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Disease and treatment burden of patients with haemophilia entering the explorer6 non-interventional study.
- Source :
-
European journal of haematology [Eur J Haematol] 2024 Nov; Vol. 113 (5), pp. 631-640. Date of Electronic Publication: 2024 Jul 19. - Publication Year :
- 2024
-
Abstract
- Objectives: We aimed to characterise baseline disease and treatment burden in a large population with haemophilia A/B, both with (HAwI/HBwI) and without (HA/HB) inhibitors.<br />Methods: The prospective, non-interventional explorer6 study included patients ≥12 years old with severe HA, severe/moderate HB or HAwI/HBwI of any severity, treated according to local standard of care (excluding previous/current exposure to concizumab or emicizumab). Baseline characteristics and historical clinical data were collected and patient-reported outcomes, including treatment burden, were assessed.<br />Results: The explorer6 study enrolled 231 patients with haemophilia (84 HAwI/HBwI) from 33 countries. At baseline, patients with HA/HB treated with prophylaxis had the lowest median annualised bleeding rates (ABRs; 2.0), irrespective of haemophilia type; of these patients, 27.5% (HA) and 31.4% (HB) had target joints. Patients with HAwI/HBwI treated episodically reported the highest treatment burden. Of these patients, 28.5% (HAwI) and 25.1% (HBwI) performed sports activities in the month before screening.<br />Conclusion: Despite receiving routine clinical care, historical and baseline information from patients enrolled in explorer6 showed that patients with HA/HB treated episodically and patients with HAwI/HBwI had higher ABRs, higher treatment burden and participated in sports less than those with HA/HB treated with prophylaxis. Emerging treatments could be beneficial in addressing these unmet medical needs.<br /> (© 2024 The Author(s). European Journal of Haematology published by John Wiley & Sons Ltd.)
- Subjects :
- Humans
Male
Adult
Adolescent
Prospective Studies
Middle Aged
Female
Hemorrhage etiology
Hemorrhage epidemiology
Cost of Illness
Hemophilia B drug therapy
Hemophilia B complications
Hemophilia B therapy
Hemophilia B epidemiology
Hemophilia B diagnosis
Child
Young Adult
Severity of Illness Index
Disease Management
Factor VIII therapeutic use
Hemophilia A drug therapy
Hemophilia A epidemiology
Hemophilia A diagnosis
Hemophilia A therapy
Subjects
Details
- Language :
- English
- ISSN :
- 1600-0609
- Volume :
- 113
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- European journal of haematology
- Publication Type :
- Academic Journal
- Accession number :
- 39030946
- Full Text :
- https://doi.org/10.1111/ejh.14277