Fanaroff Alexander C, Hasselblad Vic, Roe Matthew T, Bhatt Deepak L, James Stefan K, Steg Ph Gabriel, Gibson C Michael, Ohman E Magnus
Division of Cardiology, Duke University, Durham, NC, USA; Duke Clinical Research Institute, Duke University, Durham, NC, USA.
Duke Clinical Research Institute, Duke University, Durham, NC, USA.
Int J Cardiol. 2017 Aug 15;241:87-96. doi: 10.1016/j.ijcard.2017.03.046. Epub 2017 Mar 14.
Nine oral antithrombotic medications currently available in the United States and Europe have been studied in clinical trials for secondary prevention of cardiac events following acute coronary syndrome (ACS). Few combinations of these medications have been directly compared, and studies have used multiple different comparator regimens.
We performed a systematic review and network meta-analysis of randomized controlled trials evaluating one or more available oral antithrombotic therapies in patients with ACS or prior myocardial infarction (MI). Co-primary outcomes were all-cause and cardiovascular mortality compared with imputed placebo and aspirin monotherapy.
Forty-seven studies (196,057 subjects) met inclusion criteria and were included in the systematic review. Almost all studies tested either aspirin monotherapy compared with placebo or a combination of antithrombotic agents that included aspirin. Nearly all regimens reduced all-cause and cardiovascular mortality compared with imputed placebo. However, compared with imputed aspirin monotherapy, only combination therapy with aspirin plus ticagrelor was associated with lower cardiovascular mortality (OR 0.80, 95% CI 0.68-0.93), and triple therapy with aspirin, clopidogrel, and very low dose rivaroxaban was associated with lower all-cause mortality (OR 0.67, 95% CI 0.49-0.90). Major bleeding was increased 45-95% with dual antithrombotic therapy, and 2-6-fold with triple therapy.
Few combinations of antithrombotic therapy were associated with a reduction in mortality compared with aspirin monotherapy, highlighting the difficulty in clinical interpretation of composite ischemic endpoints. Future studies may need to focus on limiting the number of antithrombotic therapies tested in combination to best balance ischemic event reduction and bleeding.
目前在美国和欧洲可用的九种口服抗血栓药物已在临床试验中用于急性冠状动脉综合征(ACS)后心脏事件的二级预防研究。这些药物很少有组合被直接比较,并且研究使用了多种不同的对照方案。
我们对评估一种或多种可用口服抗血栓治疗对ACS或既往心肌梗死(MI)患者疗效的随机对照试验进行了系统评价和网状荟萃分析。共同主要结局是与虚拟安慰剂和阿司匹林单药治疗相比的全因死亡率和心血管死亡率。
47项研究(196,057名受试者)符合纳入标准并被纳入系统评价。几乎所有研究都测试了阿司匹林单药治疗与安慰剂相比,或包含阿司匹林的抗血栓药物组合。与虚拟安慰剂相比,几乎所有方案都降低了全因死亡率和心血管死亡率。然而,与虚拟阿司匹林单药治疗相比,只有阿司匹林加替格瑞洛的联合治疗与较低的心血管死亡率相关(OR 0.80,95%CI 0.68 - 0.93),而阿司匹林、氯吡格雷和极低剂量利伐沙班的三联治疗与较低的全因死亡率相关(OR 0.67,95%CI 0.49 - 0.90)。双联抗血栓治疗使大出血增加45% - 95%,三联治疗使其增加2 - 6倍。
与阿司匹林单药治疗相比,很少有抗血栓治疗组合与死亡率降低相关,这突出了复合缺血终点临床解读的困难。未来的研究可能需要专注于限制联合测试的抗血栓治疗数量,以最佳平衡缺血事件减少和出血。