TY - JOUR
T1 - Vaccine effectiveness against COVID-19 hospitalisation in adults (≥ 20 years) during Omicron-dominant circulation
T2 - I-MOVE-COVID-19 and VEBIS SARI VE networks, Europe, 2021 to 2022
AU - Rose, Angela Mc
AU - Nicolay, Nathalie
AU - Sandonis Martín, Virginia
AU - Mazagatos, Clara
AU - Petrović, Goranka
AU - Baruch, Joaquin
AU - Denayer, Sarah
AU - Seyler, Lucie
AU - Domegan, Lisa
AU - Launay, Odile
AU - Machado, Ausenda
AU - Burgui, Cristina
AU - Vaikutyte, Roberta
AU - Niessen, F Annabel
AU - Loghin, Isabela I
AU - Husa, Petr
AU - Aouali, Nassera
AU - Panagiotakopoulos, George
AU - Tolksdorf, Kristin
AU - Horváth, Judit Krisztina
AU - Howard, Jennifer
AU - Pozo, Francisco
AU - Gallardo, Virtudes
AU - Nonković, Diana
AU - Džiugytė, Aušra
AU - Bossuyt, Nathalie
AU - Demuyser, Thomas
AU - Duffy, Róisín
AU - Luong Nguyen, Liem Binh
AU - Kislaya, Irina
AU - Martínez-Baz, Iván
AU - Gefenaite, Giedre
AU - Knol, Mirjam J
AU - Popescu, Corneliu
AU - Součková, Lenka
AU - Simon, Marc
AU - Michelaki, Stella
AU - Reiche, Janine
AU - Ferenczi, Annamária
AU - Delgado-Sanz, Concepción
AU - Lovrić Makarić, Zvjezdana
AU - Cauchi, John Paul
AU - Barbezange, Cyril
AU - Van Nedervelde, Els
AU - O'Donnell, Joan
AU - Durier, Christine
AU - Guiomar, Raquel
AU - Castilla, Jesús
AU - Jonikaite, Indrė
AU - Bruijning-Verhagen, Patricia Cjl
AU - Lazar, Mihaela
AU - Demlová, Regina
AU - Wirtz, Gil
AU - Amerali, Marina
AU - Dürrwald, Ralf
AU - Pál Kunstár, Mihály
AU - Kissling, Esther
AU - Bacci, Sabrina
AU - Valenciano, M
N1 - Publisher Copyright:
© 2023 European Centre for Disease Prevention and Control (ECDC). All rights reserved.
PY - 2023/11/23
Y1 - 2023/11/23
N2 - IntroductionThe I-MOVE-COVID-19 and VEBIS hospital networks have been measuring COVID-19 vaccine effectiveness (VE) in participating European countries since early 2021.AimWe aimed to measure VE against PCR-confirmed SARS-CoV-2 in patients ≥ 20 years hospitalised with severe acute respiratory infection (SARI) from December 2021 to July 2022 (Omicron-dominant period).MethodsIn both networks, 46 hospitals (13 countries) follow a similar test-negative case-control protocol. We defined complete primary series vaccination (PSV) and first booster dose vaccination as last dose of either vaccine received ≥ 14 days before symptom onset (stratifying first booster into received < 150 and ≥ 150 days after last PSV dose). We measured VE overall, by vaccine category/product, age group and time since first mRNA booster dose, adjusting by site as a fixed effect, and by swab date, age, sex, and presence/absence of at least one commonly collected chronic condition.ResultsWe included 2,779 cases and 2,362 controls. The VE of all vaccine products combined against hospitalisation for laboratory-confirmed SARS-CoV-2 was 43% (95% CI: 29-54) for complete PSV (with last dose received ≥ 150 days before onset), while it was 59% (95% CI: 51-66) after addition of one booster dose. The VE was 85% (95% CI: 78-89), 70% (95% CI: 61-77) and 36% (95% CI: 17-51) for those with onset 14-59 days, 60-119 days and 120-179 days after booster vaccination, respectively.ConclusionsOur results suggest that, during the Omicron period, observed VE against SARI hospitalisation improved with first mRNA booster dose, particularly for those having symptom onset < 120 days after first booster dose.
AB - IntroductionThe I-MOVE-COVID-19 and VEBIS hospital networks have been measuring COVID-19 vaccine effectiveness (VE) in participating European countries since early 2021.AimWe aimed to measure VE against PCR-confirmed SARS-CoV-2 in patients ≥ 20 years hospitalised with severe acute respiratory infection (SARI) from December 2021 to July 2022 (Omicron-dominant period).MethodsIn both networks, 46 hospitals (13 countries) follow a similar test-negative case-control protocol. We defined complete primary series vaccination (PSV) and first booster dose vaccination as last dose of either vaccine received ≥ 14 days before symptom onset (stratifying first booster into received < 150 and ≥ 150 days after last PSV dose). We measured VE overall, by vaccine category/product, age group and time since first mRNA booster dose, adjusting by site as a fixed effect, and by swab date, age, sex, and presence/absence of at least one commonly collected chronic condition.ResultsWe included 2,779 cases and 2,362 controls. The VE of all vaccine products combined against hospitalisation for laboratory-confirmed SARS-CoV-2 was 43% (95% CI: 29-54) for complete PSV (with last dose received ≥ 150 days before onset), while it was 59% (95% CI: 51-66) after addition of one booster dose. The VE was 85% (95% CI: 78-89), 70% (95% CI: 61-77) and 36% (95% CI: 17-51) for those with onset 14-59 days, 60-119 days and 120-179 days after booster vaccination, respectively.ConclusionsOur results suggest that, during the Omicron period, observed VE against SARI hospitalisation improved with first mRNA booster dose, particularly for those having symptom onset < 120 days after first booster dose.
KW - Adult
KW - COVID-19 Vaccines
KW - COVID-19/prevention & control
KW - Europe/epidemiology
KW - Hospitalization
KW - Humans
KW - Pneumonia
KW - RNA, Messenger
KW - SARS-CoV-2
KW - Vaccine Efficacy
UR - http://www.scopus.com/inward/record.url?scp=85177865991&partnerID=8YFLogxK
U2 - 10.2807/1560-7917.ES.2023.28.47.2300187
DO - 10.2807/1560-7917.ES.2023.28.47.2300187
M3 - Article
C2 - 37997665
SN - 1560-7917
VL - 28
JO - Eurosurveillance
JF - Eurosurveillance
IS - 47
M1 - 2300187
ER -