Gynecologic Pap Test (Image-guided), Liquid-based Preparation With Reflex to Human Papillomavirus (HPV) (Aptima®) When ASC-U, ASC-H, LSIL, HSIL, AGUS
Use
Diagnose primary or metastatic neoplasm. This test aids in the diagnosis of sexually transmitted HPV infection. High-risk HPV test is used for types 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, and 68, without differentiation of the individual type.
Special Instructions
Not provided.
Limitations
The test may yield suboptimal results if ectocervical, endocervical, or vaginal cell populations are insufficient. Excessive use of lubricating jelly can interfere with cytologic examination, possibly leading to unsatisfactory results. The specimen's reprocessing or HPV testing might be limited depending on the sample's initial volume in liquid-based cytology. A negative result does not rule out HPV infection due to potential low levels of infection or sampling error. This test detects the 14 most common high-risk HPV types and cannot determine the specific type of HPV present.
Methodology
PCR-based (RT-PCR)
Biomarkers
LOINC Codes
- 47527-7
- 47528-5
- 19764-0
- 19763-2
- 52797-8
- 22636-5
- 22638-1
- 22639-9
- 19767-3
- 19769-9
- 8251-1
- 11546-9
- 11502-2
Result Turnaround Time
2-5 days
Related Documents
For more information, please review the documents below
Specimen
Cervical Swab
Volume
ThinPrep® vial
Minimum Volume
Not provided
Container
ThinPrep® vial
Collection Instructions
ThinPrep® Vial: Use a broom or brush/spatula technique. Rinse the collection device in PreservCyt® solution, and secure the cap on the ThinPrep® vial.
Patient Preparation
Avoid douches 48 to 72 hours prior. Do not collect during or shortly after menstruation.
Storage Instructions
Maintain specimen at room temperature; process within 21 days.
Causes for Rejection
Improper collection, inadequate specimen, improper labeling, leaking in transit, insufficient quantity, male patient submission, expired vials, frozen specimens, or outdated liquid-based cytology specimens.