The Canadian Atlas of Palliative Care
The British Columbia Atlas of Palliative Care
Pallium Canada has officially launched the British Columbia Edition of the Canadian Atlas of Palliative Care. This groundbreaking resource provides a comprehensive, data-driven snapshot of the status of palliative care across several domains in the province and its regions.
Mapping palliative care in British Columbia
As a member of the World Health Assembly, Canada recognizes palliative care as an essential part of every health care system. The newly launched British Columbia Edition of the Canadian Atlas of Palliative Care is a unique Canadian resource that examines palliative care at a provincial and regional level, across various domains, such as policy, services, and education. The Atlas consolidates provincial and regional level information into a single, interactive resource, providing a comprehensive view of palliative care across British Columbia.
Developed by Pallium Canada, with support from the Division of Palliative Care at McMaster University and the BC Centre for Palliative Care, the Atlas not only highlights the strengths of British Columbia’s palliative care system but also identifies some gaps.
By offering evidence-driven insights, it serves as a powerful tool to inform meaningful action and drive improvements in care. This Atlas is a pivotal step toward ensuring that every British Columbian can access compassionate, high-quality care at the end of life, no matter where they live.
Partners
The British Columbia Edition of the Canadian Atlas of Palliative Care was commissioned, supported, and collaboratively led by Pallium Canada in partnership with key stakeholders. Their contributions and expertise helped shape this resource.
What is a Palliative Care Atlas?
Palliative care atlases have proven to be powerful and transformative tools for understanding and improving palliative care systems worldwide. By offering both graphical and textual representations of the state of palliative care across different domains and indicators in a jurisdiction, they highlight areas of excellence and identify opportunities for improvement. Atlases have previously been developed for countries across Africa, Europe, the Middle East, and South America, and these Atlases have proven impactful in celebrating successes as well as driving improvements.
The Canadian Atlas of Palliative Care was first initiated by Pallium Canada in 2019, in collaboration with the Dr. Joshua Shadd Pallium Canada Research Hub at McMaster University.
About the British Columbia Edition of the Canadian Atlas of Palliative Care
The British Columbia Edition of the Canadian Atlas of Palliative Care offers a snapshot of palliative care in the province as of 2023–2024. It is informed by the insights and expertise of regional palliative care leaders from across the province, who generously contributed their time and knowledge. Drawing on global best practices, the Atlas adapts internationally recognized domains and indicators used in the international atlases to align with the Canadian health care system.
The online story map of the British Columbia Edition of the Canadian Atlas of Palliative Care is an interactive tool that allows users to explore detailed data on palliative care services across the province. This is complemented by a comprehensive PDF report of the Atlas. With the Atlas, you can:
Key findings
The following highlights the key findings and insights derived from the full version of the Atlas, offering a concise overview of the province’s palliative care landscape and the opportunities to enhance access and quality of care. These findings are crucial in guiding future policy, resource allocation, and service delivery to ensure equitable, high-quality care for all British Columbians.
Palliative care in British Columbia is robust, but regional gaps exist
Community-based palliative care is well developed, particularly in larger areas
The BC Centre for Palliative Care is a key driver of innovation and system integration
High levels of community engagement, particularly in volunteerism
Palliative care bed availability is uneven with an overall lower-than-needed availability of palliative care unit beds
- Vancouver Coastal is the only region meeting the minimum number of both PCU and hospice beds.
- Fraser Health has only half of the required minimum number of PCU beds but meets the minimum number of hospice beds.
- Northern Health and Island Health have no dedicated PCU beds and instead rely on designated PCU beds, which may be reassigned.
- Interior Health has neither dedicated nor designated PCU beds and depends entirely on hospice beds, which meet the minimum threshold, to support the region.
Hospitals provide high levels of access to specialist palliative care teams
Go beyond the key findings
The interactive British Columbia Edition of the Canadian Atlas of Palliative Care offers a comprehensive look at palliative care across the province. Explore regional data, compare service availability across different domains, and uncover insights to drive meaningful change.
Dive deeper into the British Columbia Edition of the Canadian Atlas of Palliative Care
Want to dive deeper into the findings of the British Columbia Edition of the Canadian Atlas of Palliative Care? Join an upcoming Palliative Care ECHO Project session to dig into the key findings, strengths and opportunities to improve palliative care access in BC.
Date: April 24, 2025, from 12:00–1:00 p.m. PST
Presenters: Jeffrey Moat, CEO of Pallium Canada, and Dr. Leonie Herx , MD, PhD, CCFP(PC), FCFP, Project Co-lead and Co-Principal Investigator of the British Columbia Atlas of Palliative Care
The Impact
The British Columbia Edition of the Canadian Atlas of Palliative Care identifies areas of success and celebration and serves as a catalyst for improvements, helping funders, policymakers, the media, health care analysts, health care planners, educators and the community improve their understanding of the status of palliative care in the province and its regions.
Funding
The British Columbia Edition of the Canadian Atlas of Palliative Care would not have been possible without the shared vision and generous donations by the following supporters:
Commonly asked questions
What is a palliative care atlas?
A palliative care atlas is a resource that provides a visual and text-based overview of the status of palliative care across several domains, within a specific region or country. They highlight strengths and excellence, identify gaps, and inform health care planning with the goal of improving palliative care systems.
How does this Atlas support improvements in palliative care?
By mapping the availability and accessibility of palliative care services across British Columbia, the Atlas helps identify areas where resources are needed most. It serves as a tool for advocacy, informing policy development, and guiding health care planning to strengthen palliative care services in the province.
Will there be other provincial editions of the Canadian Atlas of Palliative Care?
Yes. The British Columbia Edition of the Canadian Atlas of Palliative Care is the first provincial edition of the Canadian Atlas of Palliative Care. Future editions will expand to other provinces, with Ontario and Alberta editions set to launch in 2025.
Why doesn’t this edition of the Atlas include palliative care for Indigenous populations?
This edition of the Canadian Atlas of Palliative Care does not seek to reflect palliative care services and programs of First Nations, Inuit, or Métis peoples in Canada. Instead, with humility and in the spirit of reconciliation, Pallium Canada is dedicated to collaborating in a distinct process, led and developed by Indigenous Peoples, to describe palliative care across Turtle Island provided by, with and for Indigenous peoples. Such mapping will adhere to the First Nations Principles of Ownership, Control, Access, and Possession (OCAP®), Manitoba Métis principles of OCAS (Ownership, Control, Access and Stewardship), and Inuit Qaujimajatuqangit.
What health regions are covered in this Atlas?
The British Columbia Edition of the Canadian Atlas of Palliative Care covers five regional health authorities in the province: Interior Health, Fraser Health, Vancouver Coastal Health, Vancouver Island Health, and Northern Health.
Will this edition of the Atlas be updated?
Yes, like other palliative care atlases, the British Columbia Edition of the Canadian Atlas of Palliative Care is intended to be updated every five years. Regular updates will help track changes, improvements, and emerging needs in palliative care services across the province.
How can the Atlas be used?
The British Columbia Edition of the Canadian Atlas of Palliative Care serves as a valuable tool for policymakers, health care providers, researchers, and communities to assess the state of palliative care in the province. It helps identify successes, gaps, and opportunities for improvement, guiding decision-making and future planning to improve palliative care accessibility and quality.
Are there other palliative care atlases besides this one?
Yes, palliative care atlases have been developed for various regions worldwide. One of the earliest atlases was published in 2000, covering seven European countries. Since then, the Atlantes Program at the University of Navarra has led the development of atlases for Europe, Africa, the Middle East, North Africa, and Latin America. These atlases provide valuable insights into palliative care services, helping to drive improvements globally. The Canadian Atlas of Palliative Care follows this tradition, offering a province-by-province view to inform and improve palliative care in Canada.
What data does the British Columbia Edition of the Canadian Atlas of Palliative Care include?
The British Columbia Edition of the Canadian Atlas of Palliative Care provides a cross-sectional view of palliative care services across the province. It examines health care services, policies, system performance, education, community engagement, and professional activities. Some indicators, such as the presence of a palliative care unit or policy, are reported as “Yes,” “No,” or “Partial,” while others, including palliative care integration levels, are assessed based on expert judgment. Where possible, the Atlas applies established benchmarks, such as the recommended number of palliative care beds per population, to evaluate adequacy.
Where does the data for the British Columbia Atlas of Palliative Care come from?
The British Columbia Edition of the Canadian Atlas of Palliative Care uses a mixed-methods approach, combining surveys, interviews, and focus groups with health care professionals, policymakers, and regional palliative care leaders. Where available, publicly accessible data sources were also used. Expert input and consensus reviews helped validate findings to ensure accuracy. While some data gaps exist due to resource limitations or availability, multiple perspectives were incorporated to provide the most comprehensive overview possible.
How were the findings of this Atlas validated?
The data in this Atlas was validated through objective measures (e.g., presence of policies or services), expert judgment for harder-to-measure indicators, and established standards like the Catalonia Formula for palliative care beds. Multiple stakeholder reviews helped ensure accuracy and reduce bias.
Who contributed to the development of the British Columbia Edition of the Canadian Atlas of Palliative Care?
The British Columbia Edition of the Canadian Atlas of Palliative Care has been informed by the insights and expertise of regional palliative care leaders and practicing health care professionals from across the province. These experts generously contributed their time and knowledge to provide a comprehensive overview of the current state of palliative care in their respective regions.
Mapping the future of palliative care in Canada
The British Columbia Edition of the Canadian Atlas of Palliative Care is part of a national effort to map access to palliative care across Canada. The Ontario and Alberta editions are currently in development.
Data alone doesn’t drive change; people do. The Atlas is a vital tool for policymakers, health care leaders and communities to push for better access, stronger collaboration, and a future where high-quality palliative care is available to all. By raising awareness and supporting evidence-based decision-making, we can drive meaningful change in health equity and ensure that every Canadian has access to high-quality palliative care.