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Thematische Bibliographien / Palliative care, Canada / Zeitschriftenartikel

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Zeitschriftenartikel zum Thema „Palliative care, Canada“

Autor: Grafiati

Veröffentlicht am 4. Juni 2021

Zuletzt aktualisiert am 21. Februar 2023

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1

Smyth, Dion. "Politics and palliative care: Canada." International Journal of Palliative Nursing 17, no. 4 (April 2011): 205. http://dx.doi.org/10.12968/ijpn.2011.17.4.205.

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Heidemann, Elma G. "Palliative Care in Canada: 1986." Journal of Palliative Care 5, no. 3 (September 1989): 37–42. http://dx.doi.org/10.1177/082585978900500308.

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3

Ajemian, Ina Cummings. "Palliative Care in Canada: 1990." Journal of Palliative Care 6, no. 4 (December 1990): 47–50. http://dx.doi.org/10.1177/082585979000600410.

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Wodinsky, Harold B. "Palliative care in Canada: An overview." American Journal of Hospice Care 6, no. 6 (November 1989): 44–47. http://dx.doi.org/10.1177/104990918900600623.

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Costante, Alicia, Christina Lawand, and Clare Cheng. "Access to Palliative Care in Canada." Healthcare Quarterly 21, no. 4 (January 31, 2019): 10–12. http://dx.doi.org/10.12927/hcq.2019.25747.

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Kristjanson, Linda J., and Lynda Balneaves. "Directions for Palliative Care Nursing in Canada: Report of a National Survey." Journal of Palliative Care 11, no. 3 (September 1995): 5–8. http://dx.doi.org/10.1177/082585979501100302.

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This paper reports the results of a national survey of palliative care nurses conducted following a meeting of nurses at the Fifth Canadian Palliative Care Association Conference in 1993. The intent of the survey was to obtain information about Canadian palliative care nurses's perceptions of practice and professional issues. Eighty percent of respondents believed that palliative care nurses should form a palliative care nurses’ organization, with the majority recommending that this occur under the auspices of the Canadian Palliative Care Association. Key issues of importance to palliative car

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Czarkowski, Wiktor Maria, Dominika Agnieszka Kmita, and Marcin Janecki. "The palliative care in Australia and Canada." Palliative Medicine 14, no. 1 (2022): 9–17. http://dx.doi.org/10.5114/pm.2022.118722.

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Roy, David J. "Palliative Care Canada 1999 — A Question Period." Journal of Palliative Care 15, no. 1 (March 1999): 3–5. http://dx.doi.org/10.1177/082585979901500101.

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Morrison, R. Sean. "A National Palliative Care Strategy for Canada." Journal of Palliative Medicine 21, S1 (January 2018): S—63—S—75. http://dx.doi.org/10.1089/jpm.2017.0431.

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Widger, Kimberley, Dawn Davies, Danielle J. Drouin, Laura Beaune, Lysanne Daoust, R. Peter Farran, Nago Humbert, et al. "Pediatric Patients Receiving Palliative Care in Canada." Archives of Pediatrics & Adolescent Medicine 161, no. 6 (June 1, 2007): 597. http://dx.doi.org/10.1001/archpedi.161.6.597.

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Ley, Dorothy C. H. "Palliative Care in Canada: The First Decade and Beyond." Journal of Palliative Care 1, no. 1 (March 1985): 32–34. http://dx.doi.org/10.1177/082585978500100106.

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The first decade of palliative care in Canada has witnessed a rapid increase in programs. Originally institutional, they are now becoming community oriented. The major issues in palliative care are education, planning, development of standards and evaluative procedures, funding, and certain ethical dilemmas. The need for a sound academic base for future development is stressed. The role of the Palliative Care Foundation, both current and future, is briefly described.

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Lou Kelley, Mary. "Developing Rural Communities’ Capacity for Palliative Care: A Conceptual Model." Journal of Palliative Care 23, no. 3 (September 2007): 143–53. http://dx.doi.org/10.1177/082585970702300304.

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The population in Canada and other developing countries is aging, increasing the need for palliative care services. In rural communities, care of dying people is normally provided by health care professionals as part of a generalist practice, not by palliative care specialists. Despite a lack of specialists and resources, some rural communities have developed local palliative care programs. The goal of this research was to conceptualize rural communities’ process of developing palliative care programs using a theoretical perspective of community capacity development. Data were from nine focus

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Pilkey, Jana, James Downar, Deborah Dudgeon, Leonie Herx, Doreen Oneschuk, Cori Schroder, and Valerie Schulz. "Palliative Medicine—Becoming a Subspecialty of the Royal College of Physicians and Surgeons of Canada." Journal of Palliative Care 32, no. 3-4 (July 2017): 113–20. http://dx.doi.org/10.1177/0825859717741027.

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The discipline of palliative medicine in Canada started in 1975 with the coining of the term “palliative care.” Shortly thereafter, the provision of clinical palliative medicine services started, although the education of the discipline lagged behind. In 1993, the Canadian Society of Palliative Care Physicians (CSPCP) started to explore the option of creating an accredited training program in palliative medicine. This article outlines the process by which, over the course of 20 years, palliative medicine training in Canada went from a mission statement of the CSPCP, to a 1 year of added compet

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Brown, Catherine RL, Amy T. Hsu, Claire Kendall, Denise Marshall, Jose Pereira, Michelle Prentice, Jill Rice, et al. "How are physicians delivering palliative care? A population-based retrospective cohort study describing the mix of generalist and specialist palliative care models in the last year of life." Palliative Medicine 32, no. 8 (June 11, 2018): 1334–43. http://dx.doi.org/10.1177/0269216318780223.

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Background: To enable coordinated palliative care delivery, all clinicians should have basic palliative care skill sets (‘generalist palliative care’). Specialists should have skills for managing complex and difficult cases (‘specialist palliative care’) and co-exist to support generalists through consultation care and transfer of care. Little information exists about the actual mixes of generalist and specialist palliative care. Aim: To describe the models of physician-based palliative care services delivered to patients in the last 12 months of life. Design: This is a population-based retros

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Fassbender, Konrad, Wonita Janzen, Michelle Sims, Carleen Brenneis, and Karen Macmillan. "Palliative Care Matters: Commitment to Action Toward an Integrated Palliative Care Strategy for Canada." Journal of Pain and Symptom Management 56, no. 6 (December 2018): e24-e25. http://dx.doi.org/10.1016/j.jpainsymman.2018.10.014.

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Novik, Nuelle. "The Role of Social Work in Palliative Care." Journal of Comparative Social Work 7, no. 1 (April 2, 2012): 71–80. http://dx.doi.org/10.31265/jcsw.v7i1.81.

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A qualitative research study was conducted in northern Canada in 2007 which examined the realities and issues surrounding palliative care with seniors in remote northern settings. As a profession with a recognized role in supporting those who are dying and those who are bereaved, social work has been integral to the development of palliative care support services in northern Canada. However, in regions of the North where the social work profession is less developed and less recognized, the role for social work remains understated.

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Claxton-Oldfield, Stephen, Jennifer Tomes, Michelle Brennan, Catherine Fawcett, and Jane Claxton-Oldfield. "Palliative care volunteerism among college students in Canada." American Journal of Hospice and Palliative Medicine® 22, no. 2 (March 2005): 111–18. http://dx.doi.org/10.1177/104990910502200206.

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Collier, R. "Access to palliative care varies widely across Canada." Canadian Medical Association Journal 183, no. 2 (January 10, 2011): E87—E88. http://dx.doi.org/10.1503/cmaj.109-3763.

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Gallagher, Romayne, and Michael J. Passmore. "Canada needs equitable, earlier access to palliative care." Canadian Medical Association Journal 192, no. 20 (May 18, 2020): E559. http://dx.doi.org/10.1503/cmaj.74961.

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Mount, Balfour M., John Scott, and S. Robin Cohen. "Canada: Status of cancer pain and palliative care." Journal of Pain and Symptom Management 8, no. 6 (August 1993): 395–98. http://dx.doi.org/10.1016/0885-3924(93)90061-y.

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MacLean, Gillian, Alessia Gallipoli, and Ayla Raabis. "23 Current Trends in Canada in Neonatal Palliative Care." Paediatrics & Child Health 25, Supplement_2 (August 2020): e8-e9. http://dx.doi.org/10.1093/pch/pxaa068.022.

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Abstract Background The area of palliative care in pediatrics has been expanding, as evidence emphasizes the benefits of providing pediatric patients and their families with optimized care in cases of chronic illness and end-of-life. The majority of pediatric deaths occur in infants under one year, with significant portions of these deaths taking place in Neonatal Intensive Care Units (NICU). The expansion of palliative care into neonatal medicine is of significant importance, as symptom management and end-of-life care plays a vital role in providing complete care to these infants. Guidelines

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Pugh, Arlanna, Heather Castleden, Melissa Giesbrecht, Colleen Davison, and Valorie Crooks. "Awareness as a dimension of health care access: exploring the case of rural palliative care provision in Canada." Journal of Health Services Research & Policy 24, no. 2 (April 2019): 108–15. http://dx.doi.org/10.1177/1355819619829782.

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Objectives In Canada, the rural elderly population is increasing in size, as is their need for palliative care services in these settings. This analysis aims to identify awareness-associated barriers to delivering rural palliative care services, along with suggestions for improving service delivery from the perspective of local health care providers. Methods A total of 40 semi-structured interviews with various formal and informal health care providers were conducted in four rural and/or remote Canadian communities with limited palliative care resources. Interview data were thematically coded

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Baylis, Jared, Devin R. Harris, Charlie Chen, Daniel K. Ting, Kevin Clark, Anthony Kwan, Skye Crawford, and David Williscroft. "Palliative and end-of-life care education in Canadian emergency medicine residency programs: A national cross-sectional survey." CJEM 21, no. 2 (January 30, 2019): 219–25. http://dx.doi.org/10.1017/cem.2018.470.

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ABSTRACTObjectivesEmergency physicians play an important role in providing care at the end-of-life as well as identifying patients who may benefit from a palliative approach. Several studies have shown that emergency medicine (EM) residents desire further training in palliative care. We performed a national cross-sectional survey of EM program directors. Our primary objective was to describe the number of Canadian postgraduate EM training programs with palliative and end-of-life care curricula.MethodsA 15-question survey in English and French was sent by email to all program directors of both

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Gaudette, Leslie A., Fan Shi, Tammy Lipskie, Pierre Allard, Robin L. Fainsinger, David Maxwell, and Mike Harlos. "Developing Palliative Care Surveillance in Canada: Results of a Pilot Study." Journal of Palliative Care 18, no. 4 (December 2002): 262–69. http://dx.doi.org/10.1177/082585970201800403.

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Objective A pilot study compiled data from six palliative care centres across Canada to assess the feasibility of developing a national surveillance system. Methods Data provided for the three-year period between 1993–1997 were combined into a comparative minimum data set. Analyses included 6,369 care episodes from five centres, plus 948 patients from one centre. Results Care was provided in various settings including acute care wards, dedicated palliative care units, tertiary care, chronic care, and at home. Palliative care patients comprised equal numbers of men and women, with a median age

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Panarella, Michela, Olli Saarela, Ali Vahit Esensoy, Ahmed Jakda, and Zhihui (Amy) Liu. "Regional Variation in Palliative Care Receipt in Ontario, Canada." Journal of Palliative Medicine 22, no. 11 (November 1, 2019): 1370–77. http://dx.doi.org/10.1089/jpm.2018.0573.

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Fainsinger, Robin L., Carleen Brenneis, and Konrad Fassbender. "Edmonton, Canada: A Regional Model of Palliative Care Development." Journal of Pain and Symptom Management 33, no. 5 (May 2007): 634–39. http://dx.doi.org/10.1016/j.jpainsymman.2007.02.012.

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Turner, C. J. "P135: Canadian emergency medicine residents’ training and competency in end-of-life care: a needs assessment." CJEM 18, S1 (May 2016): S123. http://dx.doi.org/10.1017/cem.2016.309.

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Introduction: Emergency Physicians (EPs) face growing numbers of palliative care patients presenting to the emergency department (ED). Formal training for EM residents across Canada in this area is not well described. We sought to describe the training Canadian emergency medicine (EM) residents receive in end of life care issues, their attitudes toward it, self-reported knowledge and skills, and the importance they place on further training in this domain. Methods: We conducted an electronic survey across Canada. We collected demographic data, previous education in palliative care, attitudes t

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Sutcliffe, Simon B., Puneet Bains, Fraser Black, Sandra S. Broughton, Stuart Brown, Simon Colgan, Megan E. Doherty, et al. "The Two Worlds of Palliative Care: Bridging the Gap with Nepal." Nepal Journal of Science and Technology 20, no. 2 (December 31, 2021): 125–30. http://dx.doi.org/10.3126/njst.v20i2.45802.

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Despite past geo-political turbulence, Nepal has made significant progress in societal and economic initiatives, particularly in relation to social determinants of health. These improvements, however, belie the suffering of those with life-limiting disease due to pain, stigma, social and financial distress, consequent upon low patient, caregiver and health professional awareness of the need for, and availability of, appropriate care and support. Two Worlds Cancer Collaboration (INCTR-Canada) has been working with partners in Nepal to build capacity for palliative care by: (a) organizational an

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Qureshi, Maryam, Maggie C. Robinson, Aynharan Sinnarajah, Srini Chary, Janet M. de Groot, and Andrea Feldstain. "Reflecting on Palliative Care Integration in Canada: A Qualitative Report." Current Oncology 28, no. 4 (July 19, 2021): 2753–62. http://dx.doi.org/10.3390/curroncol28040240.

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Studies have identified integrated interdisciplinary care as a hallmark of effective palliative care. Although models attempt to show how integration may function, there is little literature available that practically explores how integration is fostered and maintained. In this study we asked palliative care clinicians across Canada to comment on how services are integrated across the healthcare system. This is an analysis of qualitative data from a larger study, wherein clinicians provided written responses regarding their experiences. Content analysis was used to identify response categories

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Wales, Joshua, Sumeet Kalia, Rahim Moineddin, and Amna Husain. "The Impact of Socioeconomic Status on Place of Death Among Patients Receiving Home Palliative Care in Toronto, Canada: A Retrospective Cohort Study." Journal of Palliative Care 35, no. 3 (June 16, 2019): 167–73. http://dx.doi.org/10.1177/0825859719855020.

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Background: Socioeconomic disparities in home death have been noted in the literature. Home-based palliative care increases access to home death and has been suggested as a means to decrease these disparities. Aim: Our study examines the association between socioeconomic status and other demographic factors on place of death in a population receiving home palliative care in Toronto, Canada. Design: This is a retrospective chart review of patients who died between August 2013 and August 2015 when admitted to a home-based palliative care service. Multivariate multinomial regression examined the

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Kortes-Miller, Kathy, Sonja Habjan, Mary Lou Kelley, and Marilyn Fortier. "Development of a Palliative Care Education Program in Rural Long-Term Care Facilities." Journal of Palliative Care 23, no. 3 (September 2007): 154–62. http://dx.doi.org/10.1177/082585970702300305.

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In North America, people 85 years and older are the fastest growing age cohort and long-term care homes are increasingly becoming the place of end-of-life care. This is especially true in rural communities where services are lacking. Staff in long-term care homes lack education about palliative care, but in rural areas, accessing education and the lack of relevant curricula are barriers. The focus of this paper is to describe an approach to developing and delivering a research-based palliative care education curriculum in rural long-term care homes. The approach included conducting a detailed

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Johnston, Grace, and Frederick Burge. "Analytic Framework for Clinician Provision of End-of-Life Care." Journal of Palliative Care 18, no. 3 (September 2002): 141–49. http://dx.doi.org/10.1177/082585970201800302.

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Four dimensions for the provision of end-of-life care by clinicians were identified from a review and synthesis of the Canadian family physician and palliative care literatures. These dimensions are: clinician-patient continuity, timing and location of care, community-centred services, and multidisciplinary care. Indicators of each dimension are presented along with criteria for indicator selection. The analytic framework was refined during the linkage of population-based administrative databases to identify patterns of family physician service provision in the last months of life for persons

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Kerba, Marc, Ayn Sinnarajah, M. Sarah Rose, Lynn Nicholson, Barbara Wheler, and Bert Enns. "End-of-life cancer care: Health service delivery in the last 12 months of life in Calgary, Alberta, Canada." Journal of Clinical Oncology 33, no. 29_suppl (October 10, 2015): 171. http://dx.doi.org/10.1200/jco.2015.33.29_suppl.171.

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171 Background: In Calgary, Alberta, the Calgary Zone Palliative Care Collaborative (CZPCC) undertook a study to examine the current state of cancer and palliative services and to recommend steps to address gaps in service delivery. We hypothesized that early access to palliative care services would reduce utilization of active cancer treatments and services for individuals nearing the end of life. Our study objectives were to determine the utilization and timing of acute, palliative and oncology-related services in Calgary. Methods: This retrospective study examined cancer registry and admini

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Sorensen, Anna, Lisa W. Le, Nadia Swami, Breffni Hannon, Monika K. Krzyzanowska, Kirsten Wentlandt, Gary Rodin, and Camilla Zimmermann. "Readiness for delivering early palliative care: A survey of primary care and specialised physicians." Palliative Medicine 34, no. 1 (December 18, 2019): 114–25. http://dx.doi.org/10.1177/0269216319876915.

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Background: Evidence supporting early palliative care is based on trials of specialised palliative care, but a more sustainable model might involve mainly primary providers. Aim: The aim of this study was to compare the characteristics of physicians providing primary and specialised palliative care, their attitudes towards early palliative care and their perception of having sufficient resources for its provision. Design: Survey distributed by mail and e-mail. Specialised providers were defined as both receiving palliative care referrals from other physicians and not providing palliative care

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Mak, Ernie, Patricia Murphy-Kane, and Camilla Zimmermann. "Assessing caregiver satisfaction with care on an acute palliative care unit." Journal of Clinical Oncology 35, no. 31_suppl (November 1, 2017): 51. http://dx.doi.org/10.1200/jco.2017.35.31_suppl.51.

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51 Background: Accreditation Canada has adopted four main values for hospice, palliative, and end-of-life services: dignity and respect; information sharing; partnership and participation; and collaboration . These domains, as well as communication and joint decision-making, are important for satisfaction of caregivers for patients with cancer, and can be measured using the FAMCARE questionnaire. We aimed to assess satisfaction of caregivers for patient admitted to an acute palliative care unit at a comprehensive cancer center in Toronto, Canada. Methods: The FAMCARE questionnaire was administ

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Mak, Ernie, Patricia Murphy-Kane, and Camilla Zimmermann. "Assessing caregiver satisfaction with care on an acute palliative care unit." Journal of Clinical Oncology 36, no. 30_suppl (October 20, 2018): 180. http://dx.doi.org/10.1200/jco.2018.36.30_suppl.180.

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180 Background: Accreditation Canada has adopted four main values for hospice, palliative, and end-of-life services: dignity and respect; information sharing; partnership and participation; and collaboration . These domains, as well as communication and joint decision-making, are important for satisfaction of caregivers for patients with cancer, and can be measured using the FAMCARE questionnaire. We aimed to assess satisfaction of caregivers for patient admitted to an acute palliative care unit at a comprehensive cancer center in Toronto, Canada. Methods: The FAMCARE questionnaire was adminis

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Williams, Allison M., Michelle V. Caron, Maria McMillan, Anne Litkowich, Noreen Rutter, Arlete Hartman, and John Yardley. "An evaluation of contracted palliative care home care services in Ontario, Canada." Evaluation and Program Planning 24, no. 1 (February 2001): 23–31. http://dx.doi.org/10.1016/s0149-7189(00)00044-6.

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Gilbar, Peter, and Kimberley Stefaniuk. "The Role of the Pharmacist in Palliative Care: Results of a Survey Conducted in Australia and Canada." Journal of Palliative Care 18, no. 4 (December 2002): 287–92. http://dx.doi.org/10.1177/082585970201800407.

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A survey was conducted to determine what pharmaceutical services are provided to palliative care sites in Australia and Canada, and the pharmacist's role on the interdisciplinary team. Questionnaires were sent to 100 selected sites in each country. Questions pertained to demographics and the level of duties performed. Australian 42/76 (55.3%) and Canadian 59/69 (85.5%) sites employed palliative care pharmacists. Most Australians (83.3%) and Canadians (69.8%) worked under 20 hours/week on the palliative care service. Administrative duties and basic drug supply functions were more common in Aust

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Spicer, David, Sonia Paul, Tom Tang, Charlie Chen, and Jocelyn Chase. "Survey evaluations of University of British Columbia residents’ education and attitudes regarding palliative care and physician assisted death." Canadian Medical Education Journal 8, no. 1 (February 24, 2017): e6-21. http://dx.doi.org/10.36834/cmej.36860.

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Background: Little prior research has been conducted regarding resident physicians’ opinions on the subject of Physician Assisted Death (PAD), despite past surveys ascertaining the attitudes of practicing physicians towards PAD in Canada. We solicited British Columbia residents’ opinions on the amount of education they receive about palliative care and physician assisted death, and their attitudes towards the implementation of PAD.Methods: We conducted a cross sectional, anonymous online survey with the resident physicians of British Columbia, Canada. Questions included: close-ended questions,

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Kaasalainen, Sharon, Lynn Mccleary, Shirin Vellani, and Jose Pereira. "Improving End-of-Life Care for People with Dementia in LTC Homes During the COVID-19 Pandemic and Beyond." Canadian Geriatrics Journal 24, no. 3 (July 13, 2021): 164–69. http://dx.doi.org/10.5770/cgj.24.493.

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COVID-19 pandemic has resulted in a significant increase in deaths in long-term care homes (LTCH). People with dementia living in LTCHs represent one of the most frail and marginalized populations in Canada. The surge of COVID-19 cases in LTCHs and rationing of health-care resources during the pandemic have amplified the pre-existing need for improvements in palliative and end-of-life care in LTCHs. This position statement, created by a task force commissioned by the Alzheimer Society of Canada, provides recommendations for a multipronged coordinated approach to improving palliative and end

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Sussman, Jonathan, Lisa Barbera, Daryl Bainbridge, Doris Howell, Jinghao Yang, Amna Husain, S. Lawrence Librach, Raymond Viola, and Hugh Walker. "Health system characteristics of quality care delivery: A comparative case study examination of palliative care for cancer patients in four regions in Ontario, Canada." Palliative Medicine 26, no. 4 (August 10, 2011): 322–35. http://dx.doi.org/10.1177/0269216311416697.

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Background: A number of palliative care delivery models have been proposed to address the structural and process gaps in this care. However, the specific elements required to form competent systems are often vaguely described. Aim: The purpose of this study was to explore whether a set of modifiable health system factors could be identified that are associated with population palliative care outcomes, including less acute care use and more home deaths. Design: A comparative case study evaluation was conducted of ‘palliative care’ in four health regions in Ontario, Canada. Regions were selected

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Brown, Catherine R. L., Colleen Webber, Hsien-Yeang Seow, Michelle Howard, Amy T. Hsu, Sarina R. Isenberg, Mengzhu Jiang, Glenys A. Smith, Sarah Spruin, and Peter Tanuseputro. "Impact of physician-based palliative care delivery models on health care utilization outcomes: A population-based retrospective cohort study." Palliative Medicine 35, no. 6 (April 22, 2021): 1170–80. http://dx.doi.org/10.1177/02692163211009440.

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Background: Increasing involvement of palliative care generalists may improve access to palliative care. It is unknown, however, if their involvement with and without palliative care specialists are associated with different outcomes. Aim: To describe physician-based models of palliative care and their association with healthcare utilization outcomes including: emergency department visits, acute hospitalizations and intensive care unit (ICU) admissions in last 30 days of life; and, place of death. Design: Population-based retrospective cohort study using linked health administrative data. We u

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Sirianni, Giovanna. "A Public Health Approach to Palliative Care in the Canadian Context." American Journal of Hospice and Palliative Medicine® 37, no. 7 (December 4, 2019): 492–96. http://dx.doi.org/10.1177/1049909119892591.

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Palliative care helps improve the quality of life of individuals facing life-limiting illness throughout the course of their disease. In Canada, delivery and access to palliative care has been fraught with challenges including differential availability of services based on geography, funding, language, and socioeconomic status. Many groups, including the World Health Organization, have advocated for a public health approach to palliative care as an antidote to fragmented service delivery. Multiple scholars, academics, and public health advocates have suggested that a public health approach to

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Gofton, TE, S. Stewart, J. Yeung Laiwah, VN Schulz, and A. Sarpal. "P.082 An evidence-based supportive and palliative care curriculum for Canadian neurology residents." Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques 45, s2 (June 2018): S38. http://dx.doi.org/10.1017/cjn.2018.184.

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Background: Graduating residents require general palliative care skills. In Canada, there is no standardized palliative care curriculum for specialty trained residents. The objective of this research is to develop an evidence-based palliative care curriculum designed to provide neurology residents with the general palliative care skills required for providing patient care along the continuum of life. Methods: A needs assessment was performed in Neurology at Western University using qualitative analysis techniques. Residents completed the following:. A curricular outline was developed based on

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Bélanger, Emmanuelle, Anna Towers, David Kenneth Wright, Yuexi Chen, Golda Tradounsky, and Mary Ellen Macdonald. "Of dilemmas and tensions: a qualitative study of palliative care physicians’ positions regarding voluntary active euthanasia in Quebec, Canada." Journal of Medical Ethics 45, no. 1 (October 30, 2018): 48–53. http://dx.doi.org/10.1136/medethics-2017-104339.

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ObjectivesIn 2015, the Province of Quebec, Canada passed a law that allowed voluntary active euthanasia (VAE). Palliative care stakeholders in Canada have been largely opposed to euthanasia, yet there is little research about their views. The research question guiding this study was the following: How do palliative care physicians in Quebec position themselves regarding the practice of VAE in the context of the new provincial legislation?MethodsWe used interpretive description, an inductive methodology to answer research questions about clinical practice. A total of 18 palliative care physicia

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Lee, Victor, Edward Yu, and Krzisch Claude. "Palliative Care for Chest Tumors – Hong Kong, France and Canada." Current Cancer Therapy Reviews 14, no. 2 (July 12, 2018): 167–80. http://dx.doi.org/10.2174/1573394714666180208143101.

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Scott, John F. "Palliative Care Education in Canada: Attacking Fear and Promoting Health." Journal of Palliative Care 8, no. 1 (March 1992): 47–53. http://dx.doi.org/10.1177/082585979200800111.

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Cyr, Claude, and Marie-Hélène Maisonneuve. "Paediatric palliative care in Canada: A national survey of paediatricians." Paediatrics & Child Health 20, no. 3 (April 2015): 153–54. http://dx.doi.org/10.1093/pch/20.3.153.

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Dudgeon, Deborah, Vida Vaitonis, Hsien Seow, Susan King, Helen Angus, and Carol Sawka. "Ontario, Canada: Using Networks to Integrate Palliative Care Province-Wide." Journal of Pain and Symptom Management 33, no. 5 (May 2007): 640–44. http://dx.doi.org/10.1016/j.jpainsymman.2007.02.001.

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Sévigny, Andrée, Serge Dumont, S. Robin Cohen, and Annie Frappier. "Helping Them Live Until They Die: Volunteer Practices in Palliative Home Care." Nonprofit and Voluntary Sector Quarterly 39, no. 4 (June 26, 2009): 734–52. http://dx.doi.org/10.1177/0899764009339074.

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Volunteers traditionally play an essential role in palliative care. Without them, many community and institutional programs would not survive. Despite the significant number of volunteers involved in palliative care, the nature and scope of their actions remain ambiguous. The blurred boundaries of their contribution create tensions between professionals, families, and volunteers with regards to patient care and sharing of responsibilities. This article reports on a comprehensive and descriptive qualitative study aimed at understanding volunteer practices in home palliative care in Canada throu

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