Direct Oral Anticoagulants versus Aspirin for Secondary Stroke Prevention in Patients with Embolic Stroke of Undetermined Source: An Updated Systematic Review and Meta-Analysis of Randomized Controlled Trials.

IF 1.9
Juan Armando Talavera, Larissa Teixeira, Thomas Costa Alexandre, Denilsa Navalha, Tathiane Brum Gibicoski, Nicole Fernandez, Jeffrey Healey, Luciana Armaganijan, Guilherme Dagostin de Carvalho
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Abstract

Embolic stroke of undetermined source (ESUS) accounts for around 20% of ischemic strokes. The ideal treatment for secondary prevention in ESUS remains unclear. This study aimed to perform a systematic review and meta-analysis of randomized controlled trials (RCTs) comparing the safety and efficacy of direct oral anticoagulants (DOACs) versus aspirin in patients with ESUS. A systematic search of PubMed, Embase, Cochrane, and Web of Science databases was conducted for eligible trials until March 2024. The primary outcome was recurrent stroke, while safety outcomes included major bleeding and clinically relevant non-major bleeding (CRNMB). Hazard ratios (HRs) with 95% confidence intervals (CIs) were calculated for analysis. Four RCTs were included, involving 13,970 patients, half of whom were randomized to the DOACs group. Over a mean follow-up of 16 months, DOACs did not significantly reduce recurrent stroke (HR: 0.95; 95% CI: 0.81-1.09; p=0.44), ischemic stroke (HR: 0.91; 95% CI: 0.79-1.06; p=0.23), all-cause mortality (HR: 1.11; 95% CI: 0.87-1.42; p=0.40), or major bleeding (HR: 1.56; 95% CI: 0.85%-2.86; p=0.15) compared to aspirin. However, DOACs were associated with a significantly higher risk of CRNMB (HR: 1.54; 95% CI: 1.23-1.92; p=0.0002). Subgroup analysis revealed no significant differences in stroke recurrence among patients with low or high CHA2-DS2-VASc scores. DOACs did not demonstrate superior efficacy over aspirin in preventing recurrent stroke among ESUS patients and were linked to an increased risk of CRNMB.

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来源不明的栓塞性卒中患者直接口服抗凝剂与阿司匹林预防继发性卒中:一项最新的随机对照试验系统评价和荟萃分析
来源不明的栓塞性卒中(ESUS)约占缺血性卒中的20%。ESUS二级预防的理想治疗方法尚不清楚。本研究旨在对随机对照试验(rct)进行系统回顾和荟萃分析,比较直接口服抗凝剂(DOACs)与阿司匹林在ESUS患者中的安全性和有效性。在2024年3月之前,对PubMed、Embase、Cochrane和Web of Science数据库进行了系统搜索,以获得符合条件的试验。主要结局是卒中复发,而安全结局包括大出血和临床相关的非大出血(CRNMB)。计算风险比(hr)和95%置信区间(ci)进行分析。纳入4项随机对照试验,共13970例患者,其中一半随机分为DOACs组。在平均16个月的随访中,DOACs并没有显著减少卒中复发(HR: 0.95;95% ci: 0.81-1.09;p=0.44),缺血性卒中(HR: 0.91;95% ci: 0.79-1.06;p=0.23),全因死亡率(HR: 1.11;95% ci: 0.87-1.42;p=0.40)或大出血(HR: 1.56;95% ci: 0.85%-2.86;P =0.15)。然而,DOACs与CRNMB的风险显著升高相关(HR: 1.54;95% ci: 1.23-1.92;p = 0.0002)。亚组分析显示,CHA2-DS2-VASc评分高低的患者卒中复发无显著差异。在ESUS患者中,DOACs在预防卒中复发方面没有表现出比阿司匹林更好的疗效,并且与CRNMB风险增加有关。
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