Literature DB >> 23638970

'Where do I go from here'? A cultural perspective on challenges to the use of hospice services.

Rosemary Frey1, Merryn Gott, Deborah Raphael, Stella Black, Linda Teleo-Hope, Hyeonjoo Lee, Zonghua Wang.   

Abstract

Do hospice services as shaped by a western perspective adequately fulfil the needs of persons from non-Western cultures? Based on a Western view of palliative care, the vision outlined in the New Zealand Palliative Care Strategy (2001) is to deliver palliative care services, including hospice services, to all patients and their families requiring them in the context of an increasingly pluralistic and multicultural society. It is predicted that over the next two decades the proportion of people identifying as Māori, Pacific and Asian will dramatically increase within New Zealand. Ministry of Health information provided through a GAP analysis identified hospices as facing access-to-care pressures for Māori, Pacific and Asian patients. It is therefore critical to identify the challenges to hospice service access for Māori, Asian and Pacific patients. This project involved qualitative interviews with 37 cancer patients (Māori, Pacific and Asian self-identified ethnicities), whānau/family and bereaved whanua/family, as well as 15 health professionals (e.g. referring GPs, oncologists, allied health professionals) within one District Health Board. Patients and their families included both those who utilised hospice services, as well as those non-users of hospice services identified by a health professional as having palliative care needs. Challenges to hospice service utilisation reported in the findings include a lack of awareness in the communities of available services, as well as continuing misconceptions concerning the nature of hospice services. Language barriers were particularly reported for Asian patients and their families. Issues concerning the ethnic representativeness of the hospice services staff were raised. The findings highlight the importance of patient and family knowledge of hospice care for utilisation of services. This information can be used for future planning to enable hospices to both provide high quality evidence based palliative care services for patients and families and provide consultative services to primary healthcare providers in the community.
© 2013 John Wiley & Sons Ltd.

Entities:  

Keywords:  Asian; Māori; Pacific; culture; end-of-life care; hospice services; palliative care; terminal care

Mesh:

Year:  2013        PMID: 23638970     DOI: 10.1111/hsc.12038

Source DB:  PubMed          Journal:  Health Soc Care Community        ISSN: 0966-0410


  4 in total

1.  Te Pākeketanga: living and dying in advanced age--a study protocol.

Authors:  Merryn Gott; Tess Moeke-Maxwell; Lisa Williams; Stella Black; Gabriella Trussardi; Janine Wiles; Rangimarie Mules; Anna Rolleston; Ngaire Kerse
Journal:  BMC Palliat Care       Date:  2015-12-21       Impact factor: 3.234

Review 2.  Key features of palliative care service delivery to Indigenous peoples in Australia, New Zealand, Canada and the United States: a comprehensive review.

Authors:  Shaouli Shahid; Emma V Taylor; Shelley Cheetham; John A Woods; Samar M Aoun; Sandra C Thompson
Journal:  BMC Palliat Care       Date:  2018-05-08       Impact factor: 3.234

3.  Pacific meets west in addressing palliative care for Pacific populations in Aotearoa/New Zealand: a qualitative study.

Authors:  Sunia Foliaki; Veisinia Pulu; Hayley Denison; Mark Weatherall; Jeroen Douwes
Journal:  BMC Palliat Care       Date:  2020-07-08       Impact factor: 3.234

4.  Reported Māori consumer experiences of health systems and programs in qualitative research: a systematic review with meta-synthesis.

Authors:  Suetonia C Palmer; Harriet Gray; Tania Huria; Cameron Lacey; Lutz Beckert; Suzanne G Pitama
Journal:  Int J Equity Health       Date:  2019-10-28
  4 in total

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