A qualitative study of Samoan cancer patients’ experiences

Author:

Every Alice1,Cuesta-Briand Beatriz2,Hansell Dyxon3,Burich Shelley4,Tofilua Fuamatala4,Crawford Gregory B15,Collier Aileen16

Affiliation:

1. Aged Care Rehabilitation and Palliative Care Division, Northern Adelaide Local Health Network, Adelaide, Australia

2. Rural Clinical School of Western Australia, University of Western Australia, Australia

3. World Health Organization, Samoa; National University of Samoa, Samoa

4. Samoa Cancer Society, Apia, Samoa

5. University of Adelaide, Australia

6. Flinders University, Adelaide, Australia

Abstract

To investigate the palliative care experiences of Samoan patients with cancer and the impact these experiences have on their quality of life. Methods: This qualitative interview study was part of a larger study that interviewed19 participants recruited among patients with cancer registered with Samoa Cancer Society, or patients recently discharged from the main tertiary hospital in Samoa. Interview transcripts were reviewed, and the research team identified the key palliative-care-related themes. Results: Analysis led to the generation of the following key themes: living with pain; resource constraints; support from family and faith; and interactions with healthcare professionals. Most participants were experiencing unresolved pain as a result of poor health knowledge, lack of access to medications and practical issues, such as financial limitations and lack of transport. Participants also reported a lack of resources, including financial constraints, as a significant barrier to effective healthcare. Sources of support for patients with cancer were most commonly strong family relationships and religious faith. Although it was difficult for the participants to access care from healthcare professionals, they found that honest communication about their condition was comforting. However, they were frustrated if they felt communication was unsatisfactory. Conclusion: This study provides much needed evidence on the issues that affect the quality of life patients with cancer receiving palliative care and their families in Samoa. It also highlights the intersectionality of these issues and how this compounds the patient experience. Practical recommendations for improving palliative care lie in a few key areas, including a need for improved access to opioids and support for family caregivers. However, from a systemic perspective, the way forward should lie in harnessing the strengths of Samoan culture, including the strong sense of family and the role of religion, to provide support and care for palliative patients.

Publisher

Mark Allen Group

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