首页> 外文期刊>Thrombosis Research: An International Journal on Vascular Obstruction, Hemorrhage and Hemostasis >Indirect treatment comparison of new oral anticoagulants for the treatment of acute venous thromboembolism
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Indirect treatment comparison of new oral anticoagulants for the treatment of acute venous thromboembolism

机译:新型口服抗凝剂间接治疗急性静脉血栓栓塞的比较

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Background Numerous new oral anticoagulants (NOACs) have been compared to a parenteral anticoagulant/oral vitamin K antagonist (VKA) for the treatment of acute venous thromboembolism (VTE). We aimed to conduct a systematic review and adjusted indirect comparison meta-analysis to compare the efficacy and safety of NOACs for this indication. Methods We conducted a systematic literature search through November 2013 for randomized trials that evaluated treatment of acute VTE with a NOAC including rivaroxaban, apixaban, dabigatran and edoxaban. Trials had to report at least one of the following outcomes of interest: mortality, recurrent VTE, recurrent pulmonary embolism (PE), recurrent deep vein thrombosis (DVT), or major bleeding. Included trials were evaluated for quality using the Cochrane Risk of Bias tool. We performed an adjusted indirect comparison meta-analysis to evaluate the comparative efficacy and safety of NOACs, reporting relative risks (RRs) and 95% confidence intervals for each outcome. Results Six trials (n = 27,069) met inclusion criteria, one each evaluating apixaban and edoxaban and two trials each evaluating rivaroxaban and dabigatran. Risk of bias was low for all trials. NOACS did not differ significantly in the risk of mortality, recurrent VTE, recurrent PE or recurrent DVT. Dabigatran increased major bleeding risk compared to apixaban [RR 2.69 (1.19 to 6.07)] as did edoxaban compared to apixaban [RR 2.74 (1.40 to 5.39)]. Conclusion Although NOACs do not appear to differ in the efficacy of treating acute VTE, data suggests apixaban to be the safer than some of its competitors.
机译:背景技术已经将许多新的口服抗凝剂(NOAC)与肠胃外抗凝剂/口服维生素K拮抗剂(VKA)进行了比较,以治疗急性静脉血栓栓塞(VTE)。我们旨在进行系统的审查和调整间接比较荟萃分析,以比较NOACs在该适应症中的疗效和安全性。方法我们在2013年11月之前进行了系统性文献检索,以随机试验评估利伐沙班,阿哌沙班,达比加群和依多沙班用NOAC治疗急性VTE的疗效。试验必须报告至少下列感兴趣的结果之一:死亡率,复发性VTE,复发性肺栓塞(PE),复发性深静脉血栓形成(DVT)或大出血。使用Cochrane偏倚风险工具评估了纳入试验的质量。我们进行了调整后的间接比较荟萃分析,以评估NOAC的比较疗效和安全性,报告每个结局的相对风险(RR)和95%置信区间。结果六项试验(n = 27,069)符合纳入标准,每项试验均评估阿哌沙班和依多沙班,两项试验均评估利伐沙班和达比加群。所有试验的偏倚风险均较低。 NOACS在死亡,复发性VTE,复发性PE或复发性DVT的风险方面无显着差异。与阿哌沙班相比,达比加群增加了重大出血风险[RR 2.69(1.19至6.07)],与埃多沙班相比与阿哌沙班相比[RR 2.74(1.40至5.39)]。结论尽管NOAC在治疗急性VTE的功效方面似乎没有差异,但数据表明apixaban比其某些竞争对手更安全。

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