COVID-19 Vaccine Effectiveness Among Adolescents

Author:

Poukka Eero12,Andersson Niklas Worm3,Thiesson Emilia Myrup3,Baum Ulrike1,Pihlström Nicklas4,Perälä Jori1,Kristoffersen Anja Bråthen5,Meijerink Hinta6,Starrfelt Jostein7,Ljung Rickard89,Hviid Anders310

Affiliation:

1. aInfectious Disease Control and Vaccinations Unit, Department of Health Security, Finnish Institute for Health and Welfare, Helsinki, Finland

2. bDepartment of Public Health, Faculty of Medicine, University of Helsinki, Helsinki, Finland

3. cDepartment of Epidemiology Research, Staten Serum Institut, Copenhagen, Denmark

4. dDivision of Licensing, Swedish Medical Products Agency, Uppsala, Sweden

5. eDepartment of Method Development and Analytics

6. fDepartment of Infection Control and Vaccines

7. gDepartment of Infection Control and Preparedness, Norwegian Institute of Public Health, Oslo, Norway

8. hDivision of Use and Information, Swedish Medical Products Agency, Uppsala, Sweden

9. iInstitute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden

10. jDepartment of Drug Design and Pharmacology, Pharmacovigilance Research Center, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark

Abstract

BACKGROUND For adolescents, data on the long-term effectiveness of the BNT162b2 and mRNA-1273 vaccines against severe COVID-19 outcomes are scarce. Additionally, only a few studies have evaluated vaccine effectiveness (VE) for mRNA-1273 or heterologous mRNA vaccine schedules (ie, mixing BNT162b2 and mRNA-1273). METHODS Nationwide register-based 1-to-1 matched cohort analyses were conducted in Denmark, Finland, Norway, and Sweden between May 28, 2021, and April 30, 2023, to estimate VE for primary COVID-19 vaccine (2-dose) schedules among adolescents aged 12 to 17 years. Cumulative incidences of COVID-19–related hospitalization (primary outcome) and laboratory-confirmed SARS-CoV-2 infection (secondary outcome) were compared for vaccinated and unvaccinated at 6 months of follow-up using the Kaplan-Meier estimator. Country-specific VE (1-risk ratio) and risk differences (RD) were combined by random-effects meta-analyses. RESULTS The study included 526 966 primary schedule vaccinated adolescents. VE against COVID-19–related hospitalization was 72.6% (95% confidence interval [CI], 62.5–82.7) and RD was –2.8 (95% CI, –4.5 to –1.0) per 10 000 vaccinated for BNT162b2 at 6 months of follow-up compared with unvaccinated. The corresponding VE and RD were 86.0% (95% CI, 56.8–100.0) and –2.1 (95% CI, –4.0 to –0.2) per 10 000 vaccinated for mRNA-1273 and 80.7% (95% CI, 58.0–100.0) and –5.5 (95% CI, –15.5 to 4.6) per 10 000 vaccinated for heterologous mRNA vaccine schedules. Estimates were comparable when restricting to a period of omicron predominance and extending follow-up to 12 months. CONCLUSIONS Across 4 Nordic countries, severe COVID-19 in adolescents was a rare event. Compared with unvaccinated, BNT162b2, mRNA-1273, and heterologous mRNA vaccination schedules provided high protection against COVID-19–related hospitalization, including hospitalizations during the omicron period.

Publisher

American Academy of Pediatrics (AAP)

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