Hydroxychloroquine to prevent SARS-CoV-2 infection among healthcare workers: early termination of a phase 3, randomised, open-label, controlled clinical trial

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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 =...

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Detalles Bibliográficos
Autores: 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
Formato: artículo
Fecha de Publicación:2023
Institución:Universidad Peruana de Ciencias Aplicadas
Repositorio:UPC-Institucional
Lenguaje:inglés
OAI Identifier:oai:repositorioacademico.upc.edu.pe:10757/667728
Enlace del recurso:http://hdl.handle.net/10757/667728
Nivel de acceso:acceso abierto
Materia:COVID-19
Global health
Prophylaxis
Hydroxychloroquine
SARS-CoV-2
Infection Prevention
Healthcare Workers
Clinical Trial
Control Group
Infection Incidence
Relative Risk
Adverse Events
Trial Registration
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dc.title.es_PE.fl_str_mv Hydroxychloroquine to prevent SARS-CoV-2 infection among healthcare workers: early termination of a phase 3, randomised, open-label, controlled clinical trial
title Hydroxychloroquine to prevent SARS-CoV-2 infection among healthcare workers: early termination of a phase 3, randomised, open-label, controlled clinical trial
spellingShingle 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
COVID-19
Global health
Prophylaxis
Hydroxychloroquine
Prophylaxis
SARS-CoV-2
Infection Prevention
Healthcare Workers
Clinical Trial
Control Group
Infection Incidence
Relative Risk
Adverse Events
Trial Registration
title_short Hydroxychloroquine to prevent SARS-CoV-2 infection among healthcare workers: early termination of a phase 3, randomised, open-label, controlled clinical trial
title_full Hydroxychloroquine to prevent SARS-CoV-2 infection among healthcare workers: early termination of a phase 3, randomised, open-label, controlled clinical trial
title_fullStr Hydroxychloroquine to prevent SARS-CoV-2 infection among healthcare workers: early termination of a phase 3, randomised, open-label, controlled clinical trial
title_full_unstemmed Hydroxychloroquine to prevent SARS-CoV-2 infection among healthcare workers: early termination of a phase 3, randomised, open-label, controlled clinical trial
title_sort Hydroxychloroquine to prevent SARS-CoV-2 infection among healthcare workers: early termination of a phase 3, randomised, open-label, controlled clinical trial
author Llanos-Cuentas, Alejandro
author_facet 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
author_role author
author2 Schwalb, Alvaro
Quintana, Juan Luis
Delfin, Brian
Alvarez, Fiorela
Ugarte-Gil, César
Guerra Gronerth, Rosio I.
Lucchetti, Aldo
Grogl, Max
Gotuzzo, Eduardo
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv 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
dc.subject.es_PE.fl_str_mv COVID-19
Global health
Prophylaxis
Hydroxychloroquine
Prophylaxis
SARS-CoV-2
Infection Prevention
Healthcare Workers
Clinical Trial
Control Group
Infection Incidence
Relative Risk
Adverse Events
Trial Registration
topic COVID-19
Global health
Prophylaxis
Hydroxychloroquine
Prophylaxis
SARS-CoV-2
Infection Prevention
Healthcare Workers
Clinical Trial
Control Group
Infection Incidence
Relative Risk
Adverse Events
Trial Registration
description 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).
publishDate 2023
dc.date.accessioned.none.fl_str_mv 2023-05-15T15:09:13Z
dc.date.available.none.fl_str_mv 2023-05-15T15:09:13Z
dc.date.issued.fl_str_mv 2023-12-01
dc.type.es_PE.fl_str_mv info:eu-repo/semantics/article
format article
dc.identifier.doi.none.fl_str_mv 10.1186/s13104-023-06281-7
dc.identifier.uri.none.fl_str_mv http://hdl.handle.net/10757/667728
dc.identifier.eissn.none.fl_str_mv 17560500
dc.identifier.journal.es_PE.fl_str_mv BMC Research Notes
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identifier_str_mv 10.1186/s13104-023-06281-7
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dc.language.iso.es_PE.fl_str_mv eng
language eng
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eu_rights_str_mv openAccess
rights_invalid_str_mv Attribution-NonCommercial-NoDerivatives 4.0 International
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dc.format.es_PE.fl_str_mv application/pdf
dc.publisher.es_PE.fl_str_mv BioMed Central Ltd
dc.source.es_PE.fl_str_mv Universidad Peruana de Ciencias Aplicadas (UPC)
Repositorio Academico - UPC
dc.source.none.fl_str_mv reponame:UPC-Institucional
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instname_str Universidad Peruana de Ciencias Aplicadas
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dc.source.journaltitle.none.fl_str_mv BMC Research Notes
dc.source.volume.none.fl_str_mv 16
dc.source.issue.none.fl_str_mv 1
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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. 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