COVID-19 Vaccine Effectiveness Among Adolescents

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

COVID-19 Vaccine Effectiveness Among Adolescents. / Poukka, Eero; Andersson, Niklas Worm; Thiesson, Emilia Myrup; Baum, Ulrike; Pihlström, Nicklas; Perälä, Jori; Kristoffersen, Anja Bråthen; Meijerink, Hinta; Starrfelt, Jostein; Ljung, Rickard; Hviid, Anders.

In: Pediatrics, Vol. 153, No. 2, e2023062520, 2024.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Poukka, E, Andersson, NW, Thiesson, EM, Baum, U, Pihlström, N, Perälä, J, Kristoffersen, AB, Meijerink, H, Starrfelt, J, Ljung, R & Hviid, A 2024, 'COVID-19 Vaccine Effectiveness Among Adolescents', Pediatrics, vol. 153, no. 2, e2023062520. https://doi.org/10.1542/peds.2023-062520

APA

Poukka, E., Andersson, N. W., Thiesson, E. M., Baum, U., Pihlström, N., Perälä, J., Kristoffersen, A. B., Meijerink, H., Starrfelt, J., Ljung, R., & Hviid, A. (2024). COVID-19 Vaccine Effectiveness Among Adolescents. Pediatrics, 153(2), [e2023062520]. https://doi.org/10.1542/peds.2023-062520

Vancouver

Poukka E, Andersson NW, Thiesson EM, Baum U, Pihlström N, Perälä J et al. COVID-19 Vaccine Effectiveness Among Adolescents. Pediatrics. 2024;153(2). e2023062520. https://doi.org/10.1542/peds.2023-062520

Author

Poukka, Eero ; Andersson, Niklas Worm ; Thiesson, Emilia Myrup ; Baum, Ulrike ; Pihlström, Nicklas ; Perälä, Jori ; Kristoffersen, Anja Bråthen ; Meijerink, Hinta ; Starrfelt, Jostein ; Ljung, Rickard ; Hviid, Anders. / COVID-19 Vaccine Effectiveness Among Adolescents. In: Pediatrics. 2024 ; Vol. 153, No. 2.

Bibtex

@article{9e42c818ba5e42d08a6ad7ab6af05a4d,
title = "COVID-19 Vaccine Effectiveness Among Adolescents",
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.",
author = "Eero Poukka and Andersson, {Niklas Worm} and Thiesson, {Emilia Myrup} and Ulrike Baum and Nicklas Pihlstr{\"o}m and Jori Per{\"a}l{\"a} and Kristoffersen, {Anja Br{\aa}then} and Hinta Meijerink and Jostein Starrfelt and Rickard Ljung and Anders Hviid",
year = "2024",
doi = "10.1542/peds.2023-062520",
language = "English",
volume = "153",
journal = "Pediatrics",
issn = "0031-4005",
publisher = "American Academy of Pediatrics",
number = "2",

}

RIS

TY - JOUR

T1 - COVID-19 Vaccine Effectiveness Among Adolescents

AU - Poukka, Eero

AU - Andersson, Niklas Worm

AU - Thiesson, Emilia Myrup

AU - Baum, Ulrike

AU - Pihlström, Nicklas

AU - Perälä, Jori

AU - Kristoffersen, Anja Bråthen

AU - Meijerink, Hinta

AU - Starrfelt, Jostein

AU - Ljung, Rickard

AU - Hviid, Anders

PY - 2024

Y1 - 2024

N2 - 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.

AB - 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.

U2 - 10.1542/peds.2023-062520

DO - 10.1542/peds.2023-062520

M3 - Journal article

C2 - 38196395

AN - SCOPUS:85184137349

VL - 153

JO - Pediatrics

JF - Pediatrics

SN - 0031-4005

IS - 2

M1 - e2023062520

ER -

ID: 382847897