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  • GCS Does Not Predict Cognitive Outcome 30 Years After Severe Traumatic Brain Injury

    Final Number:
    306

    Authors:
    Molly E. Hubbard MD; Abdullah Bin Zahid MD; Gabrielle Meyer DO; Kathleen Vonderhaar MD; David Y. Balser; David Darrow; Anne Kleeberger; Drake Burri; Vikalpa Dammavalam; Shivani Venkatesh; David Tupper PhD; Sarah B. Rockswold MD; Thomas A. Bergman MD; Gaylan L. Rockswold MD, PhD; Uzma Samadani MD

    Study Design:
    Other

    Subject Category:

    Meeting: Congress of Neurological Surgeons 2017 Annual Meeting

    Introduction: Traumatic brain injury (TBI) is a leading cause of morbidity and mortality in the US. The effects of TBI on quality of life may not become apparent for years after the injury. There are conflicting reports in the literature regarding long term outcomes. Physicians are often asked to predict long term functional and cognitive outcomes, with limited data available.

    Methods: Patients with severe TBI (GCS =9) who previously participated in a clinical trial during the 1980s were followed up with and compared to healthy controls without history of TBI. A health questionnaire, sports concussion assessment tool version 3 (SCAT3) and the Telephone Interview for Cognitive Status-modified (TICS-m) were completed over the phone and compared with controls using t-test. GCS at admission and 12-month GRS were used to predict to TICS-M at 30 years using linear regression.

    Results: 45 of the initial 168 subjects were confirmed alive, and 37 (13 females; mean age: 52.43 years S.D. 10.7) consented. Controls(n=58; 23 females; mean age = 54 years, S.D. 11.5) had lower symptom severity score (6.7 S.D. 12.6 versus 20.6 S.D. 25.3; p=0.005), lower total number of symptoms (3.4 S.D. 4.7 versus 7.12 S.D. 6.5; p=0.006), higher standardized assessment of concussion score (25.6 S.D. 2.8 versus 21.2 S.D. 6.9; p=0.001), and lower corrected MPAI-4 (22.3 S.D. 17.0 versus 43.7 S.D. 12.8; p<0.001). GCS at admission did not predict cognitive status at 30-years assessed using TICS-M (p=0.345). The Glasgow Outcome Scale score at 12-months was correlated to TICS-M at 30 years (R=0.548, p<0.001); each point decrease in GOS decreasing the score at TICS-M by 5.6 points.

    Conclusions: Remote history of TBI disrupts the lives of survivors long after injury. Admission GCS does not predict cognitive status 30 years after TBI. The GOS at 12-months predicted the cognitive status assessed using TICS-M score at 30 years.

    Patient Care: Better understanding of outcomes after severe TBI will help guide discussions with families, focus treatments, and develop trials to treat TBI in the future.

    Learning Objectives: 1. Reporting the long term effects of neurotrauma 2. Understanding the utility of short term outcomes for long term prediction 3. Comparing cognition in controls to patients with TBI

    References: Rockswold, G. L., Ford, S. E., Anderson, D. C., Bergman, T. a & Sherman, R. E. Results of a prospective randomized trial for treatment of severely brain-injured patients with hyperbaric oxygen. J. Neurosurg. 76, 929–934 (1992). World Health Organization (2006). Neurological Disorders: Public Health Challenges. Geneva, Switzerland. Ponsford, J. Factors contributing to outcome following traumatic brain injury. NeuroRehabilitation 32, 803–815 (2013). Sariaslan A, Sharp DJ, D’Onofrio BM, Larsson H, Fazel S: 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 Medicine 13:e1002103, 2016 Dahm, J. & Ponsford, J. Predictors of global functioning and employment 10 years following traumatic brain injury compared with orthopaedic injury traumatic brain injury compared with orthopaedic injury. 9052, (2015). Green, R. E. et al. Examining Moderators of Cognitive Recovery Trajectories After Moderate to Severe Traumatic Brain Injury. Arch. Phys. Med. Rehabil. 89, S16–S24 (2008). Dan Hoofien, Assaf Gilboa, Eli Vaki. Traumatic brain injury (TBI) 10-20 years later: a comprehensive outcome study of psychiatric symptomatology, cognitive abilities and psychosocial functioning. Brain Inj. 15, 189–209 (2001).

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