"Everyone needs a Deb": what Australian indigenous women say about breast cancer screening and treatment services.


Journal

BMC health services research
ISSN: 1472-6963
Titre abrégé: BMC Health Serv Res
Pays: England
ID NLM: 101088677

Informations de publication

Date de publication:
21 Jun 2023
Historique:
received: 13 03 2023
accepted: 01 06 2023
medline: 23 6 2023
pubmed: 22 6 2023
entrez: 21 6 2023
Statut: epublish

Résumé

Breast cancer continues to be the second most diagnosed cancer overall and the most diagnosed cancer for women in Australia. While mortality rates overall have declined in recent years, Indigenous women continue to be diagnosed at more marginal rates (0.9 times) and are more likely to die (1.2 times). The literature provides a myriad of reasons for this; however, the voices of Indigenous women are largely absent. This study sets out to understand what is happening from the perspectives of Australian Indigenous women with a view to charting culturally safer pathways that improve participation in screening and treatment by Indigenous women. This co-design study was conducted using semi-structured, in-depth interviews and focus group discussions. Recruitment of study participants was via snowball sampling. Participants were subsequently consented into the study through the Aboriginal Health Service and the research team. Interviews were audio recorded and transcribed verbatim, and data coded in NVivo12 using inductive thematic analysis. A total of 21 Indigenous women and 14 health service providers were interviewed predominantly from the same regional/rural area in NSW, with a small proportion from other states in Australia. Six major themes were identified: Access, Awareness, Community and Family, Lack of control, Negative feelings and associations and Role of services. To improve access and participation of Indigenous women and ultimately improve mortality rates, breast cancer services must explicitly address cultural and community needs.

Sections du résumé

BACKGROUND BACKGROUND
Breast cancer continues to be the second most diagnosed cancer overall and the most diagnosed cancer for women in Australia. While mortality rates overall have declined in recent years, Indigenous women continue to be diagnosed at more marginal rates (0.9 times) and are more likely to die (1.2 times). The literature provides a myriad of reasons for this; however, the voices of Indigenous women are largely absent. This study sets out to understand what is happening from the perspectives of Australian Indigenous women with a view to charting culturally safer pathways that improve participation in screening and treatment by Indigenous women.
METHODS METHODS
This co-design study was conducted using semi-structured, in-depth interviews and focus group discussions. Recruitment of study participants was via snowball sampling. Participants were subsequently consented into the study through the Aboriginal Health Service and the research team. Interviews were audio recorded and transcribed verbatim, and data coded in NVivo12 using inductive thematic analysis.
RESULTS RESULTS
A total of 21 Indigenous women and 14 health service providers were interviewed predominantly from the same regional/rural area in NSW, with a small proportion from other states in Australia. Six major themes were identified: Access, Awareness, Community and Family, Lack of control, Negative feelings and associations and Role of services.
CONCLUSION CONCLUSIONS
To improve access and participation of Indigenous women and ultimately improve mortality rates, breast cancer services must explicitly address cultural and community needs.

Identifiants

pubmed: 37344905
doi: 10.1186/s12913-023-09633-y
pii: 10.1186/s12913-023-09633-y
pmc: PMC10283162
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

672

Informations de copyright

© 2023. The Author(s).

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Auteurs

Vita Christie (V)

Djurali Centre for Aboriginal and Torres Strait Islander Health Research and Education, Macquarie University, Macquarie Park, Australia. vita.christie@mq.edu.au.

Deb Green (D)

Armajun Aboriginal Health Service, Armidale and Inverell, NSW, Australia.

John Skinner (J)

Djurali Centre for Aboriginal and Torres Strait Islander Health Research and Education, Macquarie University, Macquarie Park, Australia.

Lynette Riley (L)

Indigenous Studies & Aboriginal Education, The University of Sydney, Camperdown, NSW, Australia.

Ross O'Shea (R)

Foundation for Breast Cancer Care, Brisbane, Australia.

Karen Littlejohn (K)

Foundation for Breast Cancer Care, Brisbane, Australia.

Christopher Pyke (C)

Foundation for Breast Cancer Care, Brisbane, Australia.

Debbie McCowen (D)

Armajun Aboriginal Health Service, Armidale and Inverell, NSW, Australia.

Boe Rambaldini (B)

Djurali Centre for Aboriginal and Torres Strait Islander Health Research and Education, Macquarie University, Macquarie Park, Australia.

Kylie Gwynne (K)

Djurali Centre for Aboriginal and Torres Strait Islander Health Research and Education, Macquarie University, Macquarie Park, Australia.

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