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伊维菌素备受关注:COVID-19 患者疗效的系统评价和荟萃分析及可能引发争议的原因。

Ivermectin under scrutiny: a systematic review and meta-analysis of efficacy and possible sources of controversies in COVID-19 patients.

机构信息

Student Research Committee, Alborz University of Medical Sciences, Karaj, Iran.

School of Medicine, Alborz University of Medical Sciences, Karaj, Iran.

出版信息

Virol J. 2022 Jun 13;19(1):102. doi: 10.1186/s12985-022-01829-8.

Abstract

BACKGROUND

We conducted a systematic review and meta-analysis to evaluate the efficacy of ivermectin for COVID-19 patients based on current peer-reviewed RCTs and to address disputes over the existing evidence.

METHODS

MEDLINE (Pubmed), Scopus, Web of Science, Cochrane library, Google scholar and Clinicaltrials.gov were searched for RCTs assessing the efficacy of Ivermectin up to 20 February 2022. A systematic review and meta-analysis of studies was performed based on the PRISMA 2020 statement criteria.

RESULTS

19 and 17 studies were included in this systematic review and meta-analysis, respectively. There was no significant difference in progression to severe disease (log OR - 0.27 [95% CI - 0.61 to 0.08], I2 = 42.29%), negative RT-PCR (log OR 0.25 [95% CI - 0.18-0.68], I2 = 58.73%), recovery (log OR 0.11 [95% CI - 0.22-0.45], I2 = 13.84%), duration of hospitalization (SMD - 0.40 [95% CI - 0.85-0.06], I2 = 88.90%), time to negative RT-PCR (SMD - 0.36 [95% CI - 0.89-0.17], I2 = 46.2%), and viral load (SMD -0.17 [95% CI -0.45 to 0.12], I^2 = 0%). It is worth noting that, based on low-certainty evidence, ivermectin may possibly reduce mortality (log OR - 0.67 [95% CI - 1.20 to - 0.13], I2 = 28.96%). However, studies with a higher risk of bias were more likely to indicate positive effects on the efficacy of this drug, according to our subgroup analyses based on study quality.

CONCLUSION

Ivermectin did not have any significant effect on outcomes of COVID-19 patients and as WHO recommends, use of ivermectin should be limited to clinical trials.

摘要

背景

我们进行了一项系统评价和荟萃分析,以评估伊维菌素治疗 COVID-19 患者的疗效,该研究基于当前的同行评审 RCT,并解决了现有证据存在的争议。

方法

检索了 MEDLINE(Pubmed)、Scopus、Web of Science、Cochrane 图书馆、Google Scholar 和 Clinicaltrials.gov,以评估截至 2022 年 2 月 20 日伊维菌素疗效的 RCT。根据 PRISMA 2020 声明标准,对研究进行了系统评价和荟萃分析。

结果

本系统评价和荟萃分析分别纳入了 19 项和 17 项研究。在进展为重症疾病(logOR-0.27[95%CI-0.61 至 0.08],I2=42.29%)、RT-PCR 转阴(logOR0.25[95%CI-0.18 至 0.68],I2=58.73%)、康复(logOR0.11[95%CI-0.22 至 0.45],I2=13.84%)、住院时间(SMD-0.40[95%CI-0.85 至 0.06],I2=88.90%)、RT-PCR 转阴时间(SMD-0.36[95%CI-0.89 至 0.17],I2=46.2%)和病毒载量(SMD-0.17[95%CI-0.45 至 0.12],I^2=0%)方面,伊维菌素均无显著效果。值得注意的是,基于低质量证据,伊维菌素可能降低死亡率(logOR-0.67[95%CI-1.20 至-0.13],I2=28.96%)。然而,根据研究质量的亚组分析,偏倚风险较高的研究更有可能表明该药物疗效呈阳性。

结论

伊维菌素对 COVID-19 患者的结局没有任何显著影响,并且正如世卫组织所建议的,伊维菌素的使用应限于临床试验。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/404d/9195212/da72dbfaefeb/12985_2022_1829_Fig1_HTML.jpg

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