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Preference of treatment characteristics among people with haemophilia or their caregivers, and physicians in the Japanese healthcare environment.

Teruhisa FujiiMasataka IshimuraSatomi TakaoAyumi Deguchi
Published in: Haemophilia : the official journal of the World Federation of Hemophilia (2024)
Our study utilises real-world survey data and presents preferences for haemophilia treatment characteristics among physicians, PWH and their caregivers in Japan, which could encourage improvements in individualised treatment and disease management. Alignment between treatment approaches at HTCs and non-HTCs could facilitate improvements in the quality of care for PWH across Japan.
Keyphrases
  • healthcare
  • palliative care
  • primary care
  • quality improvement
  • machine learning
  • cross sectional
  • electronic health record
  • artificial intelligence
  • big data
  • pain management
  • affordable care act