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Updated: Jan 9, 2026

A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy
Hydroxyurea Therapy in Sickle Cell Disease: Evaluating Healthcare Costs and Utilization in a Brazilian Tertiary
La'Ron L A Browne1, Emilia Matos do Nascimento2,3, Patricia Moura2
1Department of Global Pediatric Medicine, St Jude Children's Research Hospital, Memphis, TN, United States.
Abstract:
Patients with sickle cell disease (SCD) treated with hydroxyurea, a disease-modifying agent, experience reduced hospitalizations, blood utilization, opioid use, and mortality, but how the reduced acute care utilization translates to cost-savings is understudied. This study aimed to test whether hydroxyurea reduces overall care costs for SCD patients in Brazil. Healthcare costs in Brazilian Reais (R$) were collected from patients with SCD who had at least one encounter between January 1, 2018, and June 30, 2018. The total median healthcare resource utilization included ambulatory clinic, emergency department (ED), and inpatient care. Patients were stratified by hydroxyurea use and medication adherence (MPR >50% vs. ≤50%). A total of 3331 active patients were included in the analysis, with 3032 having at least one encounter. 51% were female, and the median age was 15 years (range 0-76). 2212 (73.0%), had HbSS/Sβ°thalassemia, followed by HbSC (n=610, 20%) and HbSβ+thalassemia (n=148, 5%). 614 (20.2%) were prescribed hydroxyurea. Hydroxyurea-treated patients had higher median ambulatory visits, fewer ED visits, and fewer hospitalizations than those not on hydroxyurea. While hydroxyurea reduced acute care utilization, costs remained comparable to those of patients not using hydroxyurea suggesting that disease severity, use of expensive drugs, and chronic conditions are key factors driving costs requiring further analysis.
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