Literature DB >> 29283876

A National Palliative Care Strategy for Canada.

R Sean Morrison1.   

Abstract

OBJECTIVE: To identify barrier to achieving universal access to high quality palliative care in Canada, review published national strategies and frameworks to promote palliative care, examine key aspects that have been linked to successful outcomes, and make recommendations for Canada.
BACKGROUND: In 2014, the World Health Organization called on members to develop and implement policies to ensure palliative care is integrated into national health services.
METHODS: Rapid review supplemented by the author's personal files, outreach to colleagues within the international palliative care community, review of European Association for Palliative Care publications, and a subsequent search of the table of contents of the major palliative care journals.
RESULTS: Frameworks were found for 10 countries ranging from detailed and comprehensive multi-year strategies to more general approaches including laws guaranteeing access to palliative care services for "dying" patients or recommendations for the development of clinical infrastructure. Few formal evaluations were found minimal comparative data exist regarding the quality of care, access to palliative care services, timing of access in the disease trajectory, and patient and family satisfaction with care. Factors that appear to be associated with success include: 1) input and early involvement of senior policy makers; 2) comprehensive strategies that address major barriers to universal access and that involve the key constituents; 3) a focus on enhancing the evidence base and developing a national system of quality reporting; and 4) substantial and sustained government investment. DISCUSSION: Comprehensive national strategies appear to improve access to high quality palliative care for persons with serious illness and their families. Such strategies require sustained government funding and address barriers related to infrastructure, professional and public education, workforce shortages, and an inadequate evidence base.

Entities:  

Keywords:  Canadian framework; health policy; palliative care

Mesh:

Year:  2018        PMID: 29283876      PMCID: PMC5733738          DOI: 10.1089/jpm.2017.0431

Source DB:  PubMed          Journal:  J Palliat Med        ISSN: 1557-7740            Impact factor:   2.947


  11 in total

1.  Developing a palliative care competence framework for health and social care professionals: the experience in the Republic of Ireland.

Authors:  Michael Connolly; Karen Ryan; Karen Charnley
Journal:  BMJ Support Palliat Care       Date:  2015-12-22       Impact factor: 3.568

2.  Policy analysis: palliative care in Ireland.

Authors:  Peter May; Geralyn Hynes; Philip McCallion; Sheila Payne; Philip Larkin; Mary McCarron
Journal:  Health Policy       Date:  2013-08-08       Impact factor: 2.980

3.  Strengthening of palliative care as a component of integrated treatment throughout the life course.

Authors: 
Journal:  J Pain Palliat Care Pharmacother       Date:  2014-04-29

Review 4.  Palliative care for chronic illness: driving change.

Authors:  Graeme Rocker; James Downar; R Sean Morrison
Journal:  CMAJ       Date:  2016-08-22       Impact factor: 8.262

5.  Comparison of Site of Death, Health Care Utilization, and Hospital Expenditures for Patients Dying With Cancer in 7 Developed Countries.

Authors:  Justin E Bekelman; Scott D Halpern; Carl Rudolf Blankart; Julie P Bynum; Joachim Cohen; Robert Fowler; Stein Kaasa; Lukas Kwietniewski; Hans Olav Melberg; Bregje Onwuteaka-Philipsen; Mariska Oosterveld-Vlug; Andrew Pring; Jonas Schreyögg; Connie M Ulrich; Julia Verne; Hannah Wunsch; Ezekiel J Emanuel
Journal:  JAMA       Date:  2016-01-19       Impact factor: 56.272

6.  The PRISMA Symposium 3: lessons from beyond Europe. why invest in research and service development in palliative care? An Australian perspective.

Authors:  David C Currow
Journal:  J Pain Symptom Manage       Date:  2011-10       Impact factor: 3.612

7.  Doctors' understanding of palliative care.

Authors:  Barbara Hanratty; Derek Hibbert; Frances Mair; Carl May; Chris Ward; Ged Corcoran; Simon Capewell; Andrea Litva
Journal:  Palliat Med       Date:  2006-07       Impact factor: 4.762

8.  Interventions to manage symptoms at the end of life.

Authors:  Charles F von Gunten
Journal:  J Palliat Med       Date:  2005       Impact factor: 2.947

9.  Oncologist factors that influence referrals to subspecialty palliative care clinics.

Authors:  Yael Schenker; Megan Crowley-Matoka; Daniel Dohan; Michael W Rabow; Cardinale B Smith; Douglas B White; Edward Chu; Greer A Tiver; Sara Einhorn; Robert M Arnold
Journal:  J Oncol Pract       Date:  2013-12-03       Impact factor: 3.840

10.  Comparison of legislation, regulations and national health strategies for palliative care in seven European countries (Results from the Europall Research Group): a descriptive study.

Authors:  Karen Van Beek; Kathrin Woitha; Nisar Ahmed; Johan Menten; Birgit Jaspers; Yvonne Engels; Sam H Ahmedzai; Kris Vissers; Jeroen Hasselaar
Journal:  BMC Health Serv Res       Date:  2013-07-17       Impact factor: 2.655

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  13 in total

1.  Patterns of Care and Costs for Older Patients With Colorectal Cancer at the End of Life: Descriptive Study of the United States and Canada.

Authors:  Karen E Bremner; K Robin Yabroff; Diarmuid Coughlan; Ning Liu; Christopher Zeruto; Joan L Warren; Claire de Oliveira; Angela B Mariotto; Clara Lam; Michael J Barrett; Kelvin K-W Chan; Jeffrey S Hoch; Murray D Krahn
Journal:  JCO Oncol Pract       Date:  2019-10-24

2.  Risk Factors of Metabolic Syndrome among Polish Nurses.

Authors:  Anna Bartosiewicz; Edyta Łuszczki; Małgorzata Nagórska; Łukasz Oleksy; Artur Stolarczyk; Katarzyna Dereń
Journal:  Metabolites       Date:  2021-04-23

3.  Access to palliative care by disease trajectory: a population-based cohort of Ontario decedents.

Authors:  Hsien Seow; Erin O'Leary; Richard Perez; Peter Tanuseputro
Journal:  BMJ Open       Date:  2018-04-05       Impact factor: 2.692

4.  Development of an eHealth information resource for family carers supporting a person receiving palliative care on the island of Ireland.

Authors:  David Scott; Peter Hudson; Karen Charnley; Cathy Payne; Gareth Westcott
Journal:  BMC Palliat Care       Date:  2019-08-30       Impact factor: 3.234

5.  Diagnosing Gaps in the Development of Palliative and End-of-Life Care: A Qualitative Exploratory Study.

Authors:  Helen Y L Chan; Diana T F Lee; Jean Woo
Journal:  Int J Environ Res Public Health       Date:  2019-12-24       Impact factor: 3.390

6.  Frequency of providing a palliative approach to care in family practice: a chart review and perceptions of healthcare practitioners in Canada.

Authors:  Erin Gallagher; Daniel Carter-Ramirez; Kaitlyn Boese; Samantha Winemaker; Amanda MacLennan; Nicolle Hansen; Abe Hafid; Michelle Howard
Journal:  BMC Fam Pract       Date:  2021-03-27       Impact factor: 2.497

7.  Cultural Considerations in Palliative Care Provision: A Scoping Review of Canadian Literature.

Authors:  Erynn M Monette
Journal:  Palliat Med Rep       Date:  2021-05-20

8.  Australian GPs' perceptions of barriers and enablers to best practice palliative care: a qualitative study.

Authors:  Anne Herrmann; Mariko L Carey; Alison C Zucca; Lucy A P Boyd; Bernadette J Roberts
Journal:  BMC Palliat Care       Date:  2019-10-31       Impact factor: 3.234

9.  Burnout and resilience among Canadian palliative care physicians.

Authors:  Cindy Wang; Pamela Grassau; Peter G Lawlor; Colleen Webber; Shirley H Bush; Bruno Gagnon; Monisha Kabir; Edward G Spilg
Journal:  BMC Palliat Care       Date:  2020-11-06       Impact factor: 3.234

Review 10.  Developing an integrated model of community-based palliative care into the primary health care (PHC) for terminally ill cancer patients in Iran.

Authors:  Suzanne Hojjat-Assari; Maryam Rassouli; Maxwell Madani; Heshmatolah Heydari
Journal:  BMC Palliat Care       Date:  2021-06-28       Impact factor: 3.234

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