroprotective effects of hormones,61 it is clear that circulating estrogens may elicit a differential pain response62,63 and the reduction of progesterone concentration after TBI can lead to a withdrawal from its proposed neuroprotective properties.64

Long-Term Sequelae of Traumatic Brain Injury

Patients of all ages often present with a heterogeneous combination of symptoms that can progress in nature and involve multiple pathophysiological mechanisms after a brain injury of varying severity.6567 These biological mechanisms can cause excitotoxicity, apoptosis, inflammatory events, seizures, demyelination, white matter pathology, and neurodegeneration, resulting in prolonged motor and cognitive deficits.65,68 Some TBI symptoms may occur early and improve or worsen over time, whereas others may develop later in the course of recovery.67 Although symptoms resolve for a majority of persons who experience mTBI in ~3 months, some continue to experience symptoms at or beyond 1 year post-injury.69 Estimates indicate that between 15% and 30% of persons who experience an mTBI suffer symptoms long after exposure,7074 as indicated by imaging findings, age, population studied, time of initial assessment, and patient presentation.75 Although these percentages are likely an underestimate, studies are beginning to reveal that even a single mTBI might manifest as a measurable cognitive impairment as early as 3 months after injury. Unfortunately, research exploring the long-term consequences of mTBI remains in its infancy. Moreover, disputes in the interpretation of data have arisen because of insufficient methods to detect subtle changes, flaws in quantitative analyses,75,76 and failure to account for the heterogeneity in symptom presentation, sociodemographic factors, environmental factors, and treatment/outcome trajectories.

The sections below break down the chronicity of TBI into subpopulations, although each of these groups shows even further heterogeneity in the presentation and outcomes of the disease. Exploring the variations in presentations can facilitate approaches to achieve better follow-up over time and target therapies toward specific patient populations using precision medicine.

Long-term outcomes in children

Every year, ~500,000 children ≤14 years of age sustain TBIs severe enough to require visits to the ED,77 with young children 0–4 years of age having the highest rate of ED visits.15 Similar to the general population, symptoms subside in most pediatric patients with mTBI within a couple weeks of injury and between 70% and 80% fully recover within 3 months.7880 Those who have persistent symptoms after 3 months usually report headaches, fatigue, and frustration, with ongoing headaches being the most common symptom.81 A number of wide-ranging factors impact the persistence of symptoms, including age, sociodemographic factors (e.g., race/ethnicity), comorbidities with other mental health or neurological disorders, learning difficulties, and family and social stressors.82 These factors can lead to long-term detriments in a range of functions, including school performance and social participation,83 as well as long-term impairments in health, cognitive, emotional, behavioral, family, and other social outcomes (for a review, see a previous work45).

Relatively few studies have examined the long-term consequences of mTBI in children.15 However, delayed sequelae from mTBI have been reported in children (either from sports-related events or non-sports-related events such as falls or motor vehicle crashes). Indeed, recent reports indicate persistent or emerging deficits in cognition, behavior, and mental health39,42; these deficits appear to be independent of the injury mechanism, duration of time post-injury, and age at the time of injury.39 Emerging research has also established that after a mTBI, children (and adults) have difficulty with visual smooth pursuit, saccades, vestibular-ocular reflex, convergence, and gait at the time of diagnosis.84,85 These vestibular and oculomotor impairments may be associated with worse outcomes and, given that they can be identified early in the clinical profile, may help to better inform treatments and interventions early after an injury.84,86

Some deficits may persist or appear later in time as a result of developmental processes involved in brain maturation and might interfere with academic achievement, disrupt psychosocial functioning regardless of injury severity,42,45,87,88 or increase susceptibility to a variety of health and neuropsychiatric conditions, including learning disorders (21%), attention-deficit/hyperactivity disorder (ADHD; 21%), speech/language problems (19%), developmental delay (15%), bone, joint, or muscle problems (14%), and anxiety problems (13%).50 Importantly, these findings indicate that comorbid conditions might occur at higher rates; indeed, one study found that when a child under the age of 10 (and especially if the injury occurred before 5 years of age) experienced a mTBI sufficient to warrant temporary hospitalization, they were likely to show adverse psychosocial outcomes (e.g., hyperactivity/inattention) and present with conduct disorder behaviors at ages 10–13.42 In addition to longer-term effects, children who experience an injury across the pediatric life span, including those in elementary school, are at higher risk for exposure to additional mTBIs, which can impact their outcomes.85,89

A few studies have summarized the chronic features observed in pediatric mTBI (see an earlier work45 for a review), and a limited number of studies have assessed outcomes in adults who experienced a TBI as a child. For example, a recent study examined adults who experienced a childhood TBI in a Swedish birth cohort, comparing them to siblings who did not experience an injury.90 Findings from this and similarly designed studies indicate that persons who experience a childhood TBI have lower rates of enrollment in post-secondary education, are less likely to be employed or live independently, and are more likely to work in entry-level or low-skilled jobs when compared to those with other disabilities or persons who have not experienced a TBI.19,9096

Biological and environmental circumstances are difficult to separate as risk factors for TBI outcomes. Studies have reported a high prevalence of TBI in young persons entering the justice and prison systems. For example, a 2015 study evaluated the prevalence of TBI based on self-reported history among 93 male participants 15–18 years of age in a juvenile facility. Approximately 82% had experienced at least one TBI that resulted in being knocked out or dazed and confused, and 44% reported ongoing symptoms.97 Longitudinal studies have found associations between TBI in childhood and subsequent increased criminality and conduct problems later in life.98 Moreover, a cohort study of prison inmates found that those with a self-reported TBI history were more likely to be rearrested sooner than those without a TBI history.99 This association between TBI and criminality could be the result of long-term TBI-related impairments that affect the person’s ability to regulate behavior and affect attention capacity and/or interpersonal skills. Alternatively, the TBI might have been the result of novelty seeking and low harm avoidance in persons prone to risky behaviors. Indeed, a larger proportion of juvenile offenders who have experienced a TBI were injured because of a fight, road traffic accident, or fall compared to non-offenders.97 However, history of substance use is also associated with TBI and juvenile delinquency, making these relationships more complex.100

Although the majority of pediatric mTBI studies report on psychosocial outcomes, many gaps remain in this research. Indeed, no study to date has assessed: 1) longitudinal changes in the developing brain after mTBI; 2) age-related differences in injury mechanisms contributing to long-term consequences; 3) long-term anatomical changes associated with injury (e.g., diffuse axonal injury, swelling); and 4) genetic and sociodemographic factors contributing to long-term consequences. Further, two studies have noted that the existing research on mTBI in children suffers from severe methodological shortcomings, including: 1) variable definitions of mTBI; 2) lack of inclusion/exclusion criteria; 3) the underlying assumption that children with mTBI are a homogenous group; 4) lack of inclusion of a control group with no TBI or other injury; 5) failure to control for pre-injury risk factors; 6) inadequate sample sizes; and 7) lack of standardized tests to measure outcomes and longitudinal designs.75,80

Long-term outcomes in adults

As previously discussed, men are more likely at every age to experience TBI than women, although women are more likely to report chronic sequelae; less-educated persons and those with a previous mental health diagnosis are also more likely to report persistent symptoms.22,101 Symptoms commonly associated with chronic sequelae include cognitive (e.g., attention difficulties, memory problems, and executive dysfunction) and social deficits.102 Indeed, an age-matched prospective cohort study assessed long-term social cognition after mTBI in adult civilians.103 Four years after injury, the TBI group showed a significant reduction in social inference—interpreting verbal and non-verbal social cues—even after controlling for cognitive functioning, suggesting that even mTBI can potentially impact overall functioning. In another study using mild-to-moderately injured patients, younger adults (ages 23–63 years) reported more psychological symptoms, such as anxiety, whereas older adults (65–91 years of age) reported more physical symptoms, such as fatigue, balance, and coordination problems.44 Other studies have found that mTBI across the age span is associated with persistent headache,104 vestibular dysfunction,105 depression, and cognitive complaints.106 Adults with sports-related concussion compared to those without a concussion history showed significant cognitive deficits in verbal memory, recall, and attention 10 years after retirement.107

Studies assessing the long-term (>1 year) consequences of mTBI in adults are sparse. The paucity of longitudinal research is complicated by 1) lack of a clear definition of post-TBI brain symptoms or interpretation of individual reports; 2) lack of standard controls (many controlled studies use injured patients spared of TBI); 3) selection bias; and 4) poor follow-up. Taking many of these factors into consideration, studies have revealed that patients who have three or more symptoms at the time of injury also report new or worse symptoms 1 year post-injury.108,109 More recently, investigators from the Transforming Research and Clinical Knowledge in TBI (TRACK-TBI) study found that less than half of adults with mTBI who present to a level 1 trauma center return to pre-injury levels of daily functioning at 1 year based on self-report.56 The factors contributing to delayed or incomplete recovery include comorbid psychiatric disorders, age at time of injury (see more below), abnormal acute neuroimaging, expectation of poor outcomes, and repetitive injuries (see an earlier work110 for additional details).

It is beyond the scope of this article to explain how each factor contributes to delayed or incomplete recovery; however, it is critical to highlight two factors reported in the literature: repetitive injury and age. Although the prevalence of repetitive mTBI is less clear, it is understood that previous TBI is a risk factor for future TBI and incomplete recovery.111 Indeed, multiple insults can produce cumulative effects and lead to long-term consequences, including age-related neurodegenerative disorders.112 Repetitive injuries, including hits to the body that can cause subconcussive TBIs, occur mostly through contact sports and do not produce gross structural or detectable functional changes in the brain parenchyma. However, the cumulative effects may result in four major clusters of symptoms: cognitive, behavioral, mood, and motor disturbances.13 Repetitive injury has been assessed most thoroughly among contact sports such as American football. These athletes have increased risk for death by suicide, diminished cognitive functioning, macrostructural, microstructural, functional, and neurochemical changes, and increased propensity for death from neurodegenerative causes such as dementia or Alzheimer’s disease.19,113,114

Older persons are more likely to sustain a TBI by falling,115 be hospitalized following their injury,67,115 and suffer from severe injuries as a consequence of their fall.44,111 Given that cognitive and physical abilities in adults diminish with age, the lasting consequences of a TBI of any severity might result in a greater impact on daily living. Among persons who receive inpatient care for a moderate-to-severe TBI, older persons are more likely to die within 5 years.67 In addition, older age groups show a greater amount of decline in cognitive and motor outcomes after a TBI compared to their younger counterparts with similar-severity injuries and require more assistance or supervision with increasing age >50 years. In a similar cohort, older persons were associated with poorer medical, functional, and participation outcomes than their younger counterparts.116 These more-severe outcomes suggest that older persons are more susceptible to experiencing a TBI, have a higher incidence of ED visits for TBI, are more vulnerable to the deleterious effects of TBI, and/or have symptoms that are exacerbated by the state of their health going into the TBI.

Long-term outcomes in military populations

As in civilian populations, the majority of military-related TBIs are classified as mild.117,118 Unfortunately, the long-term clinical impact of military-related injuries remains incompletely described, most likely because the studies are restricted to single-cohort evaluations, retrospective analyses, and self-reports.119,120 Moreover, similar to civilian samples, there are few standardized requirements for diagnosis or available treatments for TBI, leaving many injuries unreported. Despite the failures of previous studies, research assessing TBI in the military population have consistently reported poorer outcomes on the Glasgow Outcome Scale-Extended compared to civilian studies at all severities.120124 One prospective study of active-duty U.S. military personnel examined longitudinal outcomes among four groups of combat-deployed service members: control (no TBI or blast), blast control (no TBI), mTBI only, and blast plus mTBI. The analyses found that service members with mTBI and those with blast plus mTBI had significant neurobehavioral impairment and more-severe depression and post-traumatic stress disorder (PTSD) symptoms compared to combat-deployed controls; outcomes for blast controls fell between those two groups and controls.120

Another longitudinal study compared 5-year clinical outcomes of active-duty U.S. military after mTBI and blast injury to combat-deployed control persons.125 Participants in the mTBI group had no previous history of TBI. The study found that global disability, satisfaction with life, neurobehavioral symptom severity, psychiatric symptom severity, and sleep impairment were significantly worse in those with blast mTBI compared with combat-deployed controls. These differences in outcomes suggest that the underlying mechanisms and etiology may differ based on the injury type and that treatment options that work in civilians may not necessarily translate to the military population.

Some aspects of the chronic impact of combat-related TBI are focused on social function. Although the majority of these studies use moderate-to-severe TBI cohorts, the trends appear to be similar even with mild injuries.126128 Community reintegration studies suggest differences in social function between civilian and military populations with TBI. Indeed, approximately half of veterans with TBI report difficulty readjusting to civilian life, with even worse social function among those who are also diagnosed with PTSD.129,130 Civilian studies have found that TBI itself, rather than mental health, is associated with less-favorable community reintegration outcomes.126128,131 Similarly, a study in veterans confirmed that military TBI exposure is associated with long-term impacts on social and family functioning, community reintegration, and the ability to return to work, even after controlling for PTSD comorbidity and combat experiences.129 Sociodemographic characteristics may also account for some of these outcomes. For example, veterans with lower education report lower levels of social support and family functioning, and women report significantly more difficulty with community reintegration compared to men.129

Comorbidities with Traumatic Brain Injury

A significant long-term consequence of TBI is the association with and susceptibility to comorbid psychiatric and neurological conditions. As described in previous sections, several health conditions are associated with risk for TBI and outcomes after TBI. These complex patterns of comorbidity complicate diagnosis and treatment and suggest that the disease course may be modifiable. Given that the field is moving toward an era of precision medicine, this raises the question: How can researchers assimilate this complexity to appropriately evaluate individual presentations and, ultimately, better treat patients and improve health outcomes?

Association of traumatic brain injury with dementia

TBI in adults has been identified as an early risk factor for Alzheimer’s disease and dementia.132 This phenomenon has been well documented in veterans who sustained a TBI of any severity.112,133138 Unfortunately, findings are mixed and can depend on the study design. For example, two prospective studies failed to find an association between TBI and Alzheimer’s disease.139,140 though the former indicated that TBI with loss of consciousness (LOC) is associated with risk for Lewy body accumulation, parkinsonism, and Parkinson’s disease, but not non-parkinsonism dementia, Alzheimer’s disease, neuritic plaques, or neurofibrillary tangles.139 By contrast, multiple retrospective studies have found significant correlations between mTBI and increased risk for dementia. Indeed, a retrospective cohort study of 188,764 U.S. veterans >55 years of age examined the association between TBI and the risk of all-cause dementia.136 mTBI was associated with a 60% increased risk of developing dementia over 9 years, after accounting for competing risks and potential confounders.136 Importantly, the results showed an additive association between mTBI and other conditions, such as PTSD and depression, on dementia risk. A subsequent study examined the role of TBI severity in the association between TBI and dementia diagnosis in veterans.112 Whereas mTBI without LOC was associated with a >2-fold increase in the risk of dementia diagnosis, consistent with an independent report,141 those with moderate or severe TBI had a nearly 4-fold risk of dementia.

Another recent study used national registries to form a very large cohort (>2 million people) and found an association between mTBI and increased risk of dementia and Alzheimer’s disease when compared to persons with non-TBI trauma.133 Risk of dementia in older adults was the highest the first 6 months after injury and increased with an increasing number of TBI events. However, age and sex must also be taken into consideration. For example, younger age of sustaining a TBI was associated with greater risk for subsequent dementia, but patients with mTBI only showed an increased risk for dementia at ≥65 years. This finding is in line with the study described above133 and other studies that only included persons >65 years of age.142 Finally, a cohort study examined whether TBI, PTSD, or depression increase dementia risk among older female veterans.143 The results showed that women with these conditions had a 50–80% increased risk of developing dementia compared to women without these diagnoses; those with more than one condition had a 2-fold increased risk of dementia. Research on the association of TBI and dementia is complex, with inconsistencies in study findings and evolving results that can be controversial.

Association of traumatic brain injury with psychiatric disorders

The long-term neuropsychiatric sequelae of TBI seldom occur in isolation, with between 30% and 50% of adults with a moderate-to-severe TBI presenting with a psychiatric illness, such as depression after trauma.144 Evidence suggests that TBI increases the risk of developing mood and anxiety disorders, substance-use disorders, and psychosis.145 In a study of 60 persons who suffered from a TBI of any severity, around half developed a new psychiatric disorder after injury, with significantly higher lifetime rates of depression (26% vs. 8%), panic disorder (8% vs. 1.6%), and psychotic disorders (8%) than base rates.146 In the Epidemiologic Catchment Area study, severe TBI with LOC or confusion was associated with major depression and anxiety disorders.147 TBI is also associated with chronic pain,148 suicidality,149 substance-use disorders,150 and sleep disturbances.151 Other studies have indicated varying rates of psychiatric disorders, including depression (18.5–61.0%),152 obsessive-compulsive disorder (1.6–18%), psychotic disorders (0.1–9.8%),153 and substance-use disorders (34.9–51.0%),154,155 in TBI of all injury severities.

Among the youth population, those with TBI show increased risk of comorbidity as well, particularly with ADHD and mental health issues.156 Children in particular are at increased risk for psychological consequences from TBI,157 including social/behavioral disorders (odds ratios ranging from 1.40 to 27.11 at 12-month follow-up),158 increased stress responses (e.g., PTSD or other anxiety disorders), and other behavioral problems.42 Most mTBI studies in children have reported these effects within a few years of injury. Although a birth cohort study has offered insight into the occurrence of health and social outcomes of TBI during childhood, it is unclear how this applies to children who experience mTBI.

Importantly, psychiatric comorbidities can affect TBI recovery and the effects of TBI over time. Persons who experience a TBI and associated comorbidities show symptom overlap, and variability in symptom presentation, making it challenging to address the chronic symptoms of a TBI. Unfortunately, despite indications that TBI increases the risk of psychiatric disorder, it remains unclear and poorly understudied how mTBI contributes to the increased risk of developing comorbid psychiatric disorders in both adults and children. A recent study that examined adults with mTBI seen in an ED setting indicated that pre-injury psychiatric issues contribute to more-severe TBI symptoms and psychiatric symptoms at 3- and 6-months post-injury,159 emphasizing the importance of taking a medical history at the time of diagnosis to better understand psychiatric outcomes related to mTBI.

Association of traumatic brain injury with post-traumatic stress disorder

Many TBIs occur as a result of traumatic events (e.g., interpersonal assaults, motor vehicle crashes, domestic violence, or military combat), and this can lead to a neuropsychiatric dimension of the brain injury. Epidemiological data confirm that PTSD can develop after a TBI within both the civilian and military populations. One study with >1000 patients presenting at a civilian trauma center reported that patients with an mTBI were twice as likely to develop PTSD 1 year later compared to those who did not have a TBI.160 Another study examined the incidence and factors associated with PTSD in participants with mTBI from the TRACK-TBI study; ~27% of patients with an mTBI screened positive for PTSD at 6 months post-injury.53 Screening positive for PTSD was significantly associated with concurrent functional disability, post-injury psychiatric symptomatology, decreased satisfaction with life, and decreased performance in visual processing and mental flexibility.

Among military personnel with a history of TBI of any severity, 32–39% meet the diagnostic criteria for PTSD.161 Indeed, in a sample of nearly 50,000 U.S. Air Force members, those who presented with mTBI (n = 5065; 10.2%) were at increased risk of PTSD.162,163 PTSD symptoms typically emerge 1–3 months after TBI and peak at ~6 months.53 With the strong association between these disorders, their symptom overlap, and their combined negative effect on outcomes, it will be important to better understand the relationship between TBI and PTSD. Existing research has applied functional neuroimaging to distinguish PTSD and TBI patients from healthy controls, identify separate signatures for TBI and PTSD, and detect their co-occurrence in highly comorbid samples112,143,164 (Wilde and colleagues, this issue). Thus, neuroimaging approaches may be useful for identifying and understanding the connections, overlap, and distinct comorbidity patterns in persons with TBI.

Conclusion

TBI is common and has a large individual and societal burden because of its high prevalence, risk for long-term effects of the injury, loss to the work force, burden to healthcare systems, and impact on enviromnetal issues such as family burden, social participation, and health inequities. Comorbidities abound, affect outcomes, and confound efforts to define outcomes that are uniquely associated with TBI. Most studies examining TBI outcomes have focused on trajectories for persons experiencing moderate-to-severe TBI at the time of injury; however, research on the longer-term consequences of mTBI is emerging across the life span and is a critical component to understanding the overall burden of TBI. Despite advances in our understanding of mTBI, including epidemiological factors contributing to disease progression, new therapies to treat the consequences of the long-term sequelae are limited. The factors associated with TBI outcomes are complex and include characteristics not only of the injury, but also of the patient, such as age, pre-injury status, sex, comorbid conditions, environment, and propensity, for resilience to support recovery. Moreover, there is limited research on adult outcomes for persons who experienced a TBI during childhood, a time of rapidly changing development. Currently available reports indicate lower levels of subsequent employment and education as well as a high rate of involvement with the justice system for adults reporting a childhood TBI. Perhaps having a clear understanding of these factors will assist future clinical research designs and allow for more personalized testing of therapeutics to treat the long-term sequelae of mTBI.

Several future research directions could advance our understanding of the epidemiology of TBI.165 For example, we lack a complete understanding of the nexus of TBI and resilience; the influence of race, ethnicity, and sex on TBI outcomes; and the interaction of genetics, biomarkers, and behavior over time. Longitudinal global assessments on incidence, recovery, and treatment would also propel the research forward. Continued long-term outcome studies should expand the work to examine mTBI in the general population across the life span. Another important need is the development of standardized, validated assessment and outcome metrics, as well as a central organization to collect and interpret results of ongoing efforts.

Finally, future work should explore the biological underpinnings of the injury and trajectories for symptom improvement while considering individual behavior, medical history, and environment. Existing taxonomies focus on severity as mild, moderate, or severe based on duration of LOC and post-traumatic amnesia and measures such as the GCS or Abbreviated Injury Scale.166168 Although each approach has demonstrated strengths, they also have weaknesses.169 For instance, an analysis of the CENTER-TBI European cohort study170 used a clustering approach with injury information and physiological data from the first 2 weeks after injury and found four severity-focused clusters that were informed not only by the GCS, but also by the mechanism of injury and presence of extracranial injury. Thus, more work is needed to use the diverse existing data available to develop a taxonomy of TBI that incorporates injury mechanisms and early biomarkers to develop standard phenotypes and improve symptom trajectories (see Pugh et al. and Wilde et al., same issue). For clinical relevance, we summarize our findings with eight takeaways and, as part of our roadmap, four trackable opportunities for next steps that include specific action items (Table 1).

  • TBI poses a large burden because of high prevalence, risk for long-term effects of the injury, loss to the work force, burden to healthcare systems, and increased impact on issues such as family burden, social participation, and health inequities. mTBI represents the highest number of cases, with significant morbidity.

  • Most studies examining TBI outcomes have focused on trajectories for persons experiencing moderate-to-severe TBI at the time of injury; however, research on the longer-term consequences of mTBI is emerging across the life span and is a critical area for focused research.

  • Research examining mTBI includes studies that examine sports-related and non-sports-related injuries. Although caused by different injury mechanisms, it is important to consolidate these findings as related to mTBI.

  • In an effort to facilitate follow-up and management, the field has described TBI as a chronic health condition based on research on moderate-to-severe cases. Research on the prolonged and longer-term health effects related to mTBI is emerging and may offer insights on the importance of follow-up and optimal management over time even for less-severe injuries.

  • Examining the vestibular and oculomotor effects of mTBI is an emerging area of clinical assessment and research that may contribute to predicting long-term outcomes.

  • Across the life span, children and adults can experience multiple mTBIs that can compound the long-term effects of mTBI.

  • The factors associated with all TBI outcomes are complex and include not only characteristics of the injury, but also age, pre-injury status, and comorbid conditions.

  • Comorbidities abound, affect outcomes, and confound efforts to define outcomes that are uniquely associated with TBI.

Table 1.

Actionable Research Opportunities for Epidemiological Studies in TBI

Roadmap: Opportunities for next steps Action
Consider how injury severity, mechanism of injury, age, and lifetime TBI history could influence chronic outcomes.
  • Develop taxonomy of TBI based on biological impact, disease mechanism, and/or longitudinal course, rather than on injury severity.

  • Consider how population characteristics affect the etiology of the course and outcome of TBI.

Consider how epidemiological factors contribute to patient diagnosis and heterogeneity.
  • Identify putative areas of interventional investigation around the presence of comorbid conditions, which suggests the potential for a shared underlying biology.

  • Consider the opportunities and challenges of patients who present with multiple health conditions in future clinical trials’ inclusion and exclusion criteria.

  • Develop longitudinal studies in diverse populations (e.g., pediatric, military, sports, and elderly) and identify outcome trajectories and differences in the mechanisms of injury.

Leverage new approaches for data collection.
  • Identify new approaches for data collection in clinical care settings, including the type of care received, use of wearable devices, and methods (e.g., machine learning, artificial intelligence) to analyze the complex data and understand persons at risk for phenotypes representing poor outcomes.

Build a national TBI registry to enable monitoring of trends in health, resources, allocation, and priority setting; ensure better data collection; and establish best practices for intervention timeliness, monitoring, and evaluation.
  • Develop a database or registry (similar to TBI Model Systems) that follows persons over time.

  • Ensure that the registry follows all severities of TBI, how patients were enrolled, and tools to track those with mild injuries or those who did not receive rehabilitation services.

TBI, traumatic brain injury.

Acknowledgments

The findings and conclusions in this report are those of the authors and do not necessarily represent the official position of the Centers for Disease Control and Prevention.

Funding Information

This work would not have been possible without the financial support provided by Cohen Veterans Bioscience through grant COH-0003 from Steven A. Cohen. Cohen Veterans Bioscience conceptualized and funded the Brain Trauma Blueprint. Additional information can be found at www.braintraumablueprint.org.

Footnotes

Author Disclosure Statement

No competing financial interests exist.

References

  • 1.Dewan MC, Rattani A, Gupta S, Baticulon RE, Hung YC, Punchak M, Agrawal A, Adeleye AO, Shrime MG, Rubiano AM, Rosenfeld JV, and Park KB (2018). Estimating the global incidence of traumatic brain injury. J. Neurosurg, doi: 10.3171/2017.10.JNS17352. [DOI] [PubMed] [Google Scholar]
  • 2.Carroll LJ, Cassidy JD, Holm L, Kraus J, and Coronado VG; WHO Collaborating Centre Task Force on Mild Traumatic Brain Injury. (2004). Methodological issues and research recommendations for mild traumatic brain injury: the WHO Collaborating Centre Task Force on Mild Traumatic Brain Injury. J. Rehabil. Med, 43 Suppl., 113–125. [DOI] [PubMed] [Google Scholar]
  • 3.Dematteo CA, Hanna SE, Mahoney WJ, Hollenberg RD, Scott LA, Law MC, Newman A, Lin CY, and Xu L (2010). “My child doesn’t have a brain injury, he only has a concussion”. Pediatrics 125, 327–334. [DOI] [PubMed] [Google Scholar]
  • 4.Gordon KE, Dooley JM, Fitzpatrick EA, Wren P, and Wood EP (2010). Concussion or mild traumatic brain injury: parents appreciate the nuances of nosology. Pediatr. Neurol 43, 253–257. [DOI] [PubMed] [Google Scholar]
  • 5.Lumba-Brown A, Yeates KO, Sarmiento K, Breiding MJ, Haegerich TM, Gioia GA, Turner M, Benzel EC, Suskauer SJ, Giza CC, Joseph M, Broomand C, Weissman B, Gordon W, Wright DW, Moser RS, McAvoy K, Ewing-Cobbs L, Duhaime AC, Putukian M, Holshouser B, Paulk D, Wade SL, Herring SA, Halstead M, Keenan HT, Choe M, Christian CW, Guskiewicz K, Raksin PB, Gregory A, Mucha A, Taylor HG, Callahan JM, DeWitt J, Collins MW, Kirkwood MW, Ragheb J, Ellenbogen RG, Spinks TJ, Ganiats TG, Sabelhaus LJ, Altenhofen K, Hoffman R, Getchius T, Gronseth G, Donnell Z, O’Connor RE, and Timmons SD (2018). Diagnosis and management of mild traumatic brain injury in children: a systematic review. JAMA Pediatr. 172, e182847. [DOI] [PubMed] [Google Scholar]
  • 6.Mild Traumatic Brain Injury Committee of the Head Injury Interdisciplinary Special Interest Group of the American Congress of Rehabilitation Medicine. (1993). Definition of mild traumatic brain injury. J. Head Trauma Rehabil 8, 87–87. [Google Scholar]
  • 7.Holm L, Cassidy JD, Carroll LJ, and Borg J; Neurotrauma Task Force on Mild Traumatic Brain Injury of the WHO Collaborating Centre. (2005). Summary of the WHO Collaborating Centre for Neurotrauma Task Force on Mild Traumatic Brain Injury. J. Rehabil. Med 37, 137–141. [DOI] [PubMed] [Google Scholar]
  • 8.Janak JC, Pugh MJ, and Langlois Orman JA (2015). Epidemiology of TBI, in: Traumatic Brain Injury Rehabilitation Medicine. Cifu DX and Eapen BC (eds). Elsevier: Philadelphia, PA, pps. 6–35. [Google Scholar]
  • 9.Cassidy JD, Carroll LJ, Peloso PM, Borg J, von Holst H, Holm L, Kraus J, and Coronado VG; WHO Collaborating Centre Task Force on Mild Traumatic Brain Injury. (2004). Incidence, risk factors and prevention of mild traumatic brain injury: results of the WHO Collaborating Centre Task Force on Mild Traumatic Brain Injury. J. Rehabil. Med 43 Suppl., 28–60. [DOI] [PubMed] [Google Scholar]
  • 10.Feigin VL, Theadom A, Barker-Collo S, Starkey NJ, McPherson K, Kahan M, Dowell A, Brown P, Parag V, Kydd R, Jones K, Jones A, and Ameratunga S; BIONIC Study Group. (2013). Incidence of traumatic brain injury in New Zealand: a population-based study. Lancet Neurol. 12, 53–64. [DOI] [PubMed] [Google Scholar]
  • 11.Leibson CL, Brown AW, Ransom JE, Diehl NN, Perkins PK, Mandrekar J, and Malec JF (2011). Incidence of traumatic brain injury across the full disease spectrum: a population-based medical record review study. Epidemiology 22, 836–844. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Nguyen R, Fiest KM, McChesney J, Kwon CS, Jette N, Frolkis AD, Atta C, Mah S, Dhaliwal H, Reid A, Pringsheim T, Dykeman J, and Gallagher C (2016). The international incidence of traumatic brain injury: a systematic review and meta-analysis. Can. J. Neurol. Sci 43, 774–785. [DOI] [PubMed] [Google Scholar]
  • 13.Numminen HJ (2011). The incidence of traumatic brain injury in an adult population—how to classify mild cases? Eur. J. Neurol 18, 460–464. [DOI] [PubMed] [Google Scholar]
  • 14.Peeters W, van den Brande R, Polinder S, Brazinova A, Steyerberg EW, Lingsma HF, and Maas AI (2015). Epidemiology of traumatic brain injury in Europe. Acta Neurochir. (Wien) 157, 1683–1696. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Centers for Disease Control and Prevention (CDC). (2019). Surveillance Report of Traumatic Brain Injury-related Emergency Department Visits, Hospitalizations, and Deaths—United States, 2014. Centers for Disease Control and Prevention, U.S. Department of Health and Human Services: Atlanta, GA. [Google Scholar]
  • 16.Bazarian JJ, McClung J, Shah MN, Cheng YT, Flesher W, and Kraus J (2005). Mild traumatic brain injury in the United States, 1998–2000. Brain Inj. 19, 85–91. [DOI] [PubMed] [Google Scholar]
  • 17.Selassie AW, Zaloshnja E, Langlois JA, Miller T, Jones P, and Steiner C (2008). Incidence of long-term disability following traumatic brain injury hospitalization, United States, 2003. J. Head Trauma Rehabil 23, 123–131. [DOI] [PubMed] [Google Scholar]
  • 18.GBD 2016 Traumatic Brain Injury and Spinal Cord Injury Collaborators. (2019). Global, regional, and national burden of traumatic brain injury and spinal cord injury, 1990–2016: a systematic analysis for the Global Burden of Disease Study 2016. Lancet Neurol. 18, 56–87. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Capizzi A, Woo J, and Verduzco-Gutierrez M (2020). Traumatic brain injury: an overview of epidemiology, pathophysiology, and medical management. Med. Clin. North Am 104, 213–238. [DOI] [PubMed] [Google Scholar]
  • 20.Sarmiento K, Thomas KE, Daugherty J, Waltzman D, Haarbauer-Krupa JK, Peterson AB, Haileyesus T, and Breiding MJ (2019). Emergency department visits for sports- and recreation-related traumatic brain injuries among children—United States, 2010–2016. MMWR Morb. Mortal Wkly. Rep 68, 237–242. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Haarbauer-Krupa J, Arbogast KB, Metzger KB, Greenspan AI, Kessler R, Curry AE, Bell JM, DePadilla L, Pfeiffer MR, Zonfrillo MR, and Master CL (2018). Variations in mechanisms of injury for children with concussion. J. Pediatr 197, 241–248. e1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Mollayeva T, Mollayeva S, and Colantonio A (2018). Traumatic brain injury: sex, gender and intersecting vulnerabilities. Nat. Rev. Neurol 14, 711–722. [DOI] [PubMed] [Google Scholar]
  • 23.Haarbauer-Krupa JK, Comstock RD, Lionbarger M, Hirsch S, Kavee A, and Lowe B (2018). Healthcare professional involvement and RTP compliance in high school athletes with concussion. Brain Inj. 32, 1337–1344. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Reid MW, and Velez CS (2015). Discriminating military and civilian traumatic brain injuries. Mol.. Cell. Neurosci 66, 123–128. [DOI] [PubMed] [Google Scholar]
  • 25.Lindquist LK, Love HC, and Elbogen EB (2017). Traumatic brain injury in Iraq and Afghanistan veterans: new results from a national random sample study. J. Neuropsychiatry Clin. Neurosci 29, 254–259. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Defense and Veterans Brain Injury Center (DVBIC). (2019). DOD Worldwide Numbers for TBI. https:health.mil/About-MHS/OASDHA/Defense-Health-Agency/ResearchandDevelopment/Traumatic-Brain-Injury-Center-of-Excellence/DOD-TBI-WorldwideNumbers.
  • 27.Bazarian JJ, Blyth B, Mookerjee S, He H, and McDermott MP (2010). Sex differences in outcome after mild traumatic brain injury. J. Neurotrauma 27, 527–539. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Bouldin ED, Swan AA, Norman RS, Tate DF, Tumminello C, Amuan ME, Eapen BC, Wang CP, Trevino A, and Pugh MJ (2020). Health phenotypes and neurobehavioral symptom severity among post-9/11 veterans with mild traumatic brain injury: a Chronic Effects of Neurotrauma Consortium Study. J. Head Trauma Rehabil doi: 10.1097/HTR.0000000000000574. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Gupte R, Brooks W, Vukas R, Pierce J,. and Harris J (2019). Sex differences in traumatic brain injury: what we know and what we should know. J. Neurotrauma 36, 3063–3091. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Iverson KM, Hendricks AM, Kimerling R, Krengel M, Meterko M, Stolzmann KL, Baker E, Pogoda TK, Vasterling JJ, and Lew HL (2011). Psychiatric diagnoses and neurobehavioral symptom severity among OEF/OIF VA patients with deployment-related traumatic brain injury: a gender comparison. Womens Health Issues 21, 4 Suppl., S210–S217. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.Juengst SB, Nabasny A, and Terhorst L (2019). Cohort differences in neurobehavioral symptoms in chronic mild to severe traumatic brain injury. Front. Neurol 10, 1342. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Kim LH, Quon JL, Sun FW, Wortman KM, Adamson MM, and Harris OA (2018). Traumatic brain injury among female veterans: a review of sex differences in military neurosurgery. Neurosurg. Focus 45, E16. [DOI] [PubMed] [Google Scholar]
  • 33.Nabasny A, Myrga JM, and Juengst SB (2020). Neurobehavioral symptoms by gender and experience of nightmares after traumatic brain injury. Rehabil. Psychol 65, 186–191. [DOI] [PubMed] [Google Scholar]
  • 34.Cogan AM, McCaughey VK, and Scholten J (2020). Gender differences in outcomes after traumatic brain injury among service members and veterans. PM R. 12, 301–314. [DOI] [PubMed] [Google Scholar]
  • 35.Pugh MJ, Swan AA, Amuan ME, Eapen BC, Jaramillo CA, Delgado R, Tate DF, Yaffe K, and Wang CP (2019). Deployment, suicide, and overdose among comorbidity phenotypes following mild traumatic brain injury: a retrospective cohort study from the Chronic Effects of Neurotrauma Consortium. PLoS One 14, e0222674. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36.Belanger HG, Curtiss G, Demery JA, Lebowitz BK, and Vanderploeg RD (2005). Factors moderating neuropsychological outcomes following mild traumatic brain injury: a meta-analysis. J. Int. Neuropsychol. Soc 11, 215–227. [DOI] [PubMed] [Google Scholar]
  • 37.Corrigan JD, and Hammond FM (2013). Traumatic brain injury as a chronic health condition. Arch. Phys. Med. Rehabil 94, 1199–1201. [DOI] [PubMed] [Google Scholar]
  • 38.Masel BE, and DeWitt DS (2010). Traumatic brain injury: a disease process, not an event. J. Neurotrauma 27, 1529–1540. [DOI] [PubMed] [Google Scholar]
  • 39.Chendrasekhar A, Kuczabski B, Cohen D, Grageda M, Genovese-Scullin D, Patwari J, and Harris L (2020). Delayed sequelae related to mild traumatic brain injury in children. Glob. Pediatr. Health 7, 2333794X20947988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Cnossen MC, van der Naalt J, Spikman JM, Nieboer D, Yue JK, Winkler EA, Manley GT, von Steinbuechel N, Polinder S, Steyerberg EW, and Lingsma HF (2018). Prediction of persistent post-concussion symptoms after mild traumatic brain injury. J. Neurotrauma 35, 2691–2698. [DOI] [PubMed] [Google Scholar]
  • 41.Moore RD, Kay JJ, and Ellemberg D (2018). The long-term outcomes of sport-related concussion in pediatric populations. Int. J. Psycho-physiol 132, 14–24. [DOI] [PubMed] [Google Scholar]
  • 42.Taylor HG, Orchinik LJ, Minich N, Dietrich A, Nuss K, Wright M, Bangert B, Rusin J, and Yeates KO (2015). Symptoms of persistent behavior problems in children with mild traumatic brain injury. J. Head Trauma Rehabil 30, 302–310. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43.Davis GA, Anderson V, Babl FE, Gioia GA, Giza CC, Meehan W, Moser RS, Purcell L, Schatz P, Schneider KJ, Takagi M, Yeates KO, and Zemek R (2017). What is the difference in concussion management in children as compared with adults? A systematic review. Br. J. Sports Med 51, 949–957. [DOI] [PubMed] [Google Scholar]
  • 44.Thompson HJ, Rivara FP, and Wang J (2020). Effect of age on longitudinal changes in symptoms, function, and outcome in the first year after mild-moderate traumatic brain injury. J. Neurosci. Nurs 52, 46–52. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 45.Babikian T, Merkley T, Savage RC, Giza CC, and Levin H (2015). Chronic aspects of pediatric traumatic brain injury: review of the literature. J. Neurotrauma 32, 1849–1860. [DOI] [PubMed] [Google Scholar]
  • 46.Schorr E, Wade SL, Taylor HG, Stancin T, and Yeates KO (2020). Parenting styles as a predictor of long-term psychosocial outcomes after traumatic brain injury (TBI) in early childhood. Disabil. Rehabil 42, 2437–2443. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 47.Anderson V, Le Brocque R, Iselin G, Eren S, Dob R, Davern TJ, McKinlay L, and Kenardy J (2012). Adaptive ability, behavior and quality of life pre and posttraumatic brain injury in childhood. Disabil. Rehabil 34, 1639–1647. [DOI] [PubMed] [Google Scholar]
  • 48.Berry JG, Bloom S, Foley S, and Palfrey JS (2010). Health inequity in children and youth with chronic health conditions. Pediatrics 126, Suppl. 3, S111–S119. [DOI] [PubMed] [Google Scholar]
  • 49.Langlois JA, Rutland-Brown W, and Thomas KE (2005). The incidence of traumatic brain injury among children in the United States: differences by race. J. Head Trauma Rehabil 20, 229–238. [DOI] [PubMed] [Google Scholar]
  • 50.Haarbauer-Krupa J, Lee AH, Bitsko RH, Zhang X, and Kresnow-Sedacca MJ (2018). Prevalence of parent-reported traumatic brain injury in children and associated health conditions. JAMA Pediatr. 172, 1078–1086. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 51.Brown JB, Kheng M, Carney NA, Rubiano AM, and Puyana JC (2019). Geographical disparity and traumatic brain injury in America: rural areas suffer poorer outcomes. J. Neurosci. Rural Pract 10, 10–15. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 52.Jones J, and Curtin M (2010). Traumatic brain injury, participation, and rural identity. Qual. Health Res 20, 942–951. [DOI] [PubMed] [Google Scholar]
  • 53.Haarbauer-Krupa J, Taylor CA, Yue JK, Winkler EA, Pirracchio R, Cooper SR, Burke JF, Stein MB, and Manley GT (2017). Screening for post-traumatic stress disorder in a civilian emergency department population with traumatic brain injury. J. Neurotrauma 34, 50–58. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 54.Sinnott AM, Kontos AP, Collins MW and Ortega J (2020). Concussion symptoms among athletes: preinjury factors predict postinjury factors. J. Head Trauma Rehabil 35, E361–E371. [DOI] [PubMed] [Google Scholar]
  • 55.Zahniser E, Temkin NR, Machamer J, Barber J, Manley GT, Markowitz AJ, and Dikmen SS; TRACK-TBI Investigators. (2019). The functional status examination in mild traumatic brain injury: a TRACK-TBI sub-study. Arch. Clin. Neuropsychol 34, 1165–1174. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 56.Nelson LD, Temkin NR, Dikmen S, Barber J, Giacino JT, Yuh E, Levin HS, McCrea MA, Stein MB, Mukherjee P, Okonkwo DO, Diaz-Arrastia R, Manley GT, and the TRACK-TBI Investigators, Adeoye O, Badjatia N, Boase K, Bodien Y, Bullock MR, Chesnut R, Corrigan JD, Crawford K, Mis, Duhaime AC, Ellenbogen R, Feeser VR, Ferguson A, Foreman B, Gardner R, Gaudette E, Gonzalez L, Gopinath S, Gullapalli R, Hemphill JC, Hotz G, Jain S, Korley F, Kramer J, Kreitzer N, Lindsell C, Machamer J, Madden C, Martin A, McAllister T, Merchant R, Noel F, Palacios E, Perl D, Puccio A, Rabinowitz M, Robertson CS, Rosand J, Sander A, Satris G, Schnyer D, Seabury S, Sherer M, Taylor S, Toga A, Valadka A, Vassar MJ, Vespa P, Wang K, Yue JK, and Zafonte R (2019). Recovery after mild traumatic brain injury in patients presenting to US Level I Trauma Centers: a Transforming Research and Clinical Knowledge in Traumatic Brain Injury (TRACK-TBI) Study. JAMA Neurol. doi: 10.1001/jamaneurol.2019.1313. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 57.Yue JK, Winkler EA, Sharma S, Vassar MJ, Ratcliff JJ, Korley FK, Seabury SA, Ferguson AR, Lingsma HF, Deng H, Meeuws S, Adeoye OM, Rick JW, Robinson CK, Duarte SM, Yuh EL, Mukherjee P, Dikmen SS, McAllister TW, Diaz-Arrastia R, Valadka AB, Gordon WA, Okonkwo DO, and Manley GT; the TRACK-TBI Investigators. (2017). Temporal profile of care following mild traumatic brain injury: predictors of hospital admission, follow-up referral and six-month outcome. Brain Inj. 31, 1820–1829. [DOI] [PubMed] [Google Scholar]
  • 58.National Institute of Neurological Disorders and Stroke. (2017). Traumatic Brain Injury in Women Workshop Summary: NIH Main Campus. National Institute of Neurological Disorders and Stroke: Bethesda, MD. [Google Scholar]
  • 59.Fabricius AM, D’Souza A, Amodio V, Colantonio A, and Mollayeva T (2020). Women’s gendered experiences of traumatic brain injury. Qual. Health Res 30, 1033–1044. [DOI] [PubMed] [Google Scholar]
  • 60.United States Government Accountability Office. (2020). Report to congressional committees. Domestic violence: improved data needed to identify the prevalence of brain injuries among victims. GAO-20–534. U.S. Government Accountability Office: Washington, D.C. [Google Scholar]
  • 61.Brotfain E, Gruenbaum SE, Boyko M, Kutz R, Zlotnik A, and Klein M (2016). Neuroprotection by estrogen and progesterone in traumatic brain injury and spinal cord injury. Curr. Neuropharmacol 14, 641–653. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 62.Covassin T, Elbin R, Kontos A, and Larson E (2010). Investigating baseline neurocognitive performance between male and female athletes with a history of multiple concussion. J. Neurol. Neurosurg. Psychiatry 81, 597–601. [DOI] [PubMed] [Google Scholar]
  • 63.Covassin T, Moran R, and Elbin RJ (2016). Sex differences in reported concussion injury rates and time loss from participation: an update of the National Collegiate Athletic Association Injury Surveillance Program from 2004–2005 through 2008–2009. J. Athl. Train 51, 189–194. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 64.Ma J, Huang S, Qin S, You C, and Zeng Y (2016). Progesterone for acute traumatic brain injury. Cochrane Database Syst. Rev 12, CD008409. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 65.Bramlett HM, and Dietrich WD (2015). Long-term consequences of traumatic brain injury: current status of potential mechanisms of injury and neurological outcomes. J. Neurotrauma 32, 1834–1848. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 66.Dams-O’Connor K, Ketchum JM, Cuthbert JP, Corrigan JD, Hammond FM, Haarbauer-Krupa J, Kowalski RG, and Miller AC (2020). Functional outcome trajectories following inpatient rehabilitation for TBI in the United States: a NIDILRR TBIMS and CDC Interagency Collaboration. J. Head Trauma Rehabil 35, 127–139. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 67.Whiteneck GG, Eagye CB, Cuthbert JP, Corrigan JD, Bell JM, Haarbauer-Krupa JK, Miller AC, Ketchum JM, Hammond FM, Dams-O’Connor K, and Harrison-Felix C (2018). One and five year outcomes after moderate-to-severe TBI requiring inpatient rehabilitation. Centers for Disease Control and Prevention: Atlanta, GA. [Google Scholar]
  • 68.Gardner RC, Byers AL, Barnes DE, Li Y, Boscardin J, and Yaffe K (2018). Mild TBI and risk of Parkinson disease: a Chronic Effects of Neurotrauma Consortium Study. Neurology 90, e1771–e1779. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 69.Daneshvar DH, Riley DO, Nowinski CJ, McKee AC, Stern RA, and Cantu RC (2011). Long-term consequences: effects on normal development profile after concussion. Phys. Med. Rehabil. Clin. N. Am 22, 683–700, ix. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 70.Lange RT, Brickell TA, Ivins B, Vanderploeg RD, and French LM (2013). Variable, not always persistent, postconcussion symptoms after mild TBI in U.S. military service members: a five-year cross-sectional outcome study. J. Neurotrauma 30, 958–969. [DOI] [PubMed] [Google Scholar]
  • 71.Lew HL, Otis JD, Tun C, Kerns RD, Clark ME, and Cifu DX (2009). Prevalence of chronic pain, posttraumatic stress disorder, and persistent postconcussive symptoms in OIF/OEF veterans: polytrauma clinical triad. J. Rehabil. Res. Dev 46, 697–702. [DOI] [PubMed] [Google Scholar]
  • 72.Rutherford WH, Merrett JD, and McDonald JR (1979). Symptoms at one year following concussion from minor head injuries. Injury 10, 225–230. [DOI] [PubMed] [Google Scholar]
  • 73.Spinos P, Sakellaropoulos G, Georgiopoulos M, Stavridi K, Apostolopoulou K, Ellul J, and Constantoyannis C (2010). Postconcussion syndrome after mild traumatic brain injury in Western Greece. J. Trauma 69, 789–794. [DOI] [PubMed] [Google Scholar]
  • 74.Sterr A, Herron KA, Hayward C, and Montaldi D (2006). Are mild head injuries as mild as we think? Neurobehavioral concomitants of chronic post-concussion syndrome. BMC Neurol. 6, 7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 75.McInnes K, Friesen CL, MacKenzie DE, Westwood DA, and Boe SG (2017). Mild traumatic brain injury (mTBI) and chronic cognitive impairment: a scoping review. PLoS One 12, e0174847. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 76.Iverson GL, Karr JE, Gardner AJ, Silverberg ND, and Terry DP (2019). Results of scoping review do not support mild traumatic brain injury being associated with a high incidence of chronic cognitive impairment: commentary on McInnes et al. 2017. PLoS One 14, e0218997. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 77.Taylor CA, Bell JM, Breiding MJ, and Xu L (2017). Traumatic brain injury-related emergency department visits, hospitalizations, and deaths—United States, 2007 and 2013. MMWR Surveill. Summ 66, 1–16. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 78.Babikian T, Satz P, Zaucha K, Light R, Lewis RS, and Asarnow RF (2011). The UCLA longitudinal study of neurocognitive outcomes following mild pediatric traumatic brain injury. J. Int. Neuropsychol. Soc 17, 886–895. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 79.Barlow KM, Crawford S, Stevenson A, Sandhu SS, Belanger F, and Dewey D (2010). Epidemiology of postconcussion syndrome in pediatric mild traumatic brain injury. Pediatrics 126, e374–e381. [DOI] [PubMed] [Google Scholar]
  • 80.Yeates KO, Taylor HG, Rusin J, Bangert B, Dietrich A, Nuss K, Wright M, Nagin DS, and Jones BL (2009). Longitudinal trajectories of postconcussive symptoms in children with mild traumatic brain injuries and their relationship to acute clinical status. Pediatrics 123, 735–743. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 81.Babcock L, Byczkowski T, Wade SL, Ho M, Mookerjee S, and Bazarian JJ (2013). Predicting postconcussion syndrome after mild traumatic brain injury in children and adolescents who present to the emergency department. JAMA Pediatr. 167, 156–161. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 82.Lumba-Brown A, Yeates KO, Sarmiento K, Breiding MJ, Haegerich TM, Gioia GA, Turner M, Benzel EC, Suskauer SJ, Giza CC, Joseph M, Broomand C, Weissman B, Gordon W, Wright DW, Moser RS, McAvoy K, Ewing-Cobbs L, Duhaime AC, Putukian M, Holshouser B, Paulk D, Wade SL, Herring SA, Halstead M, Keenan HT, Choe M, Christian CW, Guskiewicz K, Raksin PB, Gregory A, Mucha A, Taylor HG, Callahan JM, DeWitt J, Collins MW, Kirkwood MW, Ragheb J, Ellenbogen RG, Spinks TJ, Ganiats TG, Sabelhaus LJ, Altenhofen K, Hoffman R, Getchius T, Gronseth G, Donnell Z, O’Connor RE, and Timmons SD (2018). Centers for Disease Control and Prevention guideline on the diagnosis and management of mild traumatic brain injury among children. JAMA Pediatr. 172, e182853. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 83.Haarbauer-Krupa JK, Glang A, Kurowski B, and Breiding MJ (2018). Report to Congress on the management of traumatic brain injury in children. Centers for Disease Control and Prevention: Atlanta, GA. [Google Scholar]
  • 84.Kontos AP, Deitrick JM, Collins MW, and Mucha A (2017). Review of vestibular and oculomotor screening and concussion rehabilitation. J. Athl. Train 52, 256–261. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 85.Master CL, Curry AE, Pfeiffer MR, Metzger KB, Kessler RS, Haarbauer-Krupa J, DePadilla L, Greenspan A, Breiding MJ, and Arbogast KB (2020). Characteristics of concussion in elementary school-aged children: implications for clinical management. J. Pediatr 223, 128–135. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 86.Corwin DJ, Wiebe DJ, Zonfrillo MR, Grady MF, Robinson RL, Goodman AM, and Master CL (2015). Vestibular deficits following youth concussion. J. Pediatr 166, 1221–1225. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 87.Anderson V, Brown S, Newitt H, and Hoile H (2009). Educational, vocational, psychosocial, and quality-of-life outcomes for adult survivors of childhood traumatic brain injury. J. Head Trauma Rehabil 24, 303–312. [DOI] [PubMed] [Google Scholar]
  • 88.Lloyd J, Wilson ML, Tenovuo O, and Saarijarvi S (2015). Outcomes from mild and moderate traumatic brain injuries among children and adolescents: a systematic review of studies from 2008–2013. Brain Inj. 29, 539–549. [DOI] [PubMed] [Google Scholar]
  • 89.Selassie AW, Wilson DA, Pickelsimer EE, Voronca DC, Williams NR, and Edwards JC (2013). Incidence of sport-related traumatic brain injury and risk factors of severity: a population-based epidemiologic study. Ann. Epidemiol 23, 750–756. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 90.Sariaslan A, Sharp DJ, D’Onofrio BM, Larsson H, and Fazel S (2016). Long-term outcomes associated with traumatic brain injury in childhood and adolescence: a nationwide Swedish cohort study of a wide range of medical and social outcomes. PLoS Med. 13, e1002103. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 91.Koskiniemi M, Kyykka T, Nybo T, and Jarho L (1995). Long-term outcome after severe brain injury in preschoolers is worse than expected. Arch. Pediatr. Adolesc. Med 149, 249–254. [DOI] [PubMed] [Google Scholar]
  • 92.Todis B, and Glang A (2008). Redefining success: results of a qualitative study of postsecondary transition outcomes for youth with traumatic brain injury. J. Head Trauma Rehabil 23, 252–263. [DOI] [PubMed] [Google Scholar]
  • 93.Nybo T, Sainio M, and Muller K (2004). Stability of vocational outcome in adulthood after moderate to severe preschool brain injury. J. Int. Neuropsychol. Soc 10, 719–723. [DOI] [PubMed] [Google Scholar]
  • 94.Cameto R, Levine P, and Wagner M (2004). Transition Planning for Students with Disabilities. A Special Topic Report of Findings from the National Longitudinal Transition Study-2 (NLTS2). SRI International Office of Special Education Programs, U.S. Department of Education, Washington, D.C. [Google Scholar]
  • 95.Ma Z, Bayley MT, Perrier L, Dhir P, Depatie L, Comper P, Ruttan L, Lay C, and Munce SEP (2019). The association between adverse childhood experiences and adult traumatic brain injury/concussion: a scoping review. Disabil. Rehabil 41, 1360–1366. [DOI] [PubMed] [Google Scholar]
  • 96.De Netto RK, and McKinlay A (2020). Impact of childhood traumatic brain injury on educational outcomes and adult standard of living. Disabil. Rehabil 42, 2444–2450. [DOI] [PubMed] [Google Scholar]
  • 97.Chitsabesan P, Lennox C, Williams H, Tariq O, and Shaw J (2015). Traumatic brain injury in juvenile offenders: findings from the comprehensive health assessment tool study and the development of a specialist linkworker service. J. Head Trauma Rehabil 30, 106–115. [DOI] [PubMed] [Google Scholar]
  • 98.McKinlay A, Dalrymple-Alford JC, Horwood LJ, and Fergusson DM (2002). Long term psychosocial outcomes after mild head injury in early childhood. J. Neurol. Neurosurg. Psychiatry 73, 281–288. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 99.Ray B, and Richardson N (2017). TBI and recidivism among returning inmates. Crim. Justice Behav 44, 472–486. [Google Scholar]
  • 100.Perron BE, and Howard MO (2008). Prevalence and correlates of traumatic brain injury among delinquent youths. Crim. Behav. Ment. Health 18, 243–255. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 101.Mott TF, McConnon ML, and Rieger BP (2012). Subacute to chronic mild traumatic brain injury. Am. Fam. Physician 86, 1045–1051. [PubMed] [Google Scholar]
  • 102.Theadom A, Parag V, Dowell T, McPherson K, Starkey N, Barker-Collo S, Jones K, Ameratunga S, and Feigin VL; BIONIC Research Group. (2016). Persistent problems 1 year after mild traumatic brain injury: a longitudinal population study in New Zealand. Br. J. Gen. Pract 66, e16–e23. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 103.Theadom A, McDonald S, Starkey N, Barker-Collo S, Jones KM, Ameratunga S, Wilson E, and Feigin VL (2019). Social cognition four years after mild-TBI: an age-matched prospective longitudinal cohort study. Neuropsychology 33, 560–567. [DOI] [PubMed] [Google Scholar]
  • 104.Yilmaz T, Roks G, de Koning M, Scheenen M, van der Horn H, Plas G, Hageman G, Schoonman G, Spikman J, and van der Naalt J (2017). Risk factors and outcomes associated with post-traumatic headache after mild traumatic brain injury. Emerg. Med. J 34, 800–805. [DOI] [PubMed] [Google Scholar]
  • 105.Denby E, Murphy D, Busuttil W, Sakel M, and Wilkinson D (2020). Neuropsychiatric outcomes in UK military veterans with mild traumatic brain injury and vestibular dysfunction. J. Head Trauma Rehabil 35, 57–65. [DOI] [PubMed] [Google Scholar]
  • 106.Silver JM, McAllister TW, and Arciniegas DB (2009). Depression and cognitive complaints following mild traumatic brain injury. Am. J. Psychiatry 166, 653–661. [DOI] [PubMed] [Google Scholar]
  • 107.Zhang Y, Ma Y, Chen S, Liu X, Kang HJ, Nelson S, and Bell S (2019). Long-term cognitive performance of retired athletes with sport-related concussion: a systematic review and meta-analysis. Brain Sci. 9, 199. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 108.Dikmen S, Machamer J, Fann JR, and Temkin NR (2010). Rates of symptom reporting following traumatic brain injury. J. Int. Neuropsychol. Soc 16, 401–411. [DOI] [PubMed] [Google Scholar]
  • 109.Dikmen S, Machamer J, and Temkin N (2017). Mild traumatic brain injury: longitudinal study of cognition, functional status, and post-traumatic symptoms. J. Neurotrauma 34, 1524–1530. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 110.McAllister TW (2016). Mild traumatic brain injury. Focus (Am. Psychiatr. Publ.) 14, 410–421. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 111.Dams-O’Connor K, Gibbons LE, Bowen JD, McCurry SM, Larson EB, and Crane PK (2013). Risk for late-life re-injury, dementia and death among individuals with traumatic brain injury: a population-based study. J. Neurol. Neurosurg. Psychiatry 84, 177–182. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 112.Barnes DE, Byers AL, Gardner RC, Seal KH, Boscardin WJ, and Yaffe K (2018). Association of mild traumatic brain injury with and without loss of consciousness with dementia in US military veterans. JAMA Neurol. 75, 1055–1061. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 113.Lehman EJ, Hein MJ, Baron SL, and Gersic CM (2012). Neurodegenerative causes of death among retired National Football League players. Neurology 79, 1970–1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 114.Manley G, Gardner AJ, Schneider KJ, Guskiewicz KM, Bailes J, Cantu RC, Castellani RJ, Turner M, Jordan BD, Randolph C, Dvorak J, Hayden KA, Tator CH, McCrory P, and Iverson GL (2017). A systematic review of potential long-term effects of sport-related concussion. Br. J. Sports Med 51, 969–977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 115.Kannus P, Niemi S, Parkkari J, Mattila V, and Sievanen H (2020). Fall-induced hospital-treated traumatic brain injuries among elderly Finns in 1970–2017. Arch. Gerontol. Geriatr 86, 103958. [DOI] [PubMed] [Google Scholar]
  • 116.Corrigan JD, Cuthbert JP, Harrison-Felix C, Whiteneck GG, Bell JM, Miller AC, Coronado VG, and Pretz CR (2014). US population estimates of health and social outcomes 5 years after rehabilitation for traumatic brain injury. J. Head Trauma Rehabil 29, E1–E9. [DOI] [PubMed] [Google Scholar]
  • 117.Defense and Veterans Brain Injury Center (DVBIC). (2019). DoD Numbers for Traumatic Brain Injury, Worldwide—Totals, 2000–2019 Q3.
  • 118.Centers for Disease Control and Prevention. (2003). Report to Congress on mild traumatic brain injury in the United States: steps to prevent a serious public health problem. Centers for Disease Control and Prevention: Atlanta, GA. [Google Scholar]
  • 119.Boyle E, Cancelliere C, Hartvigsen J, Carroll LJ, Holm LW, and Cassidy JD (2014). Systematic review of prognosis after mild traumatic brain injury in the military: results of the International Collaboration on Mild Traumatic Brain Injury Prognosis. Arch. Phys. Med. Rehabil 95, 3 Suppl. 2, S230–S237. [DOI] [PubMed] [Google Scholar]
  • 120.Mac Donald CL, Johnson AM, Wierzechowski L, Kassner E, Stewart T, Nelson EC, Werner NJ, Adam OR, Rivet DJ, Flaherty SF, Oh JS, Zonies D, Fang R, and Brody DL (2017). Outcome trends after US military concussive traumatic brain injury. J. Neurotrauma 34, 2206–2219. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 121.Mac Donald CL, Adam OR, Johnson AM, Nelson EC, Werner NJ, Rivet DJ, and Brody DL (2015). Acute post-traumatic stress symptoms and age predict outcome in military blast concussion. Brain 138, 1314–1326. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 122.Mac Donald CL, Johnson AM, Wierzechowski L, Kassner E, Stewart T, Nelson EC, Werner NJ, Zonies D, Oh J, Fang R, and Brody DL (2014). Prospectively assessed clinical outcomes in concussive blast vs nonblast traumatic brain injury among evacuated US military personnel. JAMA Neurol. 71, 994–1002. [DOI] [PubMed] [Google Scholar]
  • 123.MacDonald CL, Johnson AM, Nelson EC, Werner NJ, Fang R, Flaherty SF, and Brody DL (2014). Functional status after blast-plus-impact complex concussive traumatic brain injury in evacuated United States military personnel. J. Neurotrauma 31, 889–898. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 124.Walker WC, Hirsch S, Carne W, Nolen T, Cifu DX, Wilde EA, Levin HS, Brearly TW, Eapen BC, and Williams R (2018). Chronic Effects of Neurotrauma Consortium (CENC) multicentre study interim analysis: differences between participants with positive versus negative mild TBI histories. Brain Inj. 32, 1079–1089. [DOI] [PubMed] [Google Scholar]
  • 125.Mac Donald CL, Barber J, Jordan M, Johnson AM, Dikmen S, Fann JR and Temkin N (2017). Early clinical predictors of 5-year outcome after concussive blast traumatic brain injury. JAMA Neurol. 74, 821–829. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 126.Dikmen S, Machamer J, and Temkin N (1993). Psychosocial outcome in patients with moderate to severe head injury: 2-year follow-up. Brain Inj. 7, 113–124. [DOI] [PubMed] [Google Scholar]
  • 127.Kersel DA, Marsh NV, Havill JH, and Sleigh JW (2001). Psychosocial functioning during the year following severe traumatic brain injury. Brain Inj. 15, 683–696. [DOI] [PubMed] [Google Scholar]
  • 128.Temkin NR, Corrigan JD, Dikmen SS, and Machamer J (2009). Social functioning after traumatic brain injury. J. Head Trauma Rehabil 24, 460–467. [DOI] [PubMed] [Google Scholar]
  • 129.Pugh MJ, Swan AA, Carlson KF, Jaramillo CA, Eapen BC, Dillahunt-Aspillaga C, Amuan ME, Delgado RE, McConnell K, Finley EP, and Grafman JH; Trajectories of, R. and Complex Comorbidity Study, T. (2018). Traumatic brain injury severity, comorbidity, social support, family functioning, and community reintegration among veterans of the Afghanistan and Iraq wars. Arch. Phys. Med. Rehabil 99, S40–S49. [DOI] [PubMed] [Google Scholar]
  • 130.Sayer NA, Orazem RJ, Noorbaloochi S, Gravely A, Frazier P, Carlson KF, Schnurr PP, and Oleson H (2015). Iraq and Afghanistan War veterans with reintegration problems: differences by Veterans Affairs healthcare user status. Adm. Policy Ment. Health 42, 493–503. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 131.Pogoda TK, Stolzmann KL, Iverson KM, Baker E, Krengel M, Lew HL, Amara JH, and Meterko M (2016). Associations between traumatic brain injury, suspected psychiatric conditions, and unemployment in Operation Enduring Freedom/Operation Iraqi Freedom veterans. J. Head Trauma Rehabil 31, 191–203. [DOI] [PubMed] [Google Scholar]
  • 132.Mortimer JA, van Duijn CM, Chandra V, Fratiglioni L, Graves AB, Heyman A, Jorm AF, Kokmen E, Kondo K, Rocca WA, Shalat SL, Soininen H, and Hofman A (1991). Head trauma as a risk factor for Alzheimer’s disease: a collaborative re-analysis of case-control studies. EURODEM Risk Factors Research Group. Int. J. Epidemiol 20, Suppl. 2, S28–S35. [DOI] [PubMed] [Google Scholar]
  • 133.Fann JR, Ribe AR, Pedersen HS, Fenger-Gron M, Christensen J, Benros ME, and Vestergaard M (2018). Long-term risk of dementia among people with traumatic brain injury in Denmark: a population-based observational cohort study. Lancet Psychiatry 5, 424–431. [DOI] [PubMed] [Google Scholar]
  • 134.LoBue C, and Cullum CM (2019). POINT/COUNTER-POINT—beyond the headlines: the actual evidence that traumatic brain injury is a risk factor for later-in-life dementia. Arch. Clin. Neuropsychol 35, 123–127. [DOI] [PubMed] [Google Scholar]
  • 135.LoBue C, Wadsworth H, Wilmoth K, Clem M, Hart J Jr., Womack KB, Didehbani N, Lacritz LH, Rossetti HC, and Cullum CM (2017). Traumatic brain injury history is associated with earlier age of onset of Alzheimer disease. Clin. Neuropsychol 31, 85–98. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 136.Barnes DE, Kaup A, Kirby KA, Byers AL, Diaz-Arrastia R, and Yaffe K (2014). Traumatic brain injury and risk of dementia in older veterans. Neurology 83, 312–319. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 137.Plassman BL, Havlik RJ, Steffens DC, Helms MJ, Newman TN, Drosdick D, Phillips C, Gau BA, Welsh-Bohmer KA, Burke JR, Guralnik JM, and Breitner JC (2000). Documented head injury in early adulthood and risk of Alzheimer’s disease and other dementias. Neurology 55, 1158–1166. [DOI] [PubMed] [Google Scholar]
  • 138.Wang HK, Lin SH, Sung PS, Wu MH, Hung KW, Wang LC, Huang CY, Lu K, Chen HJ, and Tsai KJ (2012). Population based study on patients with traumatic brain injury suggests increased risk of dementia. J. Neurol. Neurosurg. Psychiatry 83, 1080–1085. [DOI] [PubMed] [Google Scholar]
  • 139.Crane PK, Gibbons LE, Dams-O’Connor K, Trittschuh E, Leverenz JB, Keene CD, Sonnen J, Montine TJ, Bennett DA, Leurgans S, Schneider JA, and Larson EB (2016). Association of traumatic brain injury with late-life neurodegenerative conditions and neuropatho-logic findings. JAMA Neurol. 73, 1062–1069. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 140.Mehta KM, Ott A, Kalmijn S, Slooter AJ, van Duijn CM, Hofman A, and Breteler MM (1999). Head trauma and risk of dementia and Alzheimer’s disease: the Rotterdam Study. Neurology 53, 1959–1962. [DOI] [PubMed] [Google Scholar]
  • 141.Lee YK, Hou SW, Lee CC, Hsu CY, Huang YS, and Su YC (2013). Increased risk of dementia in patients with mild traumatic brain injury: a nationwide cohort study. PLoS One 8, e62422. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 142.Li Y, Li Y, Li X, Zhang S, Zhao J, Zhu X, and Tian G (2017). Head injury as a risk factor for dementia and Alzheimer’s disease: a systematic review and meta-analysis of 32 observational studies. PLoS One 12, e0169650. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 143.Yaffe K, Lwi SJ, Hoang TD, Xia F, Barnes DE, Maguen S, and Peltz CB (2019). Military-related risk factors in female veterans and risk of dementia. Neurology 92, e205–e211. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 144.Juengst SB, Kumar RG, and Wagner AK (2017). A narrative literature review of depression following traumatic brain injury: prevalence, impact, and management challenges. Psychol. Res. Behav. Manag 10, 175–186. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 145.Schwarzbold M, Diaz A, Martins ET, Rufino A, Amante LN, Thais ME, Quevedo J, Hohl A, Linhares MN, and Walz R (2008). Psychiatric disorders and traumatic brain injury. Neuropsychiatr. Dis. Treat 4, 797–816. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 146.Koponen S, Taiminen T, Portin R, Himanen L, Isoniemi H, Heinonen H, Hinkka S, and Tenovuo O (2002). Axis I and II psychiatric disorders after traumatic brain injury: a 30-year follow-up study. Am. J. Psychiatry 159, 1315–1321. [DOI] [PubMed] [Google Scholar]
  • 147.Silver JM, Kramer R, Greenwald S, and Weissman M (2001). The association between head injuries and psychiatric disorders: findings from the New Haven NIMH Epidemiologic Catchment Area Study. Brain Inj. 15, 935–945. [DOI] [PubMed] [Google Scholar]
  • 148.Lahz S, and Bryant RA (1996). Incidence of chronic pain following traumatic brain injury. Arch. Phys. Med. Rehabil 77, 889–891. [DOI] [PubMed] [Google Scholar]
  • 149.Simpson G, and Tate R (2002). Suicidality after traumatic brain injury: demographic, injury and clinical correlates. Psychol. Med 32, 687–697. [DOI] [PubMed] [Google Scholar]
  • 150.Taylor LA, Kreutzer JS, Demm SR, and Meade MA (2003). Traumatic brain injury and substance abuse: a review and analysis of the literature. Neuropsychol. Rehabil 13, 165–188. [DOI] [PubMed] [Google Scholar]
  • 151.Ouellet MC, Savard J, and Morin CM (2004). Insomnia following traumatic brain injury: a review. Neurorehabil. Neural Repair 18, 187–198. [DOI] [PubMed] [Google Scholar]
  • 152.Kim E, Lauterbach EC, Reeve A, Arciniegas DB, Coburn KL, Mendez MF, Rummans TA, Coffey EC; ANPA Committee on Research. (2007). Neuropsychiatric complications of traumatic brain injury: a critical review of the literature (a report by the ANPA Committee on Research). J. Neuropsychiatry Clin. Neurosci 19, 106–127. [DOI] [PubMed] [Google Scholar]
  • 153.David AS, and Prince M (2005). Psychosis following head injury: a critical review. J. Neurol. Neurosurg. Psychiatry 76, Suppl. 1, i53i60. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 154.Jorge RE, Starkstein SE, Arndt S, Moser D, Crespo-Facorro B, and Robinson RG (2005). Alcohol misuse and mood disorders following traumatic brain injury. Arch. Gen. Psychiatry 62, 742–749. [DOI] [PubMed] [Google Scholar]
  • 155.Kreutzer JS, Witol AD, and Marwitz JH (1996). Alcohol and drug use among young persons with traumatic brain injury. J. Learn. Disabil 29, 643–651. [DOI] [PubMed] [Google Scholar]
  • 156.Schachar RJ, Park LS, and Dennis M (2015). Mental health implications of traumatic brain injury (TBI) in children and youth. J. Can. Acad. Child Adolesc. Psychiatry 24, 100–108. [PMC free article] [PubMed] [Google Scholar]
  • 157.Weil ZM, and Karelina K (2019). Lifelong consequences of brain injuries during development: from risk to resilience. Front. Neuroendocrinol 55, 100793. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 158.Schwartz L, Taylor HG, Drotar D, Yeates KO, Wade SL, and Stancin T (2003). Long-term behavior problems following pediatric traumatic brain injury: prevalence, predictors, and correlates. J. Pediatr. Psychol 28, 251–263. [DOI] [PubMed] [Google Scholar]
  • 159.Yue JK, Cnossen MC, Winkler EA, Deng H, Phelps RRL, Coss NA, Sharma S, Robinson CK, Suen CG, Vassar MJ, Schnyer DM, Puccio AM, Gardner RC, Yuh EL, Mukherjee P, Valadka AB, Okonkwo DO, Lingsma HF, and Manley GT; TRACK-TBI Investigators. (2019). Pre-injury comorbidities are associated with functional impairment and post-concussive symptoms at 3- and 6-months after mild traumatic brain injury: a TRACK-TBI study. Front. Neurol 10, 343. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 160.Bryant RA, O’Donnell ML, Creamer M, McFarlane AC, Clark CR, and Silove D (2010). The psychiatric sequelae of traumatic injury. Am. J. Psychiatry 167, 312–320. [DOI] [PubMed] [Google Scholar]
  • 161.Carlson KF, Kehle SM, Meis LA, Greer N, Macdonald R, Rutks I, Sayer NA, Dobscha SK, and Wilt TJ (2011). Prevalence, assessment, and treatment of mild traumatic brain injury and posttraumatic stress disorder: a systematic review of the evidence. J. Head Trauma Rehabil 26, 103–115. [DOI] [PubMed] [Google Scholar]
  • 162.Miller SC, Whitehead CR, Otte CN, Wells TS, Webb TS, Gore RK, and Maynard C (2015). Risk for broad-spectrum neuropsychiatric disorders after mild traumatic brain injury in a cohort of US Air Force personnel. Occup. Environ. Med 72, 560–566. [DOI] [PubMed] [Google Scholar]
  • 163.Vasterling JJ, Jacob SN, and Rasmusson A (2018). Traumatic brain injury and posttraumatic stress disorder: conceptual, diagnostic, and therapeutic considerations in the context of co-occurrence. J. Neuropsychiatry Clin. Neurosci 30, 91–100. [DOI] [PubMed] [Google Scholar]
  • 164.Amen DG, Raji CA, Willeumier K, Taylor D, Tarzwell R, Newberg A, and Henderson TA (2015). Functional neuroimaging distinguishes posttraumatic stress disorder from traumatic brain injury in focused and large community datasets. PLoS One 10, e0129659. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 165.Dijkers MP, Harrison-Felix C, and Marwitz JH (2010). The traumatic brain injury model systems: history and contributions to clinical service and research. J. Head Trauma Rehabil 25, 81–91. [DOI] [PubMed] [Google Scholar]
  • 166.Carroll CP, Cochran JA, Price JP, Guse CE, and Wang MC (2010). The AIS-2005 revision in severe traumatic brain injury: mission accomplished or problems for future research? Ann. Adv. Automot. Med 54, 233–238. [PMC free article] [PubMed] [Google Scholar]
  • 167.Kay T, Harrington DE, Adams R, Anderson T, Berrol S, Cicerone K, Dahlberg C, Gerber D, Goka R, Harley P, Hilt J, Horn L, Lehmkuhl D, and Malec J (1993). Definition of mild traumatic brain injury. J. Head Trauma Rehabil 8, 86–87. [Google Scholar]
  • 168.Mena JH, Sanchez AI, Rubiano AM, Peitzman AB, Sperry JL, Gutierrez MI, and Puyana JC (2011). Effect of the modified Glasgow Coma Scale score criteria for mild traumatic brain injury on mortality prediction: comparing classic and modified Glasgow Coma Scale score model scores of 13. J. Trauma 71, 1185–1192; discussion, 1193. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 169.Foreman BP, Caesar RR, Parks J, Madden C, Gentilello LM, Shafi S, Carlile MC, Harper CR, and Diaz-Arrastia RR (2007). Usefulness of the abbreviated injury score and the injury severity score in comparison to the Glasgow Coma Scale in predicting outcome after traumatic brain injury. J. Trauma 62, 946–950. [DOI] [PubMed] [Google Scholar]
  • 170.Gravesteijn BY, Sewalt CA, Ercole A, Akerlund C, Nelson D, Maas AIR, Menon D, Lingsma HF, and Steyerberg EW; Collaborative European NeuroTrauma Effectiveness Research for Traumatic Brain Injury Collaborators. (2020). Toward a new multi-dimensional classification of traumatic brain injury: a Collaborative European NeuroTrauma Effectiveness Research for Traumatic Brain Injury Study. J. Neurotrauma 37, 1002–1010. [DOI] [PubMed] [Google Scholar]

RESOURCES