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dc.contributor.authorPittet, Laure F.
dc.contributor.authorMessina, Nicole L.
dc.contributor.authorMcDonald, Ellie
dc.contributor.authorOrsini, Francesca
dc.contributor.authorBarry, Simone
dc.contributor.authorBonten, Marc
dc.contributor.authorCampbell, John
dc.contributor.authorCroda, Julio
dc.contributor.authorCroda, Mariana G.
dc.contributor.authorDalcolmo, Margareth
dc.contributor.authorGardiner, Kaya
dc.contributor.authorGwee, Amanda
dc.contributor.authorJardim, Bruno
dc.contributor.authorLacerda, Marcus V.G.
dc.contributor.authorLucas, Michaela
dc.contributor.authorLynn, David J.
dc.contributor.authorManning, Laurens
dc.contributor.authorFariñas Álvarez, María del Carmen 
dc.contributor.authorGutiérrez Cuadra, Manuel
dc.contributor.authorArnaiz de las Revillas Almajano, Francisco
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2025-03-17T19:38:31Z
dc.date.available2025-03-17T19:38:31Z
dc.date.issued2024
dc.identifier.issn2589-5370
dc.identifier.urihttps://hdl.handle.net/10902/36035
dc.description.abstractBackground: Bacille Calmette-Guérin (BCG) vaccination has off-target (non-specific) effects that are associated with protection against unrelated infections and decreased all-cause mortality in infants. We aimed to determine whether BCG vaccination prevents febrile and respiratory infections in adults. Methods: This randomised controlled phase 3 trial was done in 36 healthcare centres in Australia, Brazil, the Netherlands, Spain, and the United Kingdom. Healthcare workers were randomised to receive BCG-Denmark (single 0.1 ml intradermal injection) or no BCG in a 1:1 ratio using a web-based procedure, stratified by stage, site, age, and presence of co-morbidity. The difference in occurrence of febrile or respiratory illness were measured over 12 months (prespecified secondary outcome) using the intention-to-treat (ITT) population. This trial is registered with ClinicalTrials.gov, NCT04327206. Findings: Between March 30, 2020, and April 1, 2021, 6828 healthcare workers were randomised to BCG-Denmark (n = 3417) or control (n = 3411; no intervention or placebo) groups. The 12-month adjusted estimated risk of ?1 episode of febrile or respiratory illness was 66.8% in the BCG group (95% CI 65.3%-68.2%), compared with 63.4% in the control group (95% CI 61.8%-65.0%), a difference of +3.4 percentage points (95% CI +1.3% to +5.5%; p 0.002). The adjusted estimated risk of a severe episode (defined as being incapacitated for ?3 consecutive days or hospitalised) was 19.4% in the BCG group (95% CI 18.0%-20.7%), compared with 18.8% in the control group (95% CI 17.4%-20.2%) a difference of +0.6 percentage points (95% CI -1.3% to +2.5%; p 0.6). Both groups had a similar number of episodes of illness, pneumonia, and hospitalisation. There were three deaths, all in the control group. There were no safety concerns following BCG vaccination. Interpretation: In contrast to the beneficial off-target effects reported following neonatal BCG in infants, a small increased risk of symptomatic febrile or respiratory illness was observed in the 12 months following BCG vaccination in adults. There was no evidence of a difference in the risk of severe disease. Funding: Bill & Melinda Gates Foundation, Minderoo Foundation, Sarah and Lachlan Murdoch, the Royal Children's Hospital Foundation, Health Services Union NSW, the Peter Sowerby Foundation, SA Health, the Insurance Advisernet Foundation, the NAB Foundation, the Calvert-Jones Foundation, the Modara Pines Charitable Foundation, the UHG Foundation Pty Ltd, Epworth Healthcare, the National Health and Medical Research Council, the Swiss National Science Foundation and individual donors.es_ES
dc.description.sponsorshipFunding: Bill & Melinda Gates Foundation, Minderoo Foundation, Sarah and Lachlan Murdoch, the Royal Children’s Hospital Foundation, Health Services Union NSW, the Peter Sowerby Foundation, SA Health, the Insurance Advisernet Foundation, the NAB Foundation, the Calvert-Jones Foundation, the Modara Pines Charitable Foundation, the UHG Foundation Pty Ltd, Epworth Healthcare, the National Health and Medical Research Council, the Swiss National Science Foundation and individual donorses_ES
dc.format.extent10 p.es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.rights© 2024 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/)es_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.sourceeClinicalMedicine, 2024, 72, 102616es_ES
dc.subject.otherBacille Calmette-Guérin (BCG) vaccinees_ES
dc.subject.otherImmunityes_ES
dc.subject.otherHeterologouses_ES
dc.subject.otherHealth personneles_ES
dc.subject.otherRandomised controlled triales_ES
dc.subject.otherPrimary preventiones_ES
dc.subject.otherPlaceboes_ES
dc.titleBacille Calmette-Guérin vaccination to prevent febrile and respiratory illness in adults (BRACE): secondary outcomes of a randomised controlled phase 3 triales_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttp://www.doi.org/10.1016/j.eclinm.2024.102616es_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.1016/j.eclinm.2024.102616
dc.type.versionpublishedVersiones_ES


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© 2024 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/)Excepto si se señala otra cosa, la licencia del ítem se describe como © 2024 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/)