Real-world clinical and psychosocial outcomes among people with mild or moderate haemophilia A treated on-demand in the Italian CHESS II cohort: a real-world data analysis

Real-world clinical and psychosocial outcomes among people with mild or moderate haemophilia A treated on-demand in the Italian CHESS II cohort: a real-world data analysis

The burden of severe haemophilia A (HA) has been studied extensively owing to the higher bleeding frequency and associated treatment requirements, leaving a clear unmet need for research focused on the burden of mild and moderate HA.

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Bibliographic Details
Main Authors: Castaman Giancarlo, Mancuso Maria Elisa, Di Minno Matteo Nicola Dario, Sannino Luigi, Tempre Rosaria, Bendinelli Sara, Blenkiron Tom, Burke Tom, Grazzi Enrico Ferri
Format: Article
Language:English
Published: Sciendo 2024-04-01
Series:The Journal of Haemophilia Practice
Subjects:
haemophilia a
annual bleeding rate
joint arthropathy
pain
patient-reported outcomes
health-related quality of life
psychosocial burden
Online Access:https://doi.org/10.2478/jhp-2024-0008
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