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依达拉奉联合阿替普酶治疗急性缺血性脑卒中患者的安全性和有效性:系统评价和荟萃分析。

Safety and efficacy of edaravone combined with alteplase for patients with acute ischemic stroke: A systematic review and meta-analysis.

机构信息

Department of Neurology, Clinical Medical College and The First Affiliated Hospital of Chengdu Medical College, Chengdu, China.

Department of Neurology, Clinical Medical College and The First Affiliated Hospital of Chengdu Medical College, Chengdu, China;, Email:

出版信息

Pharmazie. 2021 Feb 25;76(2):109-113. doi: 10.1691/ph.2021.0949.

Abstract

Early administration of edaravone for acute ischemic stroke patients (AIS) receiving intravenous thrombolysis (IVT) has a potential neuroprotective effect. This study aimed to estimate the safety and efficacy of edaravone for AIS patients receiving IVT. We searched PubMed, Embase, Cochrane Library and Chinese Databases (CNKI database, Weipu database, and Wanfang database) for randomized controlled trials (RCT) from the inception of the database to 20 July 2020. Efficacy outcome was reduced National Institutes of Health Stroke Scale (NIHSS) score before and after treatment. Safety outcomes were intracranial hemorrhage (ICH) and mortality. Review Manager 5.3 and Stata 14.0 was used to perform the meta-analysis. A total of 1877 AIS patients from 17 studies were included, 939 (50.03%) patients received edaravone combined with alteplase treatment. Compared with alteplase alone, combined treatment reduced the NIHSS score (MD=3.95,95% CI 2.92-4.99, I² = 92%) and ICH (OR=0.44,95% CI 0.29-0.66, I² =0%) during hospitalization. There was no significant association between combined treatment and mortality during follow-up (OR=0.43,95% CI 0.13-1.42, I² =0%). Conclusions: Edaravone combined with alteplase seems to be safe and effective for AIS patients' short term outcomes.

摘要

急性缺血性脑卒中(AIS)患者接受静脉溶栓(IVT)治疗时,早期应用依达拉奉具有潜在的神经保护作用。本研究旨在评估依达拉奉对接受 IVT 的 AIS 患者的安全性和疗效。我们检索了 PubMed、Embase、Cochrane 图书馆和中国数据库(CNKI 数据库、维普数据库和万方数据库),检索了从数据库建立到 2020 年 7 月 20 日的随机对照试验(RCT)。疗效结局为治疗前后的国立卫生研究院卒中量表(NIHSS)评分降低。安全性结局为颅内出血(ICH)和死亡率。采用 Review Manager 5.3 和 Stata 14.0 进行荟萃分析。共纳入来自 17 项研究的 1877 例 AIS 患者,其中 939 例(50.03%)患者接受了依达拉奉联合阿替普酶治疗。与阿替普酶单独治疗相比,联合治疗降低了 NIHSS 评分(MD=3.95,95%CI 2.92-4.99,I² = 92%)和住院期间的 ICH(OR=0.44,95%CI 0.29-0.66,I² =0%)。联合治疗与随访期间的死亡率之间无显著相关性(OR=0.43,95%CI 0.13-1.42,I² =0%)。结论:依达拉奉联合阿替普酶似乎对 AIS 患者的短期结局安全有效。

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