FAR-BENE Study: pharmacoeconomics and well-being in hemophilia. Monitoring outcomes in light of pharmaceutical expenditure with focus on patients undergoing therapeutic switch.

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Authors: Carola Sella, Federica Valeri, Cristina Dainese, Annamaria Porreca, Matilde Scaldaferri, Daniela Cestino, Roberta Aldieri, Giulia Soave, Sara Bergonzi, Giovanni Murante, Rebecca Pastorino, Alessandra Valpreda
+2 more Benedetto Bruno, Alessandra Borchiellini
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Abstract

BACKGROUND: Hemophilia, a rare bleeding disorder, raises significant pharmacoeconomic challenges, particularly with the emergence of innovative therapies. This study evaluates clinical and patient-reported outcomes and expenditures in hemophilia patients focusing on those who underwent therapeutic switches between 2017 and 2023. MATERIALS AND METHODS: This retrospective study included severe hemophilia patients. Expenditure was analyzed based on clotting factor consumption, while clinical well-being was assessed using ABR, NRS for pain, joint health scores (HJHS, HEAD-US) and trough plasma levels. A sub-analysis was conducted by applying different therapeutic groups. Statistical significance of differences between paired measures (pre [T0] vs post [T1]) was examined using the Wilcoxon Sum Rank test. RESULTS: Seventy patients were included. Total expenditure was € 12,947,580.44 in 2017 and € 12,967,576.92 in 2023. Among 45 patients who switched therapy, the median number of infusions/year significantly decreased from 156 to 91 (p

Fields of Study & Subjects

Hemophilia Treatment and Research Blood donation and transfusion practices Health Education and Cultural Studies

Publication details

Journal / source
PubMed
Volume
24
Issue
1
Pages
77–85
Publication date
31 January 2026
Language
EN