Department of Cardiology, Jinggangshan University, Ji'an, Jiangxi, China.
Clin Cardiol. 2021 Apr;44(4):472-480. doi: 10.1002/clc.23586. Epub 2021 Mar 7.
Several observational studies have shown that the inappropriate dosing use of direct oral anticoagulants (DOACs) in atrial fibrillation (AF) that does not conform to recommendations is becoming a widespread phenomenon. Therefore, we performed a meta-analysis and systematic review to assess the effect of non-recommended doses versus recommended doses of DOACs on the effectiveness and safety outcomes among AF patients.
The PubMed and Ovid databases were systematically searched to identify the relevant studies until December 2020. The effect estimates were hazard ratios (HRs) and 95% confidence intervals (CIs), which were pooled using a fixed-effects model (I ≤ 50%) or a random-effects model (I > 50%).
A total of 11 studies were included in this meta-analysis. Compared with recommended dosing of DOACs, non-recommended low dosing of DOACs was associated with increased risks of stroke or systemic embolism (SSE, HR = 1.29, 95% CI 1.12-1.49) and all-cause death (HR = 1.37, 95% CI 1.15-1.62), but not the ischemic stroke, myocardial infarction, gastrointestinal bleeding, intracranial bleeding, and major bleeding. Compared with recommended dosing of DOACs, non-recommended high dosing of DOACs was associated with increased risks of SSE (HR = 1.44, 95% CI 1.01-2.04), major bleeding (HR = 1.99, 95% CI 1.48-2.68), and all-cause death(HR = 1.38, 95% CI 1.02-1.87).
Compared with recommended dosing of DOACs, non-recommended low dosing of DOACs was associated with increased risks of SSE and all-cause death. Further study should confirm the findings of non-recommended high dosing versus recommended dosing of DOACs.
几项观察性研究表明,不符合推荐剂量的房颤患者不恰当地使用直接口服抗凝剂(DOAC)的现象越来越普遍。因此,我们进行了一项荟萃分析和系统评价,以评估 DOAC 不推荐剂量与推荐剂量相比,对房颤患者有效性和安全性结局的影响。
系统检索了 PubMed 和 Ovid 数据库,以确定相关研究,检索时间截至 2020 年 12 月。使用固定效应模型(I ² ≤ 50%)或随机效应模型(I ² > 50%)汇总效应估计值为风险比(HRs)和 95%置信区间(CIs)。
这项荟萃分析共纳入了 11 项研究。与 DOAC 的推荐剂量相比,DOAC 的不推荐低剂量与卒中或全身性栓塞(SSE,HR = 1.29,95%CI 1.12-1.49)和全因死亡(HR = 1.37,95%CI 1.15-1.62)风险增加相关,但与缺血性卒中和心肌梗死、胃肠道出血、颅内出血和大出血无关。与 DOAC 的推荐剂量相比,DOAC 的不推荐高剂量与 SSE(HR = 1.44,95%CI 1.01-2.04)、大出血(HR = 1.99,95%CI 1.48-2.68)和全因死亡(HR = 1.38,95%CI 1.02-1.87)风险增加相关。
与 DOAC 的推荐剂量相比,DOAC 的不推荐低剂量与 SSE 和全因死亡风险增加相关。需要进一步的研究来证实 DOAC 的不推荐高剂量与推荐剂量相比的结果。