Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Multicenter Study
. 2010 Nov 9;182(16):E747-52.
doi: 10.1503/cmaj.100131. Epub 2010 Oct 4.

Defining priorities for improving end-of-life care in Canada

Affiliations
Multicenter Study

Defining priorities for improving end-of-life care in Canada

Daren K Heyland et al. CMAJ. .

Abstract

Background: High-quality end-of-life care should be the right of every Canadian. The objective of this study was to identify aspects of end-of-life care that are high in priority as targets for improvement using feedback elicited from patients and their families.

Methods: We conducted a multicentre, cross-sectional survey involving patients with advanced, life-limiting illnesses and their family caregivers. We administered the Canadian Health Care Evaluation Project (CANHELP) questionnaire along with a global rating question to measure satisfaction with end-of-life care. We derived the relative importance of individual questions on the CANHELP questionnaire from their association with a global rating of satisfaction, as determined using Pearson correlation coefficients. To determine high-priority issues, we identified questions that had scores indicating high importance and low satisfaction.

Results: We approached 471 patients and 255 family members, of whom 363 patients and 193 family members participated, with response rates of 77% for patients and 76% for families. From the perspective of patients, high-priority areas needing improvement were related to feelings of peace, to assessment and treatment of emotional problems, to physician availability and to satisfaction that the physician took a personal interest in them, communicated clearly and consistently, and listened. From the perspective of family members, similar areas were identified as high in priority, along with the additional areas of timely information about the patient's condition and discussions with the doctor about final location of care and use of end-of-life technology.

Interpretation: End-of-life care in Canada may be improved for patients and their families by providing better psychological and spiritual support, better planning of care and enhanced relationships with physicians, especially in aspects related to communication and decision-making.

PubMed Disclaimer

Figures

Figure 1
Figure 1
The performance–importance grid, as derived from a plot of the mean score for each question on the Canadian Health Care Evaluation Project (CANHELP) questionnaire for patients (measuring satisfaction with care) and the correlation coefficient for each question’s association with overall satisfaction from the patient’s point of view. Gridlines correspond to the median of the mean scores on each question (4.12) and the median of the correlation coefficients (0.29). Note: × = the plotted value; the number closest to the × is the corresponding CANHELP question number.

References

    1. Carstairs S, Beaudoin GA. Quality end of life care: the right of every Canadian. Ottawa (ON): Senate of Canada; 2000. [(accessed 2010 July 8)]. Available: www.parl.gc.ca/36/2/parlbus/commbus/senate/com-e/upda-e/rep-e/repfinjun0....
    1. Heyland DK, Groll D, Rocker G, et al. Canadian Researchers at the End of Life Network (CARENET) End of life care in acute care hospitals in Canada: A quality finish? J Palliat Care. 2005;21:142–150. - PubMed
    1. Carstairs S. Still not there Quality end-of-life care: a progress report. Ottawa (ON): Senate of Canada; 2005. [(accessed 2010 July 8)]. Available: http://sen.parl.gc.ca/scarstairs/PalliativeCare/PalliativeCare_e.asp.
    1. Workman S, Mann OE. “No control whatsoever”: end-of-life care on a medical teaching unit from the perspective of family members. QJM. 2007;100:433–40. - PubMed
    1. Giles S. Palliative stage Parkinson’s disease: patient and family experiences of health-care services. Palliat Med. 2009;23:120–5. - PubMed

Publication types

MeSH terms