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卵圆孔未闭伴不明来源栓塞性卒中患者应用达比加群或阿司匹林治疗:RE-SPECT ESUS 研究结果。

Dabigatran or Aspirin After Embolic Stroke of Undetermined Source in Patients With Patent Foramen Ovale: Results From RE-SPECT ESUS.

机构信息

Institute for Medical Informatics, Biometry and Epidemiology, University Duisburg-Essen, Germany (H-C.D.).

Department of Medicine, Faculty of Medicine, Chulalongkorn Stroke Center, King Chulalongkorn Memorial Hospital, Chulalongkorn University, Thai Red Cross Society, Bangkok, Thailand (A.C.).

出版信息

Stroke. 2021 Mar;52(3):1065-1068. doi: 10.1161/STROKEAHA.120.031237. Epub 2021 Jan 28.

Abstract

BACKGROUND AND PURPOSE

Patent foramen ovale (PFO) may increase the risk of embolic stroke of undetermined source (ESUS). Guidelines suggest anticoagulation may be more effective than antiplatelets in preventing stroke in patients with ESUS and PFO when interventional closure is not performed.

METHODS

Patients with ESUS randomized to dabigatran (150/110 mg BID) or aspirin (100 mg QD) from the RE-SPECT ESUS study (Randomized, Double-Blind, Evaluation in Secondary Stroke Prevention Comparing the Efficacy and Safety of the Oral Thrombin Inhibitor Dabigatran Etexilate Versus Acetylsalicylic Acid in Patients With Embolic Stroke of Undetermined Source) were included. The rate of recurrent stroke (primary end point) and ischemic stroke was reported for patients with and without baseline PFO. A meta-analysis comparing the effects of anticoagulant and antiplatelet therapy on ischemic stroke in patients with PFO was updated to include RE-SPECT ESUS.

RESULTS

PFO was present in 680 of 5388 (12.6%) patients with documented PFO status. The risk of recurrent stroke with dabigatran versus aspirin was similar in patients with and without PFO ( for interaction, 0.8290). In patients with PFO, the meta-analysis found no statistically significant difference between anticoagulant and antiplatelet therapy (odds ratio, 0.70 [95% CI, 0.43-1.14]) for ischemic stroke.

CONCLUSIONS

There is insufficient evidence to recommend anticoagulation over antiplatelet therapy for patients with ESUS and a PFO. More data are needed to guide antithrombotic therapy in this population. Registration: URL: https://www.clinicaltrials.gov. Unique identifier: NCT02239120.

摘要

背景与目的

卵圆孔未闭(PFO)可能会增加不明来源栓塞性卒中(ESUS)的风险。指南建议,在未进行介入封堵的情况下,对于 ESUS 和 PFO 患者,抗凝治疗可能比抗血小板治疗更能有效预防卒中。

方法

从 RE-SPECT ESUS 研究(随机、双盲、比较口服凝血酶抑制剂达比加群酯与乙酰水杨酸在栓塞性卒中来源不明患者中的疗效和安全性的二次卒中预防研究)中随机分配至达比加群(150/110mg,每日两次)或阿司匹林(100mg,每日一次)的 ESUS 患者被纳入。报告了有和无基线 PFO 患者的复发性卒中(主要终点)和缺血性卒中的发生率。一项纳入 RE-SPECT ESUS 的比较 PFO 患者抗凝和抗血小板治疗对缺血性卒中影响的荟萃分析得到了更新。

结果

在有记录的 PFO 状态的 5388 例患者中,680 例(12.6%)存在 PFO。达比加群与阿司匹林相比,PFO 患者的复发性卒中风险相似(交互检验,0.8290)。在 PFO 患者中,荟萃分析发现抗凝治疗与抗血小板治疗在缺血性卒中方面无统计学差异(比值比,0.70 [95%CI,0.43-1.14])。

结论

尚无充分证据推荐 ESUS 和 PFO 患者使用抗凝治疗而非抗血小板治疗。需要更多数据来指导该人群的抗血栓治疗。注册:网址:https://www.clinicaltrials.gov。唯一标识符:NCT02239120。

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