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首页> 外文期刊>Journal of neurotrauma >Divergent Six Month Functional Recovery Trajectories and Predictors after Traumatic Brain Injury: Novel Insights from the Citicoline Brain Injury Treatment Trial Study
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Divergent Six Month Functional Recovery Trajectories and Predictors after Traumatic Brain Injury: Novel Insights from the Citicoline Brain Injury Treatment Trial Study

机译:出现六个月功能恢复轨迹和预测因子创伤后损伤:来自Citicoline脑损伤治疗试验研究的小说洞察

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摘要

Cross-sectional approaches to outcome assessment may not adequately capture heterogeneity in recovery after traumatic brain injury (TBI). Using latent class mixed models (LCMM), a data-driven analytic that identifies groups of patients with similar trajectories, we identified distinct 6 month functional recovery trajectories in a large cohort (n = 1046) of adults 18-70 years of age with complicated mild to severe TBI who participated in the Citicoline Brain Injury Treatment Trial (COBRIT). We used multinomial logistic fixed effect models and backward elimination, forward selection, and forward stepwise selection with several stopping rules to explore baseline predictors of functional recovery trajectory. Based on statistical and clinical considerations, the seven-class model was deemed superior. Visualization of these seven functional recovery trajectories revealed that each trajectory class started at one of three recovery levels at 1 month, which, for ease of reference we labeled groups A-C: Group A, good recovery (two classes; A1 and A2); Group B, moderate disability (two classes; B1 and B2); and Group C, severe disability (three classes; C1, C2, and C3). By 6 months, these three groups experienced dramatically divergent trajectories. Group A experienced stable good recovery (A1, n = 115) or dramatic decline (A2, n = 4); Group B experienced rapid complete recovery (B1, n = 71) or gradual recovery (B2, n = 742); Group C experienced dramatic rapid recovery (C1, n = 12), no recovery (C2, n = 91), or death (C3, n = 11). Trajectory class membership was not predicted by citicoline treatment (p = 0.57). The models identified demographic, pre-injury, and injury-related predictors of functional recovery trajectory, including: age, race, education, pre-injury employment, pre-injury diabetes, pre-injury psychiatric disorder, site, Glasgow Coma Scale (GCS) score, post-traumatic amnesia, TBI mechanism, major extracranial injury, hemoglobin, and acute computed tomographic (CT) findings. GCS was the most consistently selected predictor across all models. All models also selected at least one demographic or pre-injury medical predictor. LCMM successfully identified dramatically divergent, clinically meaningful 6 month recovery trajectories with utility to inform clinical trial design.
机译:结果评估的横截面方法可能在创伤性脑损伤(TBI)后可能无法充分捕获恢复中的异质性。使用潜在的混合模型(LCMM),一种数据驱动的分析,其识别患有类似轨迹的患者组,我们在18-70岁的大型队列(n = 1046)中鉴定了不同的6个月功能恢复轨迹,其成人的大队列(n = 1046)复杂轻度到严重的TBI参与Citicoline脑损伤治疗试验(Cobrit)。我们使用多型物流固定效果模型和向后消除,前进选择,并用几个停止规则向前选择,以探索功能恢复轨迹的基线预测因子。基于统计和临床考虑,七级模型被视为优越。可视化这七个功能恢复轨迹的可视化透露,每个轨迹类在1个月的三个恢复水平之一开始,这对于易于参考,我们标记为A-C组:A组,恢复良好(两个类; A1和A2); B组,中度残疾(两类; B1和B2);和C组,严重残疾(三类; C1,C2和C3)。到6个月,这三个组剧烈地发散了轨迹。组经验丰富的良好恢复(A1,n = 115)或戏剧性下降(A2,n = 4); B组经历了快速完全恢复(B1,N = 71)或逐渐恢复(B2,N = 742); C组经历了显着的快速恢复(C1,N = 12),无恢复(C2,N = 91)或死亡(C3,N = 11)。 Citicoline治疗未预测轨迹课程成员资格(P = 0.57)。该模型确定了功能恢复轨迹的人口统计,伤害和与伤害相关的预测因子,包括:年龄,种族,教育,伤前就业,损伤前糖尿病,伤害前精神疾病,网站,格拉斯哥昏迷(GCS )评分,创伤后的胃癌,TBI机制,主要颅外损伤,血红蛋白和急性计算的断层摄影(CT)调查结果。 GCS是所有型号中最常见的选择预测器。所有型号也至少选择了至少一个人口或伤后医疗预测因子。 LCMM已成功地识别出不同的临床有意义的6个月恢复轨迹,以便提供临床试验设计。

著录项

  • 来源
    《Journal of neurotrauma》 |2019年第17期|共12页
  • 作者单位

    Univ Calif San Franscisco Memory &

    Aging Ctr Dept Neurol San Francisco CA USA;

    Univ Calif San Francisco Deparment Epidemiol &

    Biostat San Francisco CA 94121 USA;

    Univ Calif San Francisco Dept Neurol Surg San Francisco CA 94121 USA;

    Univ Calif San Francisco Deparment Epidemiol &

    Biostat San Francisco CA 94121 USA;

    Univ Calif San Francisco Deparment Epidemiol &

    Biostat San Francisco CA 94121 USA;

    Harvard Med Sch Dept Phys Med &

    Rehabil Boston MA 02115 USA;

    Univ Calif San Francisco Dept Neurol Surg San Francisco CA 94121 USA;

    Mt Sinai Sch Med Dept Populat Hlth Sci &

    Policy New York NY USA;

    Eunice Kennedy Shriver Natl Inst Child Hlth &

    Hum Traumat Brain Injury &

    Stroke Rehabil Program;

    Univ Alabama Birmingham Dept Phys Med &

    Rehabil Birmingham AL USA;

    Columbia Univ Med Ctr Dept Biostat &

    Epidemiol New York NY USA;

    Columbia Univ Dept Epidemiol Med Ctr New York NY USA;

    Penn State Univ Milton S Hershey Med Ctr Dept Neurosurg Hershey PA 17033 USA;

    Thomas Jefferson Univ Dept Neurosurg Div Neurotrauma &

    Crit Care Jefferson Med Coll;

    Univ Maryland Sch Med Dept Neurosurg Baltimore MD 21201 USA;

    Thomas Jefferson Univ Moss Rehabil Res Inst Dept Rehabil Med Sidney Kimmel Med Coll Elkins Pk;

    NYU Dept Rehabil Med Div Psychol Rusk Inst Rehabil New York NY USA;

    Univ Penn Dept Neurol Perelman Sch Med Penn Presbyterian Med Ctr Philadelphia PA 19104 USA;

    Virginia Commonwealth Univ Sch Med Dept Anat &

    Neurobiol Ctr Rehabil Sci &

    Engn Richmond VA USA;

    Univ Washington Dept Neurol Surg Sch Publ Hlth Seattle WA 98195 USA;

    Lincoln Hosp Dept Surg Bronx NY USA;

    Univ Washington Dept Rehabil Med Seattle WA 98195 USA;

    Univ Pittsburgh Dept Neurol Surg Med Ctr Pittsburgh PA 15260 USA;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 头部及神经外科学;
  • 关键词

    functional outcome; predictors; TBI; trajectory;

    机译:功能结果;预测因子;TBI;轨迹;

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