托珠单抗治疗COVID - 19后继发微生物感染的发生率——一项匹配的回顾性队列研究

Joanna L. Moore, S. Stroever, Patricia E. Rondain, R. Scatena
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引用次数: 0

摘要

导论:免疫紊乱因子面积单位理论化,重点关注COVID - 19中的蛋白质风暴综合征。然而,对继发感染风险易感性的下游影响尚不清楚。本研究旨在找出世界卫生组织接受和未接受tocilizumab治疗的COVID - 19患者继发感染的风险变化。方法:我们倾向于在2020年3月1日至5月31日期间对康涅狄格州西部的两家大型急症护理医院进行匹配的回顾性队列研究。我们倾向于收集变量,利用手工案例历史抽象。第一个暴露变量是任何剂量的托珠单抗。第一个结果是国家护理安全网络概述的任何与医疗保健相关的微生物或真菌病。我们倾向于进行Kaplan-Meier分析,以评估暴露团队中医疗保健相关感染(HAI)的加性可能性的粗略区别。我们倾向于联合进行多变量Cox多变量分析,以确定暴露组与HAI的危害定量关系,而潜在混杂因素占主导地位。结果:Kaplan-Meier分析无可争议,在团队HAI的相加似然中没有区别。给予托珠单抗的患者发生HAI的校正风险为零。未给予托珠单抗的患者的85倍(95%置信区间= 0)。29, 2.52, P = 0.780)在相关混杂因素中占主导地位。结论:托珠单抗并未增加COVID - 19患者继发感染的发生率。更大的、不规则的试验应该将感染作为次要结果来评估,以验证这一发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Incidence of Secondary Microorganism Infections Following Utilization of Tocilizumab for the Treatment of COVID‑19 - A Matched Retrospective Cohort Study
Introduction: immunological disorder agent’s area unit theorized to focus on the protein storm syndrome in COVID‑19. However, the downstream effects concerning susceptibilities to secondary infection risk stay unknown. This study seeks to work out risk variations for secondary infections among COVID‑19 patients World Health Organization did and failed to receive tocilizumab. Methods: we have a tendency to conducted a matched retrospective cohort study from 2 giants, acute care hospitals in Western Connecticut from March 1 to May 31, 2020. we have a tendency to collected variables exploitation manual case history abstraction. the first exposure variable was any dose of tocilizumab. the first outcome was any healthcare‑associated microorganism or mycosis as outlined by the National Care Safety Network. we have a tendency to performed a Kaplan–Meier analysis to assess the crude distinction within the additive likelihood of healthcare‑associated infection (HAI) across exposure teams. we have a tendency to conjointly performed a multivariable Cox multivariate analysis to work out the hazard quantitative relation for HAI by exposure group whereas dominant for potential confounders. Results: The Kaplan–Meier analysis incontestable no distinction within the additive likelihood of HAI across teams. The adjusted hazard of HAI for patients given tocilizumab was zero.85 times that of patients not given tocilizumab (95% confidence interval = zero.29, 2.52, P = 0.780) once dominant for relevant confounders. Conclusions: Tocilizumab failed to increase the incidence of secondary infection among COVID‑19 patients. Larger, irregular trials ought to valuate infection as a secondary outcome to validate this finding.
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