首页> 外文期刊>The American heart journal >Rationale and design of the dual antiplatelet therapy study, a prospective, multicenter, randomized, double-blind trial to assess the effectiveness and safety of 12 versus 30 months of dual antiplatelet therapy in subjects undergoing percutaneous coronary intervention with either drug-eluting stent or bare metal stent placement for the treatment of coronary artery lesions.
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Rationale and design of the dual antiplatelet therapy study, a prospective, multicenter, randomized, double-blind trial to assess the effectiveness and safety of 12 versus 30 months of dual antiplatelet therapy in subjects undergoing percutaneous coronary intervention with either drug-eluting stent or bare metal stent placement for the treatment of coronary artery lesions.

机译:双重抗血小板治疗研究的原理和设计,这是一项前瞻性,多中心,随机,双盲试验,旨在评估经药物洗脱支架或裸露经皮冠状动脉介入治疗的受试者12个月与30个月双重抗血小板治疗的有效性和安全性金属支架置入术治疗冠状动脉病变。

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BACKGROUND: Dual antiplatelet therapy with aspirin and thienopyridines (clopidogrel or prasugrel) is required after placement of coronary stents to prevent thrombotic complications. Although current clinical practice guidelines recommend 12-month treatment after drug-eluting stent placement, even longer durations may prevent thrombotic events. STUDY DESIGN: The Dual Antiplatelet Therapy (DAPT) Study is comparing the benefits and risks of 12 versus 30 months of dual antiplatelet therapy in preventing stent thrombosis or major adverse cardiovascular and cerebrovascular events in subjects undergoing percutaneous coronary intervention (PCI) for the treatment of coronary artery obstructive lesions. The DAPT Study is a multicenter, international, randomized, double-blind, placebo-controlled trial that will enroll 15,245 subjects treated with drug-eluting stent (DES) and 5,400 subjects treated with bare-metal stents (BMS). All subjects will receive 12 months of open-label thienopyridine treatment in addition to aspirin. After 12 months, subjects who are free from death, myocardial infarction, or stroke (MACCE), repeat revascularization, and GUSTO (Global Use of Strategies to Open Occluded Coronary Arteries) moderate or severe bleeding events will be randomized to receive either 18 additional months of thienopyridine (clopidogrel or prasugrel) (30 month DAPT arm) or placebo (12 month DAPT arm) plus aspirin. Coprimary end points are MACCE and stent thrombosis. The primary safety end point is GUSTO moderate or severe bleeding. CONCLUSIONS: This randomized trial is designed to define the relative safety and effectiveness of 12 versus 30 months of dual antiplatelet therapy across the broad spectrum of patients receiving coronary stents.
机译:背景:在放置冠状动脉支架后,需要使用阿司匹林和噻吩并吡啶(氯吡格雷或普拉格雷)双重抗血小板治疗,以防止血栓并发症。尽管当前的临床实践指南建议在药物洗脱支架放置后进行12个月的治疗,但更长的持续时间也可以预防血栓形成事件。研究设计:双重抗血小板治疗(DAPT)研究比较了在接受经皮冠状动脉介入治疗(PCI)的受试者中预防性支架血栓形成或重大不良心血管和脑血管事件的12个月与30个月双重抗血小板治疗的收益和风险。冠状动脉阻塞性病变。 DAPT研究是一项多中心,国际,随机,双盲,安慰剂对照试验,将招募15245名接受药物洗脱支架(DES)治疗的受试者和5400名裸机支架(BMS)治疗的受试者。除阿司匹林外,所有受试者还将接受12个月的开放标签噻吩并吡啶治疗。 12个月后,无死亡,心肌梗塞或中风(MACCE),重复血运重建和GUSTO(全球使用开放性冠状动脉阻塞策略)中度或重度出血事件的受试者将被随机分配接受另外18个月的治疗噻吩吡啶(氯吡格雷或普拉格雷)(30个月DAPT组)或安慰剂(12个月DAPT组)加阿司匹林。共同的主要终点是MACCE和支架血栓形成。主要安全终点是GUSTO中度或重度出血。结论:该随机试验旨在确定在接受冠状动脉支架治疗的广泛患者中,十二个月和三十个月双重抗血小板治疗的相对安全性和有效性。

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