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新冠病毒肺炎死亡率与瑞德西韦——重症监护环境下的一项回顾性队列研究

COVID-19 Mortality and Remdesivir - A Retrospective Cohort in Intensive Care Setting.

作者信息

Xavier Elizabeth S, Nair Vishnu R, Shajahan Shahanas P, Raheem Abdul, Philips Geetha, Valsalan Praveen, Pradeep Manu

机构信息

Pulmonology, Aster Medcity, Kochi, IND.

Nephrology, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, GBR.

出版信息

Cureus. 2023 Dec 23;15(12):e51002. doi: 10.7759/cureus.51002. eCollection 2023 Dec.

Abstract

BACKGROUND

Remdesivir is a broad-spectrum antiviral drug that received emergency use authorization in the first wave of the COVID-19 pandemic. However, its effectiveness in preventing mortality in COVID-19 patients who required intensive care was unclear.

PATIENTS AND METHODS

We retrospectively analyzed clinical data of 302 patients from intensive care units of a quaternary care center with moderate to severe COVID-19 illness and followed them until discharge between March 2020 and February 2021. Participants who received at least five doses of Remdesivir were compared against participants who received standard care. The primary outcome was all-cause mortality. Secondary outcomes included invasive mechanical ventilation, clinical worsening, and intensive care stay.

RESULTS

Remdesivir use was not associated with all-cause mortality in this cohort (age and sex-adjusted OR = 0.76, 95% CI 0.4 -1.5, p = 0.409). However, when stratified for clinical severity and steroid use, Remdesivir demonstrated a strong negative association with all-cause mortality in severely ill patients (OR 0.3, 95% CI 0.1 - 0.6, p = 0.003) or when used along with intravenous Methylprednisolone (Infusion/Bolus, OR 0.2/0.3, 95% CI 0.1 - 0.9 p = 0.06). Remdesivir use was not significantly associated with invasive mechanical ventilation or clinical worsening but with prolonged ICU stay.

CONCLUSION

While Remdesivir use may not affect all-cause mortality in moderate to severely ill COVID-19 ICU patients, it may still benefit severely ill patients or when used with intravenous steroids. However, the limitations of the present study necessitate a randomized controlled trial to test this combined intervention strategy.

摘要

背景

瑞德西韦是一种广谱抗病毒药物,在新冠疫情第一波期间获得了紧急使用授权。然而,其对需要重症监护的新冠患者预防死亡的有效性尚不清楚。

患者与方法

我们回顾性分析了一家四级医疗中心重症监护病房302例中重度新冠疾病患者的临床数据,并对他们进行随访直至2020年3月至2021年2月出院。将接受至少五剂瑞德西韦的参与者与接受标准治疗的参与者进行比较。主要结局是全因死亡率。次要结局包括有创机械通气、临床恶化和重症监护住院时间。

结果

在该队列中,使用瑞德西韦与全因死亡率无关(年龄和性别调整后的比值比=0.76,95%置信区间0.4-1.5,p=0.409)。然而,按临床严重程度和类固醇使用情况分层时,瑞德西韦在重症患者中与全因死亡率呈强负相关(比值比0.3,95%置信区间0.1-0.6,p=0.003),或与静脉注射甲泼尼龙联合使用时(输注/推注,比值比0.2/0.3,95%置信区间0.1-0.9,p=0.06)。使用瑞德西韦与有创机械通气或临床恶化无显著关联,但与重症监护住院时间延长有关。

结论

虽然使用瑞德西韦可能不会影响中重度新冠重症监护患者的全因死亡率,但它可能仍使重症患者受益,或与静脉类固醇联合使用时有益。然而,本研究的局限性需要进行一项随机对照试验来检验这种联合干预策略。

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本文引用的文献

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Cochrane Database Syst Rev. 2023 Jan 25;1(1):CD014962. doi: 10.1002/14651858.CD014962.pub2.
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PLoS Comput Biol. 2022 Oct 24;18(10):e1010632. doi: 10.1371/journal.pcbi.1010632. eCollection 2022 Oct.
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