Information for doctors
- On December 1, 2017, the Cervical Screening Test (CST) replaced the Pap test
- The CST is now the only Medicare-funded routine cervical screening test, and is available to women aged 25 years and over
- Specimens must be collected by clinicians into ThinPrep® vials
- Request forms must specify the requested test PLUS the reason for test PLUS supporting clinical notes.
A risk-based approach
The CST uses an HPV DNA test to detect the presence of oncogenic HPV types known to be associated with a higher risk of developing significant cervical abnormalities. The HPV test is more sensitive than cytology, so it can be performed less frequently.
- Asymptomatic women who test negative for oncogenic HPV are at low risk of developing cervical cancer and only need to be screened every 5 years
- Asymptomatic women who test positive for oncogenic HPV will have a liquid-based cytology (LBC) test performed on the same sample (reflex LBC) and will be assessed as either intermediate risk and advised to return for further testing in 12 months, or higher risk and referred for colposcopy
- Symptomatic women and those with a history of high-grade cervical pathology will have both an HPV and LBC test (Co-test) performed, regardless of their HPV result
- Women with special circumstances identified by the program may be offered more frequent screening or a single screening test prior to age 25.
In order to help you with the changes implemented on December 1, 2017, we have created a range of resources which are available for download using the links below.
Previous information sheets
|ThinPrep Pap Test information for health care professionals|
|Cancer Council Australia Cancer Guidelines Wiki: National Cervical Screening Program |
Guidelines for the management of screen-detected abnormalities, screening in specific populations and investigation of abnormal vaginal bleeding.
For further information on the new program, please contact our Cytology Department on (03) 9287 7761.