Association of the child opportunity index with in-hospital mortality and persistence of organ dysfunction at one week after onset of Phoenix Sepsis among children admitted to the pediatric intensive care unit with suspected infection
- PMID: 40228194
- PMCID: PMC11996216
- DOI: 10.1371/journal.pdig.0000763
Association of the child opportunity index with in-hospital mortality and persistence of organ dysfunction at one week after onset of Phoenix Sepsis among children admitted to the pediatric intensive care unit with suspected infection
Abstract
The social determinants of health (SDoH) are fundamental factors that contribute to overall health and health-related outcomes. Children living in lower socioeconomic areas have a higher risk of critical illness and worse outcomes compared to children living in more socioeconomically advantaged areas. In this work, we determine whether the Child Opportunity Index (COI 3.0), a multi-dimensional child-specific indicator of neighborhood environment, is associated with in-hospital mortality or persistence of a Phoenix Sepsis Score ≥ 2 at one week following Phoenix Sepsis onset in children admitted to pediatric intensive care units (PICUs) with suspected infection. We performed a retrospective cohort analysis of 63,824 patients with suspected or confirmed infection admission diagnosis in two PICUs in Atlanta, Georgia with a Georgia residential address that could be geocoded and linked to a census tract. The primary outcome was the composite of in-hospital mortality or persistence of a Phoenix Sepsis Score ≥ 2 at one week following Phoenix Sepsis onset. Model performance measures of interest were the area under the receiver operating characteristic curve (AUROC) and the area under the precision-recall curve (AUPRC). Models developed with electronic medical record (EMR) data using Egleston (EG) or Scottish Rite (SR) as the training site achieved AUROCs of 0.81-0.84 (95% CI range: 0.8-0.85) and 0.82-0.82 (95% CI range: 0.81-0.83) and AUPRCs of 0.59-0.68 (95% CI range: 0.58-0.69) and 0.62-0.64 (95% CI range: 0.61-0.65) respectively. Despite significant differences in COI 3.0 characteristics and overall in-hospital mortality of children with Phoenix suspected infection between the EG and SR PICUs, the addition of COI 3.0 did not improve the overall model performance metrics. While children admitted to both PICUs were more often from COI 3.0 neighborhoods in the lowest two quintiles, these neighborhood features had less of an impact on the model's predictive performance compared to patient physiologic and biologic features available in the EMR.
Copyright: © 2025 Moore et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Conflict of interest statement
The authors have declared that no competing interests exist.
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