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Aboriginal and Torres Strait Islander peoples' (hereafter respectfully referred to as Indigenous Australians) experiences of health care are shaped by historical, social and cultural factors, with cultural security critical to effective care provision and engagement between services and community. Positive patient experiences are associated with better health outcomes. Consequently, it is an accreditation requirement that primary health care (PHC) services must formally gather and respond to patient feedback. However, currently available patient feedback tools were not developed with Indigenous Australians, and do not reflect their values and world views. Existing tools do not capture important experiences of care of Indigenous Australians in PHC settings, nor return information that assists services to improve care. Consistent with the principles of Indigenous Data Sovereignty, we will co-design and validate an Indigenous-specific Patient Reported Experience Measure (PREM) that produces data by and for community, suitable for use in quality improvement in comprehensive PHC services. This paper presents the protocol of the study, outlining the rationale, methodologies and associated activities that are being applied in developing the PREM. Briefly, guided by an Aboriginal and Torres Strait Islander Advisory Group, our team of Indigenous and non-Indigenous researchers, service providers and policy makers will use a combination of Indigenous methodologies, participatory, and traditional western techniques for scale development. We will engage PHC service staff and communities in eight selected sites across remote, regional, and metropolitan communities in Australia for iterative cycles of data collection and feedback throughout the research process. Yarning Circles with community members will identify core concepts to develop an "Experience of Care Framework", which will be used to develop items for the PREM. Staff members will be interviewed regarding desirable characteristics and feasibility considerations for the PREM. The PREM will undergo cognitive and psychometric testing.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9819546 | PMC |
http://dx.doi.org/10.3390/ijerph20010357 | DOI Listing |
Overview: We analysed Australian Immunisation Register (AIR) data, predominantly for National Immunisation Program funded vaccines, as at 2 April 2023 for children, adolescents and adults, focusing on the calendar year 2022 and on trends from previous years. This report aims to provide comprehensive analysis and interpretation of vaccination coverage data to inform immunisation policy and programs.
Children: Fully vaccinated coverage in Australian children in 2022 was 0.
Lancet Reg Health West Pac
August 2025
Western Australian Centre for Rural Health, University of Western Australia, 167 Fitzgerald Street, Geraldton, Western Australia, 6530, Australia.
Poorer cancer prevention and control outcomes for First Nations Australians have resulted in a need for improved health literacy, that is their capacity as individuals to access, understand, and use information in ways that promote and maintain good health. This narrative review explores the evidence on how education programs work to improve First Nations Australians' understanding of cancer, and how this leads to more effective use of prevention, screening and treatment services. Limited to the Australian context, a bibliographic search using terms structured around four main concepts: Aboriginal, Cancer, Australia, and Intervention (health literacy, health promotion) was undertaken in May 2024 for publications from January 2000.
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August 2025
Western Australian Centre for Rural Health, University of Western Australia, 167 Fitzgerald St, Geraldton, Western Australia, 6531, Australia.
Compared to adult cancer in Aboriginal and Torres Strait Islander populations, minimal research has focussed on cancer in Indigenous Australian children. This narrative review examined published information about incidence, mortality, barriers to diagnosis and treatment, and psychosocial needs and interventions for Indigenous Australian children with cancer. Most papers were epidemiological, investigating incidence and mortality.
View Article and Find Full Text PDFLancet Reg Health West Pac
August 2025
Western Australian Centre for Rural Health, University of Western Australia, 167 Fitzgerald Street, Geraldton, Western Australia 6530, Australia.
Lancet Reg Health West Pac
August 2025
Western Australian Centre for Rural Health, University of Western Australia, Geraldton, Western Australia, Australia.
Aboriginal and Torres Strait Islander (hereafter respectfully named Indigenous) Australians are diagnosed with some cancers substantially more frequently than non-Indigenous Australians implying a different risk factor landscape. Additionally, poorer outcomes for certain cancers are exacerbated by lower cancer screening rates and later diagnoses compared to non-Indigenous Australians. An improved understanding of cancer causation would allow better shaping and targeting of screening programs for those at the highest risk.
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