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Hydroxychloroquine for treatment of non-hospitalized adults with COVID-19: A meta-analysis of individual participant data of randomized trials

  • Oriol Mitjà*
  • , Gilmar Reis
  • , David R. Boulware
  • , Adam M. Spivak
  • , Ammar Sarwar
  • , Christine Johnston
  • , Brandon Webb
  • , Michael D. Hill
  • , Davey Smith
  • , Peter Kremsner
  • , Marla Curran
  • , David Carter
  • , Jim Alexander
  • , Marc Corbacho
  • , Todd C. Lee
  • , Katherine Huppler Hullsiek
  • , Emily G. McDonald
  • , Rachel Hess
  • , Michael Hughes
  • , Jared M. Baeten
  • Ilan Schwartz, Luanne Metz, Lawrence Richer, Kara W. Chew, Eric Daar, David Wohl, Michael Dunne
*Autor correspondiente de este trabajo
  • Fight AIDS and Infectious Diseases Foundation
  • Hospital Universitari Germans Trias i Pujol
  • Lihir Medical Center–International SOS
  • Pontifícia Universidade Católica de Minas Gerais
  • Cytel Inc.
  • University of Minnesota Medical School
  • University of Utah
  • Harvard University
  • University of Washington
  • University of Utah School of Medicine
  • University of Calgary
  • University of California at San Diego
  • University of Tübingen
  • Centre de Recherches Médicales de Lambaréné
  • Bill & Melinda Gates Medical Research Institute
  • MMS Holdings Inc
  • McGill University
  • University of Alberta
  • David Geffen School of Medicine at UCLA
  • University of California at Los Angeles
  • University of North Carolina at Chapel Hill

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

11 Citas (Scopus)

Resumen

Hydroxychloroquine (HCQ) was initially promoted as an oral therapy for early treatment of coronavirus disease 2019 (COVID-19). Conventional meta-analyses cannot fully address the heterogeneity of different designs and outcomes of randomized controlled trials (RCTs) assessing the efficacy of HCQ in outpatients with mild COVID-19. We conducted a pooled analysis of individual participant data from RCTs that evaluated the effect of HCQ on hospitalization and viral load reduction in outpatients with confirmed COVID-19. We evaluated the overall treatment group effect by log-likelihood ratio test (−2LL) from a generalized linear mixed model to accommodate correlated longitudinal binary data. The analysis included data from 11 RCTs. The outcome of virological effect, assessed in 1560 participants (N = 795 HCQ, N = 765 control), did not differ significantly between the two treatment groups (−2LL = 7.66; p = 0.18) when adjusting for cohort, duration of symptoms, and comorbidities. The decline in polymerase chain reaction positive tests from day 1 to 7 was 42.0 and 41.6 percentage points in the HCQ and control groups, respectively. Among the 2037 participants evaluable for hospitalization (N = 1058 HCQ, N = 979 control), we found no significant differences in hospitalization rate between participants receiving HCQ and controls (odds ratio 0.995; 95% confidence interval 0.614–1.610; −2LL = 0.0; p = 0.98) when adjusting for cohort, duration of symptoms, and comorbidities. This individual participant data meta-analysis of 11 HCQ trials that evaluated severe acute respiratory syndrome-coronavirus 2 viral clearance and COVID-19 hospitalization did not show a clinical benefit of HCQ. Our meta-analysis provides evidence to support the interruption in the use of HCQ in mild COVID-19 outpatients to reduce progression to severe disease.

Idioma originalInglés
Páginas (desde-hasta)524-535
Número de páginas12
PublicaciónClinical and Translational Science
Volumen16
N.º3
DOI
EstadoPublicada - mar. 2023
Publicado de forma externa

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