Palliative Care Flashcards

1
Q

Identify what patients want during the last stages of a terminal illness

A
  • Pain and symptom control
  • Avoid inappropriate prolongation of the dying process
  • Achieve a sense of control
  • Relieve burdens on family
  • Strengthen relationships with loved ones
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2
Q

Provide a definition of palliative care.

A
  • Palliative care is specialized medical care for people with serious illnesses. It is focused on providing patients with relief from the symptoms, pain, and stress of a serious illness – whatever the diagnosis. The goal is to improve quality of life for both the patient and the family
  • Palliative care is provided by a team of doctors, nurses, and other specialists who work together with a patient’s other doctors to provide an extra layer of support. It is appropriate at any stage in a serious illness and can be provided along with curative treatment.
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3
Q

List the seven major skills needed when delivering palliative care.

A
  • Communication
  • Decision making
  • Management of disease-related complications
  • Symptom control
  • Psychological and spiritual care
  • Care of the dying
  • Coordination of care of continuity
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4
Q

List the information needs of palliative care patients.

A
  • Understanding of their illness and treatment options
  • Unrealistic expectations
  • Help making priorities for the future
  • Care for themselves
  • Participation in treatment decisions
  • A sense of autonomy and control as a way of coping with serious illness
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5
Q

State the potential barriers to communication about serious illness care goals.

A
  • Patient factors
  • Physician factors
  • System factors
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6
Q

Patient factors that can be a barrier to communication

A

o Patient emotions

o Patient expectations

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7
Q

Physician factors that can be a barrier to communication

A

o Lack of serious illness conversation training
o Timing of conversations
o Uncertainty about prognostic accuracy
o Uncertainty of how to address patient’s and family’s psychosocial concerns

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8
Q

System factors that can be a barrier to communication

A

o Ambiguity about who is responsible
o Life-sustaining treatment is a default approach
o Lack of a systematic approach to serious illness care planning
o Variation in location and quality of documentation in electronic health records

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9
Q

Identify the questions that should be asked of or the information that should be shared with patients and their family during a conversation about serious illness

A
  • Understanding: What is your understanding now of where you are with your illness?
  • Information preferences: How much information about what is likely to be ahead with your illness would you like from me?
  • Prognosis: Share prognosis as a range, tailored to information preferences
  • Goals: If your health situation worsens, what are your most important goals?
  • Fears/Worries: What are your biggest fears and worries about the future with your health?
  • Function: What abilities are so critical to your life that you can’t imagine living without them?
  • Trade-offs: If you become sicker, how much are you willing to go through for the possibility of gaining more time?
  • Family: How much does your family know about your priorities and wishes?
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10
Q

State how using the “wish/worry/wonder” framework allows providers to connect with patients during a conversation about serious illness

A
  • “I wish . . .” statements allow for aligning with the patients hope
  • “I worry . . .” statements allow for being truthful while sensitive
  • “I wonder . . .” statements are a subtle way to make a recommendation
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11
Q

Provide a definition of shared decision-making.

A

Collaboration in which the physician shares with the patient medical knowledge and opinion, and the patient shares with the physician values and preferences

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