Lopinavir-ritonavir (LPV/r) for the Treatment of SARS-CoV-2 (COVID-19): A Systematic Review

Zhipeng Yan, K. Shum, Ching‐lung Lai
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Abstract

Background: SARS-CoV-2 is the pathogenic agent of COVID-19, which has affected more than 200 countries; infected million people and declared a global pandemic. At the time of writing, no approved definitive therapeutic treatment for COVID-19 is available. Many studies are still on-going. Lopinavir-ritonavir (LPV/r), or its combination has been advocated as a potential treatment. This study reviews the evidence of LPV/r usage in the treatment of SARS-CoV-2 infection. Methods: A systematic review protocol was written based on the PRISMA Statement Article for review selected from electronic databases (PubMed, Embase and Medline). Inclusion criteria were: full English articles published accessible peer-reviewed. The search keywords COVID, and SARS-CoV-2. Studies fulfilling the inclusion criteria were included, regardless of study designs. Data were extracted from published reports. Findings : As of 9 May 2020, 243 manuscripts were identified. Thirteen studies were included with a total of 494 patients. These consisted of clinical trials (n=2), case reports (n=5), case series (n=3), and retrospective cohort studies (n=3). In the thirteen studies, the use of LPV/r shortened the PCR negative-conversion time for SARS-CoV-2, the earliest as being 5 days (Range: 5 to 28 days), and clinical improvement was expected as early as 2 days (Range: 2 to 28 days). Interpretation : Our review shows that the use of LPV/r may be an effective treatment for non-severe COVID-19 patients, while only limited benefits were observed in severe COVID-19 patients.
洛匹那韦-利托那韦治疗SARS-CoV-2 (COVID-19)的系统评价
背景:SARS-CoV-2是COVID-19的病原体,已影响200多个国家;感染了百万人,并宣布全球大流行。在撰写本文时,还没有批准的针对COVID-19的明确治疗方法。许多研究仍在进行中。洛匹那韦-利托那韦(LPV/r)或其组合被认为是一种潜在的治疗方法。本研究回顾了LPV/r用于治疗SARS-CoV-2感染的证据。方法:从电子数据库(PubMed、Embase和Medline)中选择PRISMA声明文章进行综述,编写系统评价方案。纳入标准为:发表的可访问的同行评审的完整英文文章。搜索关键词COVID和SARS-CoV-2。无论研究设计如何,均纳入符合纳入标准的研究。数据摘自已发表的报告。结果:截至2020年5月9日,共鉴定出243份手稿。13项研究共纳入494名患者。这些研究包括临床试验(n=2)、病例报告(n=5)、病例系列(n=3)和回顾性队列研究(n=3)。在13项研究中,使用LPV/r缩短了SARS-CoV-2的PCR阴性转化时间,最早为5天(范围:5 ~ 28天),预计临床改善最早为2天(范围:2 ~ 28天)。解释:我们的综述显示,LPV/r可能是一种有效的治疗非重症COVID-19患者的方法,而在重症COVID-19患者中仅观察到有限的益处。
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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