Effectiveness of the adapted bivalent mRNA COVID-19 vaccines against hospitalisation in individuals aged ≥ 60 years during the Omicron XBB lineage-predominant period: VEBIS SARI VE network, Europe, February to August, 2023

We conducted a multicentre hospital-based test-negative case-control study to measure the effectiveness of adapted bivalent COVID-19 mRNA vaccines against PCR-confirmed SARS-CoV-2 infection during the Omicron XBB lineage-predominant period in patients aged ≥ 60 years with severe acute respiratory in...

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Veröffentlicht in:Euro surveillance : bulletin européen sur les maladies transmissibles 2024-01, Vol.29 (3)
Hauptverfasser: Antunes, Liliana, Mazagatos, Clara, Martínez-Baz, Iván, Gomez, Verónica, Borg, Maria-Louise, Petrović, Goranka, Duffy, Róisín, Dufrasne, François E, Dürrwald, Ralf, Lazar, Mihaela, Jancoriene, Ligita, Oroszi, Beatrix, Husa, Petr, Howard, Jennifer, Melo, Aryse, Pozo, Francisco, Pérez-Gimeno, Gloria, Castilla, Jesús, Machado, Ausenda, Džiugytė, Aušra, Karabuva, Svjetlana, Fitzgerald, Margaret, Fierens, Sébastien, Tolksdorf, Kristin, Popovici, Silvia-Odette, Mickienė, Auksė, Túri, Gergő, Součková, Lenka, Nicolay, Nathalie, Rose, Angela Mc
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Sprache:eng
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Zusammenfassung:We conducted a multicentre hospital-based test-negative case-control study to measure the effectiveness of adapted bivalent COVID-19 mRNA vaccines against PCR-confirmed SARS-CoV-2 infection during the Omicron XBB lineage-predominant period in patients aged ≥ 60 years with severe acute respiratory infection from five countries in Europe. Bivalent vaccines provided short-term additional protection compared with those vaccinated > 6 months before the campaign: from 80% (95% CI: 50 to 94) for 14-89 days post-vaccination, 15% (95% CI: -12 to 35) at 90-179 days, and lower to no effect thereafter.
ISSN:1560-7917
1025-496X
1560-7917
DOI:10.2807/1560-7917.ES.2024.29.3.2300708