Department of Pharmacology, All India Institute of Medical Sciences Bhopal, Bhopal, Madhya Pradesh, 462020, India.
Department of Cardiology, All India Institute of Medical Sciences Bhopal, Bhopal, Madhya Pradesh, 462020, India.
Cardiovasc Drugs Ther. 2021 Jun;35(3):561-574. doi: 10.1007/s10557-020-07056-z. Epub 2020 Aug 20.
Dual antiplatelet therapy (DAPT) with aspirin and ticagrelor or prasugrel is the mainstay of treatment for patients with acute coronary syndrome (ACS) undergoing percutaneous coronary intervention (PCI). We aimed to systematically perform a head-to-head comparison of ticagrelor vs prasugrel in terms of efficacy and safety.
We searched PubMed/Medline, EMBASE and Cochrane Central Register of Controlled Trials (CENTRAL) for relevant published randomized controlled trials (RCTs). The primary outcome was adverse cardiovascular events and secondary outcome was bleeding events. A random-effects meta-analysis was used to obtain the pooled estimate of each outcome.
Nine RCTs with a total number of 6990 patients (3550 treated with prasugrel and 3481 treated with ticagrelor) were included. No significant difference between prasugrel and ticagrelor was observed in terms of mortality (OR 0.86, 95% CI 0.66 to 1.13, P = 0.28), major adverse cardiovascular events (MACEs) (OR 0.85, 95% CI 0.70 to 1.03, P = 0.10), non-fatal myocardial infarction (OR 0.78, 95% CI 0.57 to 1.06, P = 0.11), stroke (OR 1.02, 95% CI 0.60 to 1.72, P = 0.95), stent thrombosis (OR 0.76, 95% CI 0.47 to 1.21, P = 0.25), thrombolysis in myocardial infarction (TIMI) defined major (OR 0.94, 95% CI 0.19 to 4.67, P = 0.94), minor (OR 0.35, 95% CI 0.08 to 1.62, P = 0.18) and minimal (OR 0.48, 95% CI 0.19 to 1.18, P = 0.11) bleeding and Bleeding Academic Research Consortium (BARC) defined bleeding (OR 1.06, 95% CI 0.82 to 1.36, P = 0.68).
In patients with ACS undergoing PCI, both prasugrel and ticagrelor were associated with similar cardiovascular outcomes and adverse bleeding events.
接受经皮冠状动脉介入治疗(PCI)的急性冠状动脉综合征(ACS)患者的双联抗血小板治疗(DAPT)采用阿司匹林联合替格瑞洛或普拉格雷。我们旨在系统地进行替格瑞洛与普拉格雷在疗效和安全性方面的头对头比较。
我们在 PubMed/MEDLINE、EMBASE 和 Cochrane 对照试验中心注册库(CENTRAL)中检索了相关的已发表随机对照试验(RCT)。主要结局为心血管不良事件,次要结局为出血事件。使用随机效应荟萃分析获得每个结局的汇总估计值。
纳入了 9 项 RCT,共 6990 例患者(普拉格雷组 3550 例,替格瑞洛组 3481 例)。普拉格雷和替格瑞洛在死亡率(OR 0.86,95%CI 0.66 至 1.13,P=0.28)、主要不良心血管事件(MACEs)(OR 0.85,95%CI 0.70 至 1.03,P=0.10)、非致死性心肌梗死(OR 0.78,95%CI 0.57 至 1.06,P=0.11)、卒中(OR 1.02,95%CI 0.60 至 1.72,P=0.95)、支架血栓形成(OR 0.76,95%CI 0.47 至 1.21,P=0.25)、心肌梗死溶栓治疗(TIMI)定义的主要(OR 0.94,95%CI 0.19 至 4.67,P=0.94)、次要(OR 0.35,95%CI 0.08 至 1.62,P=0.18)和最小(OR 0.48,95%CI 0.19 至 1.18,P=0.11)出血以及出血学术研究联合会(BARC)定义的出血(OR 1.06,95%CI 0.82 至 1.36,P=0.68)方面,两者无显著差异。
在接受 PCI 的 ACS 患者中,普拉格雷和替格瑞洛的心血管结局和不良出血事件相似。