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Safety outcomes following COVID-19 vaccination and infection in 5.1 million children in England.
Copland, Emma; Patone, Martina; Saatci, Defne; Handunnetthi, Lahiru; Hirst, Jennifer; Hunt, David P J; Mills, Nicholas L; Moss, Paul; Sheikh, Aziz; Coupland, Carol A C; Harnden, Anthony; Robertson, Chris; Hippisley-Cox, Julia.
Afiliación
  • Copland E; Nuffield Department of Primary Health Care Sciences, University of Oxford, Oxford, UK.
  • Patone M; Nuffield Department of Primary Health Care Sciences, University of Oxford, Oxford, UK.
  • Saatci D; Nuffield Department of Primary Health Care Sciences, University of Oxford, Oxford, UK.
  • Handunnetthi L; Centre for Human Genetics, University of Oxford, Oxford, UK.
  • Hirst J; Department of Psychiatry, University of Oxford, Oxford, UK.
  • Hunt DPJ; Nuffield Department of Primary Health Care Sciences, University of Oxford, Oxford, UK.
  • Mills NL; UK Dementia Research Institute, Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, UK.
  • Moss P; BHF/University Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, UK.
  • Sheikh A; Usher Institute, University of Edinburgh, Edinburgh, UK.
  • Coupland CAC; Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham, UK.
  • Harnden A; Nuffield Department of Primary Health Care Sciences, University of Oxford, Oxford, UK.
  • Robertson C; Usher Institute, University of Edinburgh, Edinburgh, UK.
  • Hippisley-Cox J; Nuffield Department of Primary Health Care Sciences, University of Oxford, Oxford, UK.
Nat Commun ; 15(1): 3822, 2024 May 27.
Article en En | MEDLINE | ID: mdl-38802362
ABSTRACT
The risk-benefit profile of COVID-19 vaccination in children remains uncertain. A self-controlled case-series study was conducted using linked data of 5.1 million children in England to compare risks of hospitalisation from vaccine safety outcomes after COVID-19 vaccination and infection. In 5-11-year-olds, we found no increased risks of adverse events 1-42 days following vaccination with BNT162b2, mRNA-1273 or ChAdOX1. In 12-17-year-olds, we estimated 3 (95%CI 0-5) and 5 (95%CI 3-6) additional cases of myocarditis per million following a first and second dose with BNT162b2, respectively. An additional 12 (95%CI 0-23) hospitalisations with epilepsy and 4 (95%CI 0-6) with demyelinating disease (in females only, mainly optic neuritis) were estimated per million following a second dose with BNT162b2. SARS-CoV-2 infection was associated with increased risks of hospitalisation from seven outcomes including multisystem inflammatory syndrome and myocarditis, but these risks were largely absent in those vaccinated prior to infection. We report a favourable safety profile of COVID-19 vaccination in under-18s.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Vacunación / Vacunas contra la COVID-19 / SARS-CoV-2 / COVID-19 / Vacuna BNT162 / ChAdOx1 nCoV-19 / Hospitalización Límite: Adolescent / Child / Child, preschool / Female / Humans / Male País/Región como asunto: Europa Idioma: En Revista: Nat Commun Asunto de la revista: BIOLOGIA / CIENCIA Año: 2024 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Vacunación / Vacunas contra la COVID-19 / SARS-CoV-2 / COVID-19 / Vacuna BNT162 / ChAdOx1 nCoV-19 / Hospitalización Límite: Adolescent / Child / Child, preschool / Female / Humans / Male País/Región como asunto: Europa Idioma: En Revista: Nat Commun Asunto de la revista: BIOLOGIA / CIENCIA Año: 2024 Tipo del documento: Article País de afiliación: Reino Unido