Palliative Part 1 Flashcards

1
Q

What is a hospice?

A
  • Primarily a ‘concept’ of care - not always a specific place of care, but often combined
  • E.g. specific philosophy of and/or approach to care rather than merely a type of building, service or both
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2
Q

What is palliative care?

A
  • Approach that improves the quality of life of patients and their families facing the problem associated with life-threatening illness
  • Prevention/relief of suffering by means of early identification, assessment, tx of pain and other physical, psycho-social and spiritual problems
  • Guided by principles of primary healthcare
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3
Q

What are the principles of primary health care?

A

Accessible, participatory, inter-professional, health promoting, uses appropriate technology/skills

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4
Q

What does the Canadian Hospice Palliative Care Association consider palliative care to be?

A
  • Affirms life, regards dying as a normal process
  • Neither hastens nor postpones death
  • Provides relief from pain/other symptoms
  • Integrates psychological/spiritual aspects of care
  • Offers ongoing support systems to dying pt’s and family members
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5
Q

What has brought forth the issue of palliative care as a human right?

A

An aging population, growing incidence and prevalence of cancer, and a growing HIV/AIDS epidemic, have all increased attention to palliative care as a public health issue and a human right

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6
Q

Describe the difference between curative focus and palliative focus:

A

CURATIVE: disease-specific, treatments

PALLIATIVE: comfort/supportive treatments

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7
Q

What is the focus of curative?

A
  • Dx of disease and related symptoms
  • Curing/tx of disease
  • Alleviation of symptoms
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8
Q

What is the focus of palliative?

A
  • 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
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9
Q

What are the ten guiding principles of hospice palliative care?

A

1) Person/family centered
2) Ethical
3) High quality
4) Team-based
5) Safe and effective
6) Accessible
7) Adequately resourced
8) Collaborative
9) Advocacy-based
10) Evidence-informed/knowledge-based

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10
Q

What are the goals of palliative care?

A
  • Assure pt receives excellent pain control/other symptom/comfort measures
  • Give pt information needed to participate in care decisions
  • Offer ongoing emotional/spiritual support
  • Obtain expert help in planning care outside the hospital (e.g. discharge planning)
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11
Q

What is evidence-based practice?

A
  • The conscious decision to use current evidence in making decisions about the care of individual pt’s
  • Those working in palliative care must use existing research through systematic reviews to maximize the value of data yielded in caring for pt’s/families
  • Outcome and quality of life measures need to be sensitive to wider aspects of palliative care (not merely mortality, function, etc.)
  • More difficult to measure quality of life and altered outcomes in pt’s/families whose illness or frailty make it difficult to collect data
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12
Q

What physical affects influence quality of life?

A
  • Functional ability
  • Strength/fatigue
  • Sleep/rest
  • n/v
  • Appetite
  • constipation
  • pain
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13
Q

What psychological affects influence quality of life?

A
  • Anxiety/depression
  • Enjoyment/leisure
  • Pain distress
  • Happiness
  • Fear
  • Cognition/attention
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14
Q

What social affects influence quality of life?

A
  • Financial burden
  • Caregiver burden
  • Roles/relationships
  • Affection/sexual function
  • Appearance
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15
Q

What spiritual affects influence quality of life?

A
  • Hope
  • Suffering
  • Meaning of pain
  • Religiosity
  • Transcendence
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16
Q

What is bereavement?

A
  • Time we spend adjusting to loss
  • No standard time limit, no right/wrong way to feel - everyone must learn to cope in their own way
  • Time spent in bereavement may depend on how attached the person was to the person who died, and how much time was spent anticipating the loss
  • Bereavement counseling can offer an understanding of the mourning process, explore areas that could potentially prevent you from moving on
17
Q

What are the 7 C’s of quality hospice palliative care?

A

1) Competence
2) Consistency
3) Coordination
4) Climate
5) Cooperation
6) Communication
7) Compassion

18
Q

What is the constant factor extending across hospice palliative care in different settings?

A

Nurses!

19
Q

What is the six dimensions of the supportive care model?

A

Valuing:

1) Connecting
2) Empowering
3) Doing for (what can I do for the family?)
4) Finding meaning
5) Preserving integrity
6) Self-care

20
Q

What is involved in life closure?

A
  • Completion with worldly affairs
  • Completion of community relationships
  • Meaning about one’s individual life
  • Love of self
  • Love of others
21
Q

Which clients are served by palliative services?

A
  • Pt’s and families with a life threatening illness or facing end of life issues
  • Anticipated prognosis of weeks or months rather than years
  • Primary intent of tx is improved quality of life, not curative
  • Pt/family agree to the referral or to consultative support
  • DNR/”no code” status will be required for admission to hospice unit, but not for program
22
Q

What services are available to patients in palliative settings?

A
  • Visits by home care nurse
  • Community HCP’s
  • Support from consult team for managing symptoms such as pain/nausea
  • Family conferences
  • Grief/bereavement counseling
  • Hospice volunteer visits
  • Access to hospice facility/specialized hospital beds in acute care
  • Equipment/supplies
23
Q

What is the role of the community palliative team?

A
  • Education and support to care providers, the community, individuals and families
  • Consultation around pain and symptom management, discharge planning
  • Coordination and planning of care
  • Participation in case conferences
  • Services in residential care, acute care, and in the community
24
Q

Why should HCP’s consult community palliative teams?

A
  • pain & symptom management
  • psycho-social issues
  • ineffective family or caregiver coping
  • care planning
  • end of life issues
  • assessment re: need for hospice, acute or tertiary palliative care bed
25
Q

What settings will a consultation team might appear?

A
  • Home care
  • Palliative care unit
  • Residential care
  • Hospice
  • Acute care hospital
26
Q

In what family/pt situations is it appropriate to refer to tertiary units?

A
  • difficult pain syndromes
  • complex physical symptom assessment/management
  • complex psychological/spiritual/social issues
  • significant family /caregiver distress
  • extensive support required to improve QOL
  • complex care planning exceeding resources at present community site
27
Q

Why might an acute care bed be utilized?

A
  • Short stay beds for pt’s requiring diagnostic tests and treatments
  • Consult from hospice palliative team can occur in acute care
28
Q

What is the admission criteria for hospice?

A
  • End-stage, length of stay (LOS) maximum 3 months with average expected to be 16-22 days
  • Symptom management plan in place
  • DNR (Do Not Resuscitate) must be written
  • Patient may be admitted under family physician
  • Family physician involves consultation team
  • FH resident with patient placement as close to own community as possible.
29
Q

What is the most common entry point to identifying the need for hospice palliative care support?

A

Home Care referral

30
Q

What does the BC Palliative Care Benefits program provide?

A

Medications, equipment and supplies

31
Q

When is residential care utilized?

A
  • People with many months to live who cannot remain at home can be cared for in long-term care facilities
  • Palliative care teams can be consulted to provide support to patients in a residential facility