Test Overview
Clinical Utility
This assay specifically identifies HPV 16 and HPV 18 while concurrently detecting the rest of the high risk types (31, 33, 35, 39, 45, 51, 52,56, 58, 59, 66 and 68) at clinically relevant infection levels.
Method
Polymerase chain reaction (PCR)
Result Included
HPV Detection and Genotype
Specimen
Specimen Type
Cervical CellsCollection & Handling
Collection Instructions
Additional Information
Collection supplies (with instructions and requisitions) may be obtained by contacting ICL Client Care at (416) 422-3000 ext. 300 or info@iclabs.ca. Provide the fluid source clearly on the requisition.
Performance & Interpretation
Turnaround Time
10 days
Results
Name
Units
Reference Range
Conversion
-
HPVNegative
Referral Location
Canada
Interface & Setup
HL7 Interface Codes
| Order Code | Result Name | Result Codes | Units |
|---|---|---|---|
| HPV | HPV DNA | 28266 | |
| HPV Non-16/18 Genotype | 64558 | ||
| HPV Genotype 16 | 64559 | ||
| HPV Genotype 18 | 64560 |
Test Version
Last Updated
2023-08-08