An Analysis of Journey Mapping to Create a Palliative Care Pathway in a Canadian First Nations Community: Implications for Service Integration and Policy Development.

Palliative Care Pub Date : 2017-07-21 eCollection Date: 2017-01-01 DOI:10.1177/1178224217719441
Jessica Koski, Mary Lou Kelley, Shevaun Nadin, Maxine Crow, Holly Prince, Elaine C Wiersma, Christopher J Mushquash
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引用次数: 16

Abstract

Providing palliative care in Indigenous communities is of growing international interest. This study describes and analyzes a unique journey mapping process undertaken in a First Nations community in rural Canada. The goal of this participatory action research was to improve quality and access to palliative care at home by better integrating First Nations' health services and urban non-Indigenous health services. Four journey mapping workshops were conducted to create a care pathway which was implemented with 6 clients. Workshop data were analyzed for learnings and promising practices. A follow-up focus group, workshop, and health care provider surveys identified the perceived benefits as improved service integration, improved palliative care, relationship building, communication, and partnerships. It is concluded that journey mapping improves service integration and is a promising practice for other First Nations communities. The implications for creating new policy to support developing culturally appropriate palliative care programs and cross-jurisdictional integration between the federal and provincial health services are discussed. Future research is required using an Indigenous paradigm.

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在加拿大原住民社区创建姑息治疗路径的旅程地图分析:对服务整合和政策制定的影响。
在土著社区提供姑息治疗是国际社会日益关注的问题。本研究描述和分析了在加拿大农村的第一民族社区进行的独特的旅程测绘过程。这一参与性行动研究的目标是通过更好地整合第一民族的保健服务和城市非土著的保健服务,提高在家获得姑息治疗的质量和机会。举办了四次旅程绘图研讨会,以创建一个与6个客户实施的护理路径。对研讨会数据进行了分析,以获取经验教训和有前景的实践。后续焦点小组、研讨会和卫生保健提供者调查确定了可感知的好处,包括改善服务整合、改善姑息治疗、建立关系、沟通和伙伴关系。结论是,旅程地图改善了服务整合,对其他原住民社区来说是一个很有前途的做法。讨论了制定新政策以支持发展文化上适当的姑息治疗方案和联邦和省卫生服务之间的跨司法管辖区整合的影响。未来的研究需要使用土著范式。
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15 weeks
期刊介绍: Palliative Care and Social Practice is an international, peer-reviewed, open access journal that publishes articles on all aspects of palliative care. It welcomes articles from symptom science, clinical practice, and health services research. However, its aim is also to publish cutting-edge research from the realm of social practice - from public health theory and practice, social medicine, and social work, to social sciences related to dying and its care, as well as policy, criticism, and cultural studies. We encourage reports from work with under-represented groups, community development, and studies of civic engagement in end of life issues. Furthermore, we encourage scholarly articles that challenge current thinking about dying, its current care models and practices, and current understandings of grief and bereavement. We want to showcase the next generation of palliative care innovation research and practice - in clinics and in the wider society. Relaunched in July 2019. Partnered with Public Health Palliative Care International (PHPCI) (Title 2008-2018: - Palliative Care: Research and Treatment)
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