Test Code HPVAV High-Risk Human Papilloma Virus Assay, Vaginal
Specimen and Container/Tube
Vaginal
Rejection Criteria
Random Collections ONLY.
NO preservatives or additives or sample will be rejected.
Specimen not in PreservCyt solution/container.
Specimen Type
Vaginal
Container/Tube
PreservCyt ThinPrep Pap test vial
Offsite Collection Instructions
See UCMC collection instructions
Sample in ThinPrep test vial can be stored at 2-8°C for up to 30 days prior to testing.
Test Includes
The assay detects high-risk HPV types 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, and 68 but does not discriminate among the types.
UCMC Collection Instructions
Specimen Source: Vaginal
Specimen Collection: Wipe clean of vaginal
secretions and mucus. Using a speculum with no lubricant, collect
the sample. . Please use the PreservCyt ThinPrep Pap test
vials for all HPV tests, even when a cytologic exam is not
requested. This test can be performed on the same sample collected
for liquid-based ThinPrep Pap test.
Specimen Transport: Immediate, no
refrigeration.
Microbiology Specimen Collection Tables
Please see link for Microbiology
Specimen Collection Tables;
- Category “Genital, Female, External”; Type
"Cervix"Table 1 BACTERIOLOGY, CHLAMYDIA, MYCOLOGY, MYCOBACTERIOLOGY
(AFB), VIROLOGY
Additional Information
ThinPrep collection kits are available from Hospital Stores,
Oracle #130231.
Fee Code
30687624
Synonyms
HPV
Human papillomavirus
Gen-Probe Aptima
Specimen Minimum Volume
4 mL
Day(s) Performed
Testing is performed once per week, on Friday.
STAT DAY(S) AND TIME(S) PERFORMED
Not Available
CPT
87624
Method Name
The Gen-Probe Aptima assay is a target amplification nucleic acid probe test that utilizes target capture, Transcription Mediated Amplification (TMA), and Hybridization Protection Assay (HPA) technologies for qualitative detection of Human Papillomavirus (HPV).
Test results may be affected by improper specimen collection, storage or specimen processing.
The Internal Control monitors the target capture, amplification and detection steps of the assay. It is not intended to control for cervical sampling adequacy.
A negative Aptima HPV Assay result does not exclude the possibility of cytologic abnormalities or of future or underlying CIN2, CIN3, or cancer
Reject Due To
Random Collections ONLY.
NO preservatives or additives, or sample will be rejected.
Specimen not in PreservCyt solution/container.
Pediatric Volume
4 mL
Transport Instructions
See UCMC collection instructions.
Sample in ThinPrep test vial can be stored at 2-8C for up to 30 days prior to testing.
Test Components
The assay detects high-risk HPV types 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, and 68 but does not discriminate among the types.
Methodology
The Gen-Probe Aptima assay is a target amplification nucleic acid probe test that utilizes target capture, Transcription-Mediated Amplification (TMA), and Hybridization Protection Assay (HPA) technologies for qualitative detection of Human Papillomavirus (HPV).
Test results may be affected by improper specimen collection, storage or specimen processing.
The Internal Control monitors the target capture, amplification
and detection steps of the assay. It is not intended to control
for cervical sampling adequacy.
A negative Aptima HPV Assay result does not exclude the
possibility of cytologic abnormalities or of future or
underlying
CIN2, CIN3, or cancer.
Synonyms/Key Search Words
HPV
Human papillomavirus
Gen-Probe Aptima