Efficacy and safety of ivermectin for treatment of non-hospitalized COVID-19 patients: A systematic review and meta-analysis of 12 randomized controlled trials with 7,035 participants

IF 4.9 2区 医学 Q1 INFECTIOUS DISEASES International Journal of Antimicrobial Agents Pub Date : 2024-06-20 DOI:10.1016/j.ijantimicag.2024.107248
Adrian V. Hernandez , Anna Liu , Yuani M. Roman , Paula Alejandra Burela , Vinay Pasupuleti , Priyaleela Thota , Cesar O. Carranza-Tamayo , Manuel Retamozo-Palacios , Vicente A. Benites-Zapata , Alejandro Piscoya , Jose E. Vidal
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Abstract

Introduction

We systematically assessed benefits and harms of the use of ivermectin in non-hospitalized patients with early COVID-19.

Methods

Five databases were searched until October 17, 2023, for randomized controlled trials (RCTs) in adult patients with COVID-19 treated with ivermectin against standard of care (SoC), placebo, or active drug. Primary outcomes were hospitalization, all-cause mortality, and adverse events (AEs). Secondary outcomes included mechanical ventilation (MV), clinical improvement, clinical worsening, viral clearance, and severe adverse events (SAEs). Random effects meta-analyses were performed, with quality of evidence (QoE) evaluated using GRADE methods. Pre-specified subgroup analyses (ivermectin dose, control type, risk of bias, follow-up, and country income) and trial sequential analysis (TSA) were performed.

Results

Twelve RCTs (n = 7,035) were included. The controls were placebo in nine RCTs, SoC in two RCTs, and placebo or active drug in one RCT. Ivermectin did not reduce hospitalization (relative risk [RR], 0.81, 95% confidence interval [95% CI] 0.64–1.03; 8 RCTs, low QoE), all-cause mortality (RR 0.98, 95% CI 0.73–1.33; 9 RCTs, low QoE), or AEs (RR 0.89, 95% CI 0.75–1.07; 9 RCTs, very low QoE) vs. controls. Ivermectin did not reduce MV, clinical worsening, or SAEs and did not increase clinical improvement and viral clearance vs. controls (very low QoE for secondary outcomes). Subgroup analyses were mostly consistent with main analyses, and TSA-adjusted risk for hospitalization was similar to main analysis.

Conclusions

In non-hospitalized COVID-19 patients, ivermectin did not have effect on clinical, non-clinical or safety outcomes versus controls. Ivermectin should not be recommended as treatment in non-hospitalized COVID-19 patients.

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伊维菌素治疗非住院COVID-19患者的疗效和安全性:对12项随机对照试验、7035名参与者的系统回顾和荟萃分析。
简介我们对早期COVID-19非住院患者使用伊维菌素的益处和危害进行了系统评估:截至2023年10月17日,我们在五个数据库中检索了伊维菌素与标准护理(SoC)、安慰剂或活性药物治疗COVID-19成年患者的随机对照试验(RCT)。主要结果包括住院率、全因死亡率和不良事件(AE)。次要结果包括机械通气(MV)、临床改善、临床恶化、病毒清除和严重不良事件(SAE)。研究人员进行了随机效应荟萃分析,并采用 GRADE 方法评估了证据质量(QoE)。进行了预先指定的亚组分析(伊维菌素剂量、对照类型、偏倚风险、随访和国家收入)和试验序列分析(TSA):共纳入了 12 项研究性试验(样本数:7035)。9项研究的对照组为安慰剂,2项研究的对照组为SoC,1项研究的对照组为安慰剂或活性药物。与对照组相比,伊维菌素未降低住院率(相对风险 [RR],0.81,95% 置信区间 [95%CI],0.64-1.03;8 项 RCT,低 QoE)、全因死亡率(RR,0.98,95%CI,0.73-1.33;9 项 RCT,低 QoE)或 AEs(RR,0.89,95%CI,0.75-1.07;9 项 RCT,极低 QoE)。与对照组相比,伊维菌素没有减少MV、临床恶化或SAE,也没有增加临床改善和病毒清除率(次要结果的QoE很低)。亚组分析与主要分析基本一致,TSA调整后的住院风险与主要分析相似:在未住院的COVID-19患者中,与对照组相比,伊维菌素对临床、非临床或安全性结果均无影响。不应推荐伊维菌素作为非住院COVID-19患者的治疗药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
21.60
自引率
0.90%
发文量
176
审稿时长
36 days
期刊介绍: The International Journal of Antimicrobial Agents is a peer-reviewed publication offering comprehensive and current reference information on the physical, pharmacological, in vitro, and clinical properties of individual antimicrobial agents, covering antiviral, antiparasitic, antibacterial, and antifungal agents. The journal not only communicates new trends and developments through authoritative review articles but also addresses the critical issue of antimicrobial resistance, both in hospital and community settings. Published content includes solicited reviews by leading experts and high-quality original research papers in the specified fields.
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