2024-06-04Zeitschriftenartikel
Effectiveness of COVID-19 vaccines administered in the 2023 autumnal campaigns in Europe: Results from the VEBIS primary care test-negative design study, September 2023–January 2024
Laniece Delaunay, Charlotte
Melo, Aryse
Maurel, Marine
Mazagatos, Clara
Goerlitz, Luise
O'Donnell, Joan
Oroszi, Beatrix
Sève, Noémie
Rodrigues, Ana Paula
Martínez-Baz, Iván
Meijer, Adam
Mlinarić, Ivan
Latorre-Margalef, Neus
Lazăr, Mihaela
Pérez-Gimeno, Gloria
Dürrwald, Ralf
Bennett, Charlene
Túri, Gergő
Rameix-Welti, Marie-Anne
Guiomar, Raquel
Castilla, Jesús
Hooiveld, Mariëtte
Kurečić Filipović, Sanja
Samuelsson Hagey, Tove
Dijkstra, Frederika
Borges, Vitor
Ramos Marín, Violeta
Bacci, Sabrina
Kaczmarek, Marlena
Kissling, Esther
on behalf of the European primary care VE group
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 test-negative 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.
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