有瓣膜性心脏病和无瓣膜性心脏病的心房颤动患者口服非维生素 K 拮抗剂与华法林的比较:系统综述和荟萃分析。

Arga Setyo Adji, Bryan Gervais de Liyis
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引用次数: 0

摘要

背景:心房颤动(房颤)给心脏病患者带来很大的中风风险。本系统性综述旨在评估非维生素 K 口服拮抗剂(NOACs)与维生素 K 拮抗剂(VKAs)在患有或未患有任何瓣膜性心脏病(VHD/N-VHD)的房颤患者中的疗效和安全性:在PubMed、Scopus和Google Scholar上进行了系统检索,检索时间截至2022年3月3日。对疗效和安全性参数进行了分析:本荟萃分析共纳入了 10 项研究的 85423 名受试者。NOACs 和 VKAs 对 VHD/N-VHD 房颤患者缺血性卒中的影响相似(RR 0.97;95% CI 0.72-1.30;P = 0.83),对全身性栓塞事件的影响也相似(RR 1.02;95% CI 0.83-1.25;P = 0.86)。VHD亚组和N-VHD亚组的疗效相似。两种治疗方法对VHD/N-VHD(RR 0.79;95% CI 0.49-1.26;p = 0.32)、VHD(RR 0.78;95% CI 0.59-1.02;p = 0.07)和N-VHD亚组房颤患者心肌梗死(RR 0.82;95% CI 0.30-2.21;p = 0.69)的影响相似。NOACs 可降低房颤 VHD/N-VHD 的颅内出血风险(RR 0.64;95% CI 0.54-0.77;P 结论:NOACs 对房颤 VHD 和 N-VHD 亚组有效且安全:NOACs 对 VHD/N-VHD 房颤患者的缺血性卒中、全身性栓塞事件、心肌梗死、颅内出血和消化道出血有效且安全。
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Comparison between non-vitamin K oral antagonist versus warfarin in atrial fibrillation with and without valvular heart disease: a systematic review and meta-analysis.

Background: Atrial fibrillation (AF) poses a significant stroke risk in heart disease patients. This systematic review aims to evaluate the efficacy and safety of non-vitamin K oral antagonists (NOACs) versus vitamin K antagonists (VKAs) in AF patients with and without any valvular heart disease (VHD/N-VHD).

Methods: A systematic search was conducted on PubMed, Scopus, and Google Scholar up to March 3, 2022. Efficacy and safety parameters were analyzed.

Results: A total of 85,423 subjects from 10 studies were included in this meta-analysis. NOACs and VKAs showed similar effects on ischemic stroke in AF patients with VHD/N-VHD (RR 0.97; 95% CI 0.72-1.30; p = 0.83) and also on systemic embolic events (RR 1.02; 95% CI 0.83-1.25; p = 0.86). Similar effects were seen in VHD and N-VHD subgroups. Both treatments had similar effects on myocardial infarction in AF patients with VHD/N-VHD (RR 0.79; 95% CI 0.49-1.26; p = 0.32), VHD (RR 0.78; 95% CI 0.59-1.02; p = 0.07), and N-VHD subgroups (RR 0.82; 95% CI 0.30-2.21; p = 0.69). NOACs reduced the risk of intracranial bleeding in AF VHD/N-VHD (RR 0.64; 95% CI 0.54-0.77; p < 0.0001), VHD (RR 0.59; 95% CI 0.42-0.82; p = 0.002), and N-VHD subgroups (RR 0.70; 95% CI 0.57-0.85; p = 0.0003). Additionally, NOACs reduced the risk of gastrointestinal bleeding in AF VHD/N-VHD (RR 0.80; 95% CI 0.66-0.96; p = 0.02), specifically in the VHD subgroup (RR 0.69; 95% CI 0.54-0.89; p = 0.004). Moreover, NOACs were associated with a decreased risk for minor and non-fatal bleeding in AF patients with VHD/N-VHD (RR 0.86; 95% CI 0.75-0.99; p = 0.04).

Conclusion: NOACs are effective and safe for ischemic stroke, systemic embolic events, myocardial infarction, intracranial bleeding, and gastrointestinal bleeding in AF patients with VHD/N-VHD.

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