首页> 外文OA文献 >Long-term ticagrelor monotherapy versus standard dual antiplatelet therapy followed by aspirin monotherapy in patients undergoing biolimus-eluting stent implantation: rationale and design of the GLOBAL LEADERS trial
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Long-term ticagrelor monotherapy versus standard dual antiplatelet therapy followed by aspirin monotherapy in patients undergoing biolimus-eluting stent implantation: rationale and design of the GLOBAL LEADERS trial

机译:长期替格瑞洛单药治疗与标准双重抗血小板治疗然后阿司匹林单药治疗接受生物lim洗脱支架植入的患者:GLOBAL LEADERS试验的原理和设计

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摘要

AIMSududThe GLOBAL LEADERS trial is a superiority study in patients undergoing percutaneous coronary intervention, with a uniform use of Biolimus A9-eluting stents (BES) and bivalirudin. GLOBAL LEADERS was designed to assess whether a 24-month antithrombotic regimen with ticagrelor and one month of acetylsalicylic acid (ASA), compared to conventional dual antiplatelet therapy (DAPT), improves outcomes.ududMETHODS AND RESULTSududPatients (n >16,000) are randomised (1:1 ratio) to ticagrelor 90 mg twice daily for 24 months plus ASA ≤100 mg for one month versus DAPT with either ticagrelor (acute coronary syndrome) or clopidogrel (stable coronary artery disease) for 12 months plus ASA ≤100 mg for 24 months. The primary outcome is a composite of all-cause mortality or non-fatal, new Q-wave myocardial infarction at 24 months. The key safety endpoint is investigator-reported class 3 or 5 bleeding according to the Bleeding Academic Research Consortium (BARC) definitions. Sensitivity analysis will be carried out to explore potential differences in outcome across geographic regions and according to specific angiographic and clinical risk estimates.ududCONCLUSIONSududThe GLOBAL LEADERS trial aims to assess the role of ticagrelor as a single antiplatelet agent after a short course of DAPT for the long-term prevention of cardiac adverse events, across a wide spectrum of patients, following BES implantation.
机译:AIMS ud udGLOBAL LEADERS试验是对接受经皮冠状动脉介入治疗的患者进行的一项优越性研究,其均使用Biolimus A9洗脱支架(BES)和比伐卢定。 GLOBAL LEADERS旨在评估与传统的双重抗血小板治疗(DAPT)相比,使用替格瑞洛和1个月的乙酰水杨酸(ASA)进行的24个月抗血栓治疗方案能否改善预后。 ud ud方法和结果 ud udPatients(n大于16,000的患者被随机分配(1:1比例)替卡格雷或90 mg每天两次,持续24个月,ASA≤100mg持续1个月,而DAPT合并替卡格雷(急性冠状动脉综合征)或氯吡格雷(稳定冠状动脉疾病)持续12个月ASA≤100毫克,持续24个月。主要结局是24个月全因死亡率或非致命性新Q波心肌梗死的综合结果。根据出血学术研究协会(BARC)的定义,关键的安全性终点是研究者报告的3级或5级出血。将进行敏感性分析,以探索地理区域之间结果的潜在差异,并根据具体的血管造影和临床风险评估。 ud ud结论 ud udGLOBAL LEADERS试验旨在评估替卡格雷在单药治疗后作为单一抗血小板药物的作用。 BES植入后,DAPT的短期疗程可长期预防广泛范围的患者的心脏不良事件。

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