Literature DB >> 16460364

'It's very difficult to get respite out here at the moment': Australian findings on end-of-life care for Indigenous people.

Pam McGrath1, Mary Anne Patton, Zoë McGrath, Katherine Olgivie, Robert Rayner, Hamish Holewa.   

Abstract

Whilst access to respite care has been found to represent an important source of support for terminally ill patients and their families, the availability of these services to Indigenous Australians has to date remained undocumented. This potential need for respite in Indigenous communities was explored as part of a National Health and Medical Research Council (NH&MRC) funded study designed to develop an innovative model for Indigenous palliative care. The data needed for model development were collected through a series of open-ended, qualitative interviews conducted with a cross-section of consumers and health professionals within the Northern Territory, Australia. The findings reflected a serious need for Indigenous respite services, coupled with a severe deficiency in the present availability of these services, especially within rural and regional areas. This lack of local respite services was documented to be negatively impacting upon the ability of carers to fulfil their caring duties and was found placing undue physical, emotional and economic stress upon carers, patients and their families. Furthermore, the lack of access to local respite services documented was found to be forcing rural and regional patients to relocate to metropolitan areas away from the family, community and land to which strong ties are held. The lack of Indigenous respite services was also found to obstruct patients' and carers' wishes for death to occur in the local community, rather than in far away cities. Significant obstacles were found to be hindering the provision of respite care to Indigenous Australians, namely beliefs about families looking after their own, resource restrictions, limited staff availability in local areas, as well as problems associated with hostel use in metropolitan areas. The conclusions drawn from this study suggest the importance of tackling the obstacles preventing local respite services being established in areas close to where patients and carers live.

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Year:  2006        PMID: 16460364     DOI: 10.1111/j.1365-2524.2006.00604.x

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


  6 in total

1.  A systematic review of Indigenous caregiver functioning and interventions.

Authors:  Lesli Hokanson; Michael Gerhardt Quinn; Natalie Schüz; Kristy de Salas; Jenn Scott
Journal:  Qual Life Res       Date:  2018-03-21       Impact factor: 4.147

2.  Assessment of indigenous older peoples' needs for home and community care in remote Central Australia.

Authors:  Melissa A Lindeman; Robyn P Pedler
Journal:  J Cross Cult Gerontol       Date:  2008-01-17

Review 3.  Barriers to access and minority ethnic carers' satisfaction with social care services in the community: a systematic review of qualitative and quantitative literature.

Authors:  Nan Greenwood; Ruth Habibi; Raymond Smith; Jill Manthorpe
Journal:  Health Soc Care Community       Date:  2014-08-19

4.  Improving the quality of life of palliative and chronic disease patients and carers in remote Australia with the establishment of a day respite facility.

Authors:  Timothy A Carey; Kellie Schouten; John Wakerman; John S Humphreys; Fred Miegel; Simon Murphy; Mick Arundell
Journal:  BMC Palliat Care       Date:  2016-07-18       Impact factor: 3.234

5.  Reducing hospital admissions in remote Australia through the establishment of a palliative and chronic disease respite facility.

Authors:  Timothy A Carey; Mick Arundell; Kellie Schouten; John S Humphreys; Fred Miegel; Simon Murphy; John Wakerman
Journal:  BMC Palliat Care       Date:  2017-11-21       Impact factor: 3.234

6.  Can digital stories go where palliative care research has never gone before? A descriptive qualitative study exploring the application of an emerging public health research method in an indigenous palliative care context.

Authors:  Lisa Williams; Merryn Gott; Tess Moeke-Maxwell; Stella Black; Shuchi Kothari; Sarina Pearson; Tessa Morgan; Matua Rawiri Wharemate; Whaea Whio Hansen
Journal:  BMC Palliat Care       Date:  2017-09-04       Impact factor: 3.234

  6 in total

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