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经皮冠状动脉介入治疗及抗栓治疗方案-双联抗血小板治疗 6 周与 6 个月氯吡格雷疗效对比的随机研究(ISAR-TRIPLE 研究):替格瑞洛在伴有阿司匹林和口服抗凝剂治疗的经皮冠状动脉介入治疗患者中的疗效。

Rationale and design of The Intracoronary Stenting and Antithrombotic Regimen-Testing of a six-week versus a six-month clopidogrel treatment Regimen In Patients with concomitant aspirin and oraL anticoagulant therapy following drug-Eluting stenting (ISAR-TRIPLE) study.

机构信息

Deutsches Herzzentrum, Technische Universität, Munich, Germany; DZHK (German Centre for Cardiovascular Research), partner site Munich Heart Alliance, Munich, Germany.

Deutsches Herzzentrum, Technische Universität, Munich, Germany; DZHK (German Centre for Cardiovascular Research), partner site Munich Heart Alliance, Munich, Germany.

出版信息

Am Heart J. 2014 Apr;167(4):459-465.e1. doi: 10.1016/j.ahj.2014.01.005. Epub 2014 Jan 14.

Abstract

BACKGROUND

An increasing number of patients undergoing coronary stenting need lifelong anticoagulation and therefore require a triple therapy typically consisting of aspirin, clopidogrel, and a vitamin K antagonist. Triple therapy confers an elevated bleeding risk as compared with dual therapy; however, omission of either antiplatelet or anticoagulation therapy might increase the risk of stent thrombosis or thrombembolic events. Although guidelines recommend a duration of dual antiplatelet therapy of 6 to 12months after drug-eluting stent (DES) implantation, the optimal duration of dual antiplatelet therapy in patients receiving oral anticoagulation is not known.

HYPOTHESIS

We postulate that 6-week clopidogrel therapy after DES implantation as compared with 6-month therapy is associated with improved clinical outcomes in patients undergoing DES implantation receiving concomitant aspirin and vitamin K antagonists.

STUDY DESIGN

The ISAR-TRIPLE is a randomized, open-label trial that examines the restriction of clopidogrel therapy from 6 months to 6 weeks after DES implantation in the setting of concomitant aspirin and oral anticoagulant. Patients are randomized in a 1:1 fashion to either 6-week or 6-month clopidogrel therapy. The primary end point is a composite of death, myocardial infarction, definite stent thrombosis, stroke, or major bleeding. The secondary end point comprises ischemic and bleeding complications. According to sample size calculations, a total of 600 patients are required to be enrolled. Clinical follow-up is scheduled at 6 weeks and at 6 and 9 months after randomization.

SUMMARY

There is clinical equipoise regarding the optimal duration of triple therapy after DES implantation in patients who need vitamin K antagonist therapy. The ISAR-TRIPLE trial aims to test the hypothesis that a 6-week triple therapy compared with a 6-month triple therapy improves net clinical outcomes.

摘要

背景

越来越多接受冠状动脉支架置入术的患者需要终生抗凝,因此需要三联治疗,通常包括阿司匹林、氯吡格雷和维生素 K 拮抗剂。与双联治疗相比,三联治疗会增加出血风险;然而,停用任何一种抗血小板或抗凝治疗都可能增加支架血栓或血栓栓塞事件的风险。尽管指南建议在药物洗脱支架(DES)植入后进行 6 至 12 个月的双联抗血小板治疗,但接受口服抗凝治疗的患者双联抗血小板治疗的最佳持续时间尚不清楚。

假设

与 6 个月的治疗相比,DES 植入后 6 周氯吡格雷治疗与改善接受同时使用阿司匹林和维生素 K 拮抗剂的 DES 植入患者的临床结局相关。

研究设计

ISAR-TRIPLE 是一项随机、开放标签试验,研究了在同时使用阿司匹林和口服抗凝剂的情况下,将 DES 植入后氯吡格雷治疗从 6 个月限制至 6 周对患者的影响。患者以 1:1 的比例随机分为 6 周或 6 个月氯吡格雷治疗组。主要终点是死亡、心肌梗死、明确的支架血栓形成、卒中和大出血的复合终点。次要终点包括缺血和出血并发症。根据样本量计算,需要招募总共 600 名患者。临床随访计划在随机分组后 6 周、6 个月和 9 个月进行。

总结

在需要维生素 K 拮抗剂治疗的患者中,DES 植入后三联治疗的最佳持续时间存在临床平衡。ISAR-TRIPLE 试验旨在检验以下假设,即与 6 个月三联治疗相比,6 周三联治疗可改善净临床结局。

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