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HPV High Risk with 16/18 Genotype - SurePath

Order Name HPV Hi/16/18 SP
Test Number: 5522580
Revision Date 12/19/2019
Test Name Methodology LOINC Code
HPV Genotype 16 PCR
Qualitative PCR 61372-9 
HPV Genotype 18 PCR
Qualitative PCR 61373-7 
HPV Other High Risk
Qualitative PCR 70061-7 
HPV Source
Prompt  
SPECIMEN REQUIREMENTS
Specimen Specimen Volume (min) Specimen Type Specimen Container Transport Environment
Preferred 3 mL (1.5 mL) PAP specimen SurePath Liquid Pap Container (Pap Prep) Refrigerated
Instructions Collect cervical specimen with SurePath collection kit and place in SurePath media. 
Mix well. Transfer 3mL (1.5mL) to an Sterile Transport Tube.
Unacceptable: Bloody or dark brown specimens. Specimens in any media other than indicated above. 
Specimen source required.
Stability: Ambient: 1 month; Refrigerated: 6 months; Frozen: Unacceptable
GENERAL INFORMATION
Testing Schedule Mon, Wed, Fri 
Expected TAT 1-5 days after set-up  
Clinical Use This test amplifies DNA of HPV16, HPV18 and 12 other high-risk HPV types (31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, and 68) associated with cervical cancer and its precursor lesions. Sensitivity may be affected by specimen collection methods, stage of infection, and the presence of interfering substances. Results should be interpreted in conjunction with other available laboratory and clinical data. A negative high-risk HPV result does not exclude the presence of other high-risk HPV types, the possibility of future cytologic abnormalities, underlying CIN2-3, or cancer.

This test is intended for medical purposes only and is not valid for the evaluation of suspected sexual abuse or for other forensic purposes. HPV testing should not be used for screening or management of atypical squamous cells of undetermined significance (ASCUS) in women under age 21. 
Notes Reference Lab: ARUP
Test Code: 2011933
Click Here to view information on the ARUP website.
CPT Code(s) 87624
Lab Section Reference Lab