palliative care 1c Flashcards

1
Q

Standards for providing quality
care for palliative patients in
Australia (developed 2005

A

All care, decision-making and planning are based
on the uniqueness of the patient and their families.
 Holistic care of the patient is emphasised.
 Ongoing assessment and treatment is vital
 Care is co-ordinated.
 The primary caregiver is supported and educated.
 The needs and comfort of the dying patient is
emphasised.
 Philosophy of care supplies compassionate and
competent care

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2
Q

Standards for providing quality
care for palliative patients in
Australia

A

Access to bereavement care
 Community capacity is adequate to provide
adequate care through collaboration and
partnerships.
 Quality improvement and research.
 Access to care is available regardless of geography,
diagnosis, age
 Staff are adequately trained.
 Staff are encouraged to care for themselves

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3
Q

The importance of educating
health professionals about
palliative care

A

 To correct misconceptions about palliative care
 To assist in the identification of palliative needs in their
patients
 To upskill providers in the provision of palliative care
within their scope of practice and where appropriate.
 Assist in referral to specialist palliative care services or
consultation, and when this is required
 To assist providers to work collaboratively with specialist
palliative care providers.
 Education should also increase the comfort level of
health professionals working with people approaching
the end of heir lives

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4
Q

Support for health professionals

who work in palliative care.

A

 Breaking bad news about diagnosis and/or prognosis to a
person living with a life-limiting illness and their family;
 Coping with medicine’s inability to offer these people a cure
 Repeated exposure to the death of people with whom they
may have formed relationships
 Involvement in emotional conflicts with people living with a
life-limiting illness, their families carers, or with other members of
the palliative team;
 Absorption of the anger, grief, and despair expressed by
people living with a life-limiting illness, their families and carers;
 Challenges to one’s personal belief system about the medical
network, teamwork, death, and dying.

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