Login / Signup

HRQoL and psychosocial aspects of burden on caregivers to children with moderate or severe von Willebrand disease.

Anna OlssonPia PetriniEmma Engman GrahnLinda Myrin Westesson
Published in: Haemophilia : the official journal of the World Federation of Hemophilia (2023)
This study contributes to knowledge about caregivers' HRQoL and highlights the situation of caregivers of children with moderate VWD. Furthermore, the caregiver burden was negatively affected by psychosocial aspects. Clinical follow-ups should include assessment of psychosocial aspects to identify caregivers that are at risk of high burden.
Keyphrases
  • palliative care
  • mental health
  • young adults
  • high intensity
  • healthcare
  • risk factors
  • early onset