巴西替尼作为冠状病毒病的治疗选择19:文献综述

T. Handoyo, Nurain Farhanah, Gianina Dinda Pamungkas
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摘要

背景:使用IL-6抑制剂(包括Sarilumab或Tocilizumab)治疗COVID-19可显著降低死亡风险。尽管瑞德西韦治疗有好处,但发病率和死亡率仍然很高。Baricitinib是一种JAK抑制剂,可以抑制IL-6激活途径,具有抑制疾病恶化的潜在作用。目的:评价Baricitinib在COVID-19患者中的应用。方法:本研究通过在线数据库“PubMed”和“谷歌Scholar”检索观察性和随机对照试验研究。纳入的研究必须评估Baricitinib作为治疗住院COVID-19患者的有效性。本研究共纳入11项研究(9项观察性试验和2项随机对照试验)。纳入的患者有中重度COVID-19症状。结果:Baricitinib标准剂量为4 mg / d。治疗时间在5-14天之间变化,或直到患者出院。在纳入的研究中,Baricitinib治疗与静脉注射Remdesivir、类固醇、Tocilizumab或其他补充疗法一起使用。巴西替尼住院7天内死亡率为4.4%。巴西替尼给药后有创机械通气率要求约为4%。巴西替尼给药后实验室参数明显改善:IL-6;c反应蛋白;铁蛋白;和肺动脉栓塞。在一项随机对照试验中,与Baricitinib治疗组相比,安慰剂治疗组的严重不良事件发生率更高。结论:Baricitinib治疗COVID-19患者可降低疾病进展、发病率和死亡率。需要进一步的研究来评估Baricitinib作为COVID-19主要治疗方法的益处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Baricitinib as Treatment Option for Corona Virus Disease-19: a Literature Review
Background : Treatment of COVID-19 using IL-6 inhibitors, including Sarilumab or Tocilizumab, significantly decreased mortality risk. Though, Remdesivir therapy gave benefits, morbidity and mortality remained high. Baricitinib, a JAK inhibitor, can inhibit IL-6 activation pathway and has a potential effect of inhibiting disease progression to become severe. Objective : This study aimed to evaluate the use of Baricitinib for COVID-19 patients. Methods : This study was conducted by searching for observational and randomized controlled trial studies through online databases, “PubMed” and “Google Scholar”. Studies included must evaluate Baricitinib effectivity as therapy for hospitalized COVID-19 patients. This study included 11 studies (9 observational and 2 randomized controlled trial). Patients included had moderate-to-severe symptoms of COVID-19. Results : Standard dose of Baricitinib was administered at 4 mg daily dose. Length of therapy was varied between 5-14 days, or up to patients’ discharge. Baricitinib therapy among included studies was administered with intravenous Remdesivir, Steroid, Tocilizumab, or other complement therapies. Mortality rate within 7-day of hospitalization with Baricitinib was 4.4%. Requirement of invasive mechanic ventilation rate after Baricitinib administration was approximately 4%. Laboratory parameters were significantly getting better after Baricitinib administration: IL-6; CRP; ferritin; and D-dimer. Serious adverse events in a randomized controlled trial, occurred more often in placebo treated compared to Baricitinib treated group. Conclusion : Baricitinib as therapy for COVID-19 patients can decrease progression, morbidity, and mortality of the disease. Further studies are needed to evaluate the benefit of Baricitinib as main therapy for COVID-19.
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