Efficacy of Short-term Dual Antiplatelet Therapy after Implantation of Second-generation Drug-eluting Stents: A Meta-analysis and Systematic Review.

Peisen Huang, Yuan Yu, Xikun Han, Yuejin Yang
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Abstract

Objective The benefit of short-term dual antiplatelet therapy (DAPT) following second-generation drug-eluting stents implantation has not been systematically evaluated. To bridge the knowledge gap, we did a meta-analysis to assess the efficacy of ≤6 months versus ≥12 months DAPT among patients with second-generation drug-eluting stents.Methods We searched online databases and identified randomized controlled trials that assess the clinical impact of short-term DAPT (≤6 months) published before March 3, 2016. The efficacy endpoints included the incidence of all-cause death, myocardial infarction, cerebrovascular accidents, and definite or probable stent thrombosis. Safety endpoint defined as major bleeding was also evaluated and discussed.Results We included 5 trials that randomized 9473 participants (49.8%, short-term DAPT duration vs. 50.2%, standard duration). A total of 9445 (99.7%) patients reported the efficacy endpoints, and the safety endpoint was available from 4 studies (n=8457). There was no significant difference in efficacy endpoints between short-term and standard DAPT duration (≥12 months) [risk ratio (RR) 0.96; 95% confidence intervals (CI), 0.80-1.15]. Short-term DAPT duration did not significantly increase the individual risk of all-cause death, myocardial infarction, cerebrovascular accidents, or definite or probable stent thrombosis. Although short-term DAPT obviously reduced risk of major bleeding compared with standard DAPT (RR 0.53; 95% CI, 0.29-0.96), significant publication bias was found when accessing the safety endpoint of the 4 studies (Egger's test, P=0.009).Conclusions The efficacy of short-term DAPT was comparable with that of standard duration DAPT. DAPT less than 6 months may be appropriate for patients receiving second-generation drug-eluting stents implantation.

第二代药物洗脱支架植入后短期双重抗血小板治疗的疗效:荟萃分析和系统评价。
目的对第二代药物洗脱支架植入术后短期双重抗血小板治疗(DAPT)的疗效尚未进行系统评价。为了弥合知识差距,我们进行了一项荟萃分析,以评估第二代药物洗脱支架患者≤6个月与≥12个月DAPT的疗效。方法检索在线数据库,选取2016年3月3日前发表的评估短期DAPT(≤6个月)临床影响的随机对照试验。疗效终点包括全因死亡、心肌梗死、脑血管意外和明确或可能的支架血栓形成的发生率。安全终点定义为大出血也进行了评估和讨论。我们纳入了5项试验,随机纳入9473名受试者(短期DAPT持续时间为49.8%,标准持续时间为50.2%)。共有9445例(99.7%)患者报告了疗效终点,安全终点来自4项研究(n=8457)。短期和标准DAPT持续时间(≥12个月)的疗效终点无显著差异[风险比(RR) 0.96;95%置信区间(CI), 0.80-1.15]。短期DAPT持续时间没有显著增加全因死亡、心肌梗死、脑血管意外或明确或可能的支架血栓形成的个体风险。虽然与标准DAPT相比,短期DAPT明显降低了大出血的风险(RR 0.53;95% CI, 0.29-0.96),当进入4项研究的安全终点时,发现了显著的发表偏倚(Egger检验,P=0.009)。结论短期DAPT与标准时间DAPT疗效相当。DAPT小于6个月可能适合接受第二代药物洗脱支架植入术的患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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