cpd cytology

National Cervical
Screening Program

The National Cervical Screening Program aims to prevent cervical cancer through regular testing. Women and people with a cervix from 25 to 74 years of age are encouraged to have a Cervical Screening Test (CST) every five years to check for the Human Papillomavirus (HPV). The CST checks for HPV, a common sexually transmitted infection that can lead to cell changes in the cervix. Occasionally, the presence of abnormal cells can develop into cervical cancer. We accept two patient options for HPV testing:

Self-collect HPV testing roundel
  1. Clinician-Collected Samples (including for Liquid Based Cytology/LBC)
  2. Self-Collected Samples (or Dry Swabs)
  • What age is recommended for the first HPV screening?

    Both HPV vaccinated and unvaccinated patients from the ages of 25 to 74 years should be tested.

    The age range is based on evidence that cervical cancer in young patients is rare and screening patients younger than 25 years of age has not altered the number of cervical cancer cases or deaths in this group. This measure also prevents the over-treatment of common cervical abnormalities in young patients, which usually resolve naturally. Furthermore, HPV vaccination has already and will continue to show a significant reduction of these abnormalities amongst patients in this age bracket.

    If a screening participant under the age of 25 is symptomatic, a HPV test can be requested that will be covered as a MBS item.

  • What is the cervical screening clinical management pathway?

    Patients aged 25 to 74 years are invited to have a HPV test every five years. This includes both vaccinated and unvaccinated screening participants, as the HPV vaccine protects against some but not all types of HPV.

    • If HPV is not detected, LBC will not be performed and a recommendation to repeat screening in 5 years will be made. Cytology will be performed if the patient has symptoms of cervical disease or is undergoing management of a cervical abnormality.
    • If HPV is detected, a reflex LBC/Thin Prep® will be performed on the same specimen.

    There will be a combined report for HPV and LBC results, which includes a risk category and the recommended management, in line with the guidelines. There are three risk categories:

    1. Patients who are classified as Low risk are routinely invited to re-screen in five years.
    2. Patients who are classified as Intermediate risk are routinely invited to have another HPV test in 12 months. This is to check that the infection has cleared.
    3. Patients classified as Higher risk are routinely referred directly to colposcopy for further investigation.

    Please refer to the Cervical Screening Pathway below for both clinician-collected and self-collected samples.

    Cervical Screening Pathway Flyerarrow icon
  • What is the difference between Liquid Based Cytology (LBC) and Dry Swab?

    LBC is typically performed in a medical practice for clinician-collected samples when HPV is detected. A sample of cells is collected from the cervix into the liquid-based specimen vial known as ThinPrep®, which is sent to Clinical Labs for analysis to identify the presence of HPV viral DNA at the molecular level.

    Dry Swabs are generally used for self-collection of cervical samples for HPV testing. It can be done at home or at a medical clinic. Note: Self-collected samples are not suitable for LBC testing - If HPV is detected on the self-collect dry swab, the patient will need to proceed with a clinician-collect test so that LBC can be performed.

    Please refer to table below for Clinician-Collected versus Self-Collected samples for CSTs:

    Scroll indicator
    Clinician-collected cervical sampleSelf-collected vaginal sample
    Is co-testing possible?YesNo
    Indicated for:

    • Those who are eligible and due or overdue for cervical screening, including during pregnancy
    • Other points in the pathway where only a HPV test is required, including Test of Cure after HSIL treatment
    • People who have had a total hysterectomy with history of HSIL
    YesYes
    • Those undergoing surveillance after completely excised AISYesNo
    • People who have signs and symptoms suggestive of cervical cancer
    • People who have postcoital or intermenstrual bleeding, post menopausal bleeding, or unexplained persistent vaginal discharge
    • People who were exposed to DES in utero
    YesNo
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  • How do I order a CST at Clinical Labs?

    Scroll indicator
    Patient presents asContextAgeSample typeTest typeWhat to write on the pathology request form
    AsymptomaticNational Cervical Screening Program routine five-yearly screening:
    •   Only 1 of this MBS item is claimable in a 57-month period
    ≥ 24yrs & 9mthsCervicalHPV testCervical Screening Test (CST)
    AsymptomaticScreening in specific populations:
    •   Immune-deficient
    •   Early sexual debut, prior to 14 years and not vaccinated prior to sexual debut (only 1 claimable between 20 and 24 years of age)
    Any ageCervicalHPV test•   HPV test, Immune-deficient
    •   HPV test, Early debut HPV
    Follow-up test claimable after previous positive screening test (12-month repeat)Any ageCervicalHPV testFollow-up HPV test
    FOLLOW-UP OR POST-TREATMENT FOR CLINICAL MANAGEMENT
    Following treatment of HSIL (also called “test of cure”)Any ageCervicalHPV testTest of cure
    VaginalSelf-collectSelf-collect test of cure
    VaultSelf-collectSelf-collect test of cure
    Following treatment of AISAny ageCervicalCo-testCo-test post AIS
    VaultCo-testCo-test post AIS
    DES exposed in uteroAny ageCervicalCo-testDES exposure
    VaultCo-testDES exposure
    SymptomaticFor investigation of symptoms, e.g. abnormal bleedingAny ageCervicalCo-testCo-test or HPV & LBC, Symptomatic (specify)
    Follow-up for HPV+ self-collectOnly claimable within 21 months following the detection of oncogenic HPV (any type) on a self-collected screening test>24 years and 9 monthsVaginalLBCHPV+ self-collect follow-up
    CervicalLBCHPV+ self-collect follow-up
    Repeat test following an unsatisfactory testFollowing an unsatisfactory test:
    •   Only claimable when preceded by another cervical or vaginal MBS item
    Any ageCervicalHPV testHPV test, previous result unsatisfactory
    VaginalHPV testHPV test, previous result unsatisfactory
    CervicalLBCHPV test, previous result unsatisfactory
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  • What are the LBC/ThinPrep® collection instructions at Clinical Labs?

    LBC ThinPrep Collect image

    1. Collect:
    To obtain an adequate sample, insert the central bristles of the brush into the endocervical canal. Apply sufficient pressure to gently bend the lateral bristles against the ectocervix and rotate completely three to five times in a clockwise direction. If a lubricant must be used, it should be applied sparingly on the outer portion of the speculum with great care to avoid the tip.

    LBC ThinPrep Rinse image

    2. Rinse:
    Rinse the brush in the PreservCyt® Solution vial by pushing it down against the bottom 10 times, forcing the bristles apart. Discard the collection device. Do not leave the head of the Cervex Brush in the vial. Replace the cap and tighten it so that the small black mark passes the corresponding line on the vial.

    LBC ThinPrep Record image

    3. Record:
    Record the patient’s name and date of birth on the vial, and their details and medical history on the pathology request form. Place both the vial and request form in the enclosed specimen collection bag for transport to Clinical Labs.

  • What are the self-collect instructions at Clinical Labs?

    Items required for self-collect:

    • Clinical Labs request form signed by doctor (ensure self-collect HPV test is noted).
    • Copan FLOQSwab® for vaginal self-collection (552C) (Red Top dry swab) – available from Clinical Labs.
    • Only Copan FLOQSwab 552C is validated for use.
    Copan FLOQSwab 552C for self collect

    Steps for self-collecting:

    self collect step 1

    1. Before you collect your sample, ensure you have clean hands. To avoid contamination, do not remove the swab from the container until you are ready to collect your sample and do not use any lubricant.

    self collect step 2

    2. Once you are comfortable, remove the red cap and pull the swab out of the container.

    self collect step 3

    3. There is a red line halfway along the swab. Insert the front part of the swab inside your vagina aiming for this red line.

    self collect step 4

    4. Once the swab is correctly inside your vagina, rotate it gently in a circular motion for 20-30 seconds.

    self collect step 5

    5. Remove the swab, place it back in the container and gently secure the cap.

    self collect step 6

    6. Return the self-collect swab to the medical practice or Clinical Labs collection centre with the request form with priority. Please ensure the Collection Date is labelled on the container.

  • Patient with cervical cancer symptoms

    Symptomatic patients can have a cervical sample taken at any time, regardless of their age or screening history. Patients at any age who have signs or symptoms suggestive of cervical cancer, or its precursors, will have a co-test (LBC and HPV). The presence and type of symptoms should be clearly noted on the request form to ensure cytological examination is performed on these specimens.

  • How to Order HPV Testing

    Who to test
    • Women and people with a cervix from 25 to 74 years of age should have a Cervical Screening Test every five years

    • Symptomatic patients, e.g. abnormal bleeding, genital warts

    • Asymptomatic patients with previous positive screening test

    • Doctor recommendation based on patient context

    When to Test
    • Routine five-yearly screening

    • Doctor recommendation based on patient symptoms, context and/or age (see section How do I order a CST at Clinical Labs above)

    Request Form Instructions
    • Use the Australian Clinical Labs General Pathology Request Form

    • Complete by referring to section How do I order a CST at Clinical Labs above

    • Record any Clinical Notes and tick relevant boxes under Cervical Cytology

    Specimen Details
    • Refer to section How do I order a CST at Clinical Labs for sample and test type

    • The relevant sections above also outline the processes for sample collection

    Test cost
    • Routine five-yearly screening – Only 1 MBS item is claimable in a 57-month period for those aged over 24yrs & 9mths

    • Only 1 claimable between 20 and 24 years of age

    • Follow-up test claimable after previous positive screening test (12-month repeat)

    • Only claimable within 21 months following the detection of oncogenic HPV (any type) on a self-collected screening test for those aged over 24yrs & 9mths

    • See section How do I order a CST at Clinical Labs for more details

    Additional tests to consider
    • The first Cervical Screening Test at 25 years of age is an ideal opportunity to screen for common STIs, as chlamydia and gonorrhoea testing can be performed on the same ThinPrep® vial used to collect the Cervical Screening sample. No extra specimen collection is required.