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伊维菌素作为新冠肺炎患者的一种治疗方式:对最新随机对照试验的系统评价和荟萃分析

Ivermectin as a Treatment Modality in COVID-19 Patients: A Systematic Review and Meta-Analysis of Up-To-Date RCTs.

作者信息

Maddukuri Raghava Kalyan, Desimalla Madhavi Latha, Banavathu Reshma, Arepalli Sai Pavan Kumar

机构信息

Department of Pharmacy Practice, Chebrolu Hanumaiah Institute of Pharmaceutical Sciences, Beside RVR and JC College of Engineering and Technology, Chandramoulipuram, Chowdavaram, Guntur, Andhra Pradesh, India.

出版信息

Indian J Community Med. 2025 Jan-Feb;50(1):9-19. doi: 10.4103/ijcm.ijcm_117_23. Epub 2025 Jan 23.

Abstract

The objective of this systematic review and meta-analysis is to assess the efficacy and safety of Ivermectin compared to placebo or standard of care for the treatment and prevention of COVID-19 disease. Literature search was carried out in PubMed, Scopus, and google scholar. Clinical trial registries (clinical trail.gov) and preprint servers (Medrxiv) were also searched for registered and preprint data respectively. Mortality, Clinical recovery, Clinical worsening, duration of hospital stay, and adverse events were considered as primary outcomes while viral clearance is considered as a secondary outcome. Revised Cochrane risk of bias assessment tool was used to assess the risk of bias. Random effect meta-analysis was carried out for all the outcomes. GRADE was used to rate the certainty of evidence. A total of 19 RCTs with 1111 patients were included in the analysis. Ivermectin use did was not associated with a reduction in the incidence of mortality, duration of hospitalization, clinical worsening, and incidence of adverse events nor it was associated with an increase in clinical improvement compared to either placebo or standard of care. Ivermectin also did not show any reduction in viral clearance compared to both placebo or standard of care and this was associated with substantial inconsistency. The overall certainty of the evidence was very low to low. Based on the very low to low certainty of the evidence, we consider Ivermectin ineffective in the management of COVID-19 disease, both as treatment and prophylaxis.

摘要

本系统评价和荟萃分析的目的是评估与安慰剂或标准治疗相比,伊维菌素治疗和预防新冠病毒病的疗效和安全性。在PubMed、Scopus和谷歌学术上进行了文献检索。还分别在临床试验注册库(clinicaltrial.gov)和预印本服务器(Medrxiv)中检索了注册数据和预印本数据。将死亡率、临床恢复情况、临床恶化情况、住院时间和不良事件视为主要结局,而病毒清除情况则视为次要结局。使用修订后的Cochrane偏倚风险评估工具来评估偏倚风险。对所有结局进行随机效应荟萃分析。采用GRADE对证据的确定性进行分级。分析共纳入19项随机对照试验,涉及1111名患者。与安慰剂或标准治疗相比,使用伊维菌素与死亡率、住院时间、临床恶化情况及不良事件发生率的降低无关,也与临床改善情况的增加无关。与安慰剂或标准治疗相比,伊维菌素在病毒清除方面也未显示出任何降低,且存在很大的不一致性。证据的总体确定性非常低至低。基于证据的确定性非常低至低,我们认为伊维菌素在新冠病毒病的治疗和预防中均无效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a91/11927832/0a9108c669ab/IJCM-50-9-g001.jpg

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