Coronary Care Unit and Laboratory of Clinical and Experimental Cardiology, Fondazione IRCCS Policlinico San Matteo, Viale Camillo Golgi 19, 27100, Pavia, Italy.
Department of Molecular Medicine, University of Pavia, Pavia, Italy.
Am J Cardiovasc Drugs. 2021 Mar;21(2):231-240. doi: 10.1007/s40256-020-00436-8.
In patients with atrial fibrillation (AF) receiving percutaneous coronary intervention (PCI), current guidelines recommend against combining potent oral P2Y inhibitors (i.e. ticagrelor or prasugrel) with oral anticoagulant (OAC) therapy, but the evidence is limited.
The aim of this meta-analysis was to compare the efficacy and safety of potent oral P2Y inhibitors with clopidogrel in patients receiving OAC therapy for AF after a recent PCI.
Electronic databases were searched for randomized controlled trials (RCT) reporting outcomes according to the P2Y inhibitor used. Major or clinically relevant non-major bleeding were the safety endpoints, while the efficacy outcomes were major adverse cardiovascular events (MACE). The potent oral P2Y inhibitors prasugrel and ticagrelor were compared with clopidogrel. A subgroup analysis was conducted to evaluate the differences between patients treated with dual antithrombotic therapy (DAT) versus triple antithrombotic therapy (TAT).
Four RCTs that included 10,057 patients were included in this analysis. Potent oral P2Y inhibitors were associated with a significant increase in major or clinically relevant non-major bleeding compared with clopidogrel (risk ratio [RR] 1.30, 95% confidence interval [CI] 1.06-1.59, p = 0.01; number needed to harm 18, 95% CI 12-36). This finding was consistent regardless of the concomitant antithrombotic therapy (DAT vs. TAT; p = 0.69). The risk of MACE did not differ between potent oral P2Y inhibitors and clopidogrel (RR 1.02, 95% CI 0.57-1.82).
In patients receiving OAC therapy for AF after a recent PCI, potent oral P2Y inhibitors increase the risk of clinically relevant bleeding compared with clopidogrel, with no evident benefit in terms of MACE reduction.
在接受经皮冠状动脉介入治疗(PCI)的心房颤动(AF)患者中,目前的指南建议避免将强效口服 P2Y 抑制剂(即替格瑞洛或普拉格雷)与口服抗凝剂(OAC)联合治疗,但证据有限。
本荟萃分析的目的是比较在近期 PCI 后接受 OAC 治疗的 AF 患者中,强效口服 P2Y 抑制剂与氯吡格雷的疗效和安全性。
电子数据库搜索报告根据使用的 P2Y 抑制剂进行结果的随机对照试验(RCT)。主要或临床相关非主要出血是安全性终点,而主要不良心血管事件(MACE)是疗效终点。强效口服 P2Y 抑制剂普拉格雷和替格瑞洛与氯吡格雷进行比较。进行亚组分析以评估接受双联抗血栓治疗(DAT)与三联抗血栓治疗(TAT)的患者之间的差异。
本分析纳入了四项包含 10057 例患者的 RCT。与氯吡格雷相比,强效口服 P2Y 抑制剂与主要或临床相关非主要出血的发生率显著增加(风险比 [RR] 1.30,95%置信区间 [CI] 1.06-1.59,p=0.01;危害比 18,95%CI 12-36)。无论同时使用的抗血栓治疗(DAT 与 TAT;p=0.69)如何,这一发现都是一致的。强效口服 P2Y 抑制剂与氯吡格雷在 MACE 风险方面无差异(RR 1.02,95% CI 0.57-1.82)。
在近期 PCI 后接受 OAC 治疗的 AF 患者中,与氯吡格雷相比,强效口服 P2Y 抑制剂增加了临床相关出血的风险,同时在减少 MACE 方面没有明显获益。