| Autor: |
Anna Santos Salas, Cara Bablitz, Heather Morris, Lisa Vaughn, Olga Bardales, Jennifer Easaw, Tracy Wildeman, Wendy Duggleby, Bukola Salami, Sharon M. Watanabe |
| Jazyk: |
English<br />French |
| Rok vydání: |
2023 |
| Předmět: |
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| Zdroj: |
Health Promotion and Chronic Disease Prevention in Canada, Vol 43, Iss 8, Pp 365-374 (2023) |
| Druh dokumentu: |
article |
| ISSN: |
2368-738X |
| DOI: |
10.24095/hpcdp.43.8.02 |
| Popis: |
IntroductionIn Canada, people experiencing socioeconomic inequities have higher rates of late diagnosis and lower survival rates than the general population. Palliative care services focussed on this population are scarce. We developed a community-based nursing intervention to improve access to palliative care for people experiencing socioeconomic inequities and living with life-limiting illnesses in an urban Canadian setting. MethodsThis community-based, qualitative research study combined critical and participatory research methodologies. The study was conducted in partnership with the Palliative Care Outreach Advocacy Team (PCOAT) based in Edmonton, Alberta, a team dedicated to serving populations experiencing socioeconomic inequities who require palliative care. Following an exploratory phase that served to delineate the intervention, we undertook a one-year pilot implementation during which a part-time registered nurse (RN) joined PCOAT. The RN engaged in trust building, resolution of health and practical needs and complex care coordination. Twenty-five patients participated in the intervention. Participants were interviewed at least once to explore their experiences with the intervention. Data were analyzed through thematic analysis. ResultsMost participants were men, were Indigenous and had advanced cancer. Participants had significant financial concerns, lived or had lived in precarious housing situations and had previously faced serious challenges accessing health care. Participants reported social and health needs including housing, finances, transportation, symptom control, harm reduction and end-of-life care. Participants reported improved access to health and social services and expressed satisfaction with the study intervention. ConclusionStudy findings suggest the study intervention may have contributed to improved access to palliative care, improved experiences for participants and increased equity in the delivery of care. |
| Databáze: |
Directory of Open Access Journals |
| Externí odkaz: |
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