COVID-19抗白细胞介素治疗安全性的系统评价和荟萃分析

Y. Gomon, A. Kolbin, V. V. Strizheletsky, I. G. Ivanov, F. Sultanova, Y. Balykina
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引用次数: 1

摘要

目标。通过感染并发症的风险评估抗白细胞介素药物作为COVID-19病理治疗的安全性。材料与方法。本研究系统回顾了推荐用于COVID-19患者病理治疗的抗白细胞介素药物的严重不良事件发生率和“感染与侵袭”类不良事件的安全性评价相关文献,并对相关数据进行了荟萃分析。两组间严重不良事件的危险比为0.93,95% CI为0.85;1.01,“感染与侵袭”类不良事件的危险比为0.9,95% CI为0.8;结论:本荟萃分析显示,COVID-19患者使用抗白细胞介素药物发生严重不良事件和“感染与侵袭”类不良事件的相对风险差异无统计学意义。
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A systematic review and meta-analysis of the safety of anti-interleukin therapy in COVID-19
Objective. To evaluate safety of anti-interleukin drugs used as a pathogenetic therapy of COVID-19 as assessed by risks of infectious complications. Materials and Methods. A systematic review of publications related to safety assessment of anti-interleukin drugs recommended as pathogenetic therapy in COVID-19 patients in terms of incidence of serious adverse events and adverse events of “Infections and Invasions” class and a meta-analysis of the data were performed. Results. The meta-analysis included 16 randomized and 3 non-randomized studies. The hazard ratio of serious adverse events between the comparison groups was 0.93 95% CI 0.85; 1.01, the hazard ratio of adverse event of “Infections and Invasions” class was 0.9 95% CI 0.8; 1.02, showing no differences in the incidence of those events. Conclusions. This meta-analysis did not demonstrate statistically significant differences in the relative risks of serious adverse events and adverse events of “Infections and Invasions” class for the use of antiinterleukin drugs in COVID-19 patients.
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CiteScore
0.90
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8 weeks
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