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Multi-center matched cohort study of convalescent plasma for hospitalized patients with COVID-19
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PLOS
Date
2022
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Abstract
Background Although frequently used in the early pandemic, data on the effectiveness of COVID-19 convalescent plasma (CCP) remain mixed. We investigated the effectiveness and safety of CCP in hospitalized COVID-19 patients in real-world practices during the first two waves of the pandemic in a multi-hospital healthcare system in Texas. Methods and findings Among 11,322 hospitalized patients with confirmed COVID-19 infection from July 1, 2020 to April 15, 2021, we included patients who received CCP and matched them with those who did not receive CCP within ±2 days of the transfusion date across sites within strata of sex, age groups, days and use of dexamethasone from hospital admission to the match date, and oxygen requirements 4-12 hours prior to the match date. Cox proportional hazards model estimated hazard ratios (HRs) and 95% confidence intervals (CIs) for effectiveness outcomes in a propensity score 1:1 matched cohort. Pre-defined safety outcomes were described. We included 1,245 patients each in the CCP treated and untreated groups. Oxygen support was required by 93% of patients at the baseline. The pre-defined primary effectiveness outcome of 28-day in-hospital all-cause mortality (HR = 0.85; 95%CI: 0.66,1.10) were similar between treatment groups. Sensitivity and stratified analyses found similar null results. CCP-treated patients were less likely to be discharged alive (HR = 0.82; 95%CI: 0.74, 0.91), and more likely to receive mechanical ventilation (HR = 1.48; 95%CI: 1.12, 1.96). Safety outcomes were rare and similar between treatment groups. Conclusion The findings in this large, matched cohort of patients hospitalized with COVID-19 and mostly requiring oxygen support at the time of treatment, do not support a clinical benefit in 28-day in-hospital all-cause mortality for CCP. Future studies should assess the potential benefits with specifically high-titer units in perhaps certain subgroups of patients (e.g. those with early disease or immunocompromised). © 2022 Public Library of Science. All rights reserved.
Contents
Subject
angiotensin receptor antagonist
anticoagulant agent
antithrombocytic agent
azithromycin
chloroquine
dexamethasone
dipeptidyl carboxypeptidase inhibitor
hydrocortisone
hydroxychloroquine
prednisone
remdesivir
SARS-CoV-2 convalescent plasma
tocilizumab
oxygen
adult
aged
all cause mortality
Article
artificial ventilation
clinical outcome
cohort analysis
confidence interval
controlled study
convalescent plasma transfusion
coronavirus disease 2019
drug safety
female
gender
groups by age
hazard ratio
health care system
hospital admission
hospital patient
human
hypertension
in-hospital mortality
major clinical study
male
multicenter study
oxygen therapy
pandemic
proportional hazards model
retrospective study
sensitivity analysis
Texas
thromboembolism
passive immunization
procedures
therapy
treatment outcome
Cohort Studies
COVID-19
Humans
Immunization, Passive
Oxygen
SARS-CoV-2
Treatment Outcome
anticoagulant agent
antithrombocytic agent
azithromycin
chloroquine
dexamethasone
dipeptidyl carboxypeptidase inhibitor
hydrocortisone
hydroxychloroquine
prednisone
remdesivir
SARS-CoV-2 convalescent plasma
tocilizumab
oxygen
adult
aged
all cause mortality
Article
artificial ventilation
clinical outcome
cohort analysis
confidence interval
controlled study
convalescent plasma transfusion
coronavirus disease 2019
drug safety
female
gender
groups by age
hazard ratio
health care system
hospital admission
hospital patient
human
hypertension
in-hospital mortality
major clinical study
male
multicenter study
oxygen therapy
pandemic
proportional hazards model
retrospective study
sensitivity analysis
Texas
thromboembolism
passive immunization
procedures
therapy
treatment outcome
Cohort Studies
COVID-19
Humans
Immunization, Passive
Oxygen
SARS-CoV-2
Treatment Outcome
Subject(s)
Research Projects
Organizational Units
Journal Issue
Genre
Description
Format
Department
Burnett School of Medicine