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首页> 外文期刊>International angiology: A journal of the International Union of Angiology >Comparison of efficacy and safety of dabigatran, rivaroxaban and apixaban in patients with atrial fibrillation using network meta-analysis
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Comparison of efficacy and safety of dabigatran, rivaroxaban and apixaban in patients with atrial fibrillation using network meta-analysis

机译:网络荟萃分析比较达比加群,利伐沙班和阿哌沙班在房颤患者中的疗效和安全性

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Aim. A network meta-analysis of the three new oral anticoagulants was performed from the three trials comparing dabigatran, rivaroxaban and apixaban with warfarin in patients with atrial fibrillation. Methods. Data were extracted of the RE-LY study of dabigatran 110 mg bid and dabigatran 150 mg bid, the ROCKET AF trial of rivaroxaban and the ARISTOTLE trial of apixaban for the composite outcome of ischemic stroke and systemic embolism, for major bleeding, intracerebral bleeding, mortality and myocardial infarction. Results. Dabigatran (150 mg bid) showed superior efficacy in preventing ischemic stroke plus systemic embolism to dabigatran (110 mg bid, P=0.0364) and rivaroxaban (P=0.0388). Apixaban had equivalent efficacy with rivaroxaban and dabigatran (either dose). Apixaban was safer (less major bleeding) than dabigatran (150 mg bid, P=0.036) or rivaroxaban (P=0.0002). Intracerebral hemorrhage occurred with equal frequency for all agents except for rivaroxaban (higher risk than dabigatran 110 mg bid, P=0.0070). Myocardial infarction occurred less frequently with rivaroxaban and apixaban compared to either dose of dabigatran (all P<0.05). Conclusions. All-cause mortality was not different for any agent or regimen. In the absence of head-to-head comparisons, this network meta-analysis suggests that apixaban and dabigatran 110 mg bid may offer the best benefit-risk balance for stroke prevention in non-valvular atrial fibrillation. Dabigatran 150 mg bid may be preferred for patients with a high risk for embolism.
机译:目标。对三项新的口服抗凝药进行网络荟萃分析,比较了房颤患者中的达比加群,利伐沙班和阿哌沙班与华法林的比较。方法。数据提取自达比加群110 mg每日两次和达比加群150 mg每日两次的RE-LY研究,利伐沙班的ROCKET AF试验和阿哌沙班的ARISTOTLE试验,用于缺血性中风和全身性栓塞的综合结局,用于大出血,脑出血,死亡率和心肌梗塞。结果。与达比加群(110 mg bid,P = 0.0364)和利伐沙班(P = 0.0388)相比,达比加群(150 mg bid)在预防缺血性中风和全身性栓塞方面显示出更高的疗效。阿哌沙班与利伐沙班和达比加群(两种剂量)等效。阿比沙班比达比加群(150 mg bid,P = 0.036)或利伐沙班(P = 0.0002)更安全(大出血更少)。除利伐沙班外,所有药物的脑出血发生率均相同(比达比加群110 mg bid高风险,P = 0.0070)。与两种剂量的达比加群相比,利伐沙班和阿哌沙班发生心肌梗死的频率更低(所有P <0.05)。结论对于任何药物或方案,全因死亡率没有差异。在缺乏正面比较的情况下,该网络荟萃分析表明,阿哌沙班和达比加群110 mg bid可能为非瓣膜性心房颤动的卒中预防提供最佳的获益风险平衡。对于有高栓塞风险的患者,首选达比加群150 mg bid。

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