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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...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Centers for Disease Control and Prevention
2022
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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. |
format | Online Article Text |
id | pubmed-8888205 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Centers for Disease Control and Prevention |
record_format | MEDLINE/PubMed |
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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