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High-Dose Convalescent Plasma for Treatment of Severe COVID-19

To assess whether high-dose coronavirus disease (COVID-19) convalescent plasma (CCP) transfusion may benefit patients with severe COVID-19, we conducted a multicenter randomized trial in Brazil. Patients with severe COVID-19 who were within 10 days of initial symptom onset were eligible. Patients in...

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Autores principales: De Santis, Gil C., Oliveira, Luciana Correa, Garibaldi, Pedro M.M., Almado, Carlos E.L., Croda, Julio, Arcanjo, Ghislaine G.A., Oliveira, Érika A.F., Tonacio, Adriana C., Langhi, Dante M., Bordin, José O., Gilio, Renato N., Palma, Leonardo C., Santos, Elaine V., Haddad, Simone K., Prado, Benedito P.A., Pontelli, Marjorie Cornejo, Gomes, Rogério, Miranda, Carlos H., Martins, Maria Auxiliadora, Covas, Dimas T., Arruda, Eurico, Fonseca, Benedito A.L., Calado, Rodrigo T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Centers for Disease Control and Prevention 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8888205/
https://www.ncbi.nlm.nih.gov/pubmed/35081022
http://dx.doi.org/10.3201/eid2803.212299
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author De Santis, Gil C.
Oliveira, Luciana Correa
Garibaldi, Pedro M.M.
Almado, Carlos E.L.
Croda, Julio
Arcanjo, Ghislaine G.A.
Oliveira, Érika A.F.
Tonacio, Adriana C.
Langhi, Dante M.
Bordin, José O.
Gilio, Renato N.
Palma, Leonardo C.
Santos, Elaine V.
Haddad, Simone K.
Prado, Benedito P.A.
Pontelli, Marjorie Cornejo
Gomes, Rogério
Miranda, Carlos H.
Martins, Maria Auxiliadora
Covas, Dimas T.
Arruda, Eurico
Fonseca, Benedito A.L.
Calado, Rodrigo T.
author_facet De Santis, Gil C.
Oliveira, Luciana Correa
Garibaldi, Pedro M.M.
Almado, Carlos E.L.
Croda, Julio
Arcanjo, Ghislaine G.A.
Oliveira, Érika A.F.
Tonacio, Adriana C.
Langhi, Dante M.
Bordin, José O.
Gilio, Renato N.
Palma, Leonardo C.
Santos, Elaine V.
Haddad, Simone K.
Prado, Benedito P.A.
Pontelli, Marjorie Cornejo
Gomes, Rogério
Miranda, Carlos H.
Martins, Maria Auxiliadora
Covas, Dimas T.
Arruda, Eurico
Fonseca, Benedito A.L.
Calado, Rodrigo T.
author_sort De Santis, Gil C.
collection PubMed
description To assess whether high-dose coronavirus disease (COVID-19) convalescent plasma (CCP) transfusion may benefit patients with severe COVID-19, we conducted a multicenter randomized trial in Brazil. Patients with severe COVID-19 who were within 10 days of initial symptom onset were eligible. Patients in the CCP group received 3 daily doses of CCP (600 mL/d) in addition to standard treatment; control patients received standard treatment only. Primary outcomes were death rates at days 30 and 60 of study randomization. Secondary outcomes were ventilator-free days and hospital-free days. We enrolled 107 patients: 36 CCP and 71 control. At day 30, death rates were 22% for CCP and 25% for the control group; at day 60, rates were 31% for CCP and 35% for control. Needs for invasive mechanical ventilation and durations of hospital stay were similar between groups. We conclude that high-dose CCP transfused within 10 days of symptom onset provided no benefit for patients with severe COVID-19.
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spelling pubmed-88882052022-03-02 High-Dose Convalescent Plasma for Treatment of Severe COVID-19 De Santis, Gil C. Oliveira, Luciana Correa Garibaldi, Pedro M.M. Almado, Carlos E.L. Croda, Julio Arcanjo, Ghislaine G.A. Oliveira, Érika A.F. Tonacio, Adriana C. Langhi, Dante M. Bordin, José O. Gilio, Renato N. Palma, Leonardo C. Santos, Elaine V. Haddad, Simone K. Prado, Benedito P.A. Pontelli, Marjorie Cornejo Gomes, Rogério Miranda, Carlos H. Martins, Maria Auxiliadora Covas, Dimas T. Arruda, Eurico Fonseca, Benedito A.L. Calado, Rodrigo T. Emerg Infect Dis Research To assess whether high-dose coronavirus disease (COVID-19) convalescent plasma (CCP) transfusion may benefit patients with severe COVID-19, we conducted a multicenter randomized trial in Brazil. Patients with severe COVID-19 who were within 10 days of initial symptom onset were eligible. Patients in the CCP group received 3 daily doses of CCP (600 mL/d) in addition to standard treatment; control patients received standard treatment only. Primary outcomes were death rates at days 30 and 60 of study randomization. Secondary outcomes were ventilator-free days and hospital-free days. We enrolled 107 patients: 36 CCP and 71 control. At day 30, death rates were 22% for CCP and 25% for the control group; at day 60, rates were 31% for CCP and 35% for control. Needs for invasive mechanical ventilation and durations of hospital stay were similar between groups. We conclude that high-dose CCP transfused within 10 days of symptom onset provided no benefit for patients with severe COVID-19. Centers for Disease Control and Prevention 2022-03 /pmc/articles/PMC8888205/ /pubmed/35081022 http://dx.doi.org/10.3201/eid2803.212299 Text en https://creativecommons.org/licenses/by/4.0/Emerging Infectious Diseases is a publication of the U.S. Government. This publication is in the public domain and is therefore without copyright. All text from this work may be reprinted freely. Use of these materials should be properly cited.
spellingShingle Research
De Santis, Gil C.
Oliveira, Luciana Correa
Garibaldi, Pedro M.M.
Almado, Carlos E.L.
Croda, Julio
Arcanjo, Ghislaine G.A.
Oliveira, Érika A.F.
Tonacio, Adriana C.
Langhi, Dante M.
Bordin, José O.
Gilio, Renato N.
Palma, Leonardo C.
Santos, Elaine V.
Haddad, Simone K.
Prado, Benedito P.A.
Pontelli, Marjorie Cornejo
Gomes, Rogério
Miranda, Carlos H.
Martins, Maria Auxiliadora
Covas, Dimas T.
Arruda, Eurico
Fonseca, Benedito A.L.
Calado, Rodrigo T.
High-Dose Convalescent Plasma for Treatment of Severe COVID-19
title High-Dose Convalescent Plasma for Treatment of Severe COVID-19
title_full High-Dose Convalescent Plasma for Treatment of Severe COVID-19
title_fullStr High-Dose Convalescent Plasma for Treatment of Severe COVID-19
title_full_unstemmed High-Dose Convalescent Plasma for Treatment of Severe COVID-19
title_short High-Dose Convalescent Plasma for Treatment of Severe COVID-19
title_sort high-dose convalescent plasma for treatment of severe covid-19
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8888205/
https://www.ncbi.nlm.nih.gov/pubmed/35081022
http://dx.doi.org/10.3201/eid2803.212299
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