Improving Hydroxyurea Uptake in Children: Results from a Provider Incentive Program in a Large Metropolitan Health

Insights

A provider incentive program significantly increased hydroxyurea prescriptions for children with sickle cell disease (SCD). This intervention improved medication use and fills among Medicaid-enrolled children, suggesting a path to better pediatric SCD treatment adherence.

Area of Science:

  • Hematology
  • Pediatric Medicine
  • Public Health Interventions

Background:

  • Sickle cell disease (SCD) is a genetic blood disorder affecting millions globally.
  • Hydroxyurea is a proven, safe, and effective oral medication for managing SCD in children by increasing fetal hemoglobin.
  • Suboptimal utilization and adherence to hydroxyurea therapy persist among pediatric SCD patients.

Purpose of the Study:

  • To assess the impact of a provider incentive program on hydroxyurea prescription rates in children with SCD.
  • To evaluate secondary outcomes including medication adherence, acute care utilization, and associated costs in a Medicaid-enrolled pediatric population.

Main Methods:

  • A pre-post comparison design was employed within a large metropolitan health system.
  • The primary outcome measured was the rate of active hydroxyurea prescriptions.
  • Secondary outcomes included hydroxyurea fills, adherence, and acute care utilization and costs for Medicaid beneficiaries.

Main Results:

  • The provider incentive program led to significant increases in active hydroxyurea prescriptions over time.
  • Participating providers showed greater increases in prescribing hydroxyurea.
  • Significant improvements were observed in hydroxyurea fills among children enrolled in Medicaid.

Conclusions:

  • Provider incentive programs can effectively enhance hydroxyurea utilization for pediatric sickle cell disease.
  • These interventions may improve prescribing practices and counseling, leading to better treatment adherence.
  • Findings support the implementation of similar strategies to optimize SCD management in children.

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