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Euro Surveill ; 29(3)2024 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-38240061

RESUMEN

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.


Asunto(s)
Vacunas contra la COVID-19 , COVID-19 , Humanos , Estudios de Casos y Controles , COVID-19/prevención & control , SARS-CoV-2/genética , Hospitalización , Europa (Continente)/epidemiología , ARN Mensajero
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