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血管紧张素转换酶抑制剂和血管紧张素 II 受体阻滞剂治疗 COVID-19:一项随机临床试验的实时系统评价。

Angiotensin-converting-enzyme inhibitors and angiotensin II receptor blockers for COVID-19: A living systematic review of randomized clinical trials.

机构信息

Interdisciplinary Centre for Health Studies (CIESAL), Universidad de Valparaíso, Cochrane Chile Associate Centre, Viña del Mar, Chile. ORCID: 0000-0001-9505-0358.

Interdisciplinary Centre for Health Studies (CIESAL), Universidad de Valparaíso, Cochrane Chile Associate Centre, Viña del Mar, Chile. ORCID: 0000-0001-8738-2184.

出版信息

Medwave. 2021 Mar 3;21(2):e8105. doi: 10.5867/medwave.2021.02.8105.

Abstract

OBJECTIVE

This living systematic review aims to provide a timely, rigorous, and continuously updated summary of the evidence available on the role of angiotensin-converting enzyme inhibitors (ACEi) and angiotensin II receptor blockers (ARB) in the treatment of patients with COVID-19.

DATA SOURCES

We conducted searches in PubMed/Medline, Embase, Cochrane Central Register of Controlled Trials (CENTRAL), grey literature and in a centralized repository in L·OVE (Living OVerview of Evidence), which retrieves articles from multiple sources such as PubMed/MEDLINE, Cochrane Central Register of Controlled Trials, Embase, among other pre-print and protocols repositories. In response to the COVID-19 emergency, L·OVE (Living OVerview of Evidence) was adapted to expand the range of evidence and customized to group all COVID-19 evidence in one place on a daily search basis. The search covered a period of time up to July 31, 2020.

ELIGIBILITY CRITERIA FOR SELECTING STUDIES AND METHODS

We adapted an already published standard protocol for multiple parallel living systematic reviews to this question's specificities. We included randomized trials evaluating the effect of either suspension or indication of angiotensin-converting-enzyme inhibitors or angiotensin II receptor blockers as monotherapy, or in combination versus placebo or no treatment in patients with COVID-19. We searched for randomized trials evaluating the effect of angiotensin-converting enzyme inhibitors or angiotensin II receptor blockers versus placebo or no treatment in patients with COVID-19. Two reviewers independently screened each study for eligibility, extracted data, and assessed the risk of bias. We pooled the results using meta-analysis and applied the GRADE system to assess the certainty of the evidence for each outcome. We will resubmit results every time the conclusions change or whenever there are substantial updates.

RESULTS

We screened 772 records, but none was considered for eligibility. We identified 55 ongoing studies, including 41 randomized trials evaluating angiotensin-converting enzyme inhibitors or angiotensin II receptor blockers for patients with COVID-19.

CONCLUSIONS

We did not find a randomized clinical trial meeting our inclusion criteria, and hence there is no evidence for supporting the role of angiotensin-converting enzyme inhibitors and angiotensin II receptor blockers in the treatment of patients with COVID-19. A substantial number of ongoing studies would provide valuable evidence to inform researchers and decision-makers in the near future.

PROSPERO REGISTRATION NUMBER

CRD42020182495.

PROTOCOL PREPRINT DOI

10.31219/osf.io/vp9nj.

摘要

目的

本实时系统评价旨在提供有关血管紧张素转换酶抑制剂 (ACEi) 和血管紧张素 II 受体阻滞剂 (ARB) 在治疗 COVID-19 患者中的作用的最新、严格和持续更新的证据总结。

数据来源

我们在 PubMed/Medline、Embase、Cochrane 对照试验中心注册库 (CENTRAL)、灰色文献以及 L·OVE(证据实时综合)集中存储库中进行了检索,L·OVE(证据实时综合)是一个集中存储库,可从多个来源(如 PubMed/MEDLINE、Cochrane 对照试验中心注册库、Embase 等预印本和方案存储库)检索文章。为应对 COVID-19 紧急情况,L·OVE(证据实时综合)进行了调整,以扩大证据范围,并定制了每天搜索一次将所有 COVID-19 证据集中在一个地方的功能。搜索时间截止到 2020 年 7 月 31 日。

研究选择和方法的资格标准

我们针对这个问题的具体情况,对已经发表的多平行实时系统评价标准方案进行了调整。我们纳入了评估 ACEi 或 ARB 作为单一疗法或联合治疗 COVID-19 患者时暂停或指示使用 ACEi 或 ARB 的效果的随机试验。我们搜索了评估 ACEi 或 ARB 与安慰剂或无治疗在 COVID-19 患者中的效果的随机试验。两名审查员独立筛选每个研究的资格、提取数据并评估偏倚风险。我们使用荟萃分析汇总结果,并应用 GRADE 系统评估每个结局的证据确定性。只要结论发生变化或出现实质性更新,我们将重新提交结果。

结果

我们筛选了 772 条记录,但没有一条被认为符合入选标准。我们确定了 55 项正在进行的研究,其中包括 41 项评估 ACEi 或 ARB 治疗 COVID-19 患者的随机试验。

结论

我们没有发现符合纳入标准的随机临床试验,因此没有证据支持 ACEi 和 ARB 在治疗 COVID-19 患者中的作用。大量正在进行的研究将在不久的将来为研究人员和决策者提供有价值的证据。

PROSPERO 注册号:CRD42020182495。

方案预印本 DOI:10.31219/osf.io/vp9nj。

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