Bitar Yasmin de Souza Lima, Duraes Andre Rodrigues, Roever Leonardo, Gomes Neto Mansueto, Lins-Kusterer Liliane, Bocchi Edimar Alcides
Post-graduate Program in Medicine and Health (PPgMS)/Federal University of Bahia (UFBA), Salvador, Brazil.
Federal University of Bahia, UFBA, Salvador, Brazil.
Front Cardiovasc Med. 2021 Sep 22;8:712585. doi: 10.3389/fcvm.2021.712585. eCollection 2021.
Direct oral anticoagulants (DOACS) are approved for use in non-valvular atrial fibrillation (AF). This systematic review and meta-analysis aimed to evaluate the efficacy and safety of DOACs vs. warfarin and update the evidence for treatment of AF and valvular heart disease (VHD). We identified randomized clinical trials (RCTs) and analyses comparing the use of DOACS and Warfarin in AF and VHD, including biological and mechanical heart valves (MHV), updating from 2010 to 2020. Through systematic review and meta-analysis, by using the "Rev Man" program 5.3, the primary effectiveness endpoints were stroke and systemic embolism (SE). The primary safety outcome was major bleeding, while the secondary outcome included intracranial hemorrhage. We performed prespecified subgroup analyses. Data were analyzed by risk ratio (RR) and 95% confidence interval (CI) and the I-square ( ) statistic as a quantitative measure of inconsistency. Risk of bias and methodological quality assessment of included trials was evaluated with the modified Cochrane risk-of-bias tool. We screened 326 articles and included 8 RCTs ( = 14.902). DOACs significantly reduced the risk of stroke/SE (RR 0.80, 95% CI: 0.68-0.94; = 0.008; moderate quality evidence; = 2%) and intracranial hemorrhage (RR 0.40, 95% CI: 0.24-0.66; = 0.0004; = 49%) with a similar risk of major bleeding (RR 0.83, 95% CI: 0.56-1.24; = 0.36; = 88%) compared to Warfarin. In this update, DOACs remained with similar efficacy and safety compared to warfarin in thromboprophylaxis for AF and VHD.
直接口服抗凝剂(DOACs)已被批准用于非瓣膜性心房颤动(AF)。本系统评价和荟萃分析旨在评估DOACs与华法林相比的疗效和安全性,并更新治疗AF和瓣膜性心脏病(VHD)的证据。我们检索了2010年至2020年期间比较DOACs和华法林在AF和VHD(包括生物和机械心脏瓣膜(MHV))中使用情况的随机临床试验(RCT)和分析。通过系统评价和荟萃分析,使用“Rev Man”5.3软件,主要有效性终点为卒中及全身性栓塞(SE)。主要安全性结局为大出血,次要结局包括颅内出血。我们进行了预先设定的亚组分析。数据采用风险比(RR)和95%置信区间(CI)以及I²统计量进行分析,作为不一致性的定量指标。采用改良的Cochrane偏倚风险工具评估纳入试验的偏倚风险和方法学质量。我们筛选了326篇文章,纳入了8项RCT(n = 14902)。与华法林相比,DOACs显著降低了卒中/SE风险(RR 0.80,95% CI:0.68 - 0.94;P = 0.008;中等质量证据;I² = 2%)和颅内出血风险(RR 0.40,95% CI:0.24 - 0.66;P = 0.0004;I² = 49%),大出血风险相似(RR 0.83,95% CI:0.56 - 1.24;P = 0.36;I² = 88%)。在本次更新中,与华法林相比,DOACs在AF和VHD的血栓预防中仍具有相似的疗效和安全性。