Antunes L, Mazagatos C, Martínez-Baz I, Gomez V, Borg M, Petrović G, Duffy R, Dufrasne FE, Dürrwald R, Lazar M, Jancoriene L, Oroszi B, Husa P, Howard J, Melo A, Pozo F, Pérez-Gimeno G, Castilla J, Machado A, Džiugytė A, Karabuva S, Fitzgerald M, Fierens S, Tolksdorf K, Popovici S, Mickienė A, Túri G, Součková L, Nicolay N, Rose AM, European Hospital Vaccine Effectiveness Group
Euro Surveill 29 (3) - [2024-01-00; online 2024-01-19]
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.
PubMed 38240061
DOI 10.2807/1560-7917.ES.2024.29.3.2300708
Crossref 10.2807/1560-7917.ES.2024.29.3.2300708