Department of Internal Medicine, Faculty of Medicine, School of Health Sciences, University of Thessaly, Larissa, Greece.
J Am Coll Cardiol. 2020 Jan 28;75(3):333-340. doi: 10.1016/j.jacc.2019.11.024.
The term embolic stroke of undetermined source (ESUS) was introduced in 2014 to describe patients with a nonlacunar ischemic stroke and no convincing etiology. The terms ESUS and cryptogenic stroke are not synonyms, as the latter also includes patients with multiple stroke etiologies or incomplete diagnostic work-up. ESUS involves approximately 17% of all ischemic stroke patients, and these patients are typically younger with mild strokes and an annual rate of stroke recurrence of 4% to 5%. It was hypothesized that oral anticoagulation may decrease the risk of stroke recurrence in ESUS, which was tested in 2 large randomized controlled trials: the NAVIGATE ESUS (Rivaroxaban Versus Aspirin in Secondary Prevention of Stroke and Prevention of Systemic Embolism in Patients With Recent Embolic Stroke of Undetermined Source) and the RE-SPECT ESUS (Dabigatran Etexilate for Secondary Stroke Prevention in Patients With Embolic Stroke of Undetermined Source). The present review discusses the trials of anticoagulation in patients with ESUS, suggests potential explanations for their neutral results, and highlights the rationale that supports ongoing and future research in this population aiming to reduce the associated risk for stroke recurrence.
不明来源栓塞性卒中(ESUS)一词于 2014 年提出,用于描述非腔隙性缺血性卒中和无明确病因的患者。ESUS 和隐源性卒中这两个术语并非同义词,因为后者还包括具有多种卒中病因或诊断不完整的患者。ESUS 约占所有缺血性卒中患者的 17%,这些患者通常年龄较小,卒中较轻,年卒中复发率为 4%至 5%。人们假设口服抗凝治疗可能会降低 ESUS 患者卒中复发的风险,这在两项大型随机对照试验中进行了检验:NAVIGATE ESUS(利伐沙班与阿司匹林在不明来源栓塞性卒中二级预防中的疗效比较)和 RE-SPECT ESUS(达比加群酯在不明来源栓塞性卒中二级预防中的疗效)。本文综述讨论了 ESUS 患者抗凝治疗的临床试验,提出了其中性结果的潜在解释,并强调了支持该人群正在进行和未来研究的理由,旨在降低相关卒中复发风险。