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Comparative effectiveness and safety of non-vitamin K antagonist oral anticoagulants and warfarin in patients with atrial fibrillation: propensity weighted nationwide cohort study

机译:非维生素K拮抗剂口服抗凝药和华法林在房颤患者中的比较有效性和安全性:全国人群加权倾向研究

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摘要

>Objective To study the effectiveness and safety of the non-vitamin K antagonist oral anticoagulants (novel oral anticoagulants, NOACs) dabigatran, rivaroxaban, and apixaban compared with warfarin in anticoagulant naïve patients with atrial fibrillation.>Design Observational nationwide cohort study.>Setting Three Danish nationwide databases, August 2011 to October 2015.>Participants 61 678 patients with non-valvular atrial fibrillation who were naïve to oral anticoagulants and had no previous indication for valvular atrial fibrillation or venous thromboembolism. The study population was distributed according to treatment type: warfarin (n=35 436, 57%), dabigatran 150 mg (n=12 701, 21%), rivaroxaban 20 mg (n=7192, 12%), and apixaban 5 mg (n=6349, 10%).>Main outcome measures Effectiveness outcomes defined a priori were ischaemic stroke; a composite of ischaemic stroke or systemic embolism; death; and a composite of ischaemic stroke, systemic embolism, or death. Safety outcomes were any bleeding, intracranial bleeding, and major bleeding.>Results When the analysis was restricted to ischaemic stroke, NOACs were not significantly different from warfarin. During one year follow-up, rivaroxaban was associated with lower annual rates of ischaemic stroke or systemic embolism (3.0% v 3.3%, respectively) compared with warfarin: hazard ratio 0.83 (95% confidence interval 0.69 to 0.99). The hazard ratios for dabigatran and apixaban (2.8% and 4.9% annually, respectively) were non-significant compared with warfarin. The annual risk of death was significantly lower with apixaban (5.2%) and dabigatran (2.7%) (0.65, 0.56 to 0.75 and 0.63, 0.48 to 0.82, respectively) compared with warfarin (8.5%), but not with rivaroxaban (7.7%). For the combined endpoint of any bleeding, annual rates for apixaban (3.3%) and dabigatran (2.4%) were significantly lower than for warfarin (5.0%) (0.62, 0.51 to 0.74). Warfarin and rivaroxaban had comparable annual bleeding rates (5.3%).>Conclusion All NOACs seem to be safe and effective alternatives to warfarin in a routine care setting. No significant difference was found between NOACs and warfarin for ischaemic stroke. The risks of death, any bleeding, or major bleeding were significantly lower for apixaban and dabigatran compared with warfarin.
机译:>目的研究非维生素K拮抗剂口服抗凝剂(新型口服抗凝剂,NOACs)达比加群,利伐沙班和阿哌沙班与华法林在单纯抗凝性房颤患者中的有效性和安全性。>设计全国性队列研究。>设置三个丹麦全国性数据库,2011年8月至2015年10月。>参与者 61.678名非瓣膜性心房颤动天真的患者口服抗凝药,以前没有瓣膜房颤或静脉血栓栓塞的指征。根据治疗类型分配研究人群:华法令(n = 35 436,57%),达比加群150 mg(n = 12 701,21%),利伐沙班20 mg(n = 7192,12%)和阿哌沙班5 mg (n = 6349,10%)。>主要结局指标。先验定义的疗效结局是缺血性中风;缺血性中风或全身性栓塞的复合物;死亡;并伴有缺血性中风,全身性栓塞或死亡。安全性结果是任何出血,颅内出血和大出血。>结果。当分析仅限于缺血性中风时,NOAC与华法林无显着差异。在一年的随访中,利伐沙班与缺血性中风或全身性栓塞的年发生率较低(分别为3.0%对3.3%)相比,华法林:危险比为0.83(95%置信区间为0.69至0.99)。与华法林相比,达比加群和阿哌沙班的危险率(分别为每年2.8%和4.9%)不显着。阿法沙班(5.2%)和达比加群(2.7%)(分别为0.65、0.56至0.75和0.63、0.48至0.82)的年死亡风险显着低于华法林(8.5%),但利伐沙班(7.7%)没有)。对于所有出血的综合终点,阿哌沙班(3.3%)和达比加群(2.4%)的年发生率均显着低于华法林(5.0%)(0.62,0.51至0.74)。华法林和利伐沙班的年出血率相当(5.3%)。>结论在常规护理环境中,所有NOAC似乎都是华法林的安全有效替代品。 NOAC和华法林在缺血性卒中之间无显着差异。与华法林相比,阿哌沙班和达比加群的死亡,任何出血或大出血的风险显着降低。

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