In Australia, Aboriginal and Torres Strait Islander women have poorer health than non-Indigenous women. Indigenous women have higher levels of risk factors, earlier onset of disease, and lower survival rates. Improvements in the areas of prevention, early detection and treatment can help Indigenous women to have better health outcomes.
A new national women’s health policy has been developed by the Australian Government. It addresses Indigenous women’s health needs, noting that often it is the women who look after the health of other family members and forget about their own health needs. If Indigenous women are to have better health outcomes, their history, experience, culture and rights need to be understood.
It is also important to understand that Indigenous women see health as something that covers everything important in a person’s life, including land, environment, physical body, community, relationships and law. Thus health is viewed as the social, emotional, and cultural wellbeing of the whole community.
Non-Indigenous health treatment can reduce disease in Indigenous people, but it needs to be done in a culturally sensitive manner to help with both immediate and long-term health issues for Indigenous women.
A recent report states that by June 2012 there will be approximately 300,000 Indigenous females living in Australia, which is 2.5% of the Australian female population. New South Wales (NSW) and Queensland (Qld) have the highest numbers of Indigenous females, followed by Western Australia (WA) and the Northern Territory (NT) (See Figure 1).
Figure 1: Projected Australian Indigenous female population, by jurisdiction, by June 2012

Data derived from the Australian Bureau of Statistics (2009) Experimental estimates and projections, Aboriginal and Torres Strait Islander Australians 1991 to 2021
This is where the Indigenous people of Australia live:
As the following statistics show, the Indigenous female population is much younger overall than the non-Indigenous female population (See Figure 2).
Figure 2: Age groups of Australian Indigenous and non-Indigenous female populations at 30 June 2011

Data derived from the Australian Bureau of Statistics (2009) Experimental estimates and projections, Aboriginal and Torres Strait Islander Australians 1991 to 2021 and Australian Bureau of Statistics (2008) Population projections, Australia, 2006 to 2101
The poorer health outcomes of Indigenous people are rooted in history. Modern-day factors, such as money, physical environment and social conditions also influence the health of people, families and communities as a whole. These factors are linked with education, employment, income, housing, access to services, social networks, connection with the land, racism, and imprisonment. On all these measures Indigenous people suffer poorer outcomes than non-Indigenous people. The important measures in some of these areas for Indigenous females are summarised in the following sections.
School records show us that in 2006 Indigenous females were less likely to attend school than non-Indigenous females across all age groups. The differences were the greatest in the 15 to 19 year-old age group. In 2006, school completion to year 12 was much lower for Indigenous females than for non-Indigenous females (See Figure 3).
Figure 3: Australian female school retention until year 12, by jurisdiction, 2006

Data derived from the Steering Committee for the Review of Government Service Provision (2009) Overcoming Indigenous disadvantage: key indicators 2009
A comparison of Indigenous and non-Indigenous females with respect to further education (past high school) is:
Here is a comparison of the employment of Indigenous and non-Indigenous females:
Education and employment influence a woman’s level of income. The following statistics show that Indigenous women suffer financial difficulties, given their generally lower level of education and reduced participation in employment:
Figure 4: Median gross weekly individual income for females aged 15 years and over, by Indigenous status and jurisdiction, 2006

Data derived from the Steering Committee for the Review of Government Service Provision (2009) Overcoming Indigenous disadvantage: key indicators 2009
Recent reports suggest that Indigenous females born in 2005-2007 can be expected to live to 72.9 years compared with 82.6 years expected for all females (See Figure 5). Life expectancy of Indigenous females was highest in NSW (75.0 years) and lowest in the NT (69.2 years). Due to changes in the methodology used to estimate Indigenous life expectancy, these figures are higher than previous estimates.
Figure 5: Female life expectancy in NSW, QLD, WA, NT and Australia, 2005-2007

Data derived from the Australian Bureau of Statistics (2009) Experimental life tables for Aboriginal and Torres Strait Islander Australians: 2005-2007
Understanding Indigenous death rates can be a complex task. The following points may help to explain some of the terms used:
In 2004-2008, Indigenous female deaths were between two and four times higher than age-specific death rates for the total Australian female population (See Table 1). The adjusted SMRs range from 2.16 for Indigenous females living in NSW to 3.52 for those living in the NT. This means that the actual deaths were twice as high as expected for NSW, and 3.5 times as high for the NT.
| Registered deaths | SMR | ||
|---|---|---|---|
| Registered | Number | Adjusted | |
|
Data derived from the Australian Bureau of Statistics (2009) Causes of death Australia, 2007 |
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Notes:
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| NSW | 1174 | 1.88 | 2.16 |
| Qld | 1269 | 2.29 | 2.42 |
| WA | 1028 | 3.47 | 3.12 |
| SA | 316 | 2.53 | n/a |
| NT | 1001 | 3.83 | 3.52 |
| Australia | 5056 | 2.40 | 2.61 |
In 2005-2009, death rates were higher for Indigenous females than for non-Indigenous females across all age groups. The ratio of the Indigenous rate to the non-Indigenous rate was particularly high for the age groups between 25 and 64 years (See Figure 6). Rates and rate ratios were higher for Indigenous females living in WA, SA and the NT than for those living in NSW and Qld.
Figure 6: Indigenous-non-Indigenous death rate ratios, NSW/Qld and WA/SA/NT, by age group, 2005-2009

Data derived from the Australian Bureau of Statistics (2010) Deaths Australia, 2009
In 2002-2006, of all infant female deaths in Qld, WA, SA and the NT, about one fifth were Indigenous. The infant mortality rate of 10.1 deaths per 1,000 live births for Indigenous females was 2.6 times the rate of 3.9 per 1,000 for non-Indigenous females. This means that deaths of Indigenous female infants were over two and a half times more than non-Indigenous female infants.
In 2001-2005, cardiovascular disease (i.e. diseases of the heart and circulatory system) was the leading cause of death for Indigenous females living in Qld, WA, SA and the NT. The number of Indigenous female deaths from this disease was almost three times the number of deaths expected from the rate for non-Indigenous females (SMR: 2.7)1. The next most common cause of death for Indigenous females was neoplasm (mainly cancers) (SMR: 1.6), external causes (SMR: 3.5), diabetes (SMR: 14.5), and respiratory diseases (SMR: 3.6).
In 2003-2005, of all 60 recorded maternal deaths, six were Indigenous women (10%), where Indigenous status was known (Indigenous status was not reported in 8% of the deaths).
In 2003-2005, the maternal mortality ratio for Indigenous women was 21.5 deaths per 100,000 confinements, almost three times higher than the ratio of 7.9 per 100,000 for non-Indigenous women. For direct maternal deaths, the ratio for Indigenous women was 7.2 per 100,000 compared with 3.6 per 100,000 for non-Indigenous women. This means that Indigenous women died twice as often from direct maternal deaths than non-Indigenous women.
In 2009, there were 15,825 2 births registered in Australia with one or both parents identified as Indigenous. Of these births, 7,688 were female (5% of all births registered). Indigenous status was identified as follows:
In 2009, Indigenous women had more babies than non-Indigenous women and had them at younger ages.
Figure 7: Age-specific fertility rates for Australian women, by age group, 2009

Data derived from the Australian Bureau of Statistics (2010) Births Australia, 2009
In 2009, total fertility rates were higher among the Indigenous female population. Rates for Indigenous women were 2,575 births per 1,000 and for all women were 1,901 per 1,000 (See Figure 8). The highest total fertility rates for Indigenous women were:
Figure 8: Total fertility rates for Australian women, by jurisdiction, 2009

Data derived from the Australian Bureau of Statistics (2010) Births Australia, 2009
In 2008, the average birth weight of babies born to Indigenous mothers was 3,196 grams (g), almost 200g less than the average for babies born to non-Indigenous mothers (3,385g). Babies born to Indigenous women were twice as likely to be of low birth weight (LBW) (12.3%) than were those born to non-Indigenous women (5.9%). (LBW, defined as a birth weight of less than 2,500g, increases the risk of death in infancy and other health problems.) The amount of low birth weight babies born to Indigenous women were highest for SA (16.3%) and WA (14.8%) (See Table 2).
| NSW | Vic | Qld | WA | SA | NT | Aust | |
|---|---|---|---|---|---|---|---|
|
Data derived from Laws P, Sullivan EA (2009) Australia’s mothers and babies 2008 |
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Notes:
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| Indigenous mothers | |||||||
| Mean birthweight | 3217 | 3216 | 3214 | 3107 | 3067 | 3133 | 3182 |
| % low birthweight | 11.2 | 12.0 | 11.2 | 16.2 | 16.2 | 12.5 | 12.5 |
| Non-Indigenous mothers | |||||||
| Mean birthweight | 3386 | 3370 | 3394 | 3372 | 3366 | 3390 | 3381 |
| % low birthweight | 5.5 | 6.3 | 6.0 | 5.7 | 6.1 | 4.9 | 5.9 |
Risk factors for low birth weight babies include:
Tobacco, in particular, has a major impact on birth weight. In 2001-2004, the birth weight of live babies born was:
This means that babies born to Indigenous women who smoked were over 250g lighter than babies born to Indigenous women who did not smoke.
The comparable figures for live babies born to non-Indigenous women were:
Low birth weight live-born babies occurred in the following proportions:
In 2000-2001, the Western Australian Aboriginal Child Health Survey reported slightly higher average birth weights than those reported above:
The lowest average birth weights reported in the survey were:
In 2009-10, over 171,000 Indigenous females living in NSW, Vic, Qld, WA, SA and the NT were admitted to hospital. The standardised rate for Indigenous females was 915 per 1,000, compared to 394 per 1,000 for non-Indigenous females. This means than Indigenous females were admitted to hospital more than twice that of non-Indigenous females.
In 2009-10, admission rates were higher for Indigenous females than for non-Indigenous females across all age groups, with rate ratios being particularly high for those aged between 5 and 14 years (See Figure 9).
Figure 9: Australia female Indigenous-non-Indigenous hospitalisation rate ratios, by age group, 2007-2009

Data derived from the Australian Institute of Health and Welfare (2009) Australian hospital Statistics 2007-08
The information needed to compare the causes of hospitalisation for Indigenous and non-Indigenous females is not available for recent years. It is likely that the causes for Indigenous females are similar to those documented for 1999-2000. The most common reason for hospitalisation of Indigenous females then was ‘care involving dialysis’, which was responsible for 30% of admissions. Many of these were repeat admissions; some of these people entered hospital for dialysis almost daily.
Apart from these admissions, the most common causes of hospitalisation for Indigenous females were:
More recently (2009-10), there were 305,008 hospital separations, which were identified as Indigenous, in NSW, Vic, Qld, WA, SA and the NT (3.8% of the total hospital separations). For Indigenous people, the causes of hospitalisation were:
Generally, separation rates were higher for Indigenous people than for non-Indigenous people for all main groups.
The information above shows that Indigenous women remain less healthy than non-Indigenous women. However, there is some evidence that the health status of Australia’s Indigenous females is improving slowly. For example, there have been significant reductions in recorded mortality in recent years in a number of states and territories and age-standardised death rates for Indigenous women living in WA, SA and the NT declined by around 15% over the period 1991-2006. The declines in death rates were less for Indigenous people than for non-Indigenous people, however, with Indigenous-non-Indigenous death rate ratios increasing for females.
The most recent estimate of life expectancy at birth for Indigenous females, 72.9 years in 2005-2007, is more than previous estimates, but the improvements may be due largely to revised statistical methods.
Indigenous infant mortality rates for WA, SA and the NT have declined significantly over the 16-year period 1991-2006. The Indigenous rate declined by 47% over that period, slightly more than the 34% decline of the rate for non-Indigenous people. The Indigenous-non-Indigenous rate ratio declined from 4.3 to 3.2.
There is no doubt other evidence of improvement in some measures of health status, and of deterioration in others. But, clearly, the gap between the health status of Indigenous females and that of non-Indigenous females is still unacceptably wide.