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Hydroxychloroquine to prevent SARS-CoV-2 infection among healthcare workers: early termination of a phase 3, randomised, open-label, controlled clinical trial.
Llanos-Cuentas, Alejandro; Schwalb, Alvaro; Quintana, Juan Luis; Delfin, Brian; Alvarez, Fiorela; Ugarte-Gil, César; Guerra Gronerth, Rosio I; Lucchetti, Aldo; Grogl, Max; Gotuzzo, Eduardo.
  • Llanos-Cuentas A; Instituto de Medicina Tropical Alexander Von Humboldt, Universidad Peruana Cayetano Heredia, Av. Honorio Delgado 430, San Martín de Porres, 15102, Lima, Peru. alejandro.llanos.c@upch.pe.
  • Schwalb A; Instituto de Medicina Tropical Alexander Von Humboldt, Universidad Peruana Cayetano Heredia, Av. Honorio Delgado 430, San Martín de Porres, 15102, Lima, Peru.
  • Quintana JL; School of Medicine, Universidad Peruana Cayetano Heredia, Lima, Peru.
  • Delfin B; Department of Infectious Diseases, Hospital Cayetano Heredia, Lima, Peru.
  • Alvarez F; Instituto de Medicina Tropical Alexander Von Humboldt, Universidad Peruana Cayetano Heredia, Av. Honorio Delgado 430, San Martín de Porres, 15102, Lima, Peru.
  • Ugarte-Gil C; Instituto de Medicina Tropical Alexander Von Humboldt, Universidad Peruana Cayetano Heredia, Av. Honorio Delgado 430, San Martín de Porres, 15102, Lima, Peru.
  • Guerra Gronerth RI; School of Medicine, Universidad Peruana Cayetano Heredia, Lima, Peru.
  • Lucchetti A; Centro Médico Naval Cirujano Mayor Santiago Tavara, Callao, Peru.
  • Grogl M; School of Medicine, Universidad Científica del Sur, Lima, Peru.
  • Gotuzzo E; School of Medicine, Universidad Peruana de Ciencias Aplicadas, Lima, Peru.
BMC Res Notes ; 16(1): 22, 2023 Feb 28.
Artículo en Inglés | MEDLINE | ID: covidwho-2269485
ABSTRACT

OBJECTIVE:

To assess the effectiveness and safety of hydroxychloroquine (HCQ) prophylaxis for the prevention of SARS-CoV-2 infection in healthcare workers (HCW) on duty during the COVID-19 pandemic.

RESULTS:

A total of 68 HCWs met the eligibility criteria were randomly allocated to receive HCQ (n = 36) or not (n = 32). There were no significant differences between groups in respects to age, gender, or medical history. Eight participants met the primary efficacy endpoint of SAR-CoV-2 infection during the study period; there was no difference in incidence of SARS-CoV-2 infections between both study arms (HCQ 5 vs Control 3, p = 0.538). The relative risk of SARS-CoV-2 infection in the HCQ arm was 1.69 compared to the control group (95%CI 0.41-7.11, p = 0.463); due to poor participant accrual, the resulting statistical power of the primary efficacy outcome was 11.54%. No serious adverse events occurred; however, two (2/36, 5.6%) participants no longer wished to participate in the study and withdrew consent due to recurring grade 1 and 2 adverse events. TRIAL REGISTRATION ClinicalTrials.gov ID NCT04414241. (Registered on June 4, 2020).
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Texto completo: Disponible Colección: Bases de datos internacionales Base de datos: MEDLINE Asunto principal: COVID-19 / Hidroxicloroquina Tipo de estudio: Estudio experimental / Estudio observacional / Estudio pronóstico / Ensayo controlado aleatorizado Límite: Humanos Idioma: Inglés Revista: BMC Res Notes Año: 2023 Tipo del documento: Artículo País de afiliación: S13104-023-06281-7

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Texto completo: Disponible Colección: Bases de datos internacionales Base de datos: MEDLINE Asunto principal: COVID-19 / Hidroxicloroquina Tipo de estudio: Estudio experimental / Estudio observacional / Estudio pronóstico / Ensayo controlado aleatorizado Límite: Humanos Idioma: Inglés Revista: BMC Res Notes Año: 2023 Tipo del documento: Artículo País de afiliación: S13104-023-06281-7