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首页> 外文期刊>Frontiers in Medicine >Mortality Benefit of Remdesivir in COVID-19: A Systematic Review and Meta-Analysis
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Mortality Benefit of Remdesivir in COVID-19: A Systematic Review and Meta-Analysis

机译:Covid-19中Remdesivir的死亡效果:系统审查和荟萃分析

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Importance/Background: During current public health emergency of COVID-19 pandemic, repurposing of existing antiviral drugs may be an efficient strategy since there is no proven effective treatment. Published literature shows Remdesivir has broad-spectrum antiviral activity against numerous RNA viruses and has been recently recognized as a promising therapy against SARS-CoV-2. Methods: A systematic search was conducted for full length manuscripts published between inception and July 19th, 2020 focussing on efficacy and safety of Remdesivir in COVID-19. The primary outcomes were defined as mortality rate and median days to recovery based on the available pooled data. The secondary outcome was adverse events rate and drug discontinuation rate. Statistical Analysis: All outcomes were performed using Comprehensive Meta-Analysis software package (Bio stat, Englewood, NJ, USA). Results: A total of 1,895 patients from 9 studies were included in this qualitative synthesis. In patients treated with Remdesivir, the mean recovery time was 15.84 days (95% CI 11.68–20, SE 2.12; I 2 = 97.24) and the pooled mortality rate was 11.3% (95% CI 7.9–16%; I 2 = 74.85). However, treatment with Remdesivir was associated with adverse effects (55.3%, 95% CI 31.5–76.9%; I 2 = 97.66) eventually warranting the discontinuation of the drug (17.8%, 95% CI 8.6–33.1%; I 2 = 95.64). The meta-analysis of three clinical trials indicated that administration of Remdesivir significantly reduces the mortality compared to the placebo (OR 0.70, 95% CI 0.58–0.84, p ≤ 0.001; I 2 = 16.6). Conclusions and Relevance: The result of contemporary meta-analysis suggests mortality benefit with Remdesivir in COVID-19 and median recovery time was over 2 weeks. The pooled mortality with Remdesivir was found to be very low, and this analysis can shed light on this potential treatment for COVID-19 patients.
机译:重要性/背景:在目前的Covid-19大流行的公共卫生应急期间,重新抑制现有的抗病毒药物可能是一个有效的策略,因为没有经过遗传的有效治疗方法。发表的文献表明雷德德尔对众多RNA病毒具有广泛的抗病毒活性,并且最近被认为是针对SARS-COV-2的有希望的治疗。方法:为2020年7月19日公布的全长稿件进行了系统检索,重点是Covid-19中雷迪维尔的疗效和安全性。主要结果被定义为基于可用的汇总数据恢复的死亡率和中位数。二次结果是不良事件率和药物停止率。统计分析:使用全面的Meta分析软件包(Bio Stat,Englewood,NJ,USA)进行所有结果。结果:该定性合成中共有来自9项研究的1,895名患者。在用雷替米尔治疗的患者中,平均恢复时间为15.84天(95%CI 11.68-20,SE 2.12; I 2 = 97.24)和汇集的死亡率为11.3%(95%CI 7.9-16%; I 2 = 74.85 )。然而,用雷级肽治疗与不良反应有关(55.3%,95%CI 31.5-76.9%; I 2 = 97.66)最终需要对药物的停药(17.8%,95%CI 8.6-33.1%; I 2 = 95.64 )。三种临床试验的荟萃分析表明,与安慰剂(或0.70,95%CI 0.58-0.84,P≤0.001; I 2 = 16.6),雷代肽的施用显着降低了死亡率(或0.70,95%,4 = 16.6)。结论与相关性:当代元分析的结果表明,在Covid-19中的雷德氏虫草中的死亡率效益在2周内超过2周。发现汇集的死亡率具有非常低的,并且这种分析可以在Covid-19患者的这种潜在治疗中脱亮。

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