Effectiveness of an inactivated SARS-CoV-2 vaccine in children and adolescents: a large-scale observational study.

COVID-19 Inactivated SARS-CoV-2 vaccine Paediatric cohort SARS-CoV-2 Vaccine effectiveness mRNA vaccine

Journal

Lancet regional health. Americas
ISSN: 2667-193X
Titre abrégé: Lancet Reg Health Am
Pays: England
ID NLM: 9918232503006676

Informations de publication

Date de publication:
May 2023
Historique:
received: 10 03 2022
revised: 14 10 2022
accepted: 22 03 2023
medline: 8 5 2023
pubmed: 8 5 2023
entrez: 8 5 2023
Statut: ppublish

Résumé

Policymakers urgently need evidence to adequately balance the costs and benefits of mass vaccination against COVID-19 across all age groups, including children and adolescents. In this study, we aim to assess the effectiveness of CoronaVac's primary series among children and adolescents in Chile. We used a large prospective national cohort of about two million children and adolescents 6-16 years to estimate the effectiveness of an inactivated SARS-CoV-2 vaccine (CoronaVac) in preventing laboratory-confirmed symptomatic SARS-CoV-2 infection (COVID-19), hospitalisation, and admission to an intensive care unit (ICU) associated with COVID-19. We compared the risk of individuals treated with a complete primary immunization schedule (two doses, 28 days apart) with the risk of unvaccinated individuals during the follow-up period. The study was conducted in Chile from June 27, 2021, to January 12, 2022, when the SARS-CoV-2 Delta variant was predominant but other variants of concern were co-circulating, including Omicron. We used inverse probability-weighted survival regression models to estimate hazard ratios of complete immunization over the unvaccinated status, accounting for time-varying vaccination exposure and adjusting for relevant demographic, socioeconomic, and clinical confounders. The estimated adjusted vaccine effectiveness for the inactivated SARS-CoV-2 vaccine in children aged 6-16 years was 74.5% (95% CI, 73.8-75.2), 91.0% (95% CI, 87.8-93.4), 93.8% (95% CI, 87.8-93.4) for the prevention of COVID-19, hospitalisation, and ICU admission, respectively. For the subgroup of children 6-11 years, the vaccine effectiveness was 75.8% (95% CI, 74.7-76.8) for the prevention of COVID-19 and 77.9% (95% CI, 61.5-87.3) for the prevention of hospitalisation. Our results suggest that a complete primary immunization schedule with the inactivated SARS-CoV-2 vaccine provides effective protection against severe COVID-19 disease for children 6-16 years. Agencia Nacional de Investigación y Desarrollo (ANID) Millennium Science Initiative Program and Fondo de Financiamiento de Centros de Investigación en Áreas Prioritarias (FONDAP).

Sections du résumé

Background UNASSIGNED
Policymakers urgently need evidence to adequately balance the costs and benefits of mass vaccination against COVID-19 across all age groups, including children and adolescents. In this study, we aim to assess the effectiveness of CoronaVac's primary series among children and adolescents in Chile.
Methods UNASSIGNED
We used a large prospective national cohort of about two million children and adolescents 6-16 years to estimate the effectiveness of an inactivated SARS-CoV-2 vaccine (CoronaVac) in preventing laboratory-confirmed symptomatic SARS-CoV-2 infection (COVID-19), hospitalisation, and admission to an intensive care unit (ICU) associated with COVID-19. We compared the risk of individuals treated with a complete primary immunization schedule (two doses, 28 days apart) with the risk of unvaccinated individuals during the follow-up period. The study was conducted in Chile from June 27, 2021, to January 12, 2022, when the SARS-CoV-2 Delta variant was predominant but other variants of concern were co-circulating, including Omicron. We used inverse probability-weighted survival regression models to estimate hazard ratios of complete immunization over the unvaccinated status, accounting for time-varying vaccination exposure and adjusting for relevant demographic, socioeconomic, and clinical confounders.
Findings UNASSIGNED
The estimated adjusted vaccine effectiveness for the inactivated SARS-CoV-2 vaccine in children aged 6-16 years was 74.5% (95% CI, 73.8-75.2), 91.0% (95% CI, 87.8-93.4), 93.8% (95% CI, 87.8-93.4) for the prevention of COVID-19, hospitalisation, and ICU admission, respectively. For the subgroup of children 6-11 years, the vaccine effectiveness was 75.8% (95% CI, 74.7-76.8) for the prevention of COVID-19 and 77.9% (95% CI, 61.5-87.3) for the prevention of hospitalisation.
Interpretation UNASSIGNED
Our results suggest that a complete primary immunization schedule with the inactivated SARS-CoV-2 vaccine provides effective protection against severe COVID-19 disease for children 6-16 years.
Funding UNASSIGNED
Agencia Nacional de Investigación y Desarrollo (ANID) Millennium Science Initiative Program and Fondo de Financiamiento de Centros de Investigación en Áreas Prioritarias (FONDAP).

Identifiants

pubmed: 37155483
doi: 10.1016/j.lana.2023.100487
pii: S2667-193X(23)00061-3
pmc: PMC10117174
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100487

Informations de copyright

© 2023 Published by Elsevier Ltd.

Déclaration de conflit d'intérêts

R. Araos has received consulting fees from AstraZeneca, Pfizer and research support from Sinovac. This support is not related to this article and was received after its acceptance. J.C. Flores is a non-paid member of the Servicio de Salud Metropolitano Sur Oriente's Ethics Committee, Santiago, Chile. The remaining authors have no conflicts of interest to declare.

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Auteurs

Alejandro Jara (A)

Ministry of Health, Santiago, Chile.
Facultad de Matemáticas, Pontificia Universidad Católica de Chile, Santiago, Chile.
Center for the Discovery of Structures in Complex Data (MiDaS), Santiago, Chile.

Eduardo A Undurraga (EA)

Escuela de Gobierno, Pontificia Universidad Católica de Chile, Santiago, RM, Chile.
Initiative for Collaborative Research in Bacterial Resistance (MICROB-R), Santiago, Chile.
Research Center for Integrated Disaster Risk Management (CIGIDEN), Santiago, Chile.
CIFAR Azrieli Global Scholars Program, CIFAR, Toronto, Canada.

Juan Carlos Flores (JC)

Facultad de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.

José R Zubizarreta (JR)

Department of Health Care Policy, Harvard Medical School, Boston, MA, USA.
Department of Biostatistics, Harvard T.H. School of Public Health, Boston, MA, USA.
Department of Statistics, Harvard T.H. School of Public Health, Boston, MA, USA.

Cecilia González (C)

Ministry of Health, Santiago, Chile.

Alejandra Pizarro (A)

Ministry of Health, Santiago, Chile.
Facultad de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.

Duniel Ortuño-Borroto (D)

Ministry of Health, Santiago, Chile.

Johanna Acevedo (J)

Ministry of Health, Santiago, Chile.

Katherinne Leo (K)

Ministry of Health, Santiago, Chile.

Fabio Paredes (F)

Ministry of Health, Santiago, Chile.

Tomás Bralic (T)

Ministry of Health, Santiago, Chile.

Verónica Vergara (V)

Ministry of Health, Santiago, Chile.

Francisco Leon (F)

Ministry of Health, Santiago, Chile.

Ignacio Parot (I)

Ministry of Health, Santiago, Chile.

Paulina Leighton (P)

Ministry of Health, Santiago, Chile.

Pamela Suárez (P)

Ministry of Health, Santiago, Chile.

Juan Carlos Rios (JC)

Ministry of Health, Santiago, Chile.
Facultad de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.

Heriberto García-Escorza (H)

Ministry of Health, Santiago, Chile.

Rafael Araos (R)

Ministry of Health, Santiago, Chile.
Initiative for Collaborative Research in Bacterial Resistance (MICROB-R), Santiago, Chile.
Instituto de Ciencias e Innovación en Medicina, Facultad de Medicina, Universidad del Desarrollo, Santiago, Chile.
Advanced Center for Chronic Diseases (ACCDiS), Santiago, Chile.

Classifications MeSH