Comparison of the course of multisystem inflammatory syndrome in children during different pandemic waves

Katarzyna Ptak1, Izabela Szymońska2, Anna Olchawa-Czech2

  • 1Department of Pediatrics, Jagiellonian University Medical College, ul. Wielicka 265, 30-663, Cracow, Poland. katarzyna.1.ptak@uj.edu.pl.

Insights

Multisystem inflammatory syndrome in children (MIS-C) following COVID-19 showed similar clinical courses across variants, but incidence appears to be decreasing. Management and symptoms remained consistent, with respiratory symptoms noted more in later variants.

Area of Science:

  • Pediatric Infectious Diseases
  • Epidemiology
  • Critical Care Medicine

Background:

  • The clinical presentation of COVID-19 has evolved, with Multisystem Inflammatory Syndrome in Children (MIS-C) emerging as a significant complication.
  • Subsequent pandemic waves have seen continued cases of MIS-C, necessitating an understanding of its changing characteristics.
  • The incidence of MIS-C appears to be decreasing, posing diagnostic challenges during periods of lower prevalence.

Purpose of the Study:

  • To evaluate the incidence, clinical presentation, and management strategies for MIS-C during distinct COVID-19 variant dominance periods.
  • To compare MIS-C cases during the original/Alpha variant period versus the Delta/Omicron variant periods.

Main Methods:

  • Retrospective analysis of prospectively collected data from 108 eligible pediatric patients.
  • Comparison of MIS-C incidence and clinical features between two groups based on dominant COVID-19 variants (Original/Alpha vs. Delta/Omicron).
  • Assessment of demographic data, clinical symptoms, laboratory findings, treatment modalities, and patient outcomes.

Main Results:

  • No significant differences in patient age, sex, or SARS-CoV-2 antibody positivity were observed between variant periods.
  • Fever duration and the prevalence of mucocutaneous, circulatory, neurological, and gastrointestinal symptoms were similar across groups.
  • Respiratory symptoms were more frequent during the Delta/Omicron variant period (p=0.015), while intensive care unit admission rates and mortality were comparable. Higher methylprednisolone doses were used in the Delta/Omicron group (p=0.03).

Conclusions:

  • The clinical course and management of MIS-C demonstrate remarkable similarity across different COVID-19 variant waves.
  • A potential decrease in MIS-C incidence may be occurring in later pandemic phases.
  • While overall clinical presentation is consistent, increased respiratory symptoms were noted with later variants.

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