Cytology, SurePath Liquid-Based Pap Test and Human Papillomavirus (HPV), High Risk with 16 and 18 Genotype by PCR, SurePath. (for routine co-testing in women over 30)
FDA-approved test for cotesting at 5-year intervals in individuals 25-65 years with a cervix. Recommended test is Human Papillomavirus (HPV), High Risk with 16 and 18 Genotype by PCR, SurePath (2011933).
Microscopy/Qualitative Polymerase Chain Reaction
1-7 days, add 2 days for HPV testing
New York DOH Approval Status
Cervical specimen in a SurePath collection kit, Rovers Cervex-Brush Kit (ARUP Supply #22216), PAP Perfect Plastic Spatula and Cytobrush Plus GT Collection Kit (ARUP Supply #41126), or Rovers Cervex-Brush Combi Collection Kit (ARUP Supply #45031) available online through eSupply using ARUP Connect™ or contact ARUP Client Services at (800) 522-2787. For specific instructions refer to Specimen Collection and Handling.
Transport cervical specimen in the original collection kit.
Specimens not collected in a SurePath collection kit. Expired preservative vials or vials received without the collection devices.
Ambient: 1 month; Refrigerated: 6 months; Frozen: Unacceptable
Refer to report.
In addition to the SurePath Pap Test, Human Papillomavirus (HPV), High Risk with 16 and 18 Genotype by PCR, SurePath (ARUP test code 2011933) will be performed and reported under a separate accession. The Pap Test is a screening test for cervical cancer and its precursors with an inherent false-negative rate.
87624; 88142, if reviewed by pathologist add 88141
|Component Test Code*||Component Chart Name||LOINC|
|2000473||SurePath Pap Specimen Source|
- HPV PCR
- Pap Smear and HPV testing
- Pap Test, (SurePath Liquid-Based Pap Test)
- SurePath Pap Test and HR Hybrid Capture