Palliative and End-of-Life Care[ PDF (565 KB) | Help ]
The term palliative care refers not only to the care and management of patients approaching the end of life but also addresses the reduction of suffering throughout the course of illness and, for family, into bereavement. Palliative and end-of-life care, although traditionally associated with cancer care, intersects with a number of other clinical disciplines, such as cardiology, respiratory medicine, critical care, nephrology, pediatrics and neurology. As our aging population continues to grow and modern medicine provides the means to prolong the life of individuals with a variety of life-limiting diseases and conditions, society struggles with the ethical and legal questions around "appropriate" use of health care resources. Quality of care toward and at the end of life is also a significant issue. Many of the people who could benefit from palliative and end-of-life care do not receive it. All too often it is left to patients, their families and a loosely knit community of volunteer organizations to sort through the myriad of physical, psychological, spiritual and ethical choices.
The key to change lies in rigorous scientific research that will provide the evidence for informed decision making by clinical practitioners and policy makers. Historically, palliative and end-of-life care research has been underfunded in Canada and small groups of highly committed and dedicated researchers have struggled to obtain recognition for the field as an independent health discipline.
Palliative and end-of-life care was identified by the CIHR Institute of Cancer Research (ICR) as one of its six original strategic research priorities in 2002. As a first step, ICR immediately took advantage of the opportunity to partner on two programs already approved for CIHR funding. The first was a New Emerging Team (NET) project led by Dr. Pierre Allard, from the University of Ottawa that focused on the structure, process, quality and outcomes of end-of-life care for older persons and how personal, social and environmental factors affect care. This $300,000 per year five-year project, submitted in response to a Request for Applications (RFA) launched by the CIHR Institute of Aging (IA), was jointly funded by ICR and IA. The second was a CIHR Strategic Training Program grant led by Dr. Robin Cohen of McGill University designed to give students and new researchers exposure to all aspects of palliative and end-of-life care and train them to transfer their results quickly to the clinicians who work as front line contacts in palliative care. ICR and the Canadian Cancer Society (CCS), through the National Cancer Institute of Canada (NCIC), partnered equally on the funding of this $300,000 per year six-year program.
Palliative and End-of-Life Care Initiative
In June 2003, CIHR and partners launched a palliative and end-of-life care initiative that reflected the multiple needs of the palliative care research community. The initiative was designed to support infrastructure development, enhance interdisciplinary research collaboration, encourage the development of early career researchers and attract trainees to this emerging area. This multidisciplinary initiative supported nineteen Pilot Projects, nine New Emerging Team Grants, and one Career Transition Award. This initiative along with the previously funded NET and Strategic Training Program represents a total investment of $16.5 million over six years into palliative and end-of-life care research, the largest research investment in this field ever made in Canada.
This extraordinary investment was made possible by the contributions of many partners. The support of the provincial cancer boards and agencies made it possible to fund research teams across the country, forming the basis of a national network in palliative and end-of-life care research.
Partners Supporting Palliative and End-of-Life Care Research
- Alberta Cancer Board
- British Columbia Cancer Agency
- Canadian Breast Cancer Research Alliance
- Cancer Care Manitoba
- CIHR Institute of Aboriginal Peoples' Health (IAPH)
- CIHR Institute of Aging (IA)
- CIHR Institute of Cancer Research (ICR)
- CIHR Institute of Circulator and Respiratory Health (ICRH)
- CIHR Institute of Gender and Health (IGH)
- CIHR Institute of Health Services and Policy Research (IHSPR)
- CIHR Institute of Human Development, Child and Youth Health (IHDCYH)
- CIHR Institute of Neurosciences, Mental Health and Addiction (INMHA)
- CIHR Knowledge Translation Branch Health Canada
- Heart and Stroke Foundation of Canada
- National Cancer Institute of Canada
- National Ovarian Cancer Association
ICR continued to invest in this strategic priority area through the CIHR Institute of Gender and Health-led Reducing Health Disparities & Promoting Equity for Vulnerable Populations Interdisciplinary Capacity Enhancement (ICE) grants. McMaster University's Dr. Allison Williams and Dr. Donna Wilson received funding for an ICE grant entitled "Timely access & seamless transitions in rural palliative/end-of-life care". This grant focuses on timely access to palliative care in rural communities, encompassing two of ICR's major priority areas (Palliative and End-of-Life Care and Access to Quality Cancer Care).
Results and Outcomes
Palliative and End-of-Life Care: Pilot Projects
Nineteen one-year Pilot Project grants, designed to target and assess innovative approaches in implementing palliative and end-of-life care, were funded. The purpose of these grants was to target and assess innovative approaches in implementing palliative and end-of-life care. Nineteen pilot projects were funded from across the country. The pilot projects examined a wide range of research topics including end-of-life quality indicators in lung cancer; end-of-life health care costs; pediatric palliative care surveillance; and palliative care service utilization.
|Principal Investigator||Institution Name||Project Title|
|Alibhai, Shabbir||University Health Network||A pilot study to evaluate quality of life in patients age 60 or older with newly diagnosed acute myeloid leukaemia.|
|Aubin, Michèle||Université Laval||Évaluation d'un programme de soulagement de la douleur chez les personnes âgées en perte grave d'autonomie vivant en milieu de soins de longue durée : projet pilote.|
|Baracos, Vickie||University of Alberta||Nutritional supportive care: amino acids required to support maintenance and deposition of lean body mass in patients with advanced cancer.|
|Barbera, Lisa||Sunnybrook and Women's College||Health Sciences Palliative and end-of-life quality indicators in lung cancer.|
|Duggleby, Wendy||University of Saskatchewan||A pilot study of the hope focused program for informal caregivers of palliative home care patients.|
|Fassbender, Konrad||Alberta Cancer Board||Patterns and predictors of palliative care service utilization.|
|Gagnon, Bruno||McGill University||Characterizing cognitive failure, physical retardation and hypo-active delirium in advanced cancer patients, a pilot project.|
|Grunfeld, Eva||Dalhousie University||Quality indicators for end-of-life breast cancer care: is there agreement between stakeholder groups in two provinces?|
|Grunfeld, Eva||Dalhousie University||Quality indicators for end-of life breast cancer care: testing the use of administrative databases in two provinces.|
|Hampton, Mary||University of Regina||Developing and piloting cross-cultural curriculum for delivery and utilization of end of life health care services.|
|Kiceniuk, Deborah||Dalhousie University||An examination of end-of-life health care costs in Nova Scotia.|
|Leis, Anne||University of Saskatchewan||Prevalence of palliative patients and their health services utilization in Saskatchewan: A feasibility study.|
|Schondorf, Ronald||Sir Mortimer B. Davis Jewish General Hospital||Does autonomic nervous system dysfunction contribute to the morbidity of patients with advanced gastrointestinal and non small cell lung cancer? A pilot study.|
|Simpson, John Steven||University of Calgary||A pilot project to assess the impact of a novel psychosocial intervention on the quality of life, attitudes to death and dying, and spirituality of palliative cancer patients.|
|Vigano, Antonio||McGill University||Prognostic value of the angiotensin-converting enzyme gene polymorphism in advanced cancer: A pilot study.|
|Viola, Raymond||Queen's University||Community palliative cancer care - A pilot study using linked databases.|
|Ward-Griffin, Mary||University of Western Ontario||Exploring client-family-nurse relationships in home-based palliative care for seniors.|
|Widger, Kimberley||IWK Health Centre||Pediatric palliative care surveillance pilot project.|
|Wing, Simon||McGill University||Role of lysosomal proteolysis in mediating the muscle wasting of cachexia.|
The following highlights a small selection of the outcomes from the 19 funded pilot projects.
"Developing and piloting cross-cultural curriculum for delivery and utilization of end-of-life health care services" - Dr. Mary Hampton, University of Regina
Dr. Hampton's pilot project examined the underutilization of palliative care services by Canadian Aboriginal communities. Using Community Action Research methodology Dr. Hampton's team created two videos to address the following objectives (1) inform Region's Regional Palliative and Hospice Care Service of life health care providers of culturally sensitive protocol when dealing with Aboriginal families; (2) inform the community of end-of-life care services (increase awareness); and (3) increase Aboriginal families' use of these services. Dissemination of the results of the pilot project has been achieved through the distribution of the two videos and the presentation of the research findings to a variety of audiences. The videos have been sold on a cost recovery basis to health care providers, including Aboriginal Initiatives, Canadian Cancer Society, Manitoba; Palliative Care Program, Health and Social Services, Yukon; and the Calgary Health Region's Regional Palliative and Hospice Care Service.
"A pilot study to evaluate quality of life in patients age 60 or older with newly diagnosed acute myeloid leukemia" - Dr. Shabbir M. H. Alibhai, University Health Network
Dr. Alibhai's pilot project examined the quality of life and fatigue in individuals age 60 and over who had recently been diagnosed with acute myeloid leukemia (AML). Prior to the study, little was known about the impact of intensive chemotherapy on patient's quality of life. The pilot project found that intensive chemotherapy was associated with similar or better quality of life than less aggressive treatment approaches or supportive care. Following the conclusion of the pilot project, Dr. Alibhai has received multi-year funding from CIHR to conduct a larger study looking at quality of life and fatigue in older and younger people with AML.
"A pilot study of the hope focused program for informal caregivers of palliative home care patients" - Dr. Wendy Duggleby, University of Saskatchewan
Dr. Duggleby presented the results of the pilot project on the family caregiving experience and the development of a hope intervention for these caregivers at a local workshop for the Council of Aging. This presentation resulted in media coverage for the study's outcomes, the opportunity to share the findings with a Member of Parliament, Carol Skelton, and fostered a new and active collaboration between Dr. Duggleby and a community based decision making body, the Council of Aging.
Palliative and End-of-Life Care: Career Transition Awards
The goal of the Career Transition Awards was to provide support to researchers to enable them to shift their research focus within palliative care or to transition to the field from another discipline. One, six month award was supported through the initiative.
|Principal Investigator||Institution Name||Project Title|
|Wismer, Wendy||University of Alberta||Dietary patterns, perceptions of food and motivation to eat in palliative care cancer patients.|
Dr. Wendy Wismer from the University of Alberta used her award to learn about the theory of qualitative research and apply it to research in a food and cancer setting. During the tenure of her award, Dr. Wismer attended the Summer Institute of the International Institute of Qualitative Methods at the University of Alberta; developed a research protocol for a study regarding food selection by advanced cancer patients; and contributed to a qualitative publication on the nutritional coping mechanisms of advanced care cancer patients. In her own words: "The career transition award has allowed me to develop an area of expertise that is unique and personally rewarding, and one that I anticipate will enhance the food-related quality of life for those in end of life care."
Palliative and End-of-Life Care: New Emerging Teams
The New Emerging Team (NET) grants component of the Palliative and End-of-Life Care initiative was designed to build capacity and to promote the formation of new research teams or the growth of small existing teams. Nine NET grants were supported through this initiative, in addition to Dr. Pierre Allard's NET. The five year grants began in 2004 and will be completed in 2009. Research supported through the NETs cover a wide range of research topics such as family caregiving, cancer-associated cachexia and anorexia, vulnerable populations, and improving communication and decision-making.
|Principal Investigator||Institution Name||Project Title|
|Allard, Pierre||Elizabeth Bruyère Research Institute, Ottawa||Optimizing end-of-life care for seniors.|
|Baracos, Vickie||University of Alberta||New Emerging Teams in palliative care: Cancer-associated cachexia-anorexia syndrome.|
|Chochinov, Harvey; Stienstra, Deborah||University of Manitoba||End-of-life care and vulnerable populations.|
|Doll, Richard; Kazanjian, Arminée||British Columbia Cancer Agency||Palliative care in cross-cultural context: A NET for equitable and quality cancer care for ethnically diverse populations.|
|Gagnon, Pierre||Université Laval||Developing, evaluating and implementing new interventions in palliative care.|
|Hagen, Neil; Fainsinger, Robin; Brasher, Penelope||University of Calgary||A multidisciplinary cancer pain research network to improve the classification, assessment, and management of difficult cancer pain problems.|
|Heyland, Daren||Kingston General Hospital||Understanding and improving communication and decision-making at the end-of-life.|
|Kirk, Peter; Lau Francis||University of Victoria||Overcoming barriers to communication through end-of-life and palliative transitions.|
|Siden, Harold||University of British Columbia||Transitions in pediatric palliative and end-of-life care.|
|Stajduhar, Kelli; Cohen S. Robin||University of Victoria||Family caregiving in palliative and end-of-life care: A new emerging team.|
Midway through the five year projects, the 10 NET grants collectively have over 180 publications and have made over 450 presentations. The following highlights a small selection of the mid-grant research outcomes, to date, from the ten funded NET grants.
"A multidisciplinary cancer pain research network to improve the classification, assessment, and management of difficult cancer pain problems" - Dr. Neil Hagen, Robin Fainsinger and Dr. Penelope Brasher, University of Calgary
As a component of their research grant, Drs. Hagen, Fainsinger, and Brasher's team have conducted an exhaustive literature search focused on knowledge translation for techniques aimed to improve pain management. Preliminary results show that knowledge translation interventions that target health professionals to support improved cancer pain control often fall short of their intended effect and that similar interventions aimed at patients are more likely to work. These results may inform future planning of knowledge translation strategies in cancer pain control.
"Family caregiving in palliative and end-of-life care: A new emerging team" - Dr. Kelli Stajduhar and Dr. Robin Cohen, University of Victoria
One of the studies conducted by this NET examined the factors that influence a caregiver's ability to cope while providing end-of-life care at home. Five factors were identified: (1) the caregiver's approach to life; (2) the patient's illness experience; (3) the patient's recognition of the caregivers' contribution to his or her care; (4) the quality of the relationship between the caregiver and the dying person; and (5) the caregiver's sense of security. These findings may inform health services and policies directed at enhancing family caregivers' coping abilities.
"Overcoming barriers to communication through end-of-life and palliative transitions" - Dr. Peter Kirk and Dr. Francis Lau, University of Victoria
The extensive research of this NET, led by Dr. Kirk and Dr. Lau, on the Palliative Performance Scale (PPS) has contributed to the growing evidence base needed to support the policy and practice of palliative care in Canada. The PPS measures the functional status of a patient and assigns them a Palliative Performance Value. This value also serves as a communication tool for quickly describing a patient's current functional level. As a result of their research, patients in British Columbia with a PPS of 50% (which indicated that the patient requires considerable assistance and is not able to do any work) or less are now eligible for enrolment in the Palliative Care Benefits Program which allows free prescriptions and other services for patients with a prognosis of less than six months.
To support continued growth in palliative and end-of-life care research, and in response to a growing need within the research community, CIHR created a new peer review committee that will evaluate all operating grant applications within the area of palliative and end-of-life care. Previously, such applications were reviewed by a variety of different committees. It is anticipated that interest in palliative and end of-life care research will continue to grow, and that the creation of a dedicated, multidisciplinary committee will better serve the needs of this growing scientific community. The committee also reviews proposals that address critical evaluation of ethical, legal, economic and moral issues pertaining to the utilization of health care resources and quality of care.
A full evaluation of ICR's commitment to palliative and end-of-life care research is planned following the completion of the New Emerging Team Grants. One of the primary objectives of the Palliative and End-of-Life Care initiative, however, was to increase research capacity in this area in response to an identified need. In 2001/2002 CIHR funded only 14 projects focused on palliative care for a total investment of $629,928. In 2007/2008, 58 projects were funded 250 for a total investment of $5, 854,997, almost a tenfold funding increase. In addition, the ten Principal 200 Investigators funded in 2001/2002 grew to 86 in 2007/2008, and the number of co-investigators 150 went from 23 to 201 over the same period. These figures demonstrate a dramatic increase in research 100 capacity over a six -year period, largely as a result of the sustained efforts and commitment of ICR 50 and partners.
Meetings, Planning and Dissemination Grants: Knowledge Translation
An important part of the CIHR mandate is to promote the dissemination, uptake and application of new knowledge leading to improved health outcomes. In alignment with this goal, ICR encouraged knowledge translation (KT) activities in palliative and end-of-life care through the End of Grant Knowledge Translation Supplement funding opportunity. Five KT activities were supported through this initiative by ICR, in collaboration with the CIHR Institute of Aging. Three of these teams are working closely with the Canadian Hospice Palliative Care Association to ensure the broad dissemination of KT findings.
Network Catalyst Grants
The objective of this new funding opportunity launched in August 2010 is to support the creation and/or further development of formal networks by encouraging national and/or international collaboration, resource sharing, capacity building and dissemination in the area of palliative and end-of-life care. The Network Catalyst Grants will address one of the recommendations of the impact assessment and evaluation of the palliative and end-of-life care initiative conducted in 2009 by ICR, that is, to provide funding for a sustainable palliative and end-of-life care network to support this research community. ICR will provide $600,000 over three years to support a palliative and end-of-life care network.
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