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COVID-19 和 ARDS 患者的纤维蛋白溶解治疗:系统评价和荟萃分析方案。

Fibrinolytic therapy in patients with COVID-19 and ARDS: protocol for a systematic review and meta-analysis.

机构信息

Critical Care Medicine, Hospital Sirio-Libanes, Sao Paulo, Brazil

Evidence Based Medicine, Universidade Federal de Sao Paulo, Sao Paulo, Brazil.

出版信息

BMJ Open. 2023 Jan 2;13(1):e066623. doi: 10.1136/bmjopen-2022-066623.

Abstract

INTRODUCTION

In COVID-19-related acute respiratory distress syndrome (ARDS), the clot play a role in gas exchange abnormalities. Fibrinolytic therapy can improve alveolar ventilation by restoring blood flow. In this systematic review and meta-analysis protocol, we aim to assess the safety and efficacy of fibrinolytic therapy in such a population.

METHODS

We will perform a systematic search in MEDLINE, EMBASE, Cochrane CENTRAL and LILACS databases without language restrictions for relevant randomised controlled trials (RCTs) and quasi-RCTs. Two review authors will independently perform data extraction and quality assessments of data from included studies. In case of divergence, a third author will be contacted. The Cochrane handbook will be used for guidance. If the results are not appropriate for a meta-analysis, a descriptive analysis will be performed.

DISCUSSION

This systematic review and meta-analysis protocol will provide current evidence about the safety and efficacy of fibrinolytic therapy in patients with COVID-19 and ARDS. These findings will provide if fibrinolytic therapy might be an option for a desperate clinical setting, where all medical efforts have been used.

PROSPERO REGISTRATION NUMBER

PROSPERO CRD42020187482.

ETHICS AND DISSEMINATION

Ethics committee approval is not necessary. We intend to update the public registry, report any protocol amendments and publish the results in a widely accessible journal.

摘要

简介

在 COVID-19 相关的急性呼吸窘迫综合征(ARDS)中,血栓在气体交换异常中起作用。纤维蛋白溶解疗法可通过恢复血流来改善肺泡通气。在这项系统评价和荟萃分析方案中,我们旨在评估此类人群中纤维蛋白溶解疗法的安全性和疗效。

方法

我们将在 MEDLINE、EMBASE、Cochrane CENTRAL 和 LILACS 数据库中进行系统检索,不限制语言,以检索相关的随机对照试验(RCT)和准 RCT。两名综述作者将独立地从纳入研究中提取数据并进行质量评估。如果存在分歧,将联系第三名作者。将使用 Cochrane 手册进行指导。如果结果不适合进行荟萃分析,则将进行描述性分析。

讨论

本系统评价和荟萃分析方案将提供关于 COVID-19 和 ARDS 患者纤维蛋白溶解疗法的安全性和疗效的最新证据。这些发现将提供纤维蛋白溶解疗法是否可能是一种绝望的临床情况下的选择,在这种情况下,已经用尽了所有的医疗手段。

PROSPERO 注册号:PROSPERO CRD42020187482。

伦理和传播

不需要伦理委员会批准。我们打算更新公共注册处,报告任何方案修订,并在广泛可访问的期刊上发表结果。

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本文引用的文献

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