Functional Recovery, Symptoms, and Quality of Life 1 to 5 Years After Traumatic Brain Injury

里弗米德脑震荡后症状调查表 创伤性脑损伤 格拉斯哥结局量表 医学 功能独立性测度 生活质量(医疗保健) 物理疗法 优势比 内科学 损伤严重程度评分 康复 毒物控制 伤害预防 急诊医学 精神科 护理部
作者
Lindsay D. Nelson,Nancy Temkin,Jason Barber,Benjamin L. Brett,David O. Okonkwo,Michael McCrea,Joseph T. Giacino,Yelena G. Bodien,Claudia S. Robertson,John D. Corrigan,Ramon Diaz‐Arrastia,Amy J. Markowitz,Geoffrey T. Manley
出处
期刊:JAMA network open [American Medical Association]
卷期号:6 (3): e233660-e233660 被引量:56
标识
DOI:10.1001/jamanetworkopen.2023.3660
摘要

Many level I trauma center patients experience clinical sequelae at 1 year following traumatic brain injury (TBI). Longer-term outcome data are needed to develop better monitoring and rehabilitation services.To examine functional recovery, TBI-related symptoms, and quality of life from 1 to 5 years postinjury.This cohort study enrolled trauma patients across 18 US level I trauma centers between 2014 and 2018. Eligible participants were enrolled within 24 hours of injury and followed up to 5 years postinjury. Data were analyzed January 2023.Mild TBI (mTBI), moderate-severe TBI (msTBI), or orthopedic traumatic controls (OTC).Functional independence (Glasgow Outcome Scale-Extended [GOSE] score 5 or higher), complete functional recovery (GOSE score, 8), better (ie, lower) TBI-related symptom burden (Rivermead Post Concussion Symptoms Questionnaire score of 15 or lower), and better (ie, higher) health-related quality of life (Quality of Life After Brain Injury Scale-Overall Scale score 52 or higher); mortality was analyzed as a secondary outcome.A total 1196 patients were included in analysis (mean [SD] age, 40.8 [16.9] years; 781 [65%] male; 158 [13%] Black, 965 [81%] White). mTBI and OTC groups demonstrated stable, high rates of functional independence (98% to 100% across time). While odds of independence were lower among msTBI survivors, the majority were independent at 1 year (72%), and this proportion increased over time (80% at 5 years; group × year, P = .005; independence per year: odds ratio [OR] for msTBI, 1.28; 95% CI, 1.03-1.58; OR for mTBI, 0.81; 95% CI, 0.64-1.03). For other outcomes, group differences at 1 year remained stable over time (group × year, P ≥ .44). Odds of complete functional recovery remained lower for persons with mTBI vs OTC (OR, 0.39; 95% CI, 0.28-0.56) and lower for msTBI vs mTBI (OR, 0.34; 95% CI, 0.24-0.48). Odds of better TBI-related symptom burden and quality of life were similar for both TBI subgroups and lower than OTCs. Mortality between 1 and 5 years was higher for msTBI (5.5%) than mTBI (1.5%) and OTC (0.7%; P = .02).In this cohort study, patients with previous msTBI displayed increased independence over 5 years; msTBI was also associated with increased mortality. These findings, in combination with the persistently elevated rates of unfavorable outcomes in mTBI vs controls imply that more monitoring and rehabilitation are needed for TBI.
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