The National Cardiac Registry (NCR) is committed to closing the gap in heart health by ensuring Indigenous Australians are represented in cardiac care data and improved outcomes. The NCR currently collects data on Percutaneous Coronary Intervention (PCI) and are keen to explore Rheumatic Heart Disease (RHD) as a secondary module for national reporting.
We have partnerships with State and Territory Participating Registries and are beginning a journey in partnership with Aboriginal and Torres Strait Islander peoples to ensure cardiac care is informed by inclusive data, driven by equity, and grounded in cultural respect.
The NCR is striving for Indigenous Data Sovereignty so that Indigenous decision making can be a fundamental pathway to improving Indigenous Health Services.
Join us in shaping a heart health system that listens, includes, and respects Aboriginal and Torres Strait Islander voices. Better data means stronger care, and stronger care saves lives.
For further information please contact the NCR via info@nationalcardiacregistry.org.au