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莫努匹韦治疗 COVID-19 门诊患者:一项更新的荟萃分析。

Molnupiravir for the treatment of COVID-19 outpatients: An updated meta-analysis.

机构信息

Division of Infectious Diseases, Department of Medicine, King Edward Medical University, Lahore, Pakistan.

College of Medicine, Alfaisal University, Riyadh, Saudi Arabia.

出版信息

J Microbiol Immunol Infect. 2024 Jun;57(3):396-402. doi: 10.1016/j.jmii.2024.03.002. Epub 2024 Mar 16.

Abstract

BACKGROUND

The majority of available data on molnupiravir come from an unvaccinated COVID-19 population. Therefore, we conducted this meta-analysis to integrate evidence from recent randomized controlled trials (RCTs) as well as observational studies stratified by vaccination status to determine the clinical efficacy and safety of molnupiravir in COVID-19 outpatients.

METHODS

We searched PubMed, Embase, the Cochrane Library, medRxiv, and ClinicalTrials.gov from inception to November 2023. We conducted our meta-analysis using RevMan 5.4 with risk ratio (RR) as the effect measure.

RESULTS

We included 8 RCTs and 5 observational studies in our meta-analysis. Molnupiravir reduced the risk of all-cause mortality (RR 0.28; 95% CI: 0.20-0.79, I = 0%) but did not decrease the hospitalization rate (RR 0.67; 95% CI: 0.45-1.00, I = 53%) in the overall population; in the immunized population, no benefits were observed. Molnupiravir lowered the rate of no recovery (RR 0.78; 95% CI: 0.76-0.81, I = 0%) and increased virological clearance at day 5 (RR 2.68; 95% CI: 1.94-4.22, I = 85%). There was no increase in the incidence of adverse events.

CONCLUSIONS

Molnupiravir does not decrease mortality and hospitalization rates in immunized patients with COVID-19. However, it does shorten the disease course and increases the recovery rate. The use of molnupiravir will need to be considered on a case-by-case basis in the context of the prevailing social circumstances, the resource setting, drug costs, and the healthcare burden.

摘要

背景

现有的关于莫努匹韦的多数数据均来自于未接种疫苗的 COVID-19 人群。因此,我们进行了这项荟萃分析,以整合最近的随机对照试验(RCT)和基于疫苗接种状态分层的观察性研究的证据,以确定莫努匹韦在 COVID-19 门诊患者中的临床疗效和安全性。

方法

我们从创建至 2023 年 11 月在 PubMed、Embase、Cochrane 图书馆、medRxiv 和 ClinicalTrials.gov 进行了检索。我们使用 RevMan 5.4 进行荟萃分析,以风险比(RR)作为效应量。

结果

我们的荟萃分析纳入了 8 项 RCT 和 5 项观察性研究。莫努匹韦降低了全因死亡率(RR 0.28;95%CI:0.20-0.79,I = 0%),但并未降低总体人群的住院率(RR 0.67;95%CI:0.45-1.00,I = 53%);在免疫人群中,未观察到获益。莫努匹韦降低了无恢复率(RR 0.78;95%CI:0.76-0.81,I = 0%),并增加了第 5 天的病毒学清除率(RR 2.68;95%CI:1.94-4.22,I = 85%)。不良反应发生率没有增加。

结论

莫努匹韦不能降低 COVID-19 免疫患者的死亡率和住院率。然而,它确实缩短了病程并提高了恢复率。在考虑使用莫努匹韦时,需要根据当前的社会环境、资源设置、药物成本和医疗保健负担,综合考虑具体情况。

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