Identification of Multisystem Inflammatory Syndrome in Children Classes and Development of Hyperinflammation Score in

Balagangadhar R Totapally1,2, Meghana Nadiger1, Sophia Hassor3

  • 1Division of Critical Care Medicine, Nicklaus Children's Hospital, Miami, Florida, United States.

Insights

Most children experience mild COVID-19, but critical illness affects obese adolescents. This study identifies three classes of multisystem inflammatory syndrome in children (MIS-C) and develops a predictive score for severe COVID-19 in pediatric patients.

Area of Science:

  • Pediatric Infectious Diseases
  • Critical Care Medicine
  • Epidemiology

Background:

  • COVID-19 presents with varied severity in children.
  • Multisystem inflammatory syndrome in children (MIS-C) is a significant concern.
  • Predictive tools for severe pediatric COVID-19 are needed.

Purpose of the Study:

  • To characterize pediatric COVID-19 hospitalizations.
  • To identify classes of MIS-C.
  • To develop and validate the pediatric COVID-19 associated hyperinflammation score (PcHIS).

Main Methods:

  • Retrospective cohort study of 68 pediatric patients with COVID-19.
  • Defined critical illness based on support requirements.
  • Developed PcHIS using six clinical variables.
  • Classified MIS-C using CDC criteria and latent class analysis.

Main Results:

  • Median age was 6.4 years; fever, respiratory, and GI symptoms were common.
  • MIS-C occurred in 47%, critical illness in 16%, and 25% required PICU admission.
  • Critical illness was associated with adolescents, obesity, and comorbidities.
  • PcHIS score of 3 showed 100% sensitivity and 77% specificity for critical illness.
  • Identified three MIS-C classes: without Kawasaki-like disease (47%), with respiratory disease (25%), and with Kawasaki-like disease (28%).

Conclusions:

  • Most pediatric COVID-19 cases are mild to moderate.
  • Critical COVID-19 predominantly affects obese adolescents with comorbidities.
  • Three distinct clinical classes of MIS-C were identified.
  • Further validation of PcHIS for pediatric COVID-19 is warranted.