Abstract
OBJECTIVE:
To describe and compare the recovery and disability trajectory to one-year post-injury for younger and older adults with traumatic brain injury (TBI).
DESIGN AND METHODS:
This study was a prospective longitudinal cohort study. Individuals 21 and older with mild to moderate TBI were recruited from the Emergency Department (n=33). We measured symptoms, function (Glasgow Outcome Scale-Extended [GOS-E], Functional Status Examination [FSE]) and health-related quality of life (HRQOL) at 1 week, 1, 3, 6, and 12 months post-injury.
RESULTS:
While the total number of symptoms does not differ between younger and older adults following TBI, the specific constellation of symptoms experienced does. Older adults are more likely to experience physical symptoms such as fatigue, balance and coordination problems as well as complain of being bothered by noise. Younger adults, in contrast endorse more psychological symptoms such as anxiety. Functioning as measured by the GOS-E and FSE was lower in older adults to 1-year post-injury. Physical HRQOL was consistently poorer in the year post-injury among older adults compared to younger adults following TBI. Mental HRQOL, in contrast, was higher in older adults post-TBI at 1 year.
CONCLUSIONS:
During the first year post-TBI older adults report different symptom clusters than do younger adults post-TBI. In order to foster improved recovery and HRQOL in the older adult post-TBI, nursing management strategies should focus on balance, coordination and energy conservation.
Keywords: Brain Injuries, Aged, Outcomes Assessment
Traumatic brain injury (TBI) continues to be a leading cause of death and disability worldwide. Recently the TRACK-TBI investigators found that less than half of adults with mild TBI who present to a level I trauma center returned to pre-injury levels of daily functioning at one year.1 In 2014, US adults experienced more than 2 million incident TBIs that required treatment2, representing a 53% increase over 2006. The highest rates of TBI-related ED visits, hospitalization and death are seen in adults 75 and older.2 In the US in 2014, more than 653,400 TBIs occurred among adults 65 and older; the primary cause was fall.2 The incidence of geriatric TBI continues to increase, despite a focus on injury and fall prevention.
In studies that have examined disability following TBI in older adults, there has been evidence to suggest that survivors have increased functional dependence.3–5 While this information is important, it offers little aid to clinicians who aim to diminish the problem of TBI-related disability in older adults. Although extensive research has been conducted examining recovery trajectories in younger populations, relatively few studies have been conducted in older adults with TBI.
As we age our ability to regenerate nerve tissue and recover from a brain injury diminishes, which negatively affects outcomes in these individuals compared with younger adults. This raises the question of whether expected recovery patterns are valid in an older population. Because we do not currently have a good understanding of the natural history of recovery following TBI in older adults, predicting outcomes and providing care in the older adult TBI population remains difficult. The purpose of this study is to provide an initial exploration of the natural history of symptom experience and functional recovery following a mild-moderate TBI in older and younger adults in the first year post injury. This information may improve recovery and maximize quality of life in this cohort. This study sought to answer the following research questions: 1) What symptoms, functional impairments and HRQOL issues are experienced by older adults in the first year post-TBI? and 2) How are these similar or different than those experienced by younger adults post-TBI?
Methods
Settings and Participants
Participants with mild to moderate TBI were recruited from eligible patients seeking medical treatment at Harborview Medical Center, a regional Level I trauma center. Participants met the following inclusion criteria: 1) Arrival in the ED within 24 hours of injury, 2) primary diagnosis of TBI, 3) Initial Glasgow Coma Scale (GCS) score of 9–15. In addition, participants were excluded if they had any of the following: 1) cervical spinal cord injury, 2) lower extremity fracture, 3) prior history of TBI, stroke or dementia, 4) hospitalization within the past 6 months, 5) non-English speaking. We classified TBI subjects into two categories based on age at injury: younger adult with TBI (21–64 years) and older adults (aged 65 and older). Institutional Review Board Approval was obtained for this study.
Procedures
A trained member of the research team approached participants or their legally authorized representative (LAR) to obtain written informed consent within 24 hours of injury. Once consent was obtained, a member of the research team extracted information from the electronic medical record on demographics (age, gender, race, ethnicity), mechanism of injury, type and location of brain and other injuries and comorbid health conditions. For persons who had initial consent provided by the LAR, continuing consent to participate was sought as soon as possible. Beginning at one-week post-injury, and then again at 1, 3, 6 and 12-months post injury, researchers conducted face-to-face interviews with subjects to obtain answers to questionnaires regarding recovery following TBI. Injury data extracted from the electronic medical record was later verified with the hospital trauma registry.
Measures
Symptoms.
The TBI Symptom Checklist is a 17-item questionnaire assessing status of physical and emotional symptoms. If symptom was present prior to injury, the instrument asks what is the status now (same, worse, or better?). This questionnaire also elicits severity rating of endorsed symptoms from 1=not at all a problem for me to 4=severe problem for me.6 Only symptoms that are new or worse since the injury are counted as being endorsed.
Function.
Function was measured using the Functional Status Examination (FSE) and the Glasgow Outcome Scale-Extended (GOS-E) beginning at 3 months post-injury. The FSE evaluates change in activities of everyday life as a function of an event or illness, including TBI; covers 10 activity areas: personal care, ambulation, travel, major activity involving work or school, home management, leisure/recreation, social integration, executive functioning, financial independence and standard of living.7,8 The tool is administered via structured interview. As many participants were retired, for the purposes of this study, we scored only 9 domains. Scores on each element range from 0=no change to 3=almost all activities in this domain are no longer performed due to injury. The possible total modified FSE score then ranges from 0–27 with higher scores indicating lower function following injury.
The GOS-E is a brief descriptive scale that assesses functional outcome and is administered via interview, asking participants to report any new or worsening difficulties resulting from injury. It yields an overall score ranging from 1=“dead” to 8=“upper good recovery”.9 Scores less than 8 are indicative of some functional limitation.
Health-related Quality of Life (HRQOL).
The Short Form-12 version 2 (SF-12v2) is a 12-item questionnaire that measures HRQOL and has been validated for use in TBI patients.10 Scores range from 0–100, with higher score indicating better health status. Subscales for physical component (PCS) and mental component (MCS) are produced.11
Data Analysis
Descriptive statistics, t-test and Chi-squared analyses were used to compare demographic and injury related characteristics as appropriate between younger and older groups. Differences in symptom experiences between groups were examined using Fisher’s exact tests, while differences in function and HRQOL at each time point were compared using t-tests. An alpha of 0.05 was used.
Results
A total of thirty-three subjects were recruited over a period of 16 months to participate in the study and were retained to one year post-injury [See Supplemental Digital Content Table 1 for Sample Characteristics]. The mean age of the younger TBI cohort (n=18) was 38.9 years (range 23–63), while that of the older TBI cohort was 77.5 years (range 65–91). There was a difference in gender representation across the two cohorts, with the younger cohort having a significantly higher percentage of males than the older TBI cohort (83.3% vs. 40%). Other demographic and injury characteristics did not significantly differ across groups. Falls were the predominant cause of injury in the older TBI cohort (53.3%), while motor vehicle crash (MVC) was the most common factor in younger adults.
Symptoms
At one-week post-injury, the average total number of symptoms endorsed on the TBI symptom checklist by younger and older adults following TBI was similar (6.7 and 6.4 respectively; See Table 1). While the trend was towards a more rapid improvement in the average number of symptoms endorsed over time in the younger TBI cohort compared to older cohort (e.g. 4.7 vs. 5.7 symptoms endorsed at 1-month post-injury; 3.3 vs. 6.0 at 6 months), this difference was not statistically significant. By one year post-injury both groups continued to report ongoing concerns, with younger adults endorsing 3.6 symptoms on average and older adults reporting an average of 3.9 symptoms (See Table 1).
Table 1.
Time since injury | 1 week | 1 month | 3 months | 6 months | 1 year | |||||
---|---|---|---|---|---|---|---|---|---|---|
Symptom | Younger TBI n=18 |
Older TBI n=15 |
Younger TBI | Older TBI | Younger TBI | Older TBI | Younger TBI | Older TBI | Younger TBI | Older TBI |
Headaches | 11(61.1) | 5(33.3) | 7(38.9) | 4(26.7) | 4(22.2) | 4(26.7) | 3(16.7) | 3(20.0) | 6(33.3) | 3(20.0) |
Fatigue | 9(50.0) | 10(66.7) | 8(44.4) | 10(66.7) | 9(50.0) | 9(60.0) | 4(22.2) | 10(66.7)* | 5(27.8) | 6(40.0) |
Dizziness | 9(50.0) | 9(60.0) | 9(50.0) | 8(53.3) | 4(22.2) | 4(26.7) | 3(16.7) | 6(40.0) | 5(27.8) | 3(20.0) |
Blurred Vision | 8(44.4) | 6(40.0) | 5(27.8) | 5(33.3) | 4(22.2) | 3(20.0) | 4(22.2) | 3(20.0) | 5(27.8) | 4(26.7) |
Trouble Concentrating | 8(44.4) | 6(40.0) | 7(38.9) | 6(40.0) | 4(22.2) | 4(26.7) | 3(16.7) | 4(26.7) | 3(16.7) | 3(20.0) |
Bothered by Noise | 5(27.8) | 4(26.7) | 5(27.8) | 6(40.0) | 1(5.6) | 7(46.7)* | 1(5.6) | 6(40.0)* | 2(11.1) | 5(33.3) |
Bothered by Light | 7(38.9) | 5(33.3) | 3(16.7) | 3(20.0) | 4(22.2) | 3(20.0) | 3(16.7) | 4(26.7) | 4(22.2) | 3(20.0) |
Irritability, Lack of Patience | 10(55.6) | 7(46.7) | 5(27.8) | 5(33.3) | 10(55.6) | 6(40.0) | 8(44.4) | 6(40.0) | 4(22.2) | 3(20.0) |
Lose Temper Easily | 6(33.3) | 1(6.7) | 6(33.3) | 1(6.7) | 6(33.3) | 2(13.3) | 6(33.3) | 3(20.0) | 3(16.7) | 2(13.3) |
Memory Difficulty | 7(38.9) | 7(46.7) | 6(33.3) | 7(46.7) | 7(38.9) | 7(46.7) | 6(33.3) | 7(46.7) | 7(38.9) | 4(26.7) |
Anxiety | 8(44.4) | 2(13.3) | 7(38.9) | 1(6.7)* | 5(27.8) | 4(26.7) | 5(27.8) | 5(33.3) | 6(33.3) | 2(13.3) |
Trouble with Sleep | 8(44.4) | 8(53.3) | 4(22.2) | 5(33.3) | 2(11.1) | 6(40.0) | 5(27.8) | 4(26.7) | 4(22.2) | 3(20.0) |
Balance | 11(61.1) | 11(73.3) | 5(27.8) | 10(66.7)* | 3(16.7) | 8(53.3)* | 3(16.7) | 10(66.7)** | 4(22.2) | 6(40.0) |
Sexual Difficulties | 1(5.6) | 2(13.3) | 2(11.1) | 1(6.7) | 0(0.0) | 2(13.3) | 0(0.0) | 2(13.3) | 0(0.0) | 1(6.7) |
Coordination | 1(5.6) | 4(26.7) | 1(5.6) | 6(40.0)* | 3(16.7) | 6(40.0) | 0(0.0) | 7(46.7)** | 2(11.1) | 2(14.3) |
Taste | 8(44.4) | 5(33.3) | 3(16.7) | 4(26.7) | 2(11.1) | 5(33.3) | 2(11.1) | 6(40.0) | 2(11.1) | 4(26.7) |
Smell | 4(22.2) | 4(26.7) | 2(11.1) | 4(26.7) | 2(11.1) | 4(26.7) | 3(16.7) | 4(26.7) | 3(16.7) | 4(26.7) |
Total # Symptoms endorsed Mean(SD) | 6.7(4.8) | 6.4(5.1) | 4.7(4.4) | 5.7(4.8) | 3.9(4.1) | 5.6(4.4) | 3.3(4.0) | 6.0(4.7) | 3.6(4.7) | 3.9(5.3) |
p<0.05;
p<0.01
In examining specific symptoms endorsed by the groups across the recovery trajectory, there were differences in the most common symptoms by younger and older TBI cohorts (See Table 1). For example, at one week post-injury the top three most common symptoms in younger adults were balance issues (61.1%), headache (61.1%) and irritability or lack of patience (55.6%); while older adults reported balance issues (73.3%), fatigue (66.7%) and dizziness (60%). At 1-year post-injury, balance and fatigue (40% each) remain tied as the most reported symptom in older adult TBI cohort, with being bothered by noise (33.3%) third most common. In contrast, younger adults report memory difficulty (38.9%) as the most prevalent symptom following TBI, with headache and anxiety tied for second most endorsed (33% each).
Further, there were differences in prevalence of individual symptom experienced between groups across time (Table 1). Specifically, older adults were significantly more likely to endorse balance (1, 3, 6 months) and coordination (1, 6 months) issues, being bothered by noise (3, 6 months), and experiencing fatigue (6 months) than the younger TBI cohort. In contrast, younger adults with TBI were significantly more likely to report anxiety at one month post-injury (Table 1). In examining severity of symptom endorsement, older adults had significantly higher symptom severity scores across several issues and time points. Specifically, on average, older adults reported significantly higher symptom severity scores related to fatigue (1, 6 months), balance (1, 3, 6 months), coordination (1 month), and taste (6 months) compared to younger adults following TBI (See Supplemental Digital Content Table 2).
Functional Status and HRQOL
Functional health status of older adults following mild-moderate TBI is significantly worse compared to younger adults across all time points as assessed by both the GOS-E and the FSE (Table 2). On the GOS-E, the average score on GOS-E is 6.9 (SD 1.4) indicating lower good recovery at 3 months post-injury. In contrast, older adults following TBI have an average of 5.1 (SD 2.3) indicating lower moderate disability. This trend is consistent across the 6- and 12-month assessments. Similarly, on the FSE, the older adult TBI cohort has significantly higher scores on the FSE at the 3, 6 and 12-month assessments compared to the younger cohort, indicating higher disability following injury (Table 2).
Table 2.
1 week | 1 month | 3 months | 6 months | 1 year | ||||||
---|---|---|---|---|---|---|---|---|---|---|
Younger TBI | Older TBI | Younger TBI | Older TBI | Younger TBI | Older TBI | Younger TBI | Older TBI | Younger TBI | Older TBI | |
Functional Status | ||||||||||
GOS-E | 6.9 (1.4) | 5.1 (2.3)* | 7.3 (1.4) | 5.2 (2.4)* | 7.2 (1.5) | 4.6 (2.1)** | ||||
FSE | 4.4 (6.0) | 11.0 (8.7)* | 3.4 (5.6) | 10.3 (8.6)* | 3.5 (5.8) | 11.8 (7.0)** | ||||
Health Related Quality of Life | ||||||||||
SF-12v2 PCS | 43.6 (12.2) | 34.0 (15.2)** | 41.7 (10.1) | 32.8 (9.3)** | 50.0 (14.2) | 40.5 (10.6)* | 51.1 (9.2) | 36.3 (10.9)** | 50.5 (11.7) | 33.3 (9.3)** |
SF-12v2 MCS | 47.6 (10.1) | 47.1 (15.1) | 52.6 (7.6) | 46.6 (12.3) | 48.8 (6.5) | 51.8 (9.7) | 49.9 (6.5) | 55.0 (7.2) | 49.1 (7.0) | 56.0 (9.3)* |
p<0.05,
p<0.01
There were significant differences between the two groups on physical HRQOL. Older adults with TBI reported consistently poorer overall physical HRQOL from 1 week to 1 year post-injury compared to the younger TBI cohort (Table 2). No significant differences in the mental HRQOL (MCS) scores between younger and older TBI cohorts were found from 1 week to 6 months post-injury (Table 2). However, at 1 year post-injury the older adult TBI cohort reported significantly higher average mental HRQOL (56.0) compared to the younger adult TBI cohort (49.1).
Discussion
In this study, we sought to explore the symptom experience as well as function and HRQOL in persons 65 and older in the first year post-mild-moderate TBI to assess if the recovery pattern is similar or different to those experienced by younger adults who presented to the same facility for treatment. We note that while the total number of symptoms experienced by the two groups did not differ across time, the specific constellation of symptoms experienced were different across the year post-injury. Similar to previous studies, fatigue was commonly experienced across TBI groups.1,12,13 Older adults following TBI were less likely to report headache pain, and more likely to have balance and coordination issues in the year post-injury. This is an important consideration for both rehabilitation as well as prevention of future injury. Requesting or providing the older individual with referrals to evidence-based programs to address balance and coordination is important as the primary cause of injury in older adults is falls. Further, a history of prior fall, the cause of injury in the majority of this sample, as well as balance and coordination issues place an older adult at increased risk of repeat fall and fall-related injury. Such programs include: Enhance Fitness, Tai Ji Quan: Moving for Better Balance™, and the Otago Exercise Program.14,15 The National Council on Aging provides a website that can assist individuals in finding a program in their area.16 Further, as balance and coordination are important for many ADLs/IADLs such as walking, transfers, and housekeeping, having ongoing mobility disability could be responsible for differences seen in functional measures across groups.
Our findings related to overall outcome as measured by GOSE are in line with the majority of other studies which have found that older adults have poorer overall outcome compared to younger adults following TBI.17,18 However, a recent study involving older patients from Level 1 Trauma Centers in the Netherlands reported that the majority of individuals had GOSE scores of upper good recovery at 1 year following mild TBI.19 These differences in outcome may be related to overall severity of injury in the two samples, as the mean ISS score in our sample was twice as high (17.3 vs. 8.2).19
Older adults following mild-moderate TBI had poorer physical HRQOL across all time points measured to one-year post-injury compared to younger adults. This is in contrast to prior work in severe TBI patients which found similar scores in SF-12 PCS at 3 months, but noted a trajectory of improvement over time to 12 months post-injury.18 In the current study, PCS scores were relatively stable without overall improvement. It is unclear at this time what factors other than higher overall severity of injuries may have contributed to this finding. Our findings related to overall scores of the mental component of HRQOL to six months post-injury was similar to that reported by Haller and colleagues18 following severe TBI. In contrast to that study which found that the mental component remained stable at one year in both younger and older groups18, we found that in our sample of individuals with mild TBI, the mental component of the SF-12v2 was significantly better than that of the younger cohort. This was despite higher disability and lower physical HRQOL scores in the present study, and may reflect resilience20,21, differing expectations regarding recovery in the context of aging22, ability to integrate the sequelae of injury given stage of life course23,24, and potentially exacerbation of pre-existing anxiety or depression which are more common in younger than older adults25.
Study Limitations
There are several limitations to the present study. The sample was small, and did not enable us to control for covariates like sex in the analysis. While we were not surprised at the larger percentage of women in the older adult sample given aging demographics, we were not able to address if differences seen in symptoms and function were related to age-related differences alone or a combination of age and sex. Further exploration is warranted in a larger sample that can adequately adjust for demographic covariates. Another limitation is that the results presented do not include information on treatment/management and response to inform future intervention design and nursing care. Further work, particularly integrating mixed-methods analysis to understand the symptom experience, management choices and response would be useful to aid future precision health management. Lastly, this study recruited from a single facility and may not reflect the broader older adult population. However, the trauma center serves a wide catchment area including multiple states, and is the county hospital increasing confidence in sample diversity and representation.
Conclusion
During the first year post-TBI older adults report different symptom clusters than do younger adults post-TBI. In order to foster improved recovery and HRQOL in the older adult post-TBI, nursing management should focus on balance, coordination and energy conservation. Findings from this study extend our knowledge of the natural history of recovery of older adults with a mild-moderate TBI.
Supplementary Material
Source of Funding:
Supported by the National Institutes of Health KL2RR025015 and a John A. Hartford Foundation Claire M. Fagin Fellowship 06-202, both to HJT.
Footnotes
Conflict of Interests: None.
References
- 1.Nelson LD, Temkin NR, Dikmen S, et al. 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 Neurology. 2019. doi: 10.1001/jamaneurol.2019.1313. [Epub ahead of print] [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Centers for Disease Control and Prevention. Surveillance Report of Traumatic Brain Injury-related Emergency Department Visits, Hospitalizations, and Deaths—United States, 2014. Atlanta, GA: Centers for Disease Control and Prevention; 2019. [Google Scholar]
- 3.Miller JD, Pentland B. Head injuries in elderly patients. Neurosurg Rev. 1989;12 Suppl 1:441–445. [DOI] [PubMed] [Google Scholar]
- 4.Lecours A, Sirois MJ, Ouellet MC, Boivin K, Simard JF. Long-term functional outcome of older adults after a traumatic brain injury. J Head Trauma Rehab. 2012;27(6):379–390. [DOI] [PubMed] [Google Scholar]
- 5.Mosenthal AC, Livingston DH, Lavery RF, et al. The effect of age on functional outcome in mild traumatic brain injury: 6-month report of a prospective multicenter trial. J Trauma. 2004;56(5):1042–1048. [DOI] [PubMed] [Google Scholar]
- 6.McLean A Jr., Dikmen S, Temkin N, Wyler AR, Gale JL. Psychosocial functioning at 1 month after head injury. Neurosurgery. 1984;14(4):393–399. [DOI] [PubMed] [Google Scholar]
- 7.Dikmen S, Machamer J, Miller B, Doctor J, Temkin N. Functional status examination: a new instrument for assessing outcome in traumatic brain injury. J Neurotrauma. 2001;18(2):127–140. [DOI] [PubMed] [Google Scholar]
- 8.Hudak AM, Caesar RR, Frol AB, et al. Functional outcome scales in traumatic brain injury: a comparison of the glasgow outcome scale (extended) and the functional status examination. J Neurotrauma. 2005;22(11):1319–1326. [DOI] [PubMed] [Google Scholar]
- 9.Wilson JT, Pettigrew LE, Teasdale GM. Structured interviews for the Glasgow Outcome Scale and the extended Glasgow Outcome Scale: guidelines for their use. J Neurotrauma. 1998;15(8):573–585. [DOI] [PubMed] [Google Scholar]
- 10.Findler M, Cantor J, Haddad L, Gordon W, Ashman T. The reliability and validity of the SF-36 health survey questionnaire for use with individuals with traumatic brain injury. Brain Inj. 2001;15(8):715–723. [DOI] [PubMed] [Google Scholar]
- 11.Ware J Jr., Kosinski M, Keller SD. A 12-Item Short-Form Health Survey: construction of scales and preliminary tests of reliability and validity. Med Care. 1996;34(3):220–233. [DOI] [PubMed] [Google Scholar]
- 12.van der Naalt J, Timmerman ME, de Koning ME, et al. Early predictors of outcome after mild traumatic brain injury (UPFRONT): an observational cohort study. The Lancet Neurology. 2017;16(7):532–540. [DOI] [PubMed] [Google Scholar]
- 13.Dikmen S, Machamer J, Fann JR, Temkin NR. Rates of symptom reporting following traumatic brain injury. J Int Neuropsych Soc: JINS. 2010;16(3):401–411. [DOI] [PubMed] [Google Scholar]
- 14.Stevens JA, Burns E. A CDC compendium of effective fall interventions: What works for community-dwelling older adults. Atlanta, GA: Division of Unintentional Injury Prevention; National Center for Injury Prevention and Control; Centers for Disease Control and Prevention;2015. [Google Scholar]
- 15.National Council on Aging. Evidence-based fall prevention programs. https://www.ncoa.org/healthy-aging/falls-prevention/falls-prevention-programs-for-older-adults-2/. Accessed 9/11/2019, 2019.
- 16.National Council on Aging. Find an Evidence-Based Falls Prevention Program in Your Area. https://www.ncoa.org/healthy-aging/falls-prevention/falls-prevention-awareness-day/how-to-get-involved/find-evidence-based-falls-program-area/. Accessed 12/5/2019, 2019.
- 17.Rothweiler B, Temkin NR, Dikmen SS. Aging effect on psychosocial outcome in traumatic brain injury. Arch Phys Med Rehab. 1998;79(8):881–887. [DOI] [PubMed] [Google Scholar]
- 18.Haller CS, Delhumeau C, De Pretto M, et al. Trajectory of disability and quality-of-life in non-geriatric and geriatric survivors after severe traumatic brain injury. Brain Inj. 2017;31(3):319–328. [DOI] [PubMed] [Google Scholar]
- 19.Abdulle AE, de Koning ME, van der Horn HJ, et al. Early Predictors for Long-Term Functional Outcome After Mild Traumatic Brain Injury in Frail Elderly Patients. J Head Trauma Rehab. 2018;33(6):E59–e67. [DOI] [PubMed] [Google Scholar]
- 20.Gijzel SMW, Whitson HE, van de Leemput IA, et al. Resilience in Clinical Care: Getting a Grip on the Recovery Potential of Older Adults. JAGS. 2019. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.Rapport LJ, Wong CG, Hanks RA. Resilience and well-being after traumatic brain injury. Disaband Rehab. 2019:1–7. [DOI] [PubMed] [Google Scholar]
- 22.Layman DE, Dijkers MP, Ashman TA. Exploring the impact of traumatic brain injury on the older couple: ‘yes, but how much of it is age, I can’t tell you …’. Brain Inj. 2005;19(11):909–923. [DOI] [PubMed] [Google Scholar]
- 23.Hildon Z, Montgomery SM, Blane D, Wiggins RD, Netuveli G. Examining resilience of quality of life in the face of health-related and psychosocial adversity at older ages: what is “right” about the way we age? The Gerontologist. 2010;50(1):36–47. [DOI] [PubMed] [Google Scholar]
- 24.Seery MD, Holman EA, Silver RC. Whatever does not kill us: cumulative lifetime adversity, vulnerability, and resilience. J Personality and Social Psych. 2010;99(6):1025–1041. [DOI] [PubMed] [Google Scholar]
- 25.Hasin DS, Goodwin RD, Stinson FS, Grant BF. Epidemiology of major depressive disorder: results from the National Epidemiologic Survey on Alcoholism and Related Conditions. Arch Gen Psychiatry. 2005;62(10):1097–1106. [DOI] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.