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Test ID SHPV Human Papillomavirus (HPV) DNA Detection with Genotyping, High-Risk Types by PCR, SurePath, Varies

Useful For

Detection of high-risk (HR) genotypes associated with the development of cervical cancer

 

An aid in triaging women with abnormal Pap smear test results

 

Individual genotyping of human papillomavirus (HPV)-16 and/or HPV-18, if present

 

This testing is intended for use in clinical monitoring and management of patients. It is not intended for use in medical-legal applications.

Specimen Type

Varies


Necessary Information


Specimen source, collection date, and patient identifiers are required.



Specimen Required


Supplies: Cobas PCR Media Tube w/Cap (T945)

Specimen Type: Cervical (endocervical or ectocervical) or vaginal

Specimen Volume: 3.0 mL

Collection Instructions:

1. Aliquot 3 mL SurePath specimen into Cobas PCR Media Tube w/Cap tube.

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

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


Specimen Stability Information

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

Reject Due To

SurePath enriched cell pellet Reject

Reference Values

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

Day(s) Performed

Monday through Saturday

Report Available

3 to 6 days

Performing Laboratory

Mayo Clinic Laboratories in Rochester

CPT Code Information

87626

G0476 (if appropriate)

Secondary ID

62599

Forms

If not ordering electronically, complete, print, and send a Microbiology Test Request (T244) with the specimen.