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Project: The Burden of Disease and Injury in Indigenous
Australians
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| CRCAH Project No. CP120
Administering organisation
Centre for Burden of Disease and Cost Effectiveness, University of
Queensland
Program Manager
Barbara
Beacham
Project Leader
Theo Vos (Centre for Burden of Disease and Cost Effectiveness,
University of Queensland)
Team members
Alan Lopez, Steve Begg, Bridget Barker, Lucy Stanley
Contact details
Associate Professor Theo Vos
Tel: 07 3365 5508
Fax: 07 3365 5442
Email: t.vos@sph.uq.edu.au
Funding sources
- University of Queensland
- Office of Aboriginal and Torres Strait Islander Health
(Department of Health and Ageing)
- Remote and Rural Health Division (Department of Health and
Ageing)
In-kind contributors:
CRC for Aboriginal Health
Partners involved
- University of Queensland
- Office of Aboriginal and Torres Strait Islander Health
- CRC for Aboriginal Health
- Menzies School of Health Research
- The University of Melbourne
- Indigenous community organisations (various)
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Project summary
The Indigenous Burden of Disease Study is a component of the
Australian Burden of Disease Study, which aims to describe the
health status of Australians in the year 2003. The Indigenous study
specifically looks at improving knowledge of the true level of
mortality, causes of death, non-fatal health states and risk
factors affecting Indigenous people. A previously completed pilot
burden of disease study in the Northern Territory has estimated
that health inequalities between Indigenous and non-Indigenous
Australians not only affect the length of life (three times more
years of life lost due to premature deaths among Indigenous people)
but also the health-related quality of life (almost a doubling of
disability experienced due to non-fatal disease).
Summary of projected outcomes
The primary objectives of the Burden of Disease and Injury in
Indigenous Australians project are to deliver:
- Burden of
disease estimates (deaths, years of life lost, years lived with
disability, disability-adjusted life years, incidence and
prevalence with details by age, sex and remote/non-remote
residence) that will assist health service planners and Indigenous
communities to identify those specific diseases and risk factors
that are most responsible for the gap in health status between
Indigenous and non-Indigenous Australians.
- A
platform for further analytical work on the relative
cost-effectiveness of alternative intervention options in support
of priority setting.
Summary of project implementation
The project analyses both mortality data and available survey and
epidemiological data and routine health statistics to achieve its
aims. For the mortality analyses, use is made of indirect
demographic techniques for checking completeness and reliability of
death registration relative to population estimates derived from
census counts. For the analyses of the incidence/prevalence,
average duration, remission and mortality of the 176 diseases
included in the Australian Burden of Disease study, the project
uses a standard burden of disease software program called DISMOD to
check all disease estimates for consistency. Where available,
directly observed data will determine the non-fatal disease
estimates. However, for many diseases with no directly observed
data, estimates will be derived from relative risks between
Indigenous and non-Indigenous Australians of mortality, hospital
episodes or reported disease occurrence in surveys. The
project also estimates the burden attributable to major risk
factors (including tobacco, alcohol, blood pressure, cholesterol,
obesity, unsafe sex, illicit drugs, physical inactivity, inadequate
diet, intimate partner violence) using the improved methods
developed for the 2002 World Health Report.
Related Documents
Summary Report -
The Burden of Disease and Injury in Aboriginal and Torres Strait
Islander Peoples [pdf]
Report - The
Burden of Disease and Injury in Aboriginal and Torres Strait
Islander Peoples [pdf]
Policy
Brief - The Burden of Disease and Injury in Aboriginal and Torres
Strait Islander Peoples [pdf]
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