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01.12.2012 | Study protocol | Ausgabe 1/2012 Open Access

BMC Health Services Research 1/2012

Study Protocol: establishing good relationships between patients and health care providers while providing cardiac care. Exploring how patient-clinician engagement contributes to health disparities between indigenous and non-indigenous Australians in South Australia

Zeitschrift:
BMC Health Services Research > Ausgabe 1/2012
Autoren:
Yvette L Roe, Christopher J Zeitz, Bronwyn Fredericks
Wichtige Hinweise

Electronic supplementary material

The online version of this article (doi:10.​1186/​1472-6963-12-397) contains supplementary material, which is available to authorized users.

Competing interests

The authors declare that they have no completing interests.

Authors’ contribution

YLR designed the study, negotiated support from participating health services, negotiated the Cultural Protocol for Research between herself and the Aboriginal Health Council of South Australia and drafted the manuscript. CJZ provided intellectual planning of the research, contributed to the research design and reviewed/edited the manuscript. BF participated in the designing the methodological framework of the study and thematic analysis. All authors read and approved the final manuscript.

Abstract

Background

Studies that compare Indigenous Australian and non-Indigenous patients who experience a cardiac event or chest pain are inconclusive about the reasons for the differences in-hospital and survival rates. The advances in diagnostic accuracy, medication and specialised workforce has contributed to a lower case fatality and lengthen survival rates however this is not evident in the Indigenous Australian population. A possible driver contributing to this disparity may be the impact of patient-clinician interface during key interactions during the health care process.

Methods/Design

This study will apply an Indigenous framework to describe the interaction between Indigenous patients and clinicians during the continuum of cardiac health care, i.e. from acute admission, secondary and rehabilitative care. Adopting an Indigenous framework is more aligned with Indigenous realities, knowledge, intellects, histories and experiences. A triple layered designed focus group will be employed to discuss patient-clinician engagement. Focus groups will be arranged by geographic clusters i.e. metropolitan and a regional centre. Patient informants will be identified by Indigenous status (i.e. Indigenous and non-Indigenous) and the focus groups will be convened separately. The health care provider focus groups will be convened on an organisational basis i.e. state health providers and Aboriginal Community Controlled Health Services. Yarning will be used as a research method to facilitate discussion. Yarning is in congruence with the oral traditions that are still a reality in day-to-day Indigenous lives.

Discussion

This study is nestled in a larger research program that explores the drivers to the disparity of care and health outcomes for Indigenous and non-Indigenous Australians who experience an acute cardiac admission. A focus on health status, risk factors and clinical interventions may camouflage critical issues within a patient-clinician exchange. This approach may provide a way forward to reduce the appalling health disadvantage experienced within the Indigenous Australian communities.
Zusatzmaterial
Authors’ original file for figure 1
12913_2012_2386_MOESM1_ESM.pdf
Authors’ original file for figure 2
12913_2012_2386_MOESM2_ESM.pdf
Literatur
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