– If all variables remain the same, Canada can expect to have more than 750,000 people in need of palliative home care in just over 30 years –
TORONTO, May 13 – With a rapidly ageing population and a rise in the number of individuals being diagnosed with advanced illnesses such as cancer, it is vital that all Canadians have access to programs, support and treatments that will provide them with comfort and dignity at end-of-life; however, results of a new Progress Report show that at least two thirds of Canadians (63 per cent) who are dying, do not have access to adequate hospice palliative care. Hospice Palliative Home Care in Canada: A Progress Report, released today by the Quality End-of-Life Care Coalition of Canada (QELCCC), reveals that 13 jurisdictions across Canada have in fact made progress in improving access to palliative home care services (case management, nursing, personal care and pharmaceuticals) – but there is still much more work to be done. “We gathered information from the provinces and territories through the Pan-Canadian Gold Standard for Palliative Home Care survey, and compiled it into the Progress Report in order to help jurisdictions report on the progress made in providing palliative home care,” said Sharon Baxter, QELCCC Secretariat and Executive Director, Canadian Hospice Palliative Care Association. “We have seen significant improvements in palliative home care across the country, but access to comprehensive services in most jurisdictions is limited by the lack of nurses and physicians who are trained in palliative care. While this remains problematic in most urban areas, it is even more so in rural areas.”
There is a growing trend toward Canadians wanting to die at home, yet 60 per cent of deaths in Canada occur in hospitals(1),(2). One of the main reasons that people need to be hospitalized at end-of-life is to gain access to the medications they need with no financial burden for their families. Almost all of the responding jurisdictions provide palliative home care teams with access to treatments and medical supplies; however, access is limited in rural areas.
“Although provincial and territorial governments have made considerable progress in improving access to treatments and medical supplies, provincial drug plan programs must offer access to a broader range of medications,” said Ms. Baxter. “This will help to ensure that palliative home care patients experience reduction in pain and suffering at the end-of-life.”
Only four of 13 jurisdictions (Ontario, New Brunswick, Nunavut and Yukon) report tracking wait times for patients in need of palliative home care. All jurisdictions have some form of eligibility criteria, yet several indicated that being eligible for palliative home care does not necessarily mean that patients will receive that level of care in a timely manner.
“The wait times for these essential services are not being tracked or managed by most of the jurisdictions that were surveyed – this is a serious issue given that palliative care patients are in their final moments of life and should not have to wait for care. While progress has been made in home care settings, at best, no more than 37 per cent of Canadians dying are receiving the kind of care that they require. It is clear that more needs to be done to provide care in hospitals, long-term care homes, residential hospices and to those who are homeless,” said Ms. Baxter.
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About Hospice Palliative Home Care in Canada: A Progress Report
In 2004, the federal, provincial and territorial First Ministers made a commitment to provide funding for certain palliative home care services and the CHPCA also made a commitment to report on the progress of end-of-life care at home. The CHPCA took the issue to the QELCCC who in turn asked the First Ministers to complete a survey based on The Pan-Canadian Gold Standard for Palliative Home Care.
Responses were received from 12 provinces and territories (Quebec did not participate). The federal government supplied a response for one program (Veterans Affairs Canada), but did not provide a response that addressed the other populations for which the federal government has responsibility (such as First Nations and Inuit peoples and prisoners). These responses provided an overview of palliative home care services in Canada to determine whether jurisdictions were meeting the urgent needs required by patients.
About the Quality End-of-Life Care Coalition of Canada (QELCCC)
The QELCCC believes that all Canadians have the right to quality end-of- life care that allows them to die with dignity, free of pain, surrounded by their loved ones, in a setting of their choice. The Coalition believes that achieving quality end-of-life care for all Canadians requires a well-funded, sustainable national strategy for palliative and end-of-life care. The QELCCC members work together in partnership to achieve this goal.
For more information on the QELCCC, or to download a copy of the Report Card, please visit: www.qelccc.ca.
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For further information: To receive a provincial or territorial fact sheet or to speak with a local member of the QELCCC, please contact: AnnMarie Nielsen Griffin, Secretariat for the QELCCC and Canadian Hospice Palliative Care Association, agriffin@scohs.on.ca, (613) 241-3663 ext. 229; Sarah Habib, Manning Selvage & Lee, Sarah.Habib@mslpr.ca, (416) 847-1318