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伊维菌素治疗新型冠状病毒感染的随机试验的荟萃分析

Meta-analysis of Randomized Trials of Ivermectin to Treat SARS-CoV-2 Infection.

作者信息

Hill Andrew, Garratt Anna, Levi Jacob, Falconer Jonathan, Ellis Leah, McCann Kaitlyn, Pilkington Victoria, Qavi Ambar, Wang Junzheng, Wentzel Hannah

机构信息

Department of Pharmacology and Therapeutics, University of Liverpool, Liverpool, UK.

Department of Infectious Diseases, University Hospital of Wales, Cardiff and Vale University Health Board, Cardiff, UK.

出版信息

Open Forum Infect Dis. 2021 Jul 6;8(11):ofab358. doi: 10.1093/ofid/ofab358. eCollection 2021 Nov.

Abstract

Ivermectin is an antiparasitic drug being investigated for repurposing against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Ivermectin showed in vitro activity against SARS-COV-2, but only at high concentrations. This meta-analysis investigated ivermectin in 23 randomized clinical trials (3349 patients) identified through systematic searches of PUBMED, EMBASE, MedRxiv, and trial registries. The primary meta-analysis was carried out by excluding studies at a high risk of bias. Ivermectin did not show a statistically significant effect on survival (risk ratio [RR], 0.90; 95% CI, 0.57 to 1.42; = .66) or hospitalizations (RR, 0.63; 95% CI, 0.36 to 1.11; = .11). Ivermectin displayed a borderline significant effect on duration of hospitalization in comparison with standard of care (mean difference, -1.14 days; 95% CI, -2.27 to -0.00; = .05). There was no significant effect of ivermectin on time to clinical recovery (mean difference, -0.57 days; 95% CI, -1.31 to 0.17; = .13) or binary clinical recovery (RR, 1.19; 95% CI, 0.94 to 1.50; = .15). Currently, the World Health Organization recommends the use of ivermectin only inside clinical trials. A network of large clinical trials is in progress to validate the results seen to date.

摘要

伊维菌素是一种抗寄生虫药物,目前正在研究其重新用于对抗严重急性呼吸综合征冠状病毒2(SARS-CoV-2)。伊维菌素在体外对SARS-CoV-2显示出活性,但仅在高浓度时有效。这项荟萃分析通过系统检索PUBMED、EMBASE、MedRxiv和试验注册库,对23项随机临床试验(3349名患者)中的伊维菌素进行了研究。主要的荟萃分析是通过排除存在高偏倚风险的研究来进行的。伊维菌素对生存率(风险比[RR],0.90;95%置信区间,0.57至1.42;P = 0.66)或住院率(RR,0.63;95%置信区间,0.36至1.11;P = 0.11)没有显示出统计学上的显著效果。与标准治疗相比,伊维菌素对住院时间显示出临界显著效果(平均差值,-1.14天;95%置信区间,-2.27至-0.00;P = 0.05)。伊维菌素对临床恢复时间(平均差值,-0.57天;95%置信区间,-1.31至0.17;P = 0.13)或二元临床恢复(RR,1.19;95%置信区间,0.94至1.50;P = 0.15)没有显著效果。目前,世界卫生组织仅建议在临床试验中使用伊维菌素。一个大型临床试验网络正在进行中,以验证迄今为止所观察到的结果。

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