Deutsches Herzzentrum München, Technische Universität, Klinik für Herz- und Kreislauferkrankungen, Munich, Germany.
Department of Cardiology, Aarhus University Hospital, Aarhus, Denmark.
J Am Coll Cardiol. 2015 Apr 28;65(16):1619-1629. doi: 10.1016/j.jacc.2015.02.050.
Patients receiving oral anticoagulation (OAC) who undergo drug-eluting stent (DES) implantation require additional dual antiplatelet therapy with aspirin and clopidogrel. Such triple therapy confers an elevated bleeding risk, and its optimal duration is not known.
The goal of this study was to evaluate whether shortening the duration of clopidogrel therapy from 6 months to 6 weeks after DES implantation was associated with a superior net clinical outcome in patients receiving concomitant aspirin and OAC.
In this randomized, open-label trial, we enrolled patients receiving OAC who underwent DES implantation at 3 European centers between September 2008 and December 2013. A total of 614 patients receiving concomitant aspirin and OAC were randomized to either 6-week clopidogrel therapy (n=307) or 6-month clopidogrel therapy (n=307). The primary endpoint was a composite of death, myocardial infarction (MI), definite stent thrombosis, stroke, or Thrombolysis In Myocardial Infarction (TIMI) major bleeding at 9 months.
The primary endpoint occurred in 30 patients (9.8%) in the 6-week group compared with 27 patients (8.8%) in the 6-month group (hazard ratio [HR]: 1.14; 95% CI: 0.68 to 1.91; p=0.63). There were no significant differences for the secondary combined ischemic endpoint of cardiac death, MI, definite stent thrombosis, and ischemic stroke (12 [4.0%] vs. 13 [4.3%]; HR: 0.93; 95% CI: 0.43 to 2.05; p=0.87) or the secondary bleeding endpoint of TIMI major bleeding (16 [5.3%] vs. 12 [4.0%]; HR: 1.35; 95% CI: 0.64 to 2.84; p=0.44).
Six weeks of triple therapy was not superior to 6 months with respect to net clinical outcomes. These results suggest that physicians should weigh the trade-off between ischemic and bleeding risk when choosing the shorter or longer duration of triple therapy. (Triple Therapy in Patients on Oral Anticoagulation After Drug Eluting Stent Implantation [ISAR-TRIPLE]; NCT00776633).
接受药物洗脱支架(DES)植入的口服抗凝(OAC)患者需要额外的阿司匹林和氯吡格雷双联抗血小板治疗。这种三联疗法会增加出血风险,其最佳持续时间尚不清楚。
本研究的目的是评估在接受阿司匹林和 OAC 联合治疗的患者中,将氯吡格雷治疗时间从 DES 植入后 6 个月缩短至 6 周是否与更好的净临床结局相关。
在这项随机、开放标签试验中,我们招募了 2008 年 9 月至 2013 年 12 月在欧洲 3 个中心接受 DES 植入的接受 OAC 治疗的患者。共有 614 名接受阿司匹林和 OAC 联合治疗的患者被随机分为氯吡格雷 6 周治疗组(n=307)或氯吡格雷 6 个月治疗组(n=307)。主要终点是 9 个月时死亡、心肌梗死(MI)、明确的支架血栓形成、卒中和血栓形成溶栓(TIMI)大出血的复合终点。
在 6 周组中,有 30 例(9.8%)患者发生主要终点事件,而在 6 个月组中有 27 例(8.8%)患者发生主要终点事件(风险比[HR]:1.14;95%CI:0.68 至 1.91;p=0.63)。在心脏死亡、MI、明确的支架血栓形成和缺血性卒中等次要联合缺血终点方面,两组之间没有显著差异(12 例[4.0%]与 13 例[4.3%];HR:0.93;95%CI:0.43 至 2.05;p=0.87)或 TIMI 大出血次要出血终点(16 例[5.3%]与 12 例[4.0%];HR:1.35;95%CI:0.64 至 2.84;p=0.44)。
三联疗法 6 周并不优于 6 个月,在净临床结局方面。这些结果表明,医生在选择三联疗法的较短或较长持续时间时,应权衡缺血和出血风险之间的权衡。(口服抗凝后药物洗脱支架植入患者的三联疗法[ISAR-TRIPLE];NCT00776633)。