Effectiveness and Safety of Baricitinib as a Covid-19 Drug Candidate: A Systematic Review

Y. S. Rahayu, Andi Anggriani, H. Habibie, Elly Wahyudin, M. A. Bahar
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Abstract

Baricitinib is an approved selective JAK1/JAK2 inhibitor that can potentially inhibit IL-6 as the primary driver of COVID-19-related cytokine storm syndrome. Therefore, this study aimed to assess the effectiveness and safety of baricitinib therapy in COVID-19 patients. It was reported following Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. The search for eligible articles reporting the efficacy and safety of baricitinib on COVID-19 patients, published up to May 2021, was conducted using PubMed and Embase. The research protocol was registered at PROSPERO (CDR42021235282), and data were presented in a metasynthetic (descriptive) manner. Out of 878 identified articles, seven were eligible and consisted of three randomized clinical trials, one quasi-experimental study, two before-after (pre-post) studies, and one cross-sectional study. The articles suggested that baricitinib could improve the clinical conditions of COVID-19 patients indicated by negative PCR test results, improve breathing quality, and decrease: ICU requirements, length of hospital stay, as well as the risk of death. The trial studies showed that this inhibitor works better with a loading dose of 8 mg, continued with 4 mg daily. Baricitinib could also produce synergistic effects with standard therapy such as corticosteroid and remdesivir. Therefore, it is a promising candidate therapy for COVID-19 patients, but since the number and methodological quality of the studies are low, further and better research is needed to ascertain its potential use on COVID-19.
Baricitinib作为Covid-19候选药物的有效性和安全性:一项系统评价
Baricitinib是一种被批准的选择性JAK1/JAK2抑制剂,可以潜在地抑制IL-6作为covid -19相关细胞因子风暴综合征的主要驱动因素。因此,本研究旨在评估巴西替尼治疗COVID-19患者的有效性和安全性。按照系统评价和荟萃分析(PRISMA)指南的首选报告项目进行报告。使用PubMed和Embase检索截至2021年5月发表的报告baricitinib对COVID-19患者疗效和安全性的符合条件的文章。研究方案在PROSPERO注册(CDR42021235282),数据以元合成(描述性)方式呈现。在878篇确定的文章中,有7篇符合条件,包括3项随机临床试验、1项准实验研究、2项前后对照研究和1项横断面研究。文章提示巴西替尼可改善PCR阴性的COVID-19患者的临床状况,改善呼吸质量,降低ICU需求、住院时间和死亡风险。试验研究表明,这种抑制剂在负荷剂量为8mg时效果更好,继续每天4mg。Baricitinib还可以与皮质类固醇和remdesivir等标准疗法产生协同效应。因此,它是COVID-19患者的一种有希望的候选治疗方法,但由于研究的数量和方法学质量较低,需要进一步和更好的研究来确定其对COVID-19的潜在应用。
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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