Early High-Titer Plasma Therapy to Prevent Severe Covid-19 in Older Adults

Romina Libster(Infant Foundation), Gonzalo Pérez Marc(Hospital Militar Central), Diego Wappner(Swiss Paediatric Oncology Group), Silvina Coviello(Infant Foundation), Alejandra Bianchi(Infant Foundation), Virginia Braem(Hospital Militar Central), Ignacio Esteban(Infant Foundation), Mauricio T. Caballero(Infant Foundation), Cristian Wood(Hospital Militar Central), Mabel Berrueta(Instituto de Efectividad Clínica y Sanitaria), Anibal Rondan(S.P.E.C.I.E.S.), Gabriela Lescano(S.P.E.C.I.E.S.), Pablo Jordão Alcântara Cruz(Servicio Gallego de Salud), Yvonne Ritou(S.P.E.C.I.E.S.), Valeria Fernández Viña(Hospital Zonal General De Agudos Descentralizado "Evita Pueblo"), Damián Álvarez Paggi(S.P.E.C.I.E.S.), Sebastián Esperante(Infant Foundation), Adrián Ferreti(Infant Foundation), Gastón Ofman(Infant Foundation), Álvaro Ciganda(S.P.E.C.I.E.S.), Rocío Rodríguez(Instituto de Efectividad Clínica y Sanitaria), Jorge Lantos(Swiss Paediatric Oncology Group), Ricardo Valentini(Centro de Educación Médica e Investigaciones Clínicas Norberto Quirno), Nicolás Itcovici(Hospital Militar Central), Alejandra Hintze(Hospital Militar Central), María Laura Oyarvide(Hospital Militar Central), Candela Etchegaray(Hospital Militar Central), Alejandra Neira(Hospital Militar Central), Ivonne Name(Hospital Militar Central), Julieta Alfonso(Hospital Militar Central), Rocío López Castelo(Hospital Militar Central), Gisela Caruso(Hospital Militar Central), Sofía Rapelius(Hospital Militar Central), Fernando Alvez(S.P.E.C.I.E.S.), Federico Etchenique(Swiss Paediatric Oncology Group), Federico Dimase(Hospital Militar Central), Darío Alvarez(Hospital Militar Central), Sofía S. Aranda(Infant Foundation), Clara Sánchez Yanotti(Infant Foundation), Julián De Luca(Swiss Paediatric Oncology Group), Sofía Jares Baglivo(Infant Foundation), Sofía Laudanno(Infant Foundation), Florencia Nowogrodzki(Infant Foundation), Ramiro Larrea(S.P.E.C.I.E.S.), María Dolores Silveyra(S.P.E.C.I.E.S.), Gabriel Leberzstein(Hospital Quirónsalud Sagrado Corazón), Alejandra Debonis(Ministerio de Salud - Provincia de Buenos Aires), Juan Molinos(Swiss Paediatric Oncology Group), Miguel Santiago Gonzalez(S.P.E.C.I.E.S.), Eduardo García Pérez(S.P.E.C.I.E.S.), Nicolás Kreplak(Ministerio de Salud - Provincia de Buenos Aires), Susana Pastor Argüello(Hospital Militar Central), Luz Gibbons(Instituto de Efectividad Clínica y Sanitaria), Fernando Althabe(United Nations), Eduardo Bergel(Instituto de Efectividad Clínica y Sanitaria), Fernando P. Polack(Infant Foundation)
New England Journal of Medicine
January 6, 2021
Cited by 940Open Access
Full Text

Abstract

BACKGROUND: Therapies to interrupt the progression of early coronavirus disease 2019 (Covid-19) remain elusive. Among them, convalescent plasma administered to hospitalized patients has been unsuccessful, perhaps because antibodies should be administered earlier in the course of illness. METHODS: We conducted a randomized, double-blind, placebo-controlled trial of convalescent plasma with high IgG titers against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in older adult patients within 72 hours after the onset of mild Covid-19 symptoms. The primary end point was severe respiratory disease, defined as a respiratory rate of 30 breaths per minute or more, an oxygen saturation of less than 93% while the patient was breathing ambient air, or both. The trial was stopped early at 76% of its projected sample size because cases of Covid-19 in the trial region decreased considerably and steady enrollment of trial patients became virtually impossible. RESULTS: A total of 160 patients underwent randomization. In the intention-to-treat population, severe respiratory disease developed in 13 of 80 patients (16%) who received convalescent plasma and 25 of 80 patients (31%) who received placebo (relative risk, 0.52; 95% confidence interval [CI], 0.29 to 0.94; P = 0.03), with a relative risk reduction of 48%. A modified intention-to-treat analysis that excluded 6 patients who had a primary end-point event before infusion of convalescent plasma or placebo showed a larger effect size (relative risk, 0.40; 95% CI, 0.20 to 0.81). No solicited adverse events were observed. CONCLUSIONS: Early administration of high-titer convalescent plasma against SARS-CoV-2 to mildly ill infected older adults reduced the progression of Covid-19. (Funded by the Bill and Melinda Gates Foundation and the Fundación INFANT Pandemic Fund; Dirección de Sangre y Medicina Transfusional del Ministerio de Salud number, PAEPCC19, Plataforma de Registro Informatizado de Investigaciones en Salud number, 1421, and ClinicalTrials.gov number, NCT04479163.).


Related Papers

No related papers found

Powered by citation graph analysis