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系统评价和荟萃分析早期伊维菌素治疗 SARS-CoV-2 感染的研究结果。

Results of a systematic review and meta-analysis of early studies on ivermectin in SARS-CoV-2 infection.

机构信息

Doctoral School of Clinical Medicine, University of Szeged, Szeged, Hungary.

Institute of Pharmacognosy, Faculty of Pharmacy, University of Szeged, Szeged, Hungary.

出版信息

Geroscience. 2023 Aug;45(4):2179-2193. doi: 10.1007/s11357-023-00756-y. Epub 2023 Mar 7.

Abstract

Ivermectin, an antiparasitic drug, has been repurposed for COVID-19 treatment during the SARS-CoV-2 pandemic. Although its antiviral efficacy was confirmed early in vitro and in preclinical studies, its clinical efficacy remained ambiguous. Our purpose was to assess the efficacy of ivermectin in terms of time to viral clearance based on the meta-analysis of available clinical trials at the closing date of the data search period, one year after the start of the pandemic. This meta-analysis was reported by following the PRISMA guidelines and by using the PICO format for formulating the question. The study protocol was registered on PROSPERO. Embase, MEDLINE (via PubMed), Cochrane Central Register of Controlled Trials (CENTRAL), bioRvix, and medRvix were searched for human studies of patients receiving ivermectin therapy with control groups. No language or publication status restrictions were applied. The search ended on 1/31/2021 exactly one year after WHO declared the public health emergency on novel coronavirus. The meta-analysis of three trials involving 382 patients revealed that the mean time to viral clearance was 5.74 days shorter in case of ivermectin treatment compared to the control groups [WMD = -5.74, 95% CI (-11.1, -0.39), p = 0.036]. Ivermectin has significantly reduced the time to viral clearance in mild to moderate COVID-19 diseases compared to control groups. However, more eligible studies are needed for analysis to increase the quality of evidence of ivermectin use in COVID-19.

摘要

伊维菌素是一种抗寄生虫药物,在 SARS-CoV-2 大流行期间被重新用于 COVID-19 的治疗。虽然其在体外和临床前研究中早期证实了其抗病毒功效,但临床疗效仍不明确。我们的目的是根据截止到数据检索期结束时的可用临床试验的荟萃分析,评估伊维菌素在病毒清除时间方面的疗效,这是大流行开始一年后。本荟萃分析按照 PRISMA 指南进行,并使用 PICO 格式来制定问题。研究方案已在 PROSPERO 上注册。对 Embase、MEDLINE(通过 PubMed)、Cochrane 对照试验中心注册库(CENTRAL)、bioRvix 和 medRvix 进行了检索,以查找接受伊维菌素治疗并设有对照组的患者的人类研究。未对语言或出版状态施加限制。检索于 2021 年 1 月 31 日结束,正好是世界卫生组织宣布新型冠状病毒公共卫生紧急事件一年后。涉及 382 名患者的三项试验的荟萃分析显示,与对照组相比,伊维菌素治疗的平均病毒清除时间缩短了 5.74 天[WMD=-5.74,95%CI(-11.1,-0.39),p=0.036]。与对照组相比,伊维菌素可显著缩短轻度至中度 COVID-19 疾病患者的病毒清除时间。然而,需要更多合格的研究进行分析,以提高伊维菌素在 COVID-19 中的应用证据质量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d2e/10651625/1ee4752faa64/11357_2023_756_Fig1_HTML.jpg

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