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Published on: May 11, 2015
Child Opportunity Index Influences Pediatric Pulmonary Hypertension Outcomes: Analyses From the Pediatric Health
Jai K Khurana1, Stuart Lipsitz2, Diana L Geisser3
1Department of Cardiology, Boston Children's Hospital, Boston, Massachusetts, USA.
Insights
Social determinants of health significantly impact pediatric pulmonary hypertension (PH) outcomes. Lower socioeconomic opportunity, minority race, public insurance, and longer travel distance are linked to increased PH mortality in children.
Area of Science:
- Pediatric Health Outcomes
- Social Determinants of Health
- Pulmonary Hypertension Research
Background:
- Social determinants of health (SDoH) impact pediatric pulmonary hypertension (PH) outcomes.
- Characterizing these SDoH is crucial for improving care.
Purpose of the Study:
- To examine associations between SDoH and pediatric PH outcomes.
- To identify specific SDoH factors contributing to mortality in pediatric PH patients.
Main Methods:
- Retrospective cohort study of 24,321 pediatric PH patients from 47 children's hospitals (2016-2022).
- Utilized International Classification of Diseases-10 codes for patient identification.
- Analyzed SDoH including Child Opportunity Index (COI), race/ethnicity, insurance, urbanicity, and distance, assessing their association with mortality.
Main Results:
- Mortality rate was 7.0% (1,702 deaths).
- Higher mortality observed in lower COI quintiles, with public insurance, Black/African American race, and greater home-to-hospital distance.
- Patients in the highest COI quintile had significantly lower odds of mortality (adjusted OR: 0.78; 95% CI: 0.67-0.90) compared to the lowest.
Conclusions:
- Lower Child Opportunity Index, Black/African American race, public insurance, and increased home-to-hospital distance are associated with higher mortality in pediatric PH.
- These findings highlight the critical role of SDoH in pediatric PH outcomes and underscore the need for targeted interventions.
Background:
Social determinants of health (SDoH) in pediatric pulmonary hypertension (PH) outcomes are inadequately characterized.
Objectives:
The authors examined associations between SDoH and pediatric PH outcomes.
Methods:
This retrospective cohort study utilizes the Pediatric Health Information System (47 children's hospitals). All pediatric PH patients with encounters from January 1, 2016, to December 31, 2022, were identified using International Classification of Diseases-10 codes. Demographics, therapeutics, and outcomes were compared according to SDoH including Child Opportunity Index (COI 3.0), race/ethnicity, insurance status, urbanicity, and home-to-hospital distance. Associations between SDoH and mortality were modeled, with each SDoH analyzed separately with clinical variables.
Results:
Of 24,321 pediatric PH patients, 1,702 (7.0%) died. The median age at first admission was 1 year (IQR: 0, 5) with PH groups of pulmonary arterial hypertension (n = 11,296, 46.4%), left heart disease (n = 2,332, 9.6%), lung disease (9,165, 37.7%), thromboembolic (n = 180, 0.7%), and other (n = 1,348, 5.5%). No difference in the therapy use was observed by COI. Unadjusted mortality differed by COI quintile, with the highest proportion of deaths in very low (8.5%) vs very high (6.1%, P < 0.001). Mortality was higher for patients with public insurance, Black/African American race and those living further from hospital. In multivariable models adjusting for baseline unmodifiable factors and condition severity/therapy use, patients from the very high COI quintile had significantly lower odds of mortality vs very low quintile (adjusted OR: 0.78; 95% CI: 0.67-0.90; P < 0.001).
Conclusions:
In this study of pediatric PH outcomes by SDoH at U.S. children's hospitals, lower COI, Black/African American race, public insurance, and greater home-to-hospital distance were associated with higher mortality.
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