COVID-19 vaccine effectiveness against omicron infection and hospitalization

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dc.contributor.author
Piché-Renaud, Pierre-Philippe
Swayze, Sarah
Buchan, Sarah A.
Wilson, Sarah E.
Austin, Peter C.
Morris, Shaun K.
Nasreen, Sharifa
Schwartz, Kevin L.
Tadrous, Mina
Thampi, Nisha
Wilson, Kumanan
Kwong, Jeffrey C.
Canadian Immunization Research Network (CIRN) Provincial Collaborative Investigators
dc.date.accessioned
2024-07-05T18:26:38Z
dc.date.available
2024-07-05T18:26:38Z
dc.date.issued
2023-03-03
dc.description.abstract - en
OBJECTIVES: This study aimed to provide real-world evidence on coronavirus disease 2019 vaccine effectiveness (VE) against symptomatic infection and severe outcomes caused by Omicron in children aged 5 to 11 years. METHODS: We used the test-negative study design and linked provincial databases to estimate BNT162b2 vaccine effectiveness against symptomatic infection and severe outcomes caused by Omicron in children aged 5 to 11 years between January 2 and August 27, 2022 in Ontario. We used multivariable logistic regression to estimate VE by time since the latest dose, compared with unvaccinated children, and we evaluated VE by dosing interval. RESULTS: We included 6284 test-positive cases and 8389 test-negative controls. VE against symptomatic infection declined from 24% (95% confidence interval [CI], 8% to 36%) 14 to 29 days after a first dose and 66% (95% CI, 60% to 71%) 7 to 29 days after 2 doses. VE was higher for children with dosing intervals of ≥56 days (57% [95% CI, 51% to 62%]) than 15 to 27 days (12% [95% CI, −11% to 30%]) and 28 to 41 days (38% [95% CI, 28% to 47%]), but appeared to wane over time for all dosing interval groups. VE against severe outcomes was 94% (95% CI, 57% to 99%) 7 to 29 days after 2 doses and declined to 57% (95%CI, −20% to 85%) after ≥120 days. CONCLUSIONS: In children aged 5 to 11 years, 2 doses of BNT162b2 provide moderate protection against symptomatic Omicron infection within 4 months of vaccination and good protection against severe outcomes. Protection wanes more rapidly for infection than severe outcomes. Overall, longer dosing intervals confer higher protection against symptomatic infection, however protection decreases and becomes similar to shorter dosing interval starting 90 days after vaccination.
dc.identifier.doi
https://doi.org/10.1542/peds.2022-059513
dc.identifier.issn
1098-4275
dc.identifier.pubmedID
36866446
dc.identifier.uri
https://open-science.canada.ca/handle/123456789/2659
dc.language.iso
en
dc.publisher
American Academy of Pediatrics
dc.rights - en
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0)
dc.rights - fr
Creative Commons Attribution - Pas d'utilisation commerciale - Pas de modification 4.0 International (CC BY-NC-ND 4.0)
dc.rights.openaccesslevel - en
Gold
dc.rights.openaccesslevel - fr
Or
dc.rights.uri - en
https://creativecommons.org/licenses/by-nc-nd/4.0/
dc.rights.uri - fr
https://creativecommons.org/licenses/by-nc-nd/4.0/deed.fr
dc.subject - en
Health
dc.subject - fr
Santé
dc.subject.en - en
Health
dc.subject.fr - fr
Santé
dc.title - en
COVID-19 vaccine effectiveness against omicron infection and hospitalization
dc.type - en
Article
dc.type - fr
Article
local.acceptedmanuscript.articlenum
e2022059513
local.article.journalissue
4
local.article.journaltitle
Pediatrics
local.article.journalvolume
151
local.pagination
1-12
local.peerreview - en
Yes
local.peerreview - fr
Oui
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