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dc.contributor.authorShahid, Shaouli
dc.contributor.authorTeng, T.
dc.contributor.authorBessarab, D.
dc.contributor.authorAoun, Samar
dc.contributor.authorBaxi, S.
dc.contributor.authorThompson, S.
dc.date.accessioned2017-01-30T10:59:06Z
dc.date.available2017-01-30T10:59:06Z
dc.date.created2016-06-29T19:30:16Z
dc.date.issued2016
dc.identifier.citationShahid, S. and Teng, T. and Bessarab, D. and Aoun, S. and Baxi, S. and Thompson, S. 2016. Factors contributing to delayed diagnosis of cancer among Aboriginal people in Australia: a qualitative study. BMJ Open. 6: e010909.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/7333
dc.identifier.doi10.1136/bmjopen-2015-010909
dc.description.abstract

BACKGROUND/OBJECTIVES: Delayed presentation of symptomatic cancer is associated with poorer survival. Aboriginal patients with cancer have higher rates of distant metastases at diagnosis compared with non-Aboriginal Australians. This paper examined factors contributing to delayed diagnosis of cancer among Aboriginal Australians from patient and service providers' perspectives. METHODS: In-depth, open-ended interviews were conducted in two stages (2006-2007 and 2011). Inductive thematic analysis was assisted by use of NVivo looking around delays in presentation, diagnosis and referral for cancer. PARTICIPANTS: Aboriginal patients with cancer/family members (n=30) and health service providers (n=62) were recruited from metropolitan Perth and six rural/remote regions of Western Australia. RESULTS: Three broad themes of factors were identified: (1) Contextual factors such as intergenerational impact of colonisation and racism and socioeconomic deprivation have negatively impacted on Aboriginal Australians' trust of the healthcare professionals; (2) health service-related factors included low accessibility to health services, long waiting periods, inadequate numbers of Aboriginal professionals and high staff turnover; (3) patient appraisal of symptoms and decision-making, fear of cancer and denial of symptoms were key reasons patients procrastinated in seeking help. Elements of shame, embarrassment, shyness of seeing the doctor, psychological 'fear of the whole health system', attachment to the land and 'fear of leaving home' for cancer treatment in metropolitan cities were other deterrents for Aboriginal people. Manifestation of masculinity and the belief that 'health is women's domain' emerged as a reason why Aboriginal men were reluctant to receive health checks. CONCLUSIONS: Solutions to improved Aboriginal cancer outcomes include focusing on the primary care sector encouraging general practitioners to be proactive to suspicion of symptoms with appropriate investigations to facilitate earlier diagnosis and the need to improve Aboriginal health literacy regarding cancer. Access to health services remains a critical problem affecting timely diagnosis.

dc.publisherBM J Group
dc.titleFactors contributing to delayed diagnosis of cancer among Aboriginal people in Australia: a qualitative study.
dc.typeJournal Article
dcterms.source.volume6
dcterms.source.number6
dcterms.source.startPagee010909
dcterms.source.endPagee010909
dcterms.source.titleBMJ Open
curtin.note

This open access article is distributed under the Creative Commons license http://creativecommons.org/licenses/by-nc/4.0/

curtin.departmentSchool of Nursing and Midwifery
curtin.accessStatusOpen access


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