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Test Code STPCO ThinPrep with Human Papillomavirus (HPV) Co-Test-Screen, Varies


Ordering Guidance


1. Mayo Clinic Laboratories' clients need prior laboratory approval to order cytology testing.

2. Due to the transient nature of the human Papillomavirus (HPV) in younger patients, this test is not recommended for patients under 30 years of age. STHPV / ThinPrep Screen with Human Papillomavirus (HPV) Reflex, Varies is available for women under the age of 30 with abnormal pap results.



Necessary Information


1. An acceptable cytology request form must accompany specimen containers and include the following: Patient's name, medical record number, date of birth, sex, source (exact location and procedure used), date specimen was taken, and name and pager number of ordering physician.

2. Submit any pertinent history or clinical information.



Specimen Required


Patient Preparation: For optimal interpretation, Papanicolaou smears should be collected near the middle of the menstrual cycle. No douching, lubricant use, and sexual intercourse for 24 hours prior to specimen collection.

 

Only 1 aliquot may be removed from PreservCyt sample vial prior to performing the ThinPrep Pap Test, regardless of the volume of the aliquot (maximum aliquot volume: 4 mL).

 

Submit only 1 of the following specimens:

 

Specimen Type: Cervical

Supplies: Thin Prep Media with Broom Kit (T056)

Container/Tube: ThinPrep

Specimen Volume: 16 mL

Collection Instructions:

1. Obtain adequate sampling from cervix using a broom-like collection device. If desired, use lukewarm water to warm and lubricate the speculum. Insert the central bristles of the broom into the endocervical canal deep enough to allow the shorter bristles to fully contact the ectocervix. Push gently and rotate the broom in a clockwise direction 5 times.

2. Rinse the broom as quickly as possible into the PreservCyt solution vial by pushing broom into bottom of vial 10 times, forcing the bristles apart.

3. As a final step, swirl broom vigorously to further release material. Discard the collection device.

4. Tighten cap on vial so that the torque line on the cap passes the torque line on the vial.

5. Specimen vial must be labeled with a minimum of 2 unique identifiers (patient's name and medical record number or date of birth).

6. Bag ThinPrep specimens individually as they have a tendency to leak during transport.

7. Place labels on the vial and on the bag.

 

Specimen Type: Ectocervix and endocervix

Supplies: Thin Prep Media with Spatula and Brush Kit (T434)

Container/Tube: ThinPrep

Specimen Volume: 16 mL

Collection Instructions:

1. Obtain an adequate sampling from the ectocervix using a plastic spatula. If desired, use lukewarm water to warm and lubricate the speculum. Select contoured end of plastic spatula and rotate it 360 degrees around the entire exocervix while maintaining tight contact with exocervical surface.

2. Rinse spatulas quickly as possible into the PreservCyt solution vial by swirling spatula vigorously in vial 10 times. Discard the spatula.

3. Next, obtain an adequate specimen from endocervix using an endocervical brush device. Insert the brush into the cervix until only the bottommost fibers are exposed. Slowly rotate one-quarter or one-half turn in 1 direction. Do not over rotate.

4. Rinse the brush as quickly as possible in the PreservCyt solution by rotating the device in the solution 10 times while pushing against the PreservCyt vial wall.

5. Swirl brush vigorously as final step to further release material. Discard the brush.

6. Tighten the cap so that the torque line on the cap passes the torque line on the vial.

7. Specimen vial must be labeled with a minimum of 2 unique identifiers (patient's name and medical record number or date of birth).

8. Bag ThinPrep specimens individually as they have a tendency to leak during transport.

9. Place labels on the vial and on the bag.


Useful For

Screening for cervical carcinoma or intraepithelial lesions and the presence or absence of high-risk human papillomavirus (HR-HPV) when screening women over the age of 30 for possible cervical neoplasia

 

Detection of high-risk HPV genotypes associated with the development of cervical cancer

 

Aids in triaging women with abnormal Pap smear results

 

Individual genotyping of HPV-16 or HPV-18 if present

 

Aids in triaging women with positive HR-HPV but negative Pap smear results

Reflex Tests

Test ID Reporting Name Available Separately Always Performed
TPSPC Physician Interp Screen No No
HPV HPV with Genotyping, PCR, ThinPrep Yes No
VHPV HPV Vaginal Detect / Genotyping PCR Yes No

Testing Algorithm

When this test is ordered, a ThinPrep Pap cytology screen and human papillomavirus high-risk DNA detection with genotyping by polymerase chain reaction test will be performed.

 

If ThinPrep Pap results are abnormal, a pathologist will review the case at an additional charge.

Special Instructions

Method Name

Light / Real-Time Polymerase Chain Reaction

Reporting Name

ThinPrep w/HPV Co-Test-Screen

Specimen Type

Varies

Specimen Minimum Volume

See Specimen Required

Specimen Stability Information

Specimen Type Temperature Time Special Container
Varies Ambient (preferred) 42 days THIN PREP
  Refrigerated  42 days THIN PREP

Reference Values

ThinPrep PAPANICOLAOU

Satisfactory for evaluation. Negative for intraepithelial lesion or malignancy.

 

HUMAN PAPILLOMAVIRUS (HPV)

Negative for HPV genotypes 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, and 68

Day(s) Performed

Monday through Friday

Report Available

5 to 8 days

Performing Laboratory

Mayo Clinic Laboratories in Rochester

Test Classification

This test has been cleared, approved, or is exempt by the US Food and Drug Administration and is used per manufacturer's instructions. Performance characteristics were verified by Mayo Clinic in a manner consistent with CLIA requirements.

CPT Code Information

G0123 (Government Payers)

88142  

88141-TPSPC (if appropriate)

LOINC Code Information

Test ID Test Order Name Order LOINC Value
STPCO ThinPrep w/HPV Co-Test-Screen 101822-5

 

Result ID Test Result Name Result LOINC Value
71326 Interpretation 69965-2
71327 Participated in the Interpretation No LOINC Needed
71328 Report electronically signed by 19139-5
71329 Addendum 35265-8
71330 Gross Description 22634-0
CY007 Pap Test Source 22633-2
CY008 Clinical History 22636-5
CY009 Menstrual Status (LMP, PM, Pregnant) 8678-5
CY010 Hormone Therapy/Contraceptives 8659-5
71578 Disclaimer 62364-5
71824 Case Number 80398-1