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

Abstract

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.

Keywords

• haemophilia a
• annual bleeding rate
• joint arthropathy
• pain
• patient-reported outcomes
• health-related quality of life
• psychosocial burden