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

Author:

Zambrano Laura D.1ORCID,Wu Michael J.1,Martin Lora2,Malloch Lacy2ORCID,Chen Sabrina3ORCID,Newhams Margaret M.3ORCID,Kucukak Suden3,Son Mary Beth45ORCID,Sanders Cameron2ORCID,Patterson Kayla2ORCID,Halasa Natasha6ORCID,Fitzgerald Julie C.7ORCID,Leroue Matthew K.8ORCID,Hall Mark9ORCID,Irby Katherine10ORCID,Rowan Courtney M.11ORCID,Wellnitz Kari6ORCID,Sahni Leila C.12ORCID,Loftis Laura12ORCID,Bradford Tamara T.13ORCID,Staat Mary14ORCID,Babbitt Christopher15,Carroll Christopher L.16,Pannaraj Pia S.6ORCID,Kong Michele17ORCID,Schuster Jennifer E.18ORCID,Chou Janet45ORCID,Patel Manish M.1,Randolph Adrienne G.3519ORCID,Campbell Angela P.1ORCID,Hobbs Charlotte V.2ORCID

Affiliation:

1. COVID-19 Response Team, U.S. Centers for Disease Control and Prevention, Atlanta, Georgia

2. Division of Infectious Disease, Department of Pediatrics, Children’s of Mississippi, University of Mississippi Medical Center, Jackson, Mississippi

3. Department of Anesthesiology, Critical Care, and Pain Medicine, Boston Children’s Hospital, Boston, Massachusetts

4. Division of Immunology, Department of Pediatrics, Boston Children’s Hospital, Boston, Massachusetts

5. Department of Pediatrics, Harvard Medical School, Boston, Massachusetts

6. Division of Pediatric Infectious Diseases, Department of Pediatrics, Vanderbilt University Medical Center, Nashville, Tennessee

7. Division of Critical Care Medicine, Department of Anesthesiology and Critical Care, Children’s Hospital of Philadelphia, Philadelphia, Pennsylvania

8. Department of Pediatrics, Section of Critical Care Medicine, University of Colorado School of Medicine, Aurora, Colorado

9. Division of Pediatric Critical Care Medicine, Nationwide Children’s Hospital Columbus, Ohio

10. Section of Pediatric Critical Care, Department of Pediatrics, Arkansas Children’s Hospital, Little Rock, Arkansas

11. Division of Pediatric Critical Care, Department of Pediatrics, Indiana University School of Medicine, Riley Hospital for Children, Indianapolis, Indiana

12. Department of Pediatrics, Baylor College of Medicine, Texas Children’s Hospital, Houston, Texas

13. Division of Cardiology, Department of Pediatrics, Louisiana State University Health Sciences Center and Children’s Hospital of New Orleans, New Orleans, Louisiana

14. Department of Pediatrics, University of Cincinnati College of Medicine, Division of Infectious Diseases, Cincinnati Children’s Hospital Medical Center, Cincinnati, Ohio

15. Miller Children’s and Women’s Hospital of Long Beach, Long Beach, California

16. Division of Pediatric Critical Care, Connecticut Children’s Hospital, Hartford, Connecticut

17. Department of Pediatrics, Heersink School of Medicine, The University of Alabama at Birmingham, Birmingham, Alabama

18. Department of Pediatrics, Children’s Mercy Kansas City, University of Missouri-Kansas City School of Medicine, Kansas City, Missouri

19. Department of Anesthesia, Harvard Medical School, Boston, Massachusetts.

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.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Infectious Diseases,Microbiology (medical),Pediatrics, Perinatology and Child Health

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