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Convalescent plasma for hospitalized patients with COVID-19: an open-label, randomized controlled trial.
Bégin, Philippe; Callum, Jeannie; Jamula, Erin; Cook, Richard; Heddle, Nancy M; Tinmouth, Alan; Zeller, Michelle P; Beaudoin-Bussières, Guillaume; Amorim, Luiz; Bazin, Renée; Loftsgard, Kent Cadogan; Carl, Richard; Chassé, Michaël; Cushing, Melissa M; Daneman, Nick; Devine, Dana V; Dumaresq, Jeannot; Fergusson, Dean A; Gabe, Caroline; Glesby, Marshall J; Li, Na; Liu, Yang; McGeer, Allison; Robitaille, Nancy; Sachais, Bruce S; Scales, Damon C; Schwartz, Lisa; Shehata, Nadine; Turgeon, Alexis F; Wood, Heidi; Zarychanski, Ryan; Finzi, Andrés; Arnold, Donald M.
  • Bégin P; Department of Pediatrics, CHU Sainte-Justine, Montreal, Quebec, Canada. philippe.begin.med@ssss.gouv.qc.ca.
  • Callum J; Department of Medicine, Centre Hospitalier de l'Université de Montréal, Montreal, Quebec, Canada. philippe.begin.med@ssss.gouv.qc.ca.
  • Jamula E; Department of Pathology and Molecular Medicine, Kingston Health Sciences Centre and Queen's University, Kingston, Ontario, Canada. jeannie.callum@kingstonhsc.ca.
  • Cook R; Department of Laboratory Medicine and Molecular Diagnostics, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada. jeannie.callum@kingstonhsc.ca.
  • Heddle NM; Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada. jeannie.callum@kingstonhsc.ca.
  • Tinmouth A; Canadian Blood Services, Ottawa, Ontario, Canada. jeannie.callum@kingstonhsc.ca.
  • Zeller MP; McMaster Centre for Transfusion Research, McMaster University, Hamilton, Ontario, Canada.
  • Beaudoin-Bussières G; Department of Statistics and Actuarial Science, University of Waterloo, Waterloo, Ontario, Canada.
  • Amorim L; Canadian Blood Services, Ottawa, Ontario, Canada.
  • Bazin R; McMaster Centre for Transfusion Research, McMaster University, Hamilton, Ontario, Canada.
  • Loftsgard KC; Department of Medicine, McMaster University, Hamilton, Ontario, Canada.
  • Carl R; Canadian Blood Services, Ottawa, Ontario, Canada.
  • Chassé M; Department of Medicine, University of Ottawa, Ottawa, Ontario, Canada.
  • Cushing MM; Ottawa Hospital Centre for Transfusion Research, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
  • Daneman N; Canadian Blood Services, Ottawa, Ontario, Canada.
  • Devine DV; McMaster Centre for Transfusion Research, McMaster University, Hamilton, Ontario, Canada.
  • Dumaresq J; Department of Medicine, McMaster University, Hamilton, Ontario, Canada.
  • Fergusson DA; Département de Microbiologie, Infectiologie et Immunologie, Université de Montréal, Montreal, Quebec, Canada.
  • Gabe C; CHUM Research Center, Montreal, Quebec, Canada.
  • Glesby MJ; Hemorio, Hospital and Regional Blood Center, Rio de Janeiro, Brazil.
  • Li N; Héma-Québec, Medical Affairs and Innovation, Quebec City, Quebec, Canada.
  • Liu Y; CONCOR-1 Community Advisory Committee representative, Montreal, Quebec, Canada.
  • McGeer A; Patient representative, Montreal, Quebec, Canada.
  • Robitaille N; Department of Medicine, Centre Hospitalier de l'Université de Montréal, Montreal, Quebec, Canada.
  • Sachais BS; Innovation Hub, Centre de Recherche du Centre Hospitalier de l'Université de Montréal, Montreal, Quebec, Canada.
  • Scales DC; Transfusion Medicine and Cellular Therapy, New York-Presbyterian, New York, NY, USA.
  • Schwartz L; Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, NY, USA.
  • Shehata N; Department of Medicine, Division of Infectious Diseases, Sunnybrook Health Sciences Centre, University of Toronto, Toronto, Ontario, Canada.
  • Turgeon AF; Canadian Blood Services, Vancouver, British Columbia, Canada.
  • Wood H; Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
  • Zarychanski R; Département de médecine, CISSS de Chaudière-Appalaches, Lévis, Quebec, Canada.
  • Finzi A; Département de microbiologie-infectiologie et d'immunologie, Faculté de Médecine, Université Laval, Quebec City, Quebec, Canada.
  • Arnold DM; Department of Medicine, University of Ottawa, Ottawa, Ontario, Canada.
Nat Med ; 27(11): 2012-2024, 2021 11.
Article in English | MEDLINE | ID: covidwho-1526091
ABSTRACT
The efficacy of convalescent plasma for coronavirus disease 2019 (COVID-19) is unclear. Although most randomized controlled trials have shown negative results, uncontrolled studies have suggested that the antibody content could influence patient outcomes. We conducted an open-label, randomized controlled trial of convalescent plasma for adults with COVID-19 receiving oxygen within 12 d of respiratory symptom onset ( NCT04348656 ). Patients were allocated 21 to 500 ml of convalescent plasma or standard of care. The composite primary outcome was intubation or death by 30 d. Exploratory analyses of the effect of convalescent plasma antibodies on the primary outcome was assessed by logistic regression. The trial was terminated at 78% of planned enrollment after meeting stopping criteria for futility. In total, 940 patients were randomized, and 921 patients were included in the intention-to-treat analysis. Intubation or death occurred in 199/614 (32.4%) patients in the convalescent plasma arm and 86/307 (28.0%) patients in the standard of care arm-relative risk (RR) = 1.16 (95% confidence interval (CI) 0.94-1.43, P = 0.18). Patients in the convalescent plasma arm had more serious adverse events (33.4% versus 26.4%; RR = 1.27, 95% CI 1.02-1.57, P = 0.034). The antibody content significantly modulated the therapeutic effect of convalescent plasma. In multivariate analysis, each standardized log increase in neutralization or antibody-dependent cellular cytotoxicity independently reduced the potential harmful effect of plasma (odds ratio (OR) = 0.74, 95% CI 0.57-0.95 and OR = 0.66, 95% CI 0.50-0.87, respectively), whereas IgG against the full transmembrane spike protein increased it (OR = 1.53, 95% CI 1.14-2.05). Convalescent plasma did not reduce the risk of intubation or death at 30 d in hospitalized patients with COVID-19. Transfusion of convalescent plasma with unfavorable antibody profiles could be associated with worse clinical outcomes compared to standard care.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Type of study: Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Limits: Adult / Aged / Female / Humans / Male / Middle aged Country/Region as subject: North America / South America / Brazil Language: English Journal: Nat Med Journal subject: Molecular Biology / Medicine Year: 2021 Document Type: Article Affiliation country: S41591-021-01488-2

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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Type of study: Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Limits: Adult / Aged / Female / Humans / Male / Middle aged Country/Region as subject: North America / South America / Brazil Language: English Journal: Nat Med Journal subject: Molecular Biology / Medicine Year: 2021 Document Type: Article Affiliation country: S41591-021-01488-2