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dc.creatorZhou, C. K.
dc.creatorBennett, M. M.
dc.creatorVilla, C. H.
dc.creatorHammonds, K. P.
dc.creatorLu, Y.
dc.creatorEttlinger, J.
dc.creatorPriest, E.L.
dc.creatorGottlieb, R. L.
dc.creatorDavis, S.
dc.creatorMays, E.
dc.creatorClarke, T. C.
dc.creatorShoaibi, A.
dc.creatorWong, H.-L.
dc.creatorAnderson, S. A.
dc.creatorKelly, R. J.
dc.date.accessioned2022-09-28T17:57:03Z
dc.date.available2022-09-28T17:57:03Z
dc.date.issued2022
dc.identifier.urihttps://doi.org/10.1371/journal.pone.0273223
dc.identifier.urihttps://repository.tcu.edu/handle/116099117/55826
dc.description.abstractBackground 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.
dc.languageen
dc.publisherPLOS
dc.rightsPublic Domain
dc.rights.urihttps://creativecommons.org/publicdomain/zero/1.0/
dc.sourcePLoS One
dc.subjectangiotensin receptor antagonist
dc.subjectanticoagulant agent
dc.subjectantithrombocytic agent
dc.subjectazithromycin
dc.subjectchloroquine
dc.subjectdexamethasone
dc.subjectdipeptidyl carboxypeptidase inhibitor
dc.subjecthydrocortisone
dc.subjecthydroxychloroquine
dc.subjectprednisone
dc.subjectremdesivir
dc.subjectSARS-CoV-2 convalescent plasma
dc.subjecttocilizumab
dc.subjectoxygen
dc.subjectadult
dc.subjectaged
dc.subjectall cause mortality
dc.subjectArticle
dc.subjectartificial ventilation
dc.subjectclinical outcome
dc.subjectcohort analysis
dc.subjectconfidence interval
dc.subjectcontrolled study
dc.subjectconvalescent plasma transfusion
dc.subjectcoronavirus disease 2019
dc.subjectdrug safety
dc.subjectfemale
dc.subjectgender
dc.subjectgroups by age
dc.subjecthazard ratio
dc.subjecthealth care system
dc.subjecthospital admission
dc.subjecthospital patient
dc.subjecthuman
dc.subjecthypertension
dc.subjectin-hospital mortality
dc.subjectmajor clinical study
dc.subjectmale
dc.subjectmulticenter study
dc.subjectoxygen therapy
dc.subjectpandemic
dc.subjectproportional hazards model
dc.subjectretrospective study
dc.subjectsensitivity analysis
dc.subjectTexas
dc.subjectthromboembolism
dc.subjectpassive immunization
dc.subjectprocedures
dc.subjecttherapy
dc.subjecttreatment outcome
dc.subjectCohort Studies
dc.subjectCOVID-19
dc.subjectHumans
dc.subjectImmunization, Passive
dc.subjectOxygen
dc.subjectSARS-CoV-2
dc.subjectTreatment Outcome
dc.titleMulti-center matched cohort study of convalescent plasma for hospitalized patients with COVID-19
dc.typeArticle
dc.rights.licenseCC0 1.0
local.collegeBurnett School of Medicine
local.departmentBurnett School of Medicine
local.personsGottlieb (SOM)


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