首页> 美国卫生研究院文献>BMJ Open >Prospective multicentre open-label randomised controlled trial of 3-month versus 12-month dual antiplatelet therapy after implantation of the new generation biodegradable polymer sirolimus TARGET-eluting coronary stent: protocol of the TARGET DAPT trial
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Prospective multicentre open-label randomised controlled trial of 3-month versus 12-month dual antiplatelet therapy after implantation of the new generation biodegradable polymer sirolimus TARGET-eluting coronary stent: protocol of the TARGET DAPT trial

机译:植入新一代生物可降解聚合物西罗莫司TARGET洗脱冠状动脉支架后的3个月和12个月双重抗血小板治疗的前瞻性多中心开放标签随机对照试验:TARGET DAPT试验方案

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摘要

Dual antiplatelet therapy (DAPT) with aspirin and thienopyridine is required after placement of coronary stents to prevent thrombotic complications. However, current recommendation for duration of DAPT remains controversial. Firehawk is a biodegradable polymer applied to recessed abluminal grooves, sirolimus target-eluting stent associated with early excellent healing response and almost complete strut coverage, as well as possibly reduced myocardial ischaemic events. But the optimal DAPT duration for such a new generation stent is less known. Therefore, the present trial seeks to evaluate the safety and efficacy of 3-month versus 12-month DAPT in broad patients receiving Firehawk stents.
机译:放置冠状动脉支架后需要使用阿司匹林和噻吩并吡啶进行双重抗血小板治疗(DAPT),以防止血栓并发症。但是,目前关于DAPT持续时间的建议仍存在争议。 Firehawk是一种可生物降解的聚合物,适用于凹入的空腹凹槽,西罗莫司靶洗脱支架,具有早期出色的愈合反应和几乎完全的支杆覆盖,并可能减少了心肌缺血事件。但是,这种新一代支架的最佳DAPT持续时间鲜为人知。因此,本试验旨在评估在接受Firehawk支架的广泛患者中3个月和12个月DAPT的安全性和有效性。

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