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Advisor(s)
Abstract(s)
In autumn 2023, European vaccination campaigns predominantly administered XBB.1.5 vaccine. In a European multicentre study, we estimated 2023 COVID-19 vaccine effectiveness (VE) against laboratory-confirmed symptomatic infection at primary care level between September 2023 and January 2024. Using a testnegative case–control design, we estimated VE in the target group for COVID-19 vaccination overall and by time since vaccination. We included 1057 cases and 4397 controls. Vaccine effectiveness was 40 % (95 % CI: 26–53 %) overall, 48 % (95 % CI: 31–61 %) among those vaccinated < 6 weeks of onset and 29 % (95 % CI: 3–49 %) at 6–14 weeks. Our results suggest that COVID-19 vaccines administered to target groups during the autumn 2023 campaigns showed clinically significant effectiveness against laboratory-confirmed, medically attended symptomatic SARS-CoV-2 infection in the 3 months following vaccination. A longer study period will allow for further variant-specific COVID-19 VE estimates, better understanding decline in VE and informing booster administration policies.
Description
Erratum in: Vaccine. 2024 Oct 3;42(23):126089. https://doi.org/10.1016/j.vaccine.2024.06.056. Epub 2024 Jul 8.
Keywords
COVID-19 SARS-CoV-2 Vaccine Effectiveness Multicentre Study Test-Negative Design Europe Infecções Respiratórias Investigação em Serviços de Saúde Estados de Saúde e de Doença
Pedagogical Context
Citation
Vaccine. 2024 Jul 25;42(19):3931-3937. doi: 10.1016/j.vaccine.2024.05.067. Epub 2024 Jun 4
Publisher
Elsevier
