Social Determinants of Health and Outcomes After Pediatric Ventricular Assist Device Implantation
Male
Heart Failure
Adolescent
Social Determinants of Health
Infant, Newborn
Infant
Kaplan-Meier Estimate
United States
03 medical and health sciences
Treatment Outcome
0302 clinical medicine
Child, Preschool
Humans
Female
Heart-Assist Devices
Registries
Child
Retrospective Studies
Proportional Hazards Models
DOI:
10.1111/petr.14802
Publication Date:
2024-06-10T02:04:00Z
AUTHORS (8)
ABSTRACT
ABSTRACTBackgroundLimited research exists on the influence of social determinants of health (SDOH) on outcomes in pediatric patients with advanced heart failure receiving mechanical circulatory support.MethodsLinkage of the Pediatric Interagency Registry for Mechanical Circulatory Support (Pedimacs) and Society of Thoracic Surgeon's Congenital Heart Surgery Database (STS‐CHSD) identified pediatric patients who underwent ventricular assist device (VAD) implantation from 2012 to 2022 with available residential zip codes. Utilizing the available zip codes, each patient was assigned a Childhood Opportunity Index (COI) score. Level of childhood opportunity, race, and insurance type were used as proxies for SDOH. Major outcomes included death, transplant, alive with device, and recovery. Secondary outcomes were adverse events. Statistical analyses were performed using the Kaplan–Meier survival, competing risk analyses, and multivariable Cox proportional hazards model.ResultsThree hundred seventeen patients were included in the study. Childhood opportunity level and insurance status did not significantly impact morbidity or mortality after VAD implantation. White race was associated with reduced 1‐year survival (71% in White vs. 87% in non‐White patients, p = 0.05) and increased risk of pump thrombosis (p = 0.02).ConclusionChildhood opportunity level and insurance status were not linked to morbidity and mortality in pediatric patients after VAD implantation. Notably, White race was associated with higher mortality rates. The study underscores the importance of considering SDOH in evaluating advanced therapies for pediatric heart failure and emphasizes the need for accurate socioeconomic data collection in future studies and national registries.
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