Guangdong Second Provincial General Hospital, 466 Newport Middle Road, Haizhu District, Guangzhou, 510317, Guangdong Province, China.
Department of Health Research Methods, Evidence, and Impact, McMaster University, Hamilton, Canada.
Eur J Epidemiol. 2019 Feb;34(2):173-190. doi: 10.1007/s10654-018-0415-7. Epub 2018 Jun 8.
The non-vitamin K antagonist oral anticoagulants (NOACs) have been increasingly prescribed in clinical practice for stroke prevention in patients with nonvalvular atrial fibrillation (AF). Direct comparisons between NOACs in trials are lacking, leaving an important clinical decision-making gap. We aimed to perform a systematic review and meta-analysis to summarize the evidence of observational studies for direct comparative effectiveness and safety amongst NOACs in patients with AF. Conference proceedings and electronic databases including MEDLINE, CINAHL, EMBASE and PUBMED were systematically searched. We included observational studies directly comparing individual NOACs in patients with nonvalvular AF who were aged ≥ 18 years for stroke prevention. Primary outcome included effectiveness outcome (stroke or systemic embolism) and safety outcome (major bleeding). Data were extracted in duplicated by two reviewers independently. A random-effects meta-analysis was conducted to synthesize the data from included observational studies. We used the Grading of Recommendations Assessment, Development and Evaluation (GRADE) to rate the overall quality of evidence for each outcome. Fifteen studies were included for qualitative synthesis, twelve studies for meta-analyses. It was found that rivaroxaban and dabigatran were similar with regard to risk of stroke or systemic embolism (Hazard ratio [HR] = 1.00, 95% CI 0.91-1.10; evidence quality: low), but rivaroxaban was associated with higher risk of major bleeding (HR = 1.39, 95% CI 1.28-1.50; evidence quality: moderate). Compared with apixaban, a significantly higher risk of major bleeding was observed with rivaroxaban (HR = 1.71, 95% CI 1.51-1.94; evidence quality: low). Apixaban was associated with lower risk of major bleeding, in comparison with dabigatran (HR = 0.80, 95% CI 0.68-0.95; evidence quality: low). No differences in risk of stroke or systemic embolism was observed between rivaroxaban versus apixaban, and apixaban versus dabigatran. In this study, apixaban was found to have the most favorable safety profile amongst the three NOACs. No significant difference was observed in risk of stroke or systemic embolism between the NOACs. Such findings may provide some decision-making support for physicians regarding their choices amongst NOACs in patients with AF.Registration PROSPERO (identifier: CRD42016052908).
非维生素 K 拮抗剂口服抗凝剂(NOACs)在预防非瓣膜性心房颤动(AF)患者中风方面在临床实践中越来越多地被开处。在试验中缺乏对 NOACs 的直接比较,这留下了一个重要的临床决策空白。我们旨在进行系统评价和荟萃分析,以总结 AF 患者中关于 NOACs 直接比较有效性和安全性的观察性研究证据。会议记录和电子数据库包括 MEDLINE、CINAHL、EMBASE 和 PUBMED 被系统地搜索。我们纳入了直接比较非瓣膜性 AF 患者中风预防中单独使用 NOACs 的观察性研究,这些患者年龄≥18 岁。主要结局包括有效性结局(中风或全身性栓塞)和安全性结局(大出血)。数据由两名独立审查员重复提取。使用随机效应荟萃分析对纳入的观察性研究数据进行综合分析。我们使用推荐评估、制定与评价(GRADE)来评估每个结局的总体证据质量。进行了定性综合分析的 15 项研究,进行荟萃分析的 12 项研究。结果发现,利伐沙班和达比加群在中风或全身性栓塞风险方面相似(风险比[HR] = 1.00,95%置信区间 0.91-1.10;证据质量:低),但利伐沙班与大出血风险较高相关(HR = 1.39,95%置信区间 1.28-1.50;证据质量:中)。与阿哌沙班相比,利伐沙班的大出血风险显著升高(HR = 1.71,95%置信区间 1.51-1.94;证据质量:低)。与达比加群相比,阿哌沙班的大出血风险较低(HR = 0.80,95%置信区间 0.68-0.95;证据质量:低)。利伐沙班与阿哌沙班和阿哌沙班与达比加群之间,在中风或全身性栓塞风险方面无差异。在这项研究中,阿哌沙班在三种 NOACs 中具有最有利的安全性特征。NOACs 之间在中风或全身性栓塞风险方面无显著差异。这些发现可能为医生在 AF 患者中选择 NOACs 时提供一些决策支持。注册 PROSPERO(标识符:CRD42016052908)。