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不同剂量替奈普酶治疗急性缺血性脑卒中的有效性和安全性的系统评价和荟萃分析方案。

Effectiveness and safety of different doses of tenecteplase in the treatment of acute ischemic stroke: A protocol for systematic review and meta-analysis.

机构信息

XiXi Hospital of Hangzhou, Hangzhou, Zhejiang Province, China.

出版信息

Medicine (Baltimore). 2021 Jan 22;100(3):e23805. doi: 10.1097/MD.0000000000023805.

DOI:10.1097/MD.0000000000023805
PMID:33545944
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7837936/
Abstract

BACKGROUND

Tenecteplase is a modified recombinant tissue-plasminogen activator, which is effective and safe in the treatment of acute ischemic stroke. However, the therapeutic dose of tenecteplase has been controversial. The purpose of this study is to systematically investigate the efficacy and safety of different doses of tenecteplase thrombolytic therapy for acute ischemic stroke.

METHODS

Computer retrieval of English databases (PubMed, EMBASE, Web of Science, the Cochrane Library) and Chinese databases (CNKI, Wanfang, Viper, and Chinese Biomedical Database) is conducted for a randomized controlled clinical study on thrombolytic treatment of acute ischemic stroke with different doses of tenecteplase from the establishment of the database to October 2020. Two researchers independently conduct data extraction and literature quality evaluation on the quality of the included studies, and meta-analysis is conducted on the included literatures using RevMan5.3 software.

OUTCOME

In this study, National Institute of Health Stroke Scale (NIHSS) score, Modified Rankin Scale (mRS) score scale, symptomatic intracranial hemorrhage (SICH) incidence, All-cause mortality, and so on are used to evaluate the efficacy and safety of tenecteplase thrombolytic therapy in acute ischemic stroke with different doses.

CONCLUSION

This study will provide reliable evidence-based evidence for the clinical application of different doses of tenecteplase in thrombolytic therapy for acute ischemic stroke.

OSF REGISTRATION NUMBER

DOI 10.17605/OSF.IO/2MPCW.

摘要

背景

替奈普酶是一种改良的重组组织型纤溶酶原激活剂,在治疗急性缺血性脑卒中方面有效且安全。然而,替奈普酶的治疗剂量一直存在争议。本研究旨在系统评估不同剂量替奈普酶溶栓治疗急性缺血性脑卒中的疗效和安全性。

方法

计算机检索建库至 2020 年 10 月PubMed、EMBASE、Web of Science、Cochrane 图书馆英文数据库及中国知网、万方、维普、中国生物医学文献数据库中关于不同剂量替奈普酶溶栓治疗急性缺血性脑卒中的随机对照临床研究。由 2 位研究者独立提取资料并评价纳入研究的质量后,采用 RevMan5.3 软件进行 Meta 分析。

结局

本研究采用美国国立卫生研究院卒中量表(NIHSS)评分、改良 Rankin 量表(mRS)评分、症状性颅内出血(SICH)发生率、全因死亡率等指标评价不同剂量替奈普酶溶栓治疗急性缺血性脑卒中的疗效和安全性。

结论

本研究将为不同剂量替奈普酶在急性缺血性脑卒中溶栓治疗中的临床应用提供可靠的循证医学证据。

OSF 注册号:DOI 10.17605/OSF.IO/2MPCW。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a17a/7837936/167d31cebe63/medi-100-e23805-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a17a/7837936/167d31cebe63/medi-100-e23805-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a17a/7837936/167d31cebe63/medi-100-e23805-g001.jpg

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