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1Hospice and Family Medicine Physician at the Redwood City Medical Center in CA. gurpreet.k.padam@kp.org.
The Permanente Journal
|July 16, 2015
Summary
This study explores the existential distress and quality of life in patients with end-stage lung disease. It highlights the profound psychological impact of severe illness on patient autonomy and end-of-life wishes.
Area of Science:
- Palliative Care
- Pulmonary Medicine
- Medical Ethics
Background:
- End-stage lung disease significantly impacts patients' physical and psychological well-being.
- Patient autonomy and end-of-life wishes are critical considerations in palliative care.
- Existential distress is a common yet often under-addressed aspect of severe chronic illness.
Purpose of the Study:
- To explore the lived experience of an 80-year-old male patient with end-stage lung disease.
- To understand the patient's perspective on quality of life and end-of-life care.
- To examine the intersection of severe illness, independence, and the desire for continued life.
Main Methods:
- Qualitative narrative inquiry based on a patient encounter.
- Focus on the patient's verbatim statements and observed physical presentation.
- Exploration of the patient's expressed desire regarding life-prolonging treatments.
Main Results:
- The patient expressed profound fatigue and difficulty with basic movements.
- The patient articulated a desire not to prolong life, questioning its quality.
- The patient's statement reflects a complex emotional and existential state.
Conclusions:
- End-stage lung disease presents significant challenges to a patient's quality of life and sense of self.
- Patient autonomy in end-of-life decision-making, including the refusal of life-prolonging measures, is paramount.
- Further research is needed to address existential distress and support patient autonomy in palliative care settings.