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房颤患者发生重大胃肠道出血后重启抗凝治疗与结局。

Restarting anticoagulation and outcomes after major gastrointestinal bleeding in atrial fibrillation.

机构信息

Section of Cardiovascular Medicine, Department of Internal Medicine, Wake Forest University School of Medicine, Winston-Salem, North Carolina.

Department of Internal Medicine, Henry Ford Hospital/Wayne State University School of Medicine, Detroit, Michigan.

出版信息

Am J Cardiol. 2014 Feb 15;113(4):662-8. doi: 10.1016/j.amjcard.2013.10.044. Epub 2013 Nov 23.

Abstract

Data regarding the outcomes of restarting anticoagulation in patients who develop gastrointestinal bleeding (GIB) while anticoagulated are sparse. We hypothesized that restarting anticoagulation in these patients is associated with better outcomes. This is a retrospective cohort study that enrolled subjects who developed GIB while on anticoagulation from 2005 to 2010. Atrial fibrillation was defined by history and electrocardiography on presentation. GIB was defined as a decrease in hemoglobin by 2 g, visible bleeding, or positive endoscopic evaluation. Time-to-event adjusted analyses were performed to find an association of restarting warfarin and recurrent GIB, arterial thromboembolism, and mortality. Stratified analysis by duration of interruption of warfarin was also performed. Overall, 1,329 patients (mean age 76 years, women 45%) developed major GIB. Warfarin was restarted in 653 cases (49.1%). Restarting warfarin was associated with decreased thromboembolism (hazard ratio [HR] 1.18, 95% confidence interval [CI] 0.75 to 1.84, p = 0.47) [corrected] and reduced mortality (HR 0.67, 95% CI 0.56 to 0.81, p <0.0001) but not recurrent GIB (HR 1.18, 95% CI 0.94 to 1.10, p = 0.47). When the outcomes were stratified by duration of warfarin interruption, restarting warfarin after 7 days was not associated with increased risk of GIB but was associated with decreased risk of mortality and thromboembolism compared with resuming after 30 days of interruption. Decision to restart warfarin after an episode of major GIB is associated with improved survival and decreased thromboembolism without increased risk of GIB after 7 days of interruption.

摘要

关于在抗凝治疗期间发生胃肠道出血 (GIB) 的患者重新开始抗凝治疗的结果数据较为稀少。我们假设,在这些患者中重新开始抗凝治疗与更好的结果相关。这是一项回顾性队列研究,纳入了 2005 年至 2010 年间在抗凝治疗期间发生 GIB 的患者。房颤通过就诊时的病史和心电图定义。GIB 定义为血红蛋白下降 2 g,可见出血或内镜检查阳性。进行时间依赖性调整分析,以确定重新开始使用华法林与复发性 GIB、动脉血栓栓塞和死亡率之间的关联。还进行了按华法林中断时间分层的分析。总体而言,1329 例患者(平均年龄 76 岁,女性占 45%)发生了主要 GIB。653 例(49.1%)患者重新开始使用华法林。重新开始使用华法林与血栓栓塞减少相关(风险比 [HR] 1.18,95%置信区间 [CI] 0.75 至 1.84,p = 0.47)[校正]和死亡率降低相关(HR 0.67,95%CI 0.56 至 0.81,p <0.0001),但与复发性 GIB 无关(HR 1.18,95%CI 0.94 至 1.10,p = 0.47)。当按华法林中断时间对结果进行分层时,与中断 30 天后重新开始抗凝相比,中断 7 天后重新开始华法林与 GIB 风险增加无关,但与死亡率和血栓栓塞风险降低相关。在发生严重 GIB 后决定重新开始华法林治疗与生存率提高和血栓栓塞减少相关,在中断 7 天后不会增加 GIB 风险。

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