Albrecht Jennifer S, Liu Xinggang, Baumgarten Mona, Langenberg Patricia, Rattinger Gail B, Smith Gordon S, Gambert Steven R, Gottlieb Stephen S, Zuckerman Ilene H
Department of Pharmaceutical Health Services Research, University of Maryland School of Pharmacy, Baltimore.
Department of Epidemiology and Public Health, University of Maryland School of Medicine, Baltimore.
JAMA Intern Med. 2014 Aug;174(8):1244-51. doi: 10.1001/jamainternmed.2014.2534.
The increased risk of hemorrhage associated with anticoagulant therapy following traumatic brain injury creates a serious dilemma for medical management of older patients: Should anticoagulant therapy be resumed after traumatic brain injury, and if so, when?
To estimate the risk of thrombotic and hemorrhagic events associated with warfarin therapy resumption following traumatic brain injury.
DESIGN, SETTING, AND PARTICIPANTS: Retrospective analysis of administrative claims data for Medicare beneficiaries aged at least 65 years hospitalized for traumatic brain injury during 2006 through 2009 who received warfarin in the month prior to injury (n = 10,782).
Warfarin use in each 30-day period following discharge after hospitalization for traumatic brain injury.
The primary outcomes were hemorrhagic and thrombotic events following discharge after hospitalization for traumatic brain injury. Hemorrhagic events were defined on inpatient claims using International Classification of Diseases, Ninth Revision, Clinical Modification codes and included hemorrhagic stroke, upper gastrointestinal bleeding, adrenal hemorrhage, and other hemorrhage. Thrombotic events included ischemic stroke, pulmonary embolism, deep venous thrombosis, and myocardial infarction. A composite of hemorrhagic or ischemic stroke was a secondary outcome.
Medicare beneficiaries with traumatic brain injury were predominantly female (64%) and white (92%), with a mean (SD) age of 81.3 (7.3) years, and 82% had atrial fibrillation. Over the 12 months following hospital discharge, 55% received warfarin during 1 or more 30-day periods. We examined the lagged effect of warfarin use on outcomes in the following period. Warfarin use in the prior period was associated with decreased risk of thrombotic events (relative risk [RR], 0.77 [95% CI, 0.67-0.88]) and increased risk of hemorrhagic events (RR, 1.51 [95% CI, 1.29-1.78]). Warfarin use in the prior period was associated with decreased risk of hemorrhagic or ischemic stroke (RR, 0.83 [95% CI, 0.72-0.96]).
Results from this study suggest that despite increased risk of hemorrhage, there is a net benefit for most patients receiving anticoagulation therapy, in terms of a reduction in risk of stroke, from warfarin therapy resumption following discharge after hospitalization for traumatic brain injury.
创伤性脑损伤后抗凝治疗相关的出血风险增加,给老年患者的医疗管理带来了严重困境:创伤性脑损伤后是否应恢复抗凝治疗?如果是,何时恢复?
评估创伤性脑损伤后恢复华法林治疗相关的血栓形成和出血事件风险。
设计、设置和参与者:对2006年至2009年因创伤性脑损伤住院的至少65岁医疗保险受益人的行政索赔数据进行回顾性分析,这些患者在受伤前一个月接受了华法林治疗(n = 10,782)。
创伤性脑损伤住院出院后每个30天期间使用华法林。
主要结局是创伤性脑损伤住院出院后的出血和血栓形成事件。出血事件根据国际疾病分类第九版临床修订本代码在住院索赔中定义,包括出血性中风、上消化道出血、肾上腺出血和其他出血。血栓形成事件包括缺血性中风、肺栓塞、深静脉血栓形成和心肌梗死。出血性或缺血性中风的复合情况是次要结局。
创伤性脑损伤的医疗保险受益人主要为女性(64%)和白人(92%),平均(标准差)年龄为81.3(7.3)岁,82%患有房颤。出院后的12个月内,55%的患者在1个或更多30天期间接受了华法林治疗。我们研究了华法林使用对下一时期结局的滞后效应。前期使用华法林与血栓形成事件风险降低相关(相对风险[RR],0.77[95%CI,0.67 - 0.88]),与出血事件风险增加相关(RR,1.51[95%CI,1.29 - 1.78])。前期使用华法林与出血性或缺血性中风风险降低相关(RR,0.83[95%CI,0.72 - 0.96])。
本研究结果表明,尽管出血风险增加,但对于大多数接受抗凝治疗的患者而言,创伤性脑损伤住院出院后恢复华法林治疗在降低中风风险方面有净获益。