N304: Palliative Flashcards
How are the terms “hospice & palliative care” used in Canada?
In Canada, the terms “hospice” and “palliative care” are often used interchangeably to denote a philosophy of care. In fact the term “hospice palliative care” has been adopted by the Canadian HPC Association and utilized to indicate the integration of care throughout a variety of settings. In addition, the word “hospice” may refer to a place of care.
Describe the term hospice
Primarily a ‘concept’ of care- not always a specific place of care, but often combined
i.e. a specific philosophy of and/or approach to care rather than merely a type of building or service, or both.
Describe the term palliative care
Palliative care is an approach that improves the quality of life of patients and their families facing the problem associated with life-threatening illness, through the prevention and relief of suffering by means of early identification and impeccable assessment and treatment of pain and other problems, physical, psychosocial and spiritual.
-guided by the principles of Primary Health Care: accessible, participatory, interprofessional, health promoting, uses appropriate technology/skills
What are the concepts of palliative care?
- affirms life/regards dying as normal process
- neither hastens nor postpones death (relieve suffering)
- provides relief from pain/other symptoms
- integrates psychological/spiritual aspects of care
- offers ongoing support systems to dying pts. and family members
What is mean’t by “Palliative Care is a human right”
An ageing population, a growing incidence and prevalence of cancer, and a growing HIV/AIDS epidemic has brought increased attention to palliative care as a public health issue and a human right.
What is the curative focus?
Diagnosis of disease & related symptoms
Curing of disease
Treatment of disease
Alleviation of symptoms
What is the palliative focus?
Pt/family identify unique end-of-life goals
Assess how symptoms, issues are helping/ hindering reaching goals
Interventions to assist in reaching end-of-life goals
Quality of life closure
What are the guiding principles of hospice and palliative care?
- Person/family centered = basic ‘unit of care’
- Ethical
- High Quality
- Team –based/Circle of Care
- Safe and Effective
- Accessible
- Adequately Resourced /sufficient to support HPC activities
- Collaborative
- Advocacy-Based
- Evidence-Informed/Knowledge-Based
What are the goals of palliative care?
- Assure pt. receives excellent pain control/other symptom(nausea, dyspnea, secretions)/comfort measures
- Give pt. information needed to participate in care decisions
- offer ongoing emotional/spiritual support
- obtain expert help in planning care outside hospital i.e. Discharge Planning
What is evidence based palliative care?
• Evidence-based practice is the conscious, explicit and judicious use of current evidence in making decisions about the care of individual patients.
• It is more difficult to measure quality of life and altered outcomes in patients and families whose illness or frailty make it difficult to collect data.
Outcome and quality of life measures need to be sensitive to the wider aspects of palliative care, not merely mortality, function, or absence of symptoms.
• Those working in palliative care must use existing research through appropriate systematic reviews to maximize the value of data yielded in caring for patients and families.
Why do we need to use evidence based practice?
To provide the best care possible and…
To help:
• Inform health care providers, patients and families.
• Educate health care providers and the public.
• Include all members of the health care team.
• Improve clinical decision-making.
• Reduce variation in professional practice e.g. reduce preconceived notions such as “the pt. is drug seeking”
• Ensure equitable allocation of resources.
• Measure the quality of our care.
• Identify opportunities for improvement.
• Improve management of the health care system.
• Provide a foundation for the future.
Describe quality of life
There are many models of quality of life, the important aspect is that they encompass all dimensions and focus on what is important for the patient and the ‘family’.
What are the 4 domains of quality of life?
- physical: functional ability, strength/fatigue, rest & sleep, nausea, appetite, constipation, pain.
- psychological: anxiety, depression, enjoyment, leisure, pain, distress, happiness, fear, cognition, attention.
- social: financial burden, caregiver burden, roles/relationships, affection/sexual function, appearance.
- spiritual: hope, suffering, meaning of pain, religiosity, transcendence.
What is bereavement?
- Bereavement is the time we spend adjusting to loss.
- There is no standard time limit and there is no right or wrong way to feel during the bereavement period
- everyone must learn to cope in their own way. The time spent in a period of bereavement may depend on how attached the person was to the person who died, and how much time was spent anticipating the loss.
- As with grief, it is individual and complex.
Bereavement counselling can offer an understanding of the mourning process and explore areas that could potentially prevent you from moving on.
What are the 7C’s of quality hospice palliative care
Competence Consistency Coordination Climate Cooperation Communication Compassion