Identifying and definitional attributes | |
Metadata item type: | Indicator |
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Indicator type: | Output measure |
Short name: | Bowel cancer screening rates, 2010 |
METEOR identifier: | 394292 |
Registration status: | Health, Superseded 08/06/2011 |
Description: | Screening rates for bowel cancer for people within national target groups. |
Indicator set: | National Healthcare Agreement (2010) Health, Superseded 08/06/2011 |
Outcome area: | Prevention Health, Standard 07/07/2010 |
Data quality statement: | National Healthcare Agreement: P12-Bowel cancer screening rates, 2010 QS Health, Superseded 08/06/2011 |
Collection and usage attributes | |
Population group age from: | Population aged 50, 55 and 65 years |
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Computation description: | Rates are age-specific and expressed per 100 persons. |
Computation: | 100 × (Numerator ÷ Denominator) |
Numerator: | Number of persons aged 50, 55 and 65 years who completed a faecal occult blood test supplied by the National Bowel Cancer Screening Program in the reference calendar year. |
Numerator data elements: | |
Denominator: | Population aged 50, 55 and 65 years |
Denominator data elements: | |
Disaggregation data elements: | |
Comments: | Specified disaggregation: Nationally and by state/territory: by age/sex, Indigenous status, remoteness area and SEIFA of residence. Available disaggregation: Nationally and by state/territory: by age/sex; Nationally: by remoteness area and SEIFA of residence. Data for 2009 will be available by mid-2010. Most recent data available for 2010 CRC baseline report: 2008 |
Representational attributes | |
Representation class: | Percentage |
Data type: | Real |
Unit of measure: | Person |
Format: | NN.N |
Indicator conceptual framework | |
Framework and dimensions: | Accessibility Health behaviours |
Data source attributes | |
Data sources: | |
Accountability attributes | |
Reporting requirements: | National Healthcare Agreement |
Organisation responsible for providing data: | Australian Institute of Health and Welfare |
Further data development / collection required: | Specification: Interim
A National Bowel Cancer Dataset (i.e. data dictionary) is under development. The quality of Indigenous identification needs to be assessed. Explore how to identify people who are screened outside the National Bowel Cancer Screening Program. |
Other issues caveats: | Indigenous status is self-reported by participating individuals.
Remoteness area and SEIFA of residence are based on postcode of residential address at the time of screening. Lack of inclusion of people screened outside the National Bowel Cancer Screening Program will result in an underestimate of the population screening rates in the target age groups. Disaggregation by Indigenous status, remoteness area and SEIFA of residence within individual states/territories is subject to data quality considerations. The bowel cancer screening program is guaranteed until 2010. The program is expected to expand to more age groups on a rolling basis. The National Bowel Cancer Screening Program was suspended in May 2009 due to unreliable screening kits, subsequently resuming in November 2009. |
Relational attributes | |
Related metadata references: | Has been superseded by National Healthcare Agreement: PI 12-Bowel cancer screening rates, 2011 Health, Superseded 30/10/2011 See also National Healthcare Agreement: P04-Incidence of selected cancers, 2010 Health, Superseded 08/06/2011 See also National Healthcare Agreement: P10-Breast cancer screening rates, 2010 Health, Superseded 08/06/2011 See also National Healthcare Agreement: P11-Cervical screening rates, 2010 Health, Superseded 08/06/2011 |