Skip to content
This report presents estimates of fatal burden for Aboriginal and Torres Strait Islander Australians for 2010 produced as part of the Indigenous component of the Australian burden of disease study.
Fatal burden is measured in years of life lost, which is the sum of the number of years of life lost due to premature death from disease and injury. Fatal burden estimates presented in this report are described for the Aboriginal and Torres Strait Islander population for broad disease groups, by age and sex. Estimates of the 'gap' in fatal burden between Indigenous and non-Indigenous Australians are also reported, together with selected sub-national estimates (selected states and territories, remoteness and socioeconomic disadvantage).
The Australian Institute of Health and Welfare will release a more comprehensive report on the burden of disease for Aboriginal and Torres Strait Islander peoples in 2016. It will update and extend this report with 2011 estimates of fatal and non-fatal burden for more specific causes, as well as the burden attributable to selected risk factors.
Abstract adapted from Australian Institute of Health and Welfare
This guideline provides information for GP's and practice staff about the Practice Incentives Program (PIP) Indigenous Health Incentive. This Medicare incentive aims to support general practices and Indigenous health services to provide better health care for Aboriginal and/or Torres Strait Islander patients, including best practice management of chronic disease.
The guideline provides information on:
Australian Indigenous HealthInfoNet abstract