Cargando…

Multisystem inflammatory syndrome in 1.2 million children: longitudinal cohort study of risk factors

BACKGROUND: We identified patient characteristics associated with an increased risk of developing MIS-C. METHODS: We conducted a longitudinal cohort study of 1,195,327 patients aged 0–19 years between 2006 and 2021, including the first two waves of the pandemic (February 25–August 22, 2020 and Augus...

Descripción completa

Detalles Bibliográficos
Autores principales: Auger, Nathalie, Côté-Corriveau, Gabriel, Kang, Harb, Quach, Caroline, Lo, Ernest, Lee, Ga Eun, Healy-Profitós, Jessica, Brousseau, Émilie, Luu, Thuy Mai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10191400/
https://www.ncbi.nlm.nih.gov/pubmed/37198405
http://dx.doi.org/10.1038/s41390-023-02633-y
Descripción
Sumario:BACKGROUND: We identified patient characteristics associated with an increased risk of developing MIS-C. METHODS: We conducted a longitudinal cohort study of 1,195,327 patients aged 0–19 years between 2006 and 2021, including the first two waves of the pandemic (February 25–August 22, 2020 and August 23, 2020-March 31, 2021). Exposures included prepandemic morbidity, birth outcomes, and family history of maternal disorders. Outcomes included MIS-C, Kawasaki disease, and other Covid-19 complications during the pandemic. We calculated risk ratios (RRs) and 95% confidence intervals (CIs) for the association between patient exposures and these outcomes using log-binomial regression models adjusted for potential confounders. RESULTS: Among 1,195,327 children, 84 developed MIS-C, 107 Kawasaki disease, and 330 other Covid-19 complications during the first year of the pandemic. Prepandemic hospitalizations for metabolic disorders (RR 11.3, 95% CI 5.61–22.6), atopic conditions (RR 3.34, 95% CI 1.60–6.97), and cancer (RR 8.11, 95% CI 1.13–58.3) were strongly associated with the risk of MIS-C, compared with no exposure. These same exposures were also associated with Kawasaki disease and other Covid-19 complications. However, birth characteristics and history of maternal morbidity were not associated with MIS-C development. CONCLUSIONS: Children with pre-existing morbidity have a considerably elevated risk of MIS-C. IMPACT: Morbidities that predispose children to multisystem inflammatory syndrome (MIS-C) are unclear. In this study, prepandemic hospitalizations for metabolic disorders, atopic conditions, and cancer were associated with an elevated risk of MIS-C. Birth characteristics and family history of maternal morbidity were not, however, associated with MIS-C. Pediatric morbidities may play a greater role in MIS-C onset than maternal or perinatal characteristics, and may help clinicians better recognize children at risk for this complication.