TY - JOUR
T1 - Risk Factors for Multisystem Inflammatory Syndrome in Children
T2 - A Case-control Investigation
AU - Zambrano, Laura D.
AU - Wu, Michael J.
AU - Martin, Lora
AU - Malloch, Lacy
AU - Chen, Sabrina
AU - Newhams, Margaret M.
AU - Kucukak, Suden
AU - Son, Mary Beth
AU - Sanders, Cameron
AU - Patterson, Kayla
AU - Halasa, Natasha
AU - Fitzgerald, Julie C.
AU - Leroue, Matthew K.
AU - Hall, Mark
AU - Irby, Katherine
AU - Rowan, Courtney M.
AU - Wellnitz, Kari
AU - Sahni, Leila C.
AU - Loftis, Laura
AU - Bradford, Tamara T.
AU - Staat, Mary
AU - Babbitt, Christopher
AU - Carroll, Christopher L.
AU - Pannaraj, Pia S.
AU - Kong, Michele
AU - Schuster, Jennifer E.
AU - Chou, Janet
AU - Patel, Manish M.
AU - Randolph, Adrienne G.
AU - Campbell, Angela P.
AU - Hobbs, Charlotte V.
N1 - Publisher Copyright:
© 2023 Lippincott Williams and Wilkins. All rights reserved.
PY - 2023/6/1
Y1 - 2023/6/1
N2 - 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.
AB - 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.
KW - children
KW - coronavirus disease 2019 (COVID-19)
KW - multisystem inflammatory syndrome in children
KW - risk factor s
KW - SARS-CoV-2
UR - https://www.scopus.com/pages/publications/85159770881
U2 - 10.1097/INF.0000000000003900
DO - 10.1097/INF.0000000000003900
M3 - Article
C2 - 37000922
AN - SCOPUS:85159770881
SN - 0891-3668
VL - 42
SP - E190-E196
JO - Pediatric Infectious Disease Journal
JF - Pediatric Infectious Disease Journal
IS - 6
ER -