Provide Palliative Care

Palliative care is person and family-centred care provided for a person:

  • with an active, progressive, or advanced disease
  • who has little or no prospect of cure
  • who is expected to die
  • for whom the primary goal is to optimise the quality of life. [1]

Palliative care helps people live their life as fully and as comfortably as possible with a life-limiting or terminal illness. It identifies and treats symptoms which may be physical, emotional, spiritual or social. [1]

Providing palliative care ensures the needs of the person are met and they receive timely and equitable access to end-of-life care. [2, 3] Person-centred dementia care in the context of the end of life reflects the importance of valuing the person with dementia. The acronym VIPS (very important persons) is an easy way to identify the key person-centred care principles. [4, 5]

V Value people with dementia and those who care for them promoting their citizenship rights and entitlements regardless of age or cognitive ability.
I Treat people as individuals, appreciating that all people with dementia have a unique history, personality, physical and mental health, and social and economic resources. Their positioning will affect their response to neurological impairment.
P Look at the world from the perspective of the person with dementia recognising that each person’s experience has its own psychological validity, that people with dementia act from this perspective and that empathy with this perspective has its own therapeutic potential.
S Recognise that all human life including that of people with dementia is grounded in relationships. People with dementia require an enriched social environment which both compensates for their impairment and fosters opportunities for personal growth. [4, 5]

The VIPS model of person-centred care and the principles of palliative care are aligned. The Principles of Palliative and End-of-Life Care (Principle 5) [6] states that the palliative care needs of people with dementia or cognitive impairment should be understood and met, including:

  • Dementia is recognised as a terminal illness.
  • Whenever possible, staff will promote and assist with end-of-life care planning and decision-making with early involvement of the person living with dementia, their family and carers at the time of a dementia diagnosis.
  • Appropriate care will be provided to people with dementia with related behavioural and psychological symptoms or cognitive impairment, ensuring all necessary services, including end-of-life care, are identified, documented, and accessed.
  • Substitute decision-makers are actively engaged in discussions about the needs and preferences of the person with dementia. [6]

    Palliative care is person and family-centred care provided for a person:

    • with an active, progressive, or advanced disease
    • who has little or no prospect of cure
    • who is expected to die
    • for whom the primary goal is to optimise the quality of life. [1]

    Palliative care helps people live their life as fully and as comfortably as possible with a life-limiting or terminal illness. It identifies and treats symptoms which may be physical, emotional, spiritual or social. [1]

    Providing palliative care ensures the needs of the person are met and they receive timely and equitable access to end-of-life care. [2, 3] Person-centred dementia care in the context of the end of life reflects the importance of valuing the person with dementia. The acronym VIPS (very important persons) is an easy way to identify the key person-centred care principles. [4, 5]

    V Value people with dementia and those who care for them promoting their citizenship rights and entitlements regardless of age or cognitive ability.
    I Treat people as individuals, appreciating that all people with dementia have a unique history, personality, physical and mental health, and social and economic resources. Their positioning will affect their response to neurological impairment.
    P Look at the world from the perspective of the person with dementia recognising that each person’s experience has its own psychological validity, that people with dementia act from this perspective and that empathy with this perspective has its own therapeutic potential.
    S Recognise that all human life including that of people with dementia is grounded in relationships. People with dementia require an enriched social environment which both compensates for their impairment and fosters opportunities for personal growth. [4, 5]

    The VIPS model of person-centred care and the principles of palliative care are aligned. The Principles of Palliative and End-of-Life Care (Principle 5) [6] states that the palliative care needs of people with dementia or cognitive impairment should be understood and met, including:

    • Dementia is recognised as a terminal illness.
    • Whenever possible, staff will promote and assist with end-of-life care planning and decision-making with early involvement of the person living with dementia, their family and carers at the time of a dementia diagnosis.
    • Appropriate care will be provided to people with dementia with related behavioural and psychological symptoms or cognitive impairment, ensuring all necessary services, including end-of-life care, are identified, documented, and accessed.
    • Substitute decision-makers are actively engaged in discussions about the needs and preferences of the person with dementia. [6]
  • How to provide palliative care for people with dementia

  • How to build knowledge, confidence and skills in providing palliative care for people with dementia

  • Information for families and carers

Page updated 23 September 2026