Your browser doesn't support javascript.
loading
Half dose ChAdOx1 nCoV-19 vaccine was equivalent to full doses to reduce moderate and severe COVID-19 cases.
Galvão-Lima, Leonardo J; de Medeiros Júnior, Nésio Fernandes; Jesus, Galileu S; Morais, Antônio H F; Caldeira-Silva, Gleyson J P; Queiroz Dos Santos, João Paulo; Rocha, Marcella; Marques Dos Santos, Marquiony; Freire, Pierre A; Silva, Rodrigo D; Gouvea, Maria da Penha Gomes; Neto, Lauro Ferreira Pinto; Domingues, Carla Magda Allan Santos; Teixeira-Carvalho, Andréa; Martins-Filho, Olindo Assis; Valim, Valéria; Valentim, Ricardo A M.
Afiliação
  • Galvão-Lima LJ; Laboratory of Technological Innovation in Health (LAIS), Hospital Universitário Onofre Lopes, Federal University of Rio Grande do Norte (UFRN), Natal, RN, Brazil.
  • de Medeiros Júnior NF; Programa de Pós Graduação em Saúde Coletiva (PPGSC), Universidade Federal do Espírito Santo, Vitória, Brazil.
  • Jesus GS; Laboratory of Technological Innovation in Health (LAIS), Hospital Universitário Onofre Lopes, Federal University of Rio Grande do Norte (UFRN), Natal, RN, Brazil.
  • Morais AHF; Laboratory of Technological Innovation in Health (LAIS), Hospital Universitário Onofre Lopes, Federal University of Rio Grande do Norte (UFRN), Natal, RN, Brazil.
  • Caldeira-Silva GJP; Advanced Nucleus of Technological Innovation (NAVI), Federal Institute of Rio Grande do Norte (IFRN), Natal, RN, Brazil.
  • Queiroz Dos Santos JP; Laboratory of Technological Innovation in Health (LAIS), Hospital Universitário Onofre Lopes, Federal University of Rio Grande do Norte (UFRN), Natal, RN, Brazil.
  • Rocha M; Laboratory of Technological Innovation in Health (LAIS), Hospital Universitário Onofre Lopes, Federal University of Rio Grande do Norte (UFRN), Natal, RN, Brazil.
  • Marques Dos Santos M; Advanced Nucleus of Technological Innovation (NAVI), Federal Institute of Rio Grande do Norte (IFRN), Natal, RN, Brazil.
  • Freire PA; Laboratory of Technological Innovation in Health (LAIS), Hospital Universitário Onofre Lopes, Federal University of Rio Grande do Norte (UFRN), Natal, RN, Brazil.
  • Silva RD; Laboratory of Technological Innovation in Health (LAIS), Hospital Universitário Onofre Lopes, Federal University of Rio Grande do Norte (UFRN), Natal, RN, Brazil.
  • Gouvea MDPG; Laboratory of Technological Innovation in Health (LAIS), Hospital Universitário Onofre Lopes, Federal University of Rio Grande do Norte (UFRN), Natal, RN, Brazil.
  • Neto LFP; Laboratory of Technological Innovation in Health (LAIS), Hospital Universitário Onofre Lopes, Federal University of Rio Grande do Norte (UFRN), Natal, RN, Brazil.
  • Domingues CMAS; Programa de Pós Graduação em Saúde Coletiva (PPGSC), Universidade Federal do Espírito Santo, Vitória, Brazil.
  • Teixeira-Carvalho A; Hospital Universitário Cassiano Antônio Moraes (HUCAM/UFES), Empresa Brasileira de Serviços Hospitalares (EBSERH), Vitória/ES, Brazil.
  • Martins-Filho OA; Escola Superior de Ciências da Santa Casa de Misericórdia de Vitória (EMESCAM), Vitória, Brazil.
  • Valim V; Pan-American Health Organization Consultant, Brasília/DF, Brazil.
  • Valentim RAM; Grupo Integrado de Pesquisas em Biomarcadores, Instituto René Rachou, Fundação Oswaldo Cruz (FIOCRUZ-Minas), Belo Horizonte, Brazil.
IJID Reg ; 9: 88-94, 2023 Dec.
Article em En | MEDLINE | ID: mdl-37953882
Objectives: Previously, we presented the effectiveness of ChAdOx1 nCoV-19 half-dose (HD) immunization for preventing new COVID-19 cases. Here, we evaluated the administration of an HD of ChAdOx1 nCoV-19 in the primary immunization protocol (up to two doses) in reducing moderate and severe cases, hospitalizations, and deaths when compared to the administration of full doses (FD) after a long-term follow-up. Methods: We evaluated data from 29,469 participants between January 2021 and November 2022 who received an HD or FD vaccine and crossed this information with their medical records to identify those who developed moderate or severe cases. All participants were classified into four groups according to their immunization status and followed 500 days after the last vaccine administration. Results: The propensity-score matching analysis indicates that the administration of the two HDs of ChAdOx1 nCoV-19 was equivalent to the use of two FDs to reduce moderate and severe COVID-19 cases. The relative risk of being infected and developing moderate or severe conditions after the administration of at least one HD or FD was similar 150 or 500 days after the administration of the immunizers. Conclusion: Administering two HDs can be used safely as a cost-effective alternative to the primary immunization protocol.
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article