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Europace. 2013 Jun;15(6):787-97. doi: 10.1093/europace/eut001. Epub 2013 Feb 13.
Clinical trials have shown that anticoagulation with vitamin K antagonists (VKAs), e.g. warfarin, decreases the risk of stroke in patients with atrial fibrillation (AF); however, increased bleeding risk is one of the safety concerns. The primary objective was to conduct a systematic review of the published literature, assessing the risk of major bleeding and mortality in patients with AF treated with VKAs.
Online searches of MEDLINE, EMBASE, BIOSIS, and the Cochrane Library were performed to a pre-specified protocol from 1960 to March 2012 for randomized controlled trials (RCTs) and from January 1990 to March 2012 for observational studies. A total of 47 studies (16 RCTs and 31 observational studies) were included. Cumulative follow-up was 61,563 patient-years for RCTs and 484 241 patient-years for observational studies. The overall median incidence of major bleeding was 2.1 per 100 patient-years (range, 0.9-3.4 per 100 patient-years) for RCTs and 2.0 per 100 patient-years (range, 0.2-7.6 per 100 patient-years) for observational studies. With study year as a proxy for changing management patterns, some evidence of bleeding rates and/or their reporting increasing over time was noted. Mortality rates from observational studies were inadequately reported to allow comparison with those from RCT data.
The median rate of major bleeding in observational studies and RCTs is similar. The larger heterogeneity in bleeding rates observed in a real-life setting could reflect a high variability in standard of care of patients on VKAs and/or methodological differences between observational studies and/or variability in data sources.
临床试验表明,抗凝治疗使用维生素 K 拮抗剂(VKA),如华法林,可以降低房颤(AF)患者的中风风险;然而,增加出血风险是安全性关注之一。主要目的是系统地综述已发表的文献,评估 AF 患者使用 VKA 治疗时大出血和死亡率的风险。
根据预先制定的方案,从 1960 年至 2012 年 3 月在线检索 MEDLINE、EMBASE、BIOSIS 和 Cochrane 图书馆,检索随机对照试验(RCT),从 1990 年 1 月至 2012 年 3 月检索观察性研究。共纳入 47 项研究(16 项 RCT 和 31 项观察性研究)。RCT 的累积随访时间为 61563 患者年,观察性研究为 484241 患者年。RCT 的大出血总体发生率中位数为每 100 患者年 2.1(范围为 0.9-3.4/100 患者年),观察性研究为 2.0(范围为 0.2-7.6/100 患者年)。随着研究年份作为管理模式变化的代表,有证据表明出血率和/或其报告随时间增加。观察性研究的死亡率报告不足,无法与 RCT 数据进行比较。
观察性研究和 RCT 的大出血发生率中位数相似。在实际环境中观察到的出血率更大的异质性可能反映了 VKAs 患者标准护理的高度变异性和/或观察性研究之间的方法学差异和/或数据源的变异性。