Preventive examinations by health groups
The frequency and scope of cytological screening directly depend on the woman's age and her belonging to a specific health group.
Health Group I (virtually healthy patients) A standard preventive approach with a clear age-based division is applied here:
- 21–29 years: cytology (cervical smear evaluation) is the baseline method. It must be performed at least every 3 years.
- Ages 30–65: the screening strategy changes. At this age, the priority is cotesting—simultaneous performance of the Pap smear and HPV testing. The screening interval is increased to once every 5 years.
Health Group II (presence of risk factors) This category includes women with an increased risk, primarily HPV-positive patients. Such patients are strongly advised to undergo regular PAP testing:
- If the cytology result is normal (NILM), repeat co-testing is scheduled in 1 year.
- If changes at the ASC-US level or more severe lesions are detected, the patient is strictly indicated for colposcopy.
Health Group III (benign diseases) In the presence of confirmed benign cervical diseases, the management and treatment tactics are determined by the relevant clinical guidelines.
Alternative screening option
In addition to the classical cytological approach, an alternative strategy is permitted, where HPV testing serves as the first step rather than the PAP test. The patient's pathway in this case depends on the virus status:
- HPV-negative result (-): The risk of developing pathology is minimal. The next screening HPV test is scheduled for the patient only in 5 years.
- HPV-positive result (+): High risk of intraepithelial lesions. In this situation, performing a cytological study (PAP test) to assess cellular changes in the epithelium becomes a mandatory second step.
Cytological conclusions and management algorithm
Standard or liquid-based cytology is used for analysis. In the absence of additional indications, the test is performed once every 3 years. Further actions of the physician are strictly regulated by the obtained report.
1. NILM Report Negative for Intraepithelial Lesion or Malignancy — this is a normal variant. Squamous and glandular epithelial cells show no signs of atypia.
- Tactics: Repeat the cytological examination routinely in 3 years.
2. ASC-US Report Atypical Squamous Cells of Undetermined Significance — detection of atypical squamous cells of undetermined significance.
- Primary tactics: For ASC-US and any more severe lesions, HPV testing is strictly indicated.
The further algorithm for ASC-US depends on the presence of the virus:
- If HPV test is (-): no cause for concern, repeat co-testing is indicated in 3 years.
- If HPV test is (+): the patient is referred for colposcopy.
- If abnormal findings are detected during colposcopy, a cervical biopsy is performed.
- In the absence of abnormal colposcopic findings, repeat co-testing is scheduled in 1 year.
> Clinical Note: For patients with an ASC-US result and a positive HPV test, additional diagnostic triage may be advisable. For this purpose, immunocytochemical (ICC) testing of the collected biological material for the expression of p16/Ki67 biomarkers is performed. This helps to more accurately assess the risk of high-grade dysplasia.
To memorize the management tactics for ASC-US, use the HPV test "traffic light rule": "Minus" (green light) — all clear, wait 3 years. "Plus" (red light) — danger, proceed to colposcopy immediately.
Class and exam questions
What does a NILM PAP test result mean?
The abbreviation NILM stands for Negative for Intraepithelial Lesion or Malignancy. This is a normal result indicating that routine repeat cytology should be performed in 3 years.
What is the first thing that needs to be done in case of an ASC-US result?
When atypical squamous cells of undetermined significance (ASC-US) are detected, the primary and mandatory management tactic is human papillomavirus (HPV) testing.
What is the essence of co-testing?
Co-testing is the simultaneous performance of a PAP test (cytology) and HPV testing. In women aged 30–65 without risk factors, it is performed once every 5 years.
Why is p16/Ki67 testing used?
Immunocytochemical testing for p16/Ki67 is used for additional triage of HPV-positive patients with an ASC-US result to more accurately assess the risk of high-grade dysplasia.
What else to study on this topic
- Morphological appearance of cells in ASC-US and more severe dysplasias
- Comparison of conventional and liquid-based cytology
- Colposcopic features of abnormal findings in HPV infection
- Biochemical mechanism of p16 and Ki67 protein overexpression in cells
- Management tactics for patients with LSIL and HSIL results
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