Australian Indigenous HealthBulletin
An electronic
journal from the Australian Indigenous HealthInfoNet
Vol.1 No.1
July 2001 - September
2001: ISSN 1445-7253
Reports and publications
This section of the Bulletin identifies
recent reports and publications, including book chapters. If you are
aware of material that would be appropriate for inclusion in this section
please contact us.
Australian Bureau of Statistics & Australian Institute of Health
and Welfare (2001)
The health and welfare of Australia's Aboriginal and Torres Strait
Islander peoples 2001.
Canberra: A joint program of the Australian Bureau of Statistics and the
Australian Institute of Health and Welfare.
This publication, the third of a two-yearly series that commenced in
1997, provides an up-to-date overview of Indigenous health and welfare.
The information contained in the report is drawn primarily from national
data although state and regional information is provided where quality
data is available.
The report does not purport to cover all of the many complex issues that
impact on the health and wellbeing of the Indigenous population but it
does provide a wealth of information on:
- demographic, social and economic indicators
- housing and infrastructure
- community services and housing assistance
- availability, cost and use of health services
- health status, including measures of life expectancy, mortality,
maternal and child health, mental health and hospitalisation
In addition, separate chapters provide an analysis of the nature and
prevalence of diabetes in the Indigenous population and an overview of
recent initiatives to improve the quality and availability of Indigenous
statistics.
The report provides ample evidence that Indigenous Australians continue
to suffer a greater burden of ill health than the rest of the population
- they have higher death rates, shorter life expectancy, and are more
likely to be hospitalised than other Australians. The report also documents
differences in patterns of health expenditure that reflect, in part, differences
in Indigenous and non-Indigenous access to health services . Overall,
Indigenous people continue to experience lower levels of access to health
services than the general population.
Australian Indigenous HealthInfoNet abstract
A summary
of the report is available from the ABS site. Enquiries about purchasing
a copy of this report should be directed to the ABS Bookshop in your capital
city.
AusStats subscribers and authorised Australian universities may download
the report in PDF format. If you are not an AusStats subscriber or authorised
Australian university user and would like to purchase a copy of this product,
please call the ABS National Information Service on 1300 135 070. Please
have the catalogue number (4704.0), filename and your credit card details
ready. Extra labour and handling charges may apply for ABS-assisted access
to this dataset.

Australian
Institute of Health and Welfare (2001)
Expenditures on health services for Aboriginal and Torres Strait Islander
people 1998-99.
Canberra: Australian Institute of Health and Welfare and Commonwealth
Department of Health and Aged Care.
This Australian Institute of Health and Welfare report reviews expenditure
for provision of health services to Aboriginal and Torres Strait Islander
people by Australian governments and the private sector for the 1998-1999
financial year. Its findings are similar to the first report for 1995-96
in that total expenditure per
person for health services for Aboriginal and Torres Strait Islander people
was not much higher than for the total Australian population.
Estimated total expenditure in 1998-99 was $1,245 million, which is equivalent
to $3,065 per person compared with $2,518 per person for non-Indigenous
people - a ratio of 1.22:1. When relative income position was taken into
account, public expenditure on the health of Aboriginal and Torres Strait
people appeared to be similar to that for non-Indigenous people in low-income
groups, despite the much lower health status of Aboriginal and Torres
Strait people.
The majority of Indigenous health expenditure was allocated through mainstream
health programs which generally do not, or only incompletely, document
use specifically by Aboriginal and Torres Strait Islander people. Medicare
data, for example, do not include an Indigenous identifier. The use of
surveys and other estimation techniques were used in this review, because
of inadequate or incomplete routine data.
Indigenous people were, on average, much higher users than non-Indigenous
people of publicly funded health services and State-funded health services,
particularly admitted patient services in hospitals and community health
services. Compared with non-Indigenous people, Indigenous people used
fewer private services such as doctors in private practice, private hospitals,
dentists and privately funded allied health professionals.
The Commonwealth and State governments contributed very similar amounts
to health services for Aboriginal and Torres Strait Islander people. Over
50% of the Commonwealth's contribution was indirect through its contribution
to public hospital funding. Expenditures were much lower for Aboriginal
and Torres Strait Islander people than for other Australians in the major
Commonwealth-funded health programs, Medicare and the Pharmaceutical Benefits
Scheme. Per person expenditure on Indigenous people was 37% of that for
non-Indigenous people.
The report noted that the ratio of Indigenous to non-Indigenous service
use would be lower that the expenditure ratio of 1.22:1 if the higher
costs of providing service in remote areas could be factored in. The analysis
documented decreasing levels of access to Medicare funded services and
pharmaceutical benefits as remoteness increased, but admitted patient
expenditure increased with increasing remoteness.
The report noted also that there were problems in comparing expenditures
for 1998-99 with those for 1995-96 because of changes in methodology and
data availability. It concluded, however, that, after controlling for
population and inflation, there are areas in which there had been increases
in funding and service provision.
Australian Indigenous HealthInfoNet Abstract
Click
here to view the full text document
Click
here to view the media release
To enquire about obtaining a hard copy of this report, contact the Australian
Institute of Health through their Internet site: http://www.aihw.gov.au.
The report may be available also from Commonwealth Government Info Shops
and agents in capital cities.

Condon
JR, Warman G, Arnold L (2001)
The health and welfare of Territorians.
Casuarina: Territory Health Services.
This publication summarises the available information on the current
health status of the people of the Northern Territory, many of the important
determinants of their health status, and the health services available
to them. Throughout this publication statistics are presented separately
for Aboriginal and non-Aboriginal people. There are five sections which
cover:
- determinants of health;
- specific health issues;
- the health of particular groups;
- health services; and
- death statistics.
Non-Aboriginal Territorians are in most respects at least as healthy
as other Australians, but most (not all) Aboriginal people in the Northern
Territory and throughout Australia have much worse social and economic
circumstances, living conditions and health status than other Australians.
Northern Territory Aboriginal death rates are more than three times higher
than Australian rates, and life expectancy is approximately 20 years less
than that of other Australians.
Australian Indigenous HealthInfoNet abstract
Enquiries about obtaining a copy of this report should be directed to
Public Affairs, Social Services, Territory Health Services, PO Box 40596,
Casuarina, NT 0811; ph: 899 2400; fax: 8999 2700; Internet: http://www.nt.gov.au/nths
The full report is available
from the Territory Health Services site in PDF format.

Dance P, Brown R, Bammer G, Sibthorpe B (2000)
Needs for residential aged care and other services by the older Indigenous
population in the ACT and Region.
Canberra: National Centre for Epidemiology & Population Health.
The ACT Office of the Commonwealth Department of Health and Aged Care
commissioned researchers at the National Centre for Epidemiology and Population
Health at the Australian National University to conduct an analysis of
needs of older Indigenous people in the ACT and region. The aim of the
research was to provide a picture of aged care needs and strategies to
improve access to aged care programs and services over the next five years.
Ninety eight Indigenous people aged 45 years and older were interviewed.
Sociodemographic data and the physical, mental and social health problems
and needs of the people interviewed are also included in the report. Fifty
per cent of respondents preferred an arrangement where an existing mainstream
provider of aged care 'clustered' Indigenous people together in the same
facility. Thirty two per cent would prefer an Indigenous-run organisation.
The report also includes twelve recommendations to improve aged care and
services for Indigenous people.
Australian Indigenous HealthInfoNet abstract
Gulash A, Saunders J, White P
(1999)
'Tell the story'. Barriers to effective communication
in mental health assessments for Aboriginal and Torres Strait Islander
Peoples. The development of culturally appropriate assessments for Aboriginal
and Torres Strait Islander Mental Health Consumers.
Wacol: Queensland Centre for Schizophrenia
Research.
Current mental health assessment processes
have been identified by Aboriginal and Torres Strait Islander people as
contributing to the over-representation of Aboriginal and Torres Strait
Islander peoples in mental health facilities, including forensic facilities.
This report summarises the views of Aboriginal and Torres Strait Islander
project participants on how assessment processes can be modified.
The report outlines a number of recommendations
which centre around making Aboriginal and Torres Strait Islander communities
more aware of mental health issues in general. It summarises also specific
ways to empower communities to recognise and, in time, develop methods
of community self-management for mental health issues. Strategies need
to be developed by Aboriginal and Torres Strait Islander people in partnership
with mainstream service providers, rather than imposing mainstream methods
on communities.
Australian Indigenous HealthInfoNet abstract
The full report is available
in html format on the Queensland Centre for
Schizophrenia Research's Internet site, or may be downloaded in
word format.
Copies may also be available from the Queensland
Centre for Schizophrenia Research, Wolston Park Hospital, Wolston Park
Road, Wacol, Qld 4076: ph: (07) 3271 8592; fax: (07) 3271 8567; Internet:
http://www.qcsr.uq.edu.au/

Matthews
S, Jenkin R, Frommer M, Tjhin M, Rubin, G (2001)
When research reports and academic journals are clearly not enough.
Strengthening the links between Aboriginal health research and health
outcomes.
Casuarina: Cooperative Research Centre for Aboriginal and Tropical
Health.
The Cooperative Research Centre for Aboriginal and Tropical Health (CRCATH)
was established in 1997 as a collaborative research organisation. This
paper documents the steps that were undertaken to support the development
of a health-outcomes-oriented research culture. The paper is divided into
three sections, which cover:
- the establishment phase of the organisation from 1997 to 1999;
- the links between Aboriginal health research, policy and practice;
and
- the development phase of the organisation from 1999 to 2000.
The second section addresses the question:
'How should the CRCATH set research priorities which are likely to
lead to improvements in Aboriginal health, not just increases in knowledge?'
Three main recommendations resulted from this discussion paper with the
principal recommendation being that the CRCATH should divide its investment
in research between:
- 'research projects and programs; and
- the development and support of models of research organisation designed
to promote the implementation of research findings which are likely
to lead to improvements in Aboriginal health.'
Australian Indigenous HealthInfoNet abstract
Enquiries about obtaining a copy of this report should be directed to
the Cooperative Research Centre for Aboriginal and Tropical Health, PO
Box 41096, Casuarina, NT 0820; Internet: http://www.crcah.org.au

New South Wales Health (2000)
From the ground up. Summary NSW Aboriginal health regional plans.
December 2000.
This report was developed by the New South Wales Aboriginal Health Forum
to inform funding, policy development and service development and administration
processes in NSW. It provides a summary of the seventeen Aboriginal Health
Regional Plans for NSW and links these to the NSW Aboriginal Health Strategic
Plan. The summary is divided into ten sections. The first section provides
a background to the regional planning process and places the regional
plans in the context of other Aboriginal health planning processes occurring
in NSW. The Population Overview in Section 2 provides regional comparisons
of household income, occupation, unemployment and school leaving age.
Section 3 is the Health Overview which contains a brief summary of hospitalisation
data for NSW and an estimate of overall expenditure on Aboriginal health
in NSW. The key issues for NSW are outlined in Section 4, with these issues
being discussed in greater detail in the next five sections. Section 10
provides a summary of the major issues by region.
Australian Indigenous HealthInfoNet abstract

Ogilvie E, Van Zyl A (2001)
Young Indigenous males, custody and the rites of passage.
Canberra: Australian Institute of Criminology.
The over-representation of Indigenous people in Australian prisons and
detention centres is well documented, with the Indigenous prison population
growing faster than the non-Indigenous prison population. This paper examines
the concept of incarceration as an alternative 'rite of passage' for young
Indigenous males in the Northern Territory. Both anthropological and criminological
concepts of rites of passage are discussed in related to young Indigenous'
males experiences of incarceration in the Northern Territory. Interviews
were conducted with incarcerated juveniles and adults, custodial staff
and judicial officials over a period of six months. These interviews were
aimed at identifying the background factors related to the imprisonment
of the interviewees. The interviews point to detention being seen by the
young people as an opportunity for a different experience from that available
in the remote communities. While there may be issues of status associated
with incarceration, the adolescent criminality in the Northern Territory
is primarily born out of boredom, resulting from marginalisation and lack
of access to resources.
Australian Indigenous HealthInfoNet abstract

Thomson
N, Irvine J (2001)
A review of cancer among Aboriginal people in Western Australia.
Perth: Cancer Foundation of Western Australia.
This review was undertaken by the Australian Indigenous HealthInfoNet
for the Cancer Foundation of Western Australia to assist the Foundation
in planning its activities with Indigenous communities in WA.
In the five-year period 1993-1997, the age-standardised incidence rate
for cancer was significantly lower for Indigenous than non-Indigenous
males but the rate for Indigenous females was slightly higher than that
for non-Indigenous females. Age-standardised death rates were higher for
Indigenous than non-Indigenous people.
The most common specific cancers among Indigenous people were also the
most common among non-Indigenous people but comprised smaller proportions
of all cancers - prostate cancer for males, and breast cancer for females.
Of other specific cancers, incidence and death rates for lung cancer were
much lower for Indigenous than non-Indigenous males, but the rates were
similar for Indigenous and non-Indigenous females. Incidence and death
rates for cervical cancer were much higher for Indigenous than non-Indigenous
females. Incidence and death rates for liver cancer were much higher for
Indigenous than non-Indigenous people. Incidence and death rates for pancreatic
cancer were much higher for Indigenous than non-Indigenous people.
Australian Indigenous HealthInfoNet abstract
Enquiries about obtaining a copy of this report should be directed to
the Cancer Foundation of Western Australia Inc, 46 Ventnor Avenue, West
Perth, WA 6005; ph: (08) 9212 4333; fax: (08) 9212 4334.

The Tiwi Health Board (2001)
The Tiwi Health Board story.
Stuart Park: Tiwi Health Board.
The Tiwi Islands, Bathurst and Melville, are located sixty kilometres
north of Darwin. The Tiwi Health Board was created in 1996 to empower
Tiwi people to improve health by taking control of service delivery. This
document summarises the aims and achievements of the Tiwi Health Board
and its programs.
Australian Indigenous HealthInfoNet abstract
Enquiries about obtaining a copy of this report should be directed to
the Tiwi Island Health Board, Bishop Street, Stuart Park, NT 0811; ph:
(08) 8941 5331.

Trudgen R (2000)
Why warriors lie down and die. Towards an understanding of why the
Aboriginal people of Arnhem land face the greatest crisis in health and
education since European contact.
Darwin: Aboriginal Resource and Development Services Inc.
View
book review

Youth Suicide Advisory Committee (2000)
Working together to stop Aboriginal suicide and self-harm in Western
Australia.
Perth: Youth Suicide Advisory Committee.
The rate of suicide among WA Aboriginal youth is double that of their
non-Aboriginal counterparts. The WA Youth Suicide Advisory Committee in
consultation with a range of Aboriginal individuals, groups and organisations
developed a number of recommendations for policy and programs to prevent
suicide and suicidal behaviour among Aboriginal youth in Western Australia.
This report outlines these recommendations and overall goals and strategies
for prevention.
The four overall goals proposed to prevent Aboriginal youth suicide were:
- to prevent both fatal and non-fatal suicidal behaviour among Aboriginal
people aged 25 years or less;
- to reduce the impact of suicide and suicidal behaviour on individuals,
families and communities;
- to improve access and availability of appropriate prevention services
for vulnerable youth groups and high-risk individuals; and
- to encourage the development of Aboriginal family and community networks
to support young people at risk and to promote their resilience and
emotional wellbeing.
Australian Indigenous HealthInfoNet abstract
Enquiries about obtaining a copy of this report should be directed to
the Health Department of WA, PO Box 8172, Perth Business Centre, Perth,
WA 6849; ph: (08) 9222 4222; fax: (08) 9222 4046.
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