End of Life

Analyze the impact of the Patient Self-Determination Act on the end-of-life decision-making process.
What is it?
Why was it developed? What issues influenced its conception?
How does it impact patient rights?
How does it impact healthcare facilities?
Describe the impact of state law on advance directives and end-of-life decisions.
How do laws vary state by state?
What impact have they had on the “right to die” of an individual?
How have they affected pain management and care (e.g., medical marijuana, palliative care)?
Explain what advance care planning and advance directives are and how they are related.
What documentation is needed as a part of advance planning and directives?
Who is involved in the process (e.g., lawyers, doctors, family, patient)?
What decisions have to be made?
How explicit does planning have to be?
How does age impact planning?
Discuss the implications of missing directives for dying patients.
How are decisions made?
Who is responsible?
How does the facility where treatment is provided impact the level/type of care?
Discuss the intersection between medical ethics, religious/cultural beliefs, and regulations in healthcare as they relate to end-of-life decisions.
What are some similarities and differences in views on dying?
How do ethics, beliefs, and regulations impact recommendations for certain treatments or a course of action/care?
How do they impact funding or coverage of care?
What impact do they have on allowing interventions to begin, removing interventions such as life support, and dealing with the body once someone is dead?

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