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Safety and effectiveness of dabigatran and warfarin in routine care of patients with atrial fibrillation

机译:达比加群和华法林在房颤患者常规治疗中的安全性和有效性

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The RE-LY study demonstrated the safety and efficacy of dabigatran relative to warfarin for stroke prevention in non-valvular atrial fibrillation. It is important to further evaluate safety and effectiveness of drugs in routine care. This study used a sequential cohort design with propensity score matching to compare dabigatran with warfarin among patients in two commercial health insurance databases. New users of these anticoagulants were followed from initiation until discontinuation, the end of the study, or the occurrence of a study outcome (primary study outcomes were stroke and major bleeding). Proportional hazards regression was conducted separately within each data source and results were pooled. Among 19,189 matched dabigatran and warfarin initiators (mean age: 68 years, 36 % female), astreated follow-up (average of 5 months for dabigatran, 4 months for warfarin) identified 62 and 69 strokes, respectively (pooled HR = 0.77; 95 % CI = 0.54 to 1.09), and 354 and 395 major haemorrhages, respectively (HR = 0.75; 0.65 to 0.87). No meaningful heterogeneity was identified across subgroups, but numeric trends suggest more pronounced stroke prevention by dabigatran relative to warfarin among patients age 75+ (HR = 0.57; 0.33 to 0.97) or with <6 months of use (HR = 0.51; 0.19 to 1.42). Major bleeds were reduced more by dabigatran among patients aged <55 (HR = 0.51; 0.30 to 0.87) and with CHADS(2) < 2 (HR = 0.58; 0.44 to 0.77). In conclusion, in routine care of patients with non-valvular atrial fibrillation, dabigatran treatment resulted in improved health outcomes compared with warfarin.
机译:RE-LY研究证明达比加群相对于华法林在非瓣膜性房颤中预防卒中的安全性和有效性。进一步评估常规护理中药物的安全性和有效性非常重要。这项研究采用了具有倾向得分匹配的连续队列设计,以比较两个商业健康保险数据库中患者的达比加群和华法林。这些抗凝剂的新使用者从开始到终止,研究结束或研究结果发生(主要研究结果为中风和大出血)开始接受随访。在每个数据源中分别进行了比例风险回归,并汇总了结果。在19,189例匹配的达比加群和华法林引发剂(平均年龄:68岁,女性36%)中,经随访(达比加群平均5个月,华法林为4个月),分别确定了62和69例卒中(合并HR = 0.77; 95)。 %CI = 0.54至1.09),以及354和395次大出血(HR = 0.75; 0.65至0.87)。在亚组之间未发现有意义的异质性,但是数字趋势表明,达比加群相对于华法林的卒中预防在75岁以上(HR = 0.57; 0.33至0.97)或使用6个月以下的患者(HR = 0.51; 0.19至1.42) )。达比加群在小于55岁(HR = 0.51; 0.30至0.87)和CHADS(2)<2(HR = 0.58; 0.44至0.77)的患者中大出血的发生率有所降低。总之,在非瓣膜性房颤患者的常规治疗中,达比加群治疗与华法林相比可改善健康状况。

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