From the Department of Neurology, Chang Gung University College of Medicine, Chang Gung Memorial Hospital, Chiayi, Taiwan (M.L., Y.-L.W.); Stroke Center, University of California, Los Angeles (J.L.S., N.M.R.); Department of Neurology, Ilsan Paik Hospital, Inje University, Gimhae, South Korea (K.-S.H.); and Department of Neurology, Medical University of South Carolina, Charleston (B.O.).
Stroke. 2017 Sep;48(9):2610-2613. doi: 10.1161/STROKEAHA.117.017895. Epub 2017 Jul 12.
Optimal antiplatelet therapy after an ischemic stroke or transient ischemic attack while on aspirin is uncertain. We, therefore, conducted a systematic review and meta-analysis.
We searched PubMed (1966 to August 2016) and bibliographies of relevant published original studies to identify randomized trials and cohort studies reporting patients who were on aspirin at the time of an index ischemic stroke or transient ischemic attack and reported hazard ratio for major adverse cardiovascular events or recurrent stroke associated with a switch to or addition of another antiplatelet agent versus maintaining aspirin monotherapy. Estimates were combined using a random effects model.
Five studies with 8723 patients with ischemic stroke or transient ischemic attack were identified. Clopidogrel was used in 4 cohorts, and ticagrelor was used in 1 cohort. Pooling results showed that addition of or a switch to another antiplatelet agent, versus aspirin monotherapy, was associated with reduced risks of major adverse cardiovascular events (hazard ratio, 0.68; 95% confidence interval, 0.54-0.85) and recurrent stroke (hazard ratio, 0.70; 95% confidence interval, 0.54-0.92). Each of the strategies of addition of and switching another antiplatelet agent showed benefit versus continued aspirin monotherapy, and studies with regimen initiation in the first days after index event showed more homogenous evidence of benefit.
Among patients who experience an ischemic stroke or transient ischemic attack while on aspirin monotherapy, the addition of or a switch to another antiplatelet agent, especially in the first days after index event, is associated with fewer future vascular events, including stroke.
在服用阿司匹林的缺血性卒中和短暂性脑缺血发作后,最佳的抗血小板治疗方案仍不确定。因此,我们进行了一项系统评价和荟萃分析。
我们检索了 PubMed(1966 年至 2016 年 8 月)和相关已发表原始研究的参考文献,以确定报告在索引性缺血性卒中和短暂性脑缺血发作时正在服用阿司匹林且报告与转换或添加另一种抗血小板药物与维持阿司匹林单药治疗相比,主要不良心血管事件或复发性卒中风险的比值比的随机试验和队列研究。使用随机效应模型对估计值进行合并。
确定了 5 项包含 8723 例缺血性卒中和短暂性脑缺血发作患者的研究。4 项队列研究中使用了氯吡格雷,1 项队列研究中使用了替格瑞洛。汇总结果表明,与阿司匹林单药治疗相比,添加或转换另一种抗血小板药物与降低主要不良心血管事件(风险比,0.68;95%置信区间,0.54-0.85)和复发性卒中(风险比,0.70;95%置信区间,0.54-0.92)的风险相关。添加另一种抗血小板药物和转换另一种抗血小板药物的策略均与继续阿司匹林单药治疗相比具有获益,且起始方案在索引事件后最初几天的研究显示出更一致的获益证据。
在服用阿司匹林单药治疗的缺血性卒中和短暂性脑缺血发作患者中,添加或转换另一种抗血小板药物,尤其是在索引事件后最初几天,与未来血管事件(包括卒中等)的发生减少相关。