Effect of amubarvimab-romlusevimab for treatment of severe COVID-19 in intensive care units: A retrospective cohort study

被引:0
|
作者
Qu, Peng [1 ,4 ]
Lou, Anni [1 ]
Rong, Dan [1 ]
Wang, Canmin [3 ]
Zhong, Qinglei [1 ]
Cui, Wanfu [1 ]
Gong, Jiacheng [1 ]
Xu, Qihan [1 ]
Chen, Zhuoer [1 ]
Bathaiian, Luqman Sadat [5 ]
Li, Xu [1 ]
Chen, Cheng [2 ]
机构
[1] Southern Med Univ, Nanfang Hosp, Dept Emergency Med, Guangzhou 510515, Peoples R China
[2] Southern Med Univ, Nanfang Hosp, Dept Crit Care Med, Baiyun Branch, Guangzhou, Peoples R China
[3] Guangdong Second Prov Gen Hosp, Intens Care Unit, Guangzhou 510317, Peoples R China
[4] Southern Med Univ, Nanfang Hosp, Dept Gastroenterol, Guangdong Prov Key Lab Gastroenterol, Guangzhou, Peoples R China
[5] Southern Med Univ, Sch Interatibnal Educgtior, Guangzhou, Peoples R China
关键词
COVID-19; SARS-CoV-2; Amubarvimab; Romlusevimab; Antibody therapy; Intensive care Units;
D O I
10.1016/j.heliyon.2024.e37663
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Amubarvimab-romlusevimab is a commonly recommended antiviral treatment in China for adult patients with mild or moderate SARS-CoV-2 infections, especially for patients with a high risk factor for progression to severe COVID-19. However, its exact efficacy in patients with severe Covid-19 is not yet known.This is a single-center retrospective cohort study, in which we collected the general data, laboratory tests, radiological characteristics, viral conversion status, and prognosis of the disease from patients with COVID-19 hospitalized, from December 2022 to March 2023 in the Department of Critical Care Medicine. The amubarvimab-romlusevimab therapy can reduce the 28-day mortality (29.79 % vs 51.35 %, p = 0.02), and ICU mortality (29.79 % vs 55.41 %, p = 0.006) of severe COVID-19.A 1:1 PSM (Propensity Score Matching) was performed to reduce bias, in order to ensure the two groups were balanced and comparable. In the matched population (n = 47), there were no statistically significant differences between the mAbs (monoclonal antibody)group and the Non-antiviral group in 28-day, and thromboembolic events in COVID-19 patients. The 40-day survival analysis shows that mAbs therapy can improve patient prognosis (HR = 0.45, 95%CI = 0.26-0.76, p = 0.008). However, no significant intergroup difference in the 40-day cumulative viral conversion rate. In a univariate Cox regression analysis, The Amubarvimab - romlusevimab therapy(HR:0.464; CI:[0.252-0.853]; p:0.013) is a protective factor and CRP, PCT, PLT, Lactate, PT, PT-INR, and pt% level at admission were risk factors for clinical prognosis. After including the above covariates, Multifactorial COX regression shows that the Amubarvimab - romlusevimab therapy(HR:0.392; CI:[0.211-0.729]; p:0.003), CRP, Lactate and PT-INR at admission are independent factors for mortality of severe COVID-19. Based on the current data, we conclude that amubarvimab-romlusevimab therapy is beneficial for patients with severe COVID-19.
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页数:8
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