ARUP's Laboratory Test Directory

Human Papillomavirus (HPV) DNA Probe, High Risk SurePath® (AutoCyte) with Reflex to Genotyping : 0060817

Mnemonic: SP HPVHI R

Methodology: Nucleic Acid Probe/Polymerase Chain Reaction
Performed: Tues, Thurs
Reported: 2-7 days
Specimen Required: Collect:  and Transport: SurePath® PAP specimen transport media collection device. Refer to Cytology, SurePath Pap Test (AutoCyte PREP® System) Specimen Collection in the Laboratory Test Directory for collection
guidlines. (Min: 2 mL)


Transport:  

Submit specimen according to Biological Substance, Category B, shipping guidelines.


Pediatric Collection/Transport:  

Submit specimen according to Biological Substance, Category B, shipping guidelines.


Unacceptable Conditions:  Swabs or specimens in any other transport media. For specimens in ThinPrep® Test transport media refer to test code 0060816. For cervical brush specimens in Digene specimen transport media, refer to test code 0060818. Samples other than cervical are not acceptable for children under age 12.

Stability:  Ambient: 1 month; Refrigerated: 6 months; Frozen: Unacceptable
Interpretive Data: Test Information:
The high-risk HPV test detects HPV genotypes 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, and 68, which are associated with cervical cancer and its precursor lesions. However, cross-reactions with other genotypes may occur. Results should be correlated with cytologic and histologic findings. Sensitivity may be affected by cellularity of specimen.

Please refer to Statement B in the Compliance Statements section in the front of the Laboratory Test Directory.
Note: If the Human Papillomavirus (HPV) DNA Probe test is positive Genotyping is performed.  Genotyping is not performed on specimens yielding negative or equivocal results on the Human Papillomavirus (HPV) DNA Probe test.
CPT Code(s): 87621 DNA Probe; if reflexed, add 87621 x10
 
 

 

 

 
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