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Risk Factors for Multisystem Inflammatory Syndrome in Children: A Case-control Investigation

  • Laura D. Zambrano
  • , Michael J. Wu
  • , Lora Martin
  • , Lacy Malloch
  • , Sabrina Chen
  • , Margaret M. Newhams
  • , Suden Kucukak
  • , Mary Beth Son
  • , Cameron Sanders
  • , Kayla Patterson
  • , Natasha Halasa
  • , Julie C. Fitzgerald
  • , Matthew K. Leroue
  • , Mark Hall
  • , Katherine Irby
  • , Courtney M. Rowan
  • , Kari Wellnitz
  • , Leila C. Sahni
  • , Laura Loftis
  • , Tamara T. Bradford
  • Mary Staat, Christopher Babbitt, Christopher L. Carroll, Pia S. Pannaraj, Michele Kong, Jennifer E. Schuster, Janet Chou, Manish M. Patel, Adrienne G. Randolph, Angela P. Campbell, Charlotte V. Hobbs
  • Centers for Disease Control and Prevention
  • University of Mississippi
  • Boston Children's Hospital
  • Harvard University
  • Vanderbilt University
  • The Children's Hospital of Philadelphia
  • University of Colorado School of Medicine
  • Nationwide Children’s Hospital
  • University of Arkansas for Medical Sciences
  • Indiana University Bloomington
  • University of Iowa
  • Texas Children's Hospital Houston
  • Louisiana State University Health Sciences Center
  • University of Cincinnati
  • MemorialCare Miller Children's and Women's Hospital Long Beach
  • Connecticut Children’s Hospital
  • University of Southern California
  • University of Alabama at Birmingham
  • University of Missouri at Kansas City

Research output: Contribution to journalArticlepeer-review

10 Scopus citations

Abstract

Background: In a 2020 pilot case-control study using medical records, we reported that non-Hispanic Black children were more likely to develop multisystem inflammatory syndrome in children (MIS-C) after adjustment for sociodemographic factors and underlying medical conditions. Using structured interviews, we investigated patient, household, and community factors underlying MIS-C likelihood. Methods: MIS-C case patients hospitalized in 2021 across 14 US pediatric hospitals were matched by age and site to outpatient controls testing positive for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) within 3 months of the admission date. Caregiver interviews queried race/ethnicity, medical history, and household and potential community exposures 1 month before MIS-C hospitalization (case-patients) or after SARS-CoV-2 infection (controls). We calculated adjusted odds ratios (aOR) using mixed-effects multivariable logistic regression. Results: Among 275 case patients and 496 controls, race/ethnicity, social vulnerability and patient or family history of autoimmune/rheumatologic disease were not associated with MIS-C. In previously healthy children, MIS-C was associated with a history of hospitalization for an infection [aOR: 4.8; 95% confidence interval (CI): 2.1-11.0]. Household crowding (aOR: 1.7; 95% CI: 1.2-2.6), large event attendance (aOR: 1.7; 95% CI: 1.3-2.1), school attendance with limited masking (aOR: 2.6; 95% CI: 1.1-6.6), public transit use (aOR: 1.8; 95% CI: 1.4-2.4) and co-resident testing positive for SARS-CoV-2 (aOR: 2.2; 95% CI: 1.3-3.7) were associated with increased MIS-C likelihood, with risk increasing with the number of these factors. Conclusions: From caregiver interviews, we clarify household and community exposures associated with MIS-C; however, we did not confirm prior associations between sociodemographic factors and MIS-C.

Original languageEnglish
Pages (from-to)E190-E196
JournalPediatric Infectious Disease Journal
Volume42
Issue number6
DOIs
StatePublished - 1 Jun 2023
Externally publishedYes

Keywords

  • children
  • coronavirus disease 2019 (COVID-19)
  • multisystem inflammatory syndrome in children
  • risk factor s
  • SARS-CoV-2

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