Meta-analysis of the efficacy andsafety of COVID-19 treatment by human immunoglobulin forintravenous injection

  • 曹起超 冯洁 孙振宇 宋悦 费梅芳 刘枫荻
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  • Department of Quality Administration, Sinopharm Shanghai Plasma-derived Biotherapies Co., Ltd., Shanghai 200051, China

Online published: 2025-08-16

Abstract

Objective  To investigate the efficacy and safety of human immunoglobulin for intravenous injection (IVIG) in treating COVID-19 patients by Meta-analysis. Methods Between 1 January 2020 and 31 July 2021, randomized controlled trials (RCTs) and cohort studies referred to IVIG and COVID-19 were searched from Cochrane Library, PubMed, China National Knowledge Infrastructure (CNKI) and China Biology Medicine disc (CBM). Quality evaluation was performed according to Cochrane Handbook for Systematic Reviews and Meta-analysis was conducted with RevMan 5.3 Software. Results Eleven studies were retrieved, including 4 RCTs and 7 cohort studies. The result of the Meta-analysis showed that the mortality rate of critical ill COVID-19 patients could be relieved significantly by IVIG [risk ratio (RR)=0.67, 95% confidence interval (CI): 0.52-0.85, P=0.001, I2=7%].In severe patients, IVIG could also improve patients’ survival though significant statistical difference was not achieved [RR=0.78, 95% CI: 0.52-1.18, P=0.24, I2=49%]. The incidence of adverse reactions of IVIG in patients with COVID-19 was 0.0%-5.9%, and the majority was manifested in mild to moderate palpitation, dizziness, rash, and swelling at infusion site. Conclusion IVIG can improve the survival of critical ill COVID-19 patients effectively, with excellent safety. In severe patients, it is necessary to further explore the starting time and recommended dosage of IVIG, thus serving clinical practice better.

Cite this article

曹起超 冯洁 孙振宇 宋悦 费梅芳 刘枫荻 . Meta-analysis of the efficacy andsafety of COVID-19 treatment by human immunoglobulin forintravenous injection[J]. International Journal of Biologicals, 2022 , 45(1) : 30 -36 . DOI: 10.3760/cma.j.cn311962-20211008-00059

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