Bereaved family member perceptions of patient-focused family-centred care during the last 30 days of life using a mortality follow-back survey: Does location matter?

Fred Burge, Beverley Lawson, Grace Johnston, Yukiko Asada, Paul F. McIntyre, Eva Grunfeld, Gordon Flowerdew

Research output: Contribution to journalReview articlepeer-review

42 Citations (Scopus)

Abstract

Background: Improving end-of-life care is an important international issue. Recently Nova Scotia researchers conducted a mortality follow-back survey to provide a population-based description of care provided to adults during their last 30 days of life as perceived by knowledgeable bereaved family members. Here we describe the relationship between the location where the decedent received the majority of care during their last 30 days and the informant's perception of the extent of unmet need, as defined by multiple domains of patient-focused, family-centred care. Method. Death certificate identified informants (next-of-kin) of eligible adults who died between June 2009 and May 2011, in Nova Scotia, Canada were invited to participate in a telephone interview based on the After-Death Bereaved Family Member Interview. Whether or not the informant expressed unmet need or concerns for six patient-focused, family-centred care domains were assessed in relation to the location where the majority of care occurred during the decedent's last 30 days. Results: 1358 informants took part (25% response rate). Results of 1316 eligible interviews indicated home (39%) was the most common location of care, followed by long-term care (29%), hospital (23%) and hospital-based palliative-care units (9%). Unmet need ranged from 5.6% for dyspnea help to 66% for the emotional and spiritual needs of the family. Although the mean score for overall satisfaction was high (mean = 8.7 in 1-10 scale; SD 1.8), 57% were not completely satisfied. Compared to home, adjusted results indicated greater dissatisfaction with overall care and greater communication concerns in the hospital. Greater unmet need occurred at home for dyspnea. Less overall dissatisfaction and unmet need were expressed about care provided in long-term care facilities and hospital-based palliative-care units. Conclusion: Bereaved informants were generally highly satisfied with the decedent's care during their last 30 days but variations were evident. Overall, no one location stood out as exceptionally different in terms of perceived unmet need within each of the patient-focused, family-centred care domains. Communication in various forms and family emotional and spiritual support were consistently viewed as lacking in all locations and identified as targeted areas for impacting quality care at end of life.

Original languageEnglish
Article number25
JournalBMC Palliative Care
Volume13
Issue number1
DOIs
Publication statusPublished - May 14 2014

Bibliographical note

Funding Information:
A mortality follow-back survey design was used to gather information about the experience of care provided to adults who died in the province of Nova Scotia, Canada, during their last 30 days of life, as perceived by a knowledgeable informant. Nova Scotia is a small, eastern province (population 950,000) with the highest proportion of residents aged 65 years and older in Canada [18] and with one of the highest population rates of cancer and diabetes [19,20]. Physician, hospital and homecare services are government supported as are medications for those 65 years of age and older. Long-term care (nursing home) residency is subsidized for those with insufficient income. Ethical approval for this research was provided by the Capital Health Research Ethics Board, Halifax Nova Scotia.

Funding Information:
We wish to thank the management and staff of Nova Scotia Vital Statistics for their invaluable help with this project and all the people of Nova Scotia contacted by us to participate. We would also like to acknowledge our two survey interviewers, Jillian Demmons and Cassandra Yonder for their devotion to the bereaved and their compassionate listening skills. Funding for this study was provided by an operating grant awarded from the Canadian Institute for Health Research, MOP-93711. Additional support for the data collection phase was provided by the Network of End of Life Studies (NELS-ICE), Dalhousie University, through a Canadian Institutes of Health Research, Interdisciplinary Capacity Enhancement Grant – Reducing Health Disparities and Promoting Equity for Vulnerable Populations, FRN-80067.

ASJC Scopus Subject Areas

  • General Medicine

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