Chronic Medication Burden After Cardiac Surgery for Pediatric Medicaid Beneficiaries

Joyce L Woo1, Katherine A Nash2, Kacie Dragan3

  • 1Division of Pediatric Cardiology, Ann and Robert H. Lurie Children's Hospital of Chicago, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA; Division of Pediatric Cardiology, NewYork-Presbyterian/Columbia University Irving Medical Center, New York, New York, USA.

Insights

Children with congenital heart defects have a high medication burden throughout childhood. This study highlights the significant medication use and costs in these pediatric patients, informing care for this complex group.

Area of Science:

  • Pediatric Cardiology
  • Health Services Research
  • Pharmacoeconomics

Background:

  • Congenital heart defects (CHDs) are the most common and costly birth defects.
  • Increasing survival rates for children with CHDs necessitate understanding their long-term health and resource needs.

Purpose of the Study:

  • To analyze chronic outpatient prescription medication use and expenditures in New York State pediatric Medicaid enrollees.
  • To compare medication patterns between children undergoing cardiac surgery and the general pediatric population.

Main Methods:

  • Retrospective cohort study of pediatric Medicaid enrollees (2006-2019).
  • Utilized the New York State Congenital Heart Surgery Collaborative for Longitudinal Outcomes and Utilization of Resources database.
  • Primary outcomes included chronic medication use (per person-year) and associated expenditures.

Main Results:

  • Over 40% of children undergoing cardiac surgery used chronic medications vs. 10% of the general pediatric population.
  • Medication expenditures were 10 times higher per person-year for children with CHDs.
  • Disease severity correlated with medication use; infants had highest use, but nearly half of adolescents used chronic medications.

Conclusions:

  • Children who undergo cardiac surgery face a substantial and persistent medication burden throughout childhood.
  • Findings can guide clinicians and policymakers in optimizing care and value for medically complex pediatric populations with CHDs.
Abstract

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