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About:
Convalescent plasma for patients with severe COVID-19: a matched cohort study
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schema:ScholarlyArticle
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covidontheweb.inria.fr
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Academic Article
research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
title
Convalescent plasma for patients with severe COVID-19: a matched cohort study
Creator
Ph, M
Bailey, Jeffrey
Eng, M
Mylona, Evangelia
Mylonakis, Eleftherios
Shehadeh, Fadi
Touzard-Romo, Francine
Rich, Josiah
Geffert, Sara
Larkin, Jerome
Lu, Shaolei
Neill, Marguerite
Rogers, Ralph
Sweeney, Joseph
source
MedRxiv
abstract
Background The efficacy of convalescent plasma (CP) for the treatment of COVID-19 remains unclear. Methods A matched cohort analysis of hospitalized patients with severe COVID-19. The impact of CP treatment on all cause in-hospital mortality was evaluated using univariate and multivariate Cox proportional-hazards models, and the impact of CP treatment on the time to hospital discharge was assessed using a stratified log-rank analysis. Results 64 patients who received CP a median of 7 days after symptom onset were compared to a matched control group of 177 patients. Overall in-hospital mortality was 14.9%. There was no significant difference in the risk of in-hospital mortality between the two groups (adjusted hazard ratio [aHR] 0.93, 95% confidence interval [CI] 0.39 - 2.20). There was also no significant difference in the overall rate of hospital discharge (rate ratio [RR} 1.28, 95% CI 0.91 - 1.81), but a subgroup analysis of patients 65-years-old or greater who received CP demonstrated a significantly increased hospital discharge rate among these patients (RR 1.86, 95% CI 1.03 - 3.36). There was a greater than expected frequency of transfusion reactions in the CP group (2.8% reaction rate observed per unit transfused). Conclusions The use of CP in this study was a safe treatment for COVID-19. There was no overall significant reduction of in-hospital mortality or increased rate of hospital discharge associated with the use of CP in this study, although there was a signal for improved outcomes among the elderly. Further adequately powered randomized studies should target this subgroup when assessing the efficacy CP treatment.
has issue date
2020-08-21
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bibo:doi
10.1101/2020.08.18.20177402
has license
medrxiv
sha1sum (hex)
39d72bd0fe3295fccb92f1a34498aea32ba4cfe4
schema:url
https://doi.org/10.1101/2020.08.18.20177402
resource representing a document's title
Convalescent plasma for patients with severe COVID-19: a matched cohort study
resource representing a document's body
covid:39d72bd0fe3295fccb92f1a34498aea32ba4cfe4#body_text
is
schema:about
of
named entity 'plasma'
named entity 'cohort study'
named entity 'cohort study'
named entity 'COVID-19'
named entity 'preprint'
named entity 'antibody'
named entity 'transfusion'
named entity 'critically ill patients'
named entity 'clinical outcomes'
named entity 'preprint'
named entity 'preprint'
named entity 'preprint'
named entity 'COVID-19'
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named entity 'peer review'
named entity 'medRxiv'
named entity 'clinical outcomes'
named entity 'COVID'
named entity 'electronic health record'
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named entity 'thrombosis'
named entity 'preprint'
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named entity 'copyright holder'
named entity 'preprint'
named entity 'transfusion reactions'
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named entity 'remdesivir'
named entity 'medRxiv'
named entity 'TRALI'
named entity 'subgroup analysis'
named entity 'placebo'
named entity 'control group'
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