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Published on: February 16, 2011
Quality end-of-life care: patients' perspectives
P A Singer1, D K Martin, M Kelner
1Toronto Hospital and the Department of Medicine, Joint Centre for Bioethics, University of Toronto, Ontario, Canada. peter.singer@utoronto.ca
Context:
Quality end-of-life care is increasingly recognized as an ethical obligation of health care providers, both clinicians and organizations. However, this concept has not been examined from the perspective of patients.
Objective:
To identify and describe elements of quality end-of-life care from the patient's perspective.
Design:
Qualitative study using in-depth, open-ended, face-to-face interviews and content analysis.
Setting:
Toronto, Ontario.
Participants:
A total of 126 participants from 3 patient groups: dialysis patients (n = 48), people with human immunodeficiency virus infection (n = 40), and residents of a long-term care facility (n = 38).
Outcome Measures:
Participants' views on end-of-life issues.
Results:
Participants identified 5 domains of quality end-of-life care: receiving adequate pain and symptom management, avoiding inappropriate prolongation of dying, achieving a sense of control, relieving burden, and strengthening relationships with loved ones.
Conclusion:
These domains, which characterize patients' perspectives on end-of-life care, can serve as focal points for improving the quality of end-of-life care.
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