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Early Anti-SARS-CoV-2 Convalescent Plasma in Patients Admitted for COVID-19: A Randomized Phase II Clinical Trial
María Elvira Balcells; Luis Rojas; Nicole Le Corre; Constanza Martínez-Valdebenito; María Elena Ceballos; Marcela Ferrés; Mayling Chang; Cecilia Vizcaya; Sebastián Mondaca; Álvaro Huete; Ricardo Castro; Mauricio Sarmiento; Luis Villarroel; Alejandra Pizarro; Patricio Ross; Jaime Santander; Bárbara Lara; Marcela Ferrada; Sergio Vargas-Salas; Carolina Beltrán-Pavez; Ricardo Soto-Rifo; Fernando Valiente-Echeverría; Christian Caglevic; Mauricio Mahave; Carolina Selman; Raimundo Gazitúa; José Luis Briones; Franz Villarroel-Espindola; Carlos Balmaceda; Manuel A. Espinoza; Jaime Pereira; Bruno Nervi.
Afiliação
  • María Elvira Balcells; Department of Infectious Diseases. School of Medicine. Pontificia Universidad Católica de Chile.
  • Luis Rojas; Department of Internal Medicine. School of Medicine. Pontificia Universidad Católica de Chile
  • Nicole Le Corre; Department of Pediatric Infectious Diseases and Immunology. School of Medicine. Pontificia Universidad Católica de Chile.
  • Constanza Martínez-Valdebenito; Diagnostic Virology Laboratory. Red de Salud UC Christus.
  • María Elena Ceballos; Department of Infectious Diseases. School of Medicine. Pontificia Universidad Católica de Chile
  • Marcela Ferrés; Department of Pediatric Infectious Diseases and Immunology. School of Medicine. Pontificia Universidad Católica de Chile
  • Mayling Chang; Department of Hematology and Oncology. School of Medicine. Pontificia Universidad Católica de Chile
  • Cecilia Vizcaya; Department of Pediatric Infectious Diseases and Immunology. School of Medicine. Pontificia Universidad Católica de Chile.
  • Sebastián Mondaca; Department of Hematology and Oncology. School of Medicine. Pontificia Universidad Católica de Chile.
  • Álvaro Huete; Department of Radiology. School of Medicine. Pontificia Universidad Católica de Chile.
  • Ricardo Castro; Department of Intensive Care Medicine. School of Medicine. Pontificia Universidad Católica de Chile
  • Mauricio Sarmiento; Department of Hematology and Oncology. School of Medicine. Pontificia Universidad Católica de Chile.
  • Luis Villarroel; Department of Public Health. School of Medicine. Pontificia Universidad Católica de Chile.
  • Alejandra Pizarro; Department of Infectious Diseases. School of Medicine. Pontificia Universidad Católica de Chile.
  • Patricio Ross; Department of Internal Medicine. School of Medicine. Pontificia Universidad Católica de Chile.
  • Jaime Santander; Department of Psychiatry. School of Medicine. Pontificia Universidad Católica de Chile.
  • Bárbara Lara; Emergency Medicine Section. School of Medicine. Pontificia Universidad Católica de Chile.
  • Marcela Ferrada; Clinical Research Center. School of Medicine. Pontificia Universidad Católica de Chile.
  • Sergio Vargas-Salas; Department of Hematology and Oncology. School of Medicine. Pontificia Universidad Católica de Chile.
  • Carolina Beltrán-Pavez; Laboratory of Molecular and Cellular Virology, Virology Program, Institute of Biomedical Sciences. Faculty of Medicine. Universidad de Chile. HIV/AIDS Work Grou
  • Ricardo Soto-Rifo; Laboratory of Molecular and Cellular Virology, Virology Program, Institute of Biomedical Sciences, Faculty of Medicine, Universidad de Chile. HIV/AIDS Work Grou
  • Fernando Valiente-Echeverría; Laboratory of Molecular and Cellular Virology, Virology Program, Institute of Biomedical Sciences, Faculty of Medicine, Universidad de Chile. HIV/AIDS Work Grou
  • Christian Caglevic; Instituto Oncológico Fundación Arturo López Pérez (FALP) Santiago, Chile
  • Mauricio Mahave; Instituto Oncológico Fundación Arturo López Pérez (FALP) Santiago, Chile
  • Carolina Selman; Instituto Oncológico Fundación Arturo López Pérez (FALP) Santiago, Chile
  • Raimundo Gazitúa; Instituto Oncológico Fundación Arturo López Pérez (FALP) Santiago, Chile
  • José Luis Briones; Instituto Oncológico Fundación Arturo López Pérez (FALP) Santiago, Chile
  • Franz Villarroel-Espindola; Instituto Oncológico, Fundación Arturo López Pérez (FALP). Translational Medicine Research Laboratory, Fundación Arturo López Pérez (FALP), Chile
  • Carlos Balmaceda; Health Technology Assessment Unit, Clinical Research Center, School of Medicine, Pontificia Universidad Católica de Chile
  • Manuel A. Espinoza; Department of Public Health. School of Medicine. Pontificia Universidad Católica de Chile.
  • Jaime Pereira; Department of Hematology and Oncology. School of Medicine. Pontificia Universidad Católica de Chile.
  • Bruno Nervi; Department of Hematology and Oncology. School of Medicine. Pontificia Universidad Católica de Chile.
Preprint em Inglês | medRxiv | ID: ppmedrxiv-20196212
ABSTRACT

Background:

Convalescent plasma (CP), despite limited evidence on its efficacy, is being widely used as a compassionate therapy for hospitalized patients with COVID-19. We aimed to evaluate the efficacy and safety of early CP therapy in COVID-19 progression.

Methods:

Open-label, single-center, randomized clinical trial performed in an academic center in Santiago, Chile from May 10, 2020, to July 18, 2020, with final follow-up August 17, 2020. The trial included patients hospitalized within the first 7 days of COVID-19 symptoms onset, presenting risk factors for illness progression and not on mechanical ventilation. The intervention consisted in immediate CP (early plasma group) versus no CP unless developing pre-specified criteria of deterioration (deferred plasma group). Additional standard treatment was allowed in both arms. The primary outcome was a composite of mechanical ventilation, hospitalization for >14 days or death. Key secondary outcomes included time to respiratory failure, days of mechanical ventilation, hospital length-of-stay, mortality at 30 days, and SARS-CoV-2 RT-PCR clearance rate.

Results:

Of 58 randomized patients (mean age, 65.8 years, 50% male), 57 (98.3%) completed the trial. A total of 13 (43.3%) participants from the deferred group received plasma based on clinical aggravation. We found no benefit in the primary outcome (32.1% vs 33.3%, OR 0.95, 95% CI 0.32-2.84, p>0.99) in the early versus deferred CP group. In-hospital mortality rate was 17.9% vs 6.7% (OR 3.04, 95% CI 0.54-17.2, p=0.25), mechanical ventilation 17.9% vs 6.7% (OR 3.04, 95% CI 0.54-17.2, p=0.25), and prolonged hospitalization 21.4% vs 30% (OR 0.64, 95%CI, 0.19-2.1, p=0.55) in early versus deferred CP group, respectively. Viral clearance rate on day 3 (26% vs 8%, p=0.20) and day 7 (38% vs 19%, p=0.37) did not differ between groups. Two patients experienced serious adverse events within 6 or less hours after plasma transfusion.

Conclusion:

Immediate addition of CP therapy in early stages of COVID-19 -compared to its use only in case of patient deterioration- did not confer benefits in mortality, length of hospitalization or mechanical ventilation requirement.
Licença
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Texto completo: Disponível Coleções: Preprints Base de dados: medRxiv Tipo de estudo: Cohort_studies / Experimental_studies / Estudo prognóstico / Rct Idioma: Inglês Ano de publicação: 2020 Tipo de documento: Preprint
Texto completo: Disponível Coleções: Preprints Base de dados: medRxiv Tipo de estudo: Cohort_studies / Experimental_studies / Estudo prognóstico / Rct Idioma: Inglês Ano de publicação: 2020 Tipo de documento: Preprint
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