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An observational study of haemophilia A patients without inhibitors using the French national claims (SNDS) database.
- Source :
- Hematology; Dec2024, Vol. 29 Issue 1, p1-9, 9p
- Publication Year :
- 2024
-
Abstract
- Objectives: To describe clinical characteristics, factor consumption, and events of interest in patients with haemophilia A without inhibitors receiving prophylaxis in France, and the clinical impact of switching to Elocta® in this population. Methods: This retrospective, observational study using the Système National des Données de Santé database, analysed data from patients with haemophilia A without inhibitors using prophylactic factor VIII (FVIII) replacement therapy during 2016–2019. Clinical characteristics, treatment patterns and switches, factor consumption, and rate of events of interest were determined. In a sub-cohort of patients treated with Elocta®, clinical characteristics, factor consumption, and rate of events of interest before and after switching to Elocta® were compared. Results: For 545 patients, with mean age (standard deviation [SD]) 25.4 (17.8) years, Elocta® was the most used treatment. Bleeding events and articular non-bleeding events leading to hospitalization occurred in 15.4% and 13.9% of patients, respectively, and 9.9% of patients had surgeries or procedures related to haemophilic arthropathy. The mean (SD) FVIII product consumption was 344 (93) IU/kg/month for extended half-life treatment, and 331 (98) IU/kg/month for standard half-life products. For the sub-cohort of 146 patients, bleeding events (SD) decreased from 0.32 (2.2) to 0.09 (0.42) events/patient/year (p = 0.227) after switching to Elocta®. There was no statistically significant difference in rates of factor consumption or articular non-bleeding events before and after initiation of Elocta®. Conclusion: This study provides real-world insights that advance the understanding of treatment patterns and events of interest in patients with haemophilia A on prophylactic regimens in France. [ABSTRACT FROM AUTHOR]
- Subjects :
- HEMOPHILIACS
BLOOD coagulation factor VIII
DATABASES
STANDARD deviations
HEMOPHILIA
Subjects
Details
- Language :
- English
- ISSN :
- 10245332
- Volume :
- 29
- Issue :
- 1
- Database :
- Complementary Index
- Journal :
- Hematology
- Publication Type :
- Academic Journal
- Accession number :
- 181626697
- Full Text :
- https://doi.org/10.1080/16078454.2024.2320610