Peer-reviewed article
Incidence and clinical phenotype of multisystem inflammatory syndrome in children after infection with the SARS-CoV-2 delta variant by vaccination status: a Danish nationwide prospective cohort study
Ulrikka Nygaard, Mette Holm, Ulla Birgitte Hartling, Jonathan Peter Glenthøj, Lisbeth Samsø Schmidt et al. ·
Summary
Written by AI, not yet AICS's view · claude-haiku-4-5-20251001This study tracked cases of multisystem inflammatory syndrome in children (MIS-C), a serious complication that can follow SARS-CoV-2 infection, in Denmark during the delta variant wave from August 2021 to February 2022. Researchers found that unvaccinated children had a much higher rate of MIS-C than vaccinated children, with vaccination providing 94% protection against the condition. The clinical features of MIS-C during the delta wave were similar to those seen earlier in the pandemic.
Key points
- 51 MIS-C cases occurred in unvaccinated individuals compared to 1 case in fully vaccinated adolescents during the study period
- Incidence of MIS-C was 1 per 3,400 unvaccinated infected individuals versus 1 per 9,900 vaccinated individuals with breakthrough infection
- Vaccine effectiveness against MIS-C was 94% (95% CI 55-99%) in children aged 5-17 years
- Clinical presentation of MIS-C during delta variant was comparable to the pre-delta era
- Study used nationwide prospective data collection from all 18 paediatric departments in Denmark
Limitations
The study was conducted in Denmark only and may not be generalizable to populations with different infection rates, vaccination coverage, or healthcare systems. The small number of MIS-C cases in vaccinated individuals (n=1) limits statistical precision for that group.
Abstract
BACKGROUND: Multisystem inflammatory syndrome in children (MIS-C) occurs after infection with SARS-CoV-2 and its incidence is likely to depend on multiple factors, including the variant of the preceding SARS-CoV-2 infection and vaccine effectiveness. We aimed to estimate the incidence of MIS-C, and describe the clinical phenotype, following the delta variant of SARS-CoV-2 (B.1.617.2 and sublineages) according to vaccination status. We aimed to compare the incidence and clinical phenotype of MIS-C from our cohort during the pre-delta era. METHODS: This prospective, population-based cohort study included patients aged 0-17 years hospitalised with MIS-C in Denmark, according to the US Centers for Disease Control and Prevention case definition, from Aug 1, 2021, to Feb 1, 2022, a period dominated by the delta variant. We identified MIS-C cases via a nationwide research collaboration involving real-time data collection from all 18 paediatric departments. Aggregated number of SARS-CoV-2 infections by vaccination status was obtained from the Danish COVID-19 surveillance registries. The incidence of MIS-C was calculated using the estimated number of infected individuals by vaccination status. We calculated the incidence of MIS-C per 1 000 000 vaccinated and unvaccinated person-years, and estimated vaccine effectiveness as 1-incidence rate ratio using Poisson regression. Incidence and phenotype of MIS-C were compared with MIS-C cases from the first year of the pandemic. This study is registered at ClinicalTrials.gov, NCT05186597. FINDINGS: We identified 51 MIS-C cases among unvaccinated individuals and one in a fully vaccinated adolescent. The incidence of MIS-C was one in 3400 unvaccinated individuals (95% CI 2600-4600) with the delta variant and one in 9900 vaccinated individuals (95% CI 1800-390 000) with breakthrough infection. The estimated vaccine effectiveness against MIS-C after the delta variant was 94% (95% CI 55-99; p=0·0061) in individuals aged 5-17 years. The clinical phenotype during the delta wave was comparable to the pre-delta era. INTERPRETATION: We found the incidence and phenotype of MIS-C in unvaccinated children during the delta wave to be similar to the incidence during the first year of the pandemic. We found vaccine effectiveness to be high against MIS-C, which we suggest was due to protection from infection and, possibly, a decreased incidence of MIS-C after breakthrough infection. Knowledge of the incidence of MIS-C after different SARS-CoV-2 variants and the effect of vaccination might contribute to the elucidation of the extent to which MIS-C is a vaccine-preventable disease. FUNDING: National Ministry of Higher Education and Science and Innovation Fund Denmark.
Findings the Hub has extracted
Each claim below is labelled by its type of design and links back to this report.
Problem
Multisystem inflammatory syndrome in children (MIS-C) following SARS-CoV-2 delta variant infection
- Intervention
- COVID-19 vaccination
- Population
- Children aged 0-17 years in Denmark during delta variant dominance (August 2021 to February 2022)
Key finding
Vaccine effectiveness against MIS-C was 94% (95% CI 55-99%) in ages 5-17 years
Nygaard et al. · The Lancet Child & Adolescent Health · 6 May 2022