TY - JOUR
T1 - Effectiveness of complete primary vaccination against COVID-19 at primary care and community level during predominant Delta circulation in Europe
T2 - multicentre analysis, I-MOVE-COVID-19 and ECDC networks, July to August 2021
AU - Kissling, Esther
AU - Hooiveld, Mariette
AU - Martinez-Baz, Ivan
AU - Mazagatos, Clara
AU - William, Naoma
AU - Vilcu, Ana Maria
AU - Kooijman, Marjolein N.
AU - Ilic, Maja
AU - Domegan, Lisa
AU - Machado, Ausenda
AU - De Lusignan, Simon
AU - Lazar, Mihaela
AU - Meijer, Adam
AU - Brytting, Mia
AU - Casado, Itziar
AU - Larrauri, Amparo
AU - Murray, Josephine L.K.
AU - Behillil, Sylvie
AU - De Gier, Brechje
AU - Mlinaric, Ivan
AU - O'Donnell, Joan
AU - Rodrigues, Ana Paula
AU - Tsang, Ruby
AU - Timnea, Olivia
AU - De Lange, Marit
AU - Riess, Maximilian
AU - Castilla, Jesus
AU - Pozo, Francisco
AU - Hamilton, Mark
AU - Falchi, Alessandra
AU - Knol, Mirjam J.
AU - Filipovic, Sanja Kurecic
AU - Dunford, Linda
AU - Guiomar, Raquel
AU - Cogdale, Jade
AU - Cherciu, Carmen
AU - Jansen, Tessa
AU - Enkirch, Theresa
AU - Basile, Luca
AU - Connell, Jeff
AU - Gomez, Veronica
AU - Martin, Virginia Sandonis
AU - Bacci, Sabrina
AU - Rose, Angela M.C.
AU - Celentano, Lucia Pastore
AU - Valenciano, Marta
AU - Kislaya, Irina
AU - Nunes, Baltazar
N1 - Funding Information:
This project received funding from the European Centre for Disease Prevention and Control (ECDC) under the contract ECD.11486.
Funding Information:
This project has received funding from the European Union’s Horizon 2020 research and innovation programme under grant agreement No 101003673.
Publisher Copyright:
© 2022 European Centre for Disease Prevention and Control (ECDC). All rights reserved.
PY - 2022/5/26
Y1 - 2022/5/26
N2 - Introduction: In July and August 2021, the SARS-CoV-2 Delta variant dominated in Europe. Aim: Using a multicentre test-negative study, we measured COVID-19 vaccine effectiveness (VE) against symptomatic infection. Methods: Individuals with COVID-19 or acute respiratory symptoms at primary care/community level in 10 European countries were tested for SARS-CoV-2. We measured complete primary course overall VE by vaccine brand and by time since vaccination. Results: Overall VE was 74% (95% CI: 69-79), 76% (95% CI: 71-80), 63% (95% CI: 48-75) and 63% (95% CI: 16-83) among those aged 30-44, 45-59, 60-74 and ≥ 75 years, respectively. VE among those aged 30-59 years was 78% (95% CI: 75-81), 66% (95% CI: 58-73), 91% (95% CI: 87-94) and 52% (95% CI: 40-61), for Comirnaty, Vaxzevria, Spikevax and COVID-19 Vaccine Janssen, respectively. VE among people 60 years and older was 67% (95% CI: 52-77), 65% (95% CI: 48-76) and 83% (95% CI: 64-92) for Comirnaty, Vaxzevria and Spikevax, respectively. Comirnaty VE among those aged 30-59 years was 87% (95% CI: 83-89) at 14-29 days and 65% (95% CI: 56-71%) at ≥ 90 days between vaccination and onset of symptoms. Conclusions: VE against symptomatic infection with the SARS-CoV-2 Delta variant varied among brands, ranging from 52% to 91%. While some waning of the vaccine effect may be present (sample size limited this analysis to only Comirnaty), protection was 65% at 90 days or more between vaccination and onset.
AB - Introduction: In July and August 2021, the SARS-CoV-2 Delta variant dominated in Europe. Aim: Using a multicentre test-negative study, we measured COVID-19 vaccine effectiveness (VE) against symptomatic infection. Methods: Individuals with COVID-19 or acute respiratory symptoms at primary care/community level in 10 European countries were tested for SARS-CoV-2. We measured complete primary course overall VE by vaccine brand and by time since vaccination. Results: Overall VE was 74% (95% CI: 69-79), 76% (95% CI: 71-80), 63% (95% CI: 48-75) and 63% (95% CI: 16-83) among those aged 30-44, 45-59, 60-74 and ≥ 75 years, respectively. VE among those aged 30-59 years was 78% (95% CI: 75-81), 66% (95% CI: 58-73), 91% (95% CI: 87-94) and 52% (95% CI: 40-61), for Comirnaty, Vaxzevria, Spikevax and COVID-19 Vaccine Janssen, respectively. VE among people 60 years and older was 67% (95% CI: 52-77), 65% (95% CI: 48-76) and 83% (95% CI: 64-92) for Comirnaty, Vaxzevria and Spikevax, respectively. Comirnaty VE among those aged 30-59 years was 87% (95% CI: 83-89) at 14-29 days and 65% (95% CI: 56-71%) at ≥ 90 days between vaccination and onset of symptoms. Conclusions: VE against symptomatic infection with the SARS-CoV-2 Delta variant varied among brands, ranging from 52% to 91%. While some waning of the vaccine effect may be present (sample size limited this analysis to only Comirnaty), protection was 65% at 90 days or more between vaccination and onset.
UR - http://www.scopus.com/inward/record.url?scp=85130872682&partnerID=8YFLogxK
U2 - 10.2807/1560-7917.ES.2022.27.21.2101104
DO - 10.2807/1560-7917.ES.2022.27.21.2101104
M3 - Article
C2 - 35620997
AN - SCOPUS:85130872682
SN - 1025-496X
VL - 27
JO - Eurosurveillance
JF - Eurosurveillance
IS - 21
M1 - A1
ER -