Direct Oral Anticoagulants in Patients Undergoing Urgent Reperfusion for Nonvalvular Atrial Fibrillation-Related Ischemic Stroke: A Brief Report on Literature Evidence.

IF 1.7 Q4 NEUROSCIENCES Neurology Research International Pub Date : 2019-02-24 eCollection Date: 2019-01-01 DOI:10.1155/2019/9657073
Luca Masotti, Elisa Grifoni, Alessandro Dei, Vieri Vannucchi, Federico Moroni, Grazia Panigada, Costanza Nicotra, Stefano Spolveri, Giancarlo Landini
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引用次数: 5

Abstract

Introduction: The optimal timing for starting anticoagulation in the early phase of nonvalvular atrial fibrillation (NVAF)-related acute ischemic stroke (AIS) remains a challenge, especially in patients undergoing urgent reperfusion by systemic thrombolysis or mechanical thrombectomy. The aim of our study was to review the literature evidence reporting on safety of direct oral anticoagulants (DOACs) starting in the early phase of NVAF-related AIS undergoing systemic thrombolysis and/or mechanical thrombectomy.

Materials and methods: We reviewed the PubMed databases searching articles reporting on efficacy and safety of DOACs starting time within two weeks from AIS onset in patients undergoing systemic thrombolysis and/or mechanical thrombectomy.

Results: Three studies were selected, overall including one hundred and six patients (62 females, 58.4%). Median National Institute of Health Stroke Scale (NIHSS) score at hospital admission ranged from 9 to 13 points. Median DOACs starting time ranged from 2 to 6 days. Median CHA2DS2-VASC score ranged from 4 to 6 points. Follow-up was limited to 14 days in one study, 30 days in another, and 90 days in a third one. Overall, stroke recurrence and/or intracranial bleeding occurred in two patients (1.9%) and no patient died at follow-up.

Conclusion: Small sample size real life studies seem to demonstrate that the introduction of DOACs in the early phase of NVAF-related AIS undergoing urgent reperfusion is efficacious and safe. Prospective RCTs are necessary to confirm these findings.

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直接口服抗凝剂在非瓣膜性房颤相关缺血性卒中紧急再灌注患者中的应用:文献证据的简要报告
在非瓣膜性心房颤动(NVAF)相关的急性缺血性卒中(AIS)早期开始抗凝的最佳时机仍然是一个挑战,特别是在通过全身溶栓或机械取栓进行紧急再灌注的患者中。本研究的目的是回顾有关非瓣膜性房颤相关AIS患者早期开始接受全身溶栓和/或机械取栓的直接口服抗凝剂(DOACs)安全性的文献证据。材料和方法:我们回顾了PubMed数据库,检索了报道在AIS发病后两周内进行全身溶栓和/或机械取栓的患者使用DOACs的有效性和安全性的文章。结果:共纳入3项研究,共纳入106例患者(女性62例,58.4%)。入院时美国国立卫生研究院卒中量表(NIHSS)得分中位数在9到13分之间。DOACs起始时间中位数为2 ~ 6天。CHA2DS2-VASC评分中位数为4 ~ 6分。一项研究的随访时间为14天,另一项为30天,第三项为90天。总体而言,2例患者(1.9%)发生脑卒中复发和/或颅内出血,随访期间无患者死亡。结论:小样本量的现实生活研究似乎表明,在紧急再灌注的nvaf相关AIS早期引入DOACs是有效和安全的。需要前瞻性随机对照试验来证实这些发现。
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来源期刊
CiteScore
3.50
自引率
0.00%
发文量
10
审稿时长
17 weeks
期刊介绍: Neurology Research International is a peer-reviewed, Open Access journal that publishes original research articles, review articles, and clinical studies focusing on diseases of the nervous system, as well as normal neurological functioning. The journal will consider basic, translational, and clinical research, including animal models and clinical trials.
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