Evidence map›Paper›PMID 39315175›Full record

ArticleHeliyon2024

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 and 2 more

Abstract read
In one paragraph

Article in Heliyon, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Peng QuDepartment of Emergency Medicine, Southern Medical University Nanfang Hospital, Guangzhou, China.
Anni LouDepartment of Emergency Medicine, Southern Medical University Nanfang Hospital, Guangzhou, China.
Dan RongDepartment of Emergency Medicine, Southern Medical University Nanfang Hospital, Guangzhou, China.
Canmin WangIntensive Care Unit, Guangdong Second Provincial General Hospital, Guangzhou 510317, China.
Qinglei ZhongDepartment of Emergency Medicine, Southern Medical University Nanfang Hospital, Guangzhou, China.
Wanfu CuiDepartment of Emergency Medicine, Southern Medical University Nanfang Hospital, Guangzhou, China.
Jiacheng GongDepartment of Emergency Medicine, Southern Medical University Nanfang Hospital, Guangzhou, China.
Qihan XuDepartment of Emergency Medicine, Southern Medical University Nanfang Hospital, Guangzhou, China.
Zhuoer ChenDepartment of Emergency Medicine, Southern Medical University Nanfang Hospital, Guangzhou, China.
Luqman Sadat BathaiianSchool of Interatibnal Educgtior,Southern Medical University, Guangzhou, China.
Xu LiDepartment of Emergency Medicine, Southern Medical University Nanfang Hospital, Guangzhou, China.
Cheng ChenDepartment of Critical Care Medicine, Baiyun Branch, Nanfang Hospital, Southern Medical University, Guangzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

AmubarvimabAntibody therapyCOVID-19Intensive care UnitsRomlusevimabSARS-CoV-2

Identifiers

PMID39315175
PMCPMC11417170

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.