What matters most in end-of-life care: perceptions of seriously ill patients and their family members
- PMID: 16505458
- PMCID: PMC1389825
- DOI: 10.1503/cmaj.050626
What matters most in end-of-life care: perceptions of seriously ill patients and their family members
Abstract
Background: Initiatives to improve end-of-life care are hampered by our nascent understanding of what quality care means to patients and their families. The primary purpose of this study was to describe what seriously ill patients in hospital and their family members consider to be the key elements of quality end-of-life care.
Methods: After deriving a list of 28 elements related to quality end-of-life care from existing literature, focus groups with experts and interviews with patients, we administered a face-to-face questionnaire to older patients with advanced cancer and chronic end-stage medical disease and their family members in 5 hospitals across Canada to assess their perspectives on the importance. We compared differences in ratings across various subgroups of patients and family members.
Results: Of 569 eligible patients and 176 family members, 440 patients (77%) and 160 relations (91%) agreed to participate. The elements rated as "extremely important" most frequently by the patients were "To have trust and confidence in the doctors looking after you" (55.8% of respondents), "Not to be kept alive on life support when there is little hope for a meaningful recovery" (55.7%), "That information about your disease be communicated to you by your doctor in an honest manner" (44.1%) and "To complete things and prepare for life's end - life review, resolving conflicts, saying goodbye" (43.9%). Significant differences in ratings of importance between patient groups and between patients and their family members were found for many elements of care.
Interpretation: Seriously ill patients and family members have defined the importance of various elements related to quality end-of-life care. The most important elements related to trust in the treating physician, avoidance of unwanted life support, effective communication, continuity of care and life completion. Variation in the perception of what matters the most indicates the need for customized or individualized approaches to providing end-of-life care.
Comment in
-
"You can't always get what you want"--or can you?CMAJ. 2006 Feb 28;174(5):643-4. doi: 10.1503/cmaj.060029. CMAJ. 2006. PMID: 16505460 Free PMC article. No abstract available.
-
End-of-life care in Canada.CMAJ. 2006 Sep 12;175(6):619-20; author reply 620. doi: 10.1503/cmaj.1060101. CMAJ. 2006. PMID: 16966667 Free PMC article. No abstract available.
-
End-of-life care in Canada.CMAJ. 2006 Sep 12;175(6):620; author reply 620. doi: 10.1503/cmaj.1060096. CMAJ. 2006. PMID: 16966670 Free PMC article. No abstract available.
References
-
- Open Society Institute. Project on death in America. Available: www.soros.org/initiatives/pdia (accessed 2005 Dec 5).
-
- University of Montana. Promoting palliative care excellence in intensive care. Available: www.promotingexcellence.org (accessed 2005 Dec 5).
-
- Carstairs S, Beaudoin GA; Subcommittee to Update “Of Life and Death” of the Standing Senate Committee on Social Affairs, Science and Technology. Quality end-of-life care: the right of every Canadian. Final report. Ottawa: Senate of Canada; 2000. Available: www.parl.gc.ca/36/2/parlbus/commbus/senate/com-e/upda-e/rep-e/repfinjun0... (accessed 2006 Feb 1).
-
- Cohen SR, Mount BM, Strobel MG, et al. The McGill Quality of Life Questionnaire: a measure of quality of life appropriate for people with advanced disease. A preliminary study of validity and acceptability. Palliat Med 1995;9:201-19. - PubMed
-
- Liao Y, McGee DL, Cao G, et al. Quality of the last year of life of older adults: 1986 vs 1993. JAMA 2000;283:512-8. - PubMed
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Medical