TY - JOUR
T1 - Vaccine effectiveness against COVID-19 hospitalisation in adults (≥ 20 years) during Omicron-dominant circulation
T2 - I-MOVECOVID-19 and VEBIS SARI VE networks, Europe, 2021 to 2022
AU - Rose, Angela M.C.
AU - Nicolay, Nathalie
AU - Martín, Virginia Sandonis
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 - Nguyen, Liem Binh Luong
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 - Makarić, Zvjezdana Lovrić
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 - Alexandre, Myriam
AU - I-MOVE-COVID-19 hospital study team
AU - VEBIS hospital study team
N1 - Publisher Copyright:
© 2023 European Centre for Disease Prevention and Control (ECDC). All rights reserved.
PY - 2023/11/23
Y1 - 2023/11/23
N2 - Introduction: The I-MOVE-COVID-19 and VEBIS hospital networks have been measuring COVID-19 vaccine effectiveness (VE) in participating European countries since early 2021. Aim: We 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). Methods: In 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. Results: We 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. Conclusions: Our 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 - Introduction: The I-MOVE-COVID-19 and VEBIS hospital networks have been measuring COVID-19 vaccine effectiveness (VE) in participating European countries since early 2021. Aim: We 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). Methods: In 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. Results: We 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. Conclusions: Our 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.
UR - https://www.scopus.com/pages/publications/85177865991
U2 - 10.2807/1560-7917.ES.2023.28.47.2300187
DO - 10.2807/1560-7917.ES.2023.28.47.2300187
M3 - Article
C2 - 37997665
AN - SCOPUS:85177865991
SN - 1025-496X
VL - 28
JO - Eurosurveillance
JF - Eurosurveillance
IS - 47
M1 - 2300187
ER -