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Examining the Association Between MIS-C and the Child Opportunity Index at a Single Center
Jordan Tyris1,2, Kaitlyn Boggs3, James Bost1
1Division of Hospital Medicine.
Insights
Children in areas with low Child Opportunity Index (COI) scores face higher risks for multisystem inflammatory syndrome in childhood (MIS-C). This highlights how neighborhood factors influence MIS-C diagnosis in children.
Area of Science:
- Pediatric Health
- Environmental Epidemiology
- Social Determinants of Health
Background:
- Multisystem inflammatory syndrome in childhood (MIS-C) is a serious condition affecting children.
- Understanding risk factors for MIS-C is crucial for public health interventions.
- Socioeconomic and environmental factors may play a role in MIS-C development.
Purpose of the Study:
- To investigate the association between the Child Opportunity Index (COI) and MIS-C diagnosis.
- To determine if neighborhood-level opportunity impacts MIS-C risk in hospitalized children.
Main Methods:
- Retrospective case-control study of children hospitalized between March 2020 and June 2021.
- Compared 111 children diagnosed with MIS-C against 61 controls with alternative diagnoses.
- Utilized census tract-level COI based on patient addresses as the exposure variable.
Main Results:
- A significant difference in overall COI distribution was observed between MIS-C cases and controls (P = .03).
- Children in very low to low overall COI census tracts had significantly higher odds of MIS-C diagnosis (OR = 2.82).
- Children in very low to low health/environment COI census tracts also had significantly higher odds of MIS-C diagnosis (OR = 4.69).
Conclusions:
- Child Opportunity Index is associated with MIS-C diagnosis in hospitalized children.
- Place-based determinants, reflected by COI, significantly contribute to MIS-C development.
- This suggests that neighborhood conditions are important factors in pediatric MIS-C risk.
Objective:
To describe associations between the Child Opportunity Index (COI) and multisystem inflammatory syndrome of childhood (MIS-C) diagnosis among hospitalized children.
Methods:
We used a retrospective case control study design to examine children ≤21 years hospitalized at a single, tertiary care children's hospital between March 2020 and June 2021. Our study population included children diagnosed with MIS-C (n = 111) and a control group of children hospitalized for MIS-C evaluation who had an alternative diagnosis (n = 61). Census tract COI was the exposure variable, determined using the patient's home address mapped to the census tract. Our outcome measure was MIS-C diagnosis. Odds ratios measured associations between COI and MIS-C diagnosis.
Results:
Our study population included 111 children diagnosed with MIS-C and 61 children evaluated but ruled out for MIS-C. The distribution of census tract overall COI differed significantly between children diagnosed with MIS-C compared with children with an alternate diagnosis (P = .03). Children residing in census tracts with very low to low overall COI (2.82, 95% confidence interval [CI]: 1.29-6.17) and very low to low health/environment COI (4.69, 95% CI 2.21-9.97) had significantly higher odds of being diagnosed with MIS-C compared with children living in moderate and high to very high COI census tracts, respectively.
Conclusion:
Census tract child opportunity is associated with MIS-C diagnosis among hospitalized children suggesting an important contribution of place-based determinants in the development of MIS-C.
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