Palliative Care Flashcards
Identify what patients want during the last stages of a terminal illness
- 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
Provide a definition of palliative care.
- 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.
List the seven major skills needed when delivering palliative care.
- Communication
- Decision making
- Management of disease-related complications
- Symptom control
- Psychological and spiritual care
- Care of the dying
- Coordination of care of continuity
List the information needs of palliative care patients.
- 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
State the potential barriers to communication about serious illness care goals.
- Patient factors
- Physician factors
- System factors
Patient factors that can be a barrier to communication
o Patient emotions
o Patient expectations
Physician factors that can be a barrier to communication
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
System factors that can be a barrier to communication
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
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
- 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?
State how using the “wish/worry/wonder” framework allows providers to connect with patients during a conversation about serious illness
- “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
Provide a definition of shared decision-making.
Collaboration in which the physician shares with the patient medical knowledge and opinion, and the patient shares with the physician values and preferences