ARUP's Laboratory Test Directory

Hepatitis C Virus RNA Quantitative, Real-Time PCR : 0098268

Mnemonic: HEPCQNT

Methodology: Quantitative Real-Time Polymerase Chain Reaction
Performed: Sun-Sat
Reported: 1-3 days
Specimen Required: Collect: lavender (EDTA), pink (K2EDTA), plasma preparation tube, serum separator tube.

Specimen Preparation: Separate from cells within 6 hours. (Min: 1.5 mL)
PPT:
Transport 3 mL plasma in original collection container. (Min: 1.5 mL)
All others:
Transfer 3 mL serum or plasma to an ARUP Standard Transport Tube.


Storage/Transport Temperature: Frozen. Separate specimens must be submitted when multiple tests are ordered.

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


Unacceptable Conditions: Heparinized specimens.

Stability (collection to initiation of testing): On Cells: Ambient: 6 hours. After separation from cells: Refrigerated: 72 hours; Frozen: 6 weeks
Reference Interval:
Not Detected
Interpretive Data: The quantitative range of this assay is 1.6 - 7.8 log IU/mL (43- 69,000,000 IU/mL).

An interpretation of "Not Detected" does not rule out the presence of PCR inhibitors in the patient specimen or hepatitis C virus RNA concentrations below the level of detection of the assay. Care should be taken when interpreting any single viral load determination.

This assay should not be used for blood donor screening, associated re-entry protocols, or for screening Human Cell, Tissues and Cellular Tissue-Based Products (HCT/P).

Note: The limit of quantification for this RNA assay is 1.6 log IU/mL (43 IU/mL). If the assay DID NOT DETECT the virus, the test result will be reported as "<1.6 log IU/mL (<43 IU/mL)." If the assay DETECTED the presence of the virus but was not able to accurately quantify the number of copies, the test result will be reported as "Not Quantified."

Specimens received with less than minimum volume for testing will automatically be run with a dilution according to the guidelines below:
-Specimens with 500-1000 µL will be diluted resulting in a modification of the quantitative range of the assay to 1.9-8.1 log IU/mL (88-140,000,000 IU/mL).
-Specimens with 200-500 µL will be diluted resulting in a modification of the quantitative range of the assay to 2.3-8.5 log IU/mL (219-350,000,000 IU/mL).

This test is intended for use in conjunction with clinical presentation and other laboratory markers as an indicator of disease prognosis. This test is also used in assessing viral response to antiretroviral treatment as measured by changes in HCV RNA levels.
CPT Code(s): 87522
Cross References: HCV Viral Load (Hepatitis C Virus RNA Quantitative, Real-Time PCR)
 
 

 

 

 
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