Aboriginal and/or Torres Strait Islander people

Indigenous Australians had a lower estimated participation rate than non-Indigenous Australians. They also experienced a higher screening positivity rate but have a lower follow-up diagnostic assessment rate and a longer median time between a positive screen and an assessment. Indigenous Australians had higher age-standardised bowel cancer incidence rates and higher mortality rates compared with non-Indigenous Australians (Table 4.3).

Reasons for differences in screening outcomes between Indigenous and non-Indigenous Australians are not known; however, the fact that higher proportions of Indigenous Australians live in Remote and Very remote locations and in lower socioeconomic areas, where access to relevant services can be an issue, may be contributing factors.

Table 4.3: Summary of performance indicators for Indigenous and non-Indigenous Australians

Indicator

Summary of performance indicators for Indigenous Australians compared with non-Indigenous Australians

Indigenous

Non-Indigenous

PI 1 - Participation rate(a)

Lower participation rate

37.7%

41.9%

PI 2 - Screening positivity rate

Higher screening positivity rate

8%

6%

PI 3 - Diagnostic assessment rate

Lower diagnostic assessment follow-up rate

78%

86%

PI 4 - Time between positive screen and diagnostic assessment

Longer median time

78 days

62 days

PI 9 - Adverse events –hospital admission

Comparison not published

n.p.

n.p.

PI 10 - Incidence of bowel cancer(b)(c)

Higher age-standardised incidence rate

122 per 100,000

110 per 100,000

PI 11 - Mortality from bowel cancer(c)(d)

Higher age-standardised mortality rate

39 per 100,000

27 per 100,000


References

ACSQHC (Australian Commission on Safety and Quality in Health Care) (2020) Colonoscopy Clinical Care Standard, Australian Commission on Safety and Quality in Health Care, Sydney, accessed 14 May 2025.