Project Lead

Associate Professor Luke Burchill

Full Bio

Lead partner

The University of Melbourne


Melbourne Health; Northern Health; Peter MacCallum Cancer Centre

This is a collaboration that partners Indigenous health researchers and clinicians with data scientists, biostatisticians and health economists. We will link clinical data collected by Australian general practices, hospitals, and government agencies to determine how variation in CV risk, clinical events and treatment influences Indigenous and non-Indigenous health outcomes. We will answer several important questions including:

  • What factors place Indigenous Australians at increased risk of CV disease?
  • Are existing risk assessment scores accurate and, if not, can we create a new score that more accurately predicts CV risk among Indigenous Australians?
  • How does current implementation of evidence-based CV care differ for Indigenous vs non-Indigenous Australians?
  • Does evidence-based CV care improve health outcomes among Indigenous Australians and, if so, by what magnitude?
  • How can administrative health services data be used to advance Victorian Aboriginal nation building efforts?

The findings of this research will be shared with stakeholders including peak Aboriginal & Torres Strait Islander health organizations, primary health care organizations and health agencies at the state and federal level. Working with these stakeholders the research team will devise strategies for improving implementation of evidence-based-care for Indigenous Australians with a focus on short- to medium-term improvements in CV care.

This research will reveal how CV disease is currently treated in Aboriginal & Torres Strait Islander communities. Demonstrating improvements following implementation of evidence-based CV care will have high translational impact and is an important step toward a national Indigenous CV implementation science initiative with potential for scalability and direct community benefit.

Expansion activities include introducing new sites to capture additional Aboriginal communities to increase diversity and generalisability of the study results; and increasing dissemination of the results across a larger number of Aboriginal health and research organisations through community engagement.