National Healthcare Agreement: PI 11-Cervical screening rates, 2012
Identifying and definitional attributes | |
Metadata item type:![]() | Indicator |
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Indicator type:![]() | Output measure |
Short name:![]() | PI 11-Cervical screening rates, 2012 |
METEOR identifier:![]() | 435845 |
Registration status:![]() |
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Description:![]() | Rates of cervical screening for women within national target age group. |
Indicator set:![]() | National Healthcare Agreement (2012) Health, Superseded 25/06/2013 |
Outcome area:![]() | Prevention Health, Standard 07/07/2010 |
Quality statement:![]() | National Healthcare Agreement: PI 11-Cervical screening rates, 2012 QS Health, Retired 14/01/2015 |
Collection and usage attributes | |
Population group age from:![]() | 20 years |
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Population group age to:![]() | 69 years |
Computation description:![]() | Denominator is adjusted to exclude the estimated number of women who have had a hysterectomy, using national hysterectomy fractions. Rates directly age-standardised to the 2001 Australian population. Analysis by remoteness and SEIFA Index of Relative Socio-economic Disadvantage (IRSD) is based on postcode of residential address at the time of screening. Presented as a percentage. |
Computation:![]() | 100 × (Numerator ÷ Denominator) |
Numerator:![]() | Number of women aged 20–69 years who have been screened in a 2 year period. |
Numerator data elements:![]() | |
Denominator:![]() | Population of women aged 20–69 years |
Denominator data elements:![]() | |
Disaggregation:![]() | 2007–2008 and 2008–2009 (revised for new hysterectomy fractions), 2009–2010—State and territory, by:
2007–2008 and 2008–2009 (revised for new hysterectomy fractions), 2009–2010—Nationally, by:
State and territory, by Indigenous status (no new data) Some disaggregation may result in numbers too small for publication. |
Disaggregation data elements:![]() | |
Comments:![]() | Most recent data available for 2012 CRC report: 2009–2010 (calendar years: total population); 2004–05 (Indigenous status: NATSIHS). Screening rates for Indigenous women are based on the ABS National Aboriginal and Torres Strait Islander Health Survey (NATSIHS). |
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:![]() | ABS Estimated resident population (total population) Frequency Quarterly Quality statement ABS Estimated resident population (total population), QS Data custodian Australian Bureau of Statistics National Hospital Morbidity Database (NHMD) Frequency Annual Data custodian Australian Institute of Health and Welfare ABS 2004-05 National Aboriginal and Torres Strait Islander Health Survey (NATSIHS) Frequency Every 6 years Data custodian Australian Bureau of Statistics |
Accountability attributes | |
Reporting requirements:![]() | National Healthcare Agreement |
Organisation responsible for providing data:![]() | Australian Institute of Health and Welfare |
Further data development / collection required:![]() | Specification: Long-term |
Source and reference attributes | |
Relational attributes | |
Related metadata references:![]() | See also National Healthcare Agreement: PI 04-Incidence of selected cancers, 2012
See also National Healthcare Agreement: PI 10-Breast cancer screening rates, 2012
Supersedes National Healthcare Agreement: PI 11-Cervical screening rates, 2011
See also National Healthcare Agreement: PI 12-Bowel cancer screening rates, 2012
See also National Healthcare Agreement: PI 44-Survival of people diagnosed with cancer, 2012
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