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Which has more influence on a family's assessment of the quality of dying of their long-term care resident with dementia: Frequency of symptoms or quality of communication with healthcare team?

Olivia Charest-DrapeauVéronique ProvencherLise TrottierGuillaume LéonardMachelle WilcheskyGina Bravonull null
Published in: Palliative & supportive care (2022)
Our findings show that healthcare providers' ability to engage in the end-of-life conversations with families outweighs the frequency of symptoms in family assessments of the quality of dying of their relative with dementia. Enhancing healthcare providers' ability to communicate with families about the end-of-life care could improve families' perceptions of the quality of dying of their relative with dementia and, consequently, ease their grieving process.
Keyphrases
  • healthcare
  • palliative care
  • quality improvement
  • mild cognitive impairment
  • cognitive impairment
  • long term care
  • physical activity
  • depressive symptoms
  • social media