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

Sep 2024  
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Mortality 46% Improvement Relative Risk Viral clearance 4% Amubarvimab/r.. for COVID-19  Qu et al.  ICU PATIENTS Is very late treatment with amubarvimab beneficial for COVID-19? PSM retrospective 121 patients in China (December 2022 - March 2023) Lower mortality with amubarvimab (not stat. sig., p=0.058) c19early.org Qu et al., Heliyon, September 2024 Favorsamubarvimab Favorscontrol 0 0.5 1 1.5 2+
Retrospective 121 severe ICU COVID-19 patients in China showing lower 28-day mortality and ICU mortality with amubarvimab-romlusevimab treatment compared to no antiviral treatment. No significant differences were found in viral conversion rate or thromboembolic events. After propensity score matching to balance baseline characteristics, the mortality differences were no longer statistically significant.
Efficacy is variant dependent.
Viral load measured by PCR may not accurately reflect infectious virus measured by viral culture. Porter et al. show that viral load early in infection was correlated with infectious virus, but viral load late in infection could be high even with low or undetectable infectious virus. Assessing viral load later in infection may underestimate reductions in infectious virus with treatment.
risk of death, 46.0% lower, HR 0.54, p = 0.06, treatment 47, control 47, propensity score matching, Kaplan–Meier, day 40.
risk of no viral clearance, 3.8% lower, HR 0.96, p = 0.89, treatment 47, control 47, inverted to make HR<1 favor treatment, propensity score matching, Kaplan–Meier, day 40.
Effect extraction follows pre-specified rules prioritizing more serious outcomes. Submit updates
Qu et al., 30 Sep 2024, retrospective, China, peer-reviewed, 12 authors, study period December 2022 - March 2023. Contact: qp136896991@163.com, mylx99@163.com, cc17702067789@outlook.com.
This PaperAmubarv../r..All
Effect of amubarvimab-romlusevimab for treatment of severe COVID-19 in intensive care units: A retrospective cohort study
Peng Qu, Anni Lou, Dan Rong, Canmin Wang, Qinglei Zhong, Wanfu Cui, Jiacheng Gong, Qihan Xu, Zhuoer Chen, Luqman Sadat Bathaiian, Xu Li, Cheng Chen
Heliyon, doi:10.1016/j.heliyon.2024.e37663
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.
Ethics approval and consent to participate This study was approved by the Ethics Committee of Baiyun Branch, Nanfang Hospital (2023004). Consent for publication All authors approved the final manuscript and the submission to this journal. Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
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Late treatment
is less effective
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