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Hepatitis C Virus (HCV), Quantitative, Real-time PCR (Nongraphical)

CPT

87522

Synonyms
  • HCV RNA Quantitation, TaqMan®

Test Details

Methodology

cobas® HCV (Roche Molecular Systems)

Result Turnaround Time

3 - 5 days

Turnaround time is defined as the usual number of days from the date of pickup of a specimen for testing to when the result is released to the ordering provider. In some cases, additional time should be allowed for additional confirmatory or additional reflex tests. Testing schedules may vary.

Related Documents

Use

This test is used to determine the number of international units (IU) of hepatitis C virus (HCV) RNA per milliliter in serum or plasma in known HCV-positive patients.

Special Instructions

This procedure does not provide serial monitoring; it is intended for one-time use only. If serial monitoring is required, please order Hepatitis C Virus (HCV), Quantitative, Real-time PCR (Graphical) [550070].

Limitations

The quantifiable range of the assay is 15 IU/mL to 100,000,000 IU/mL.

Specimen Requirements

Specimen

Serum or plasma

Volume

2.5 mL

Minimum Volume

700 μL (Note: This volume does not allow for repeat testing.)

Container

Gel-barrier tube, lavender-top (EDTA) tube or plasma preparation tube (PPT™)

Collection Instructions

Centrifuge sample within 24 hours of collection. Transfer serum/plasma to a screw-cap polypropylene transport tube. Ship frozen (preferred). Plasma from a PPT™ can be frozen and shipped in situ. To avoid delays in turnaround time when requesting multiple tests on frozen samples, please submit a separate frozen specimen for each test requested.

Stability Requirements

TemperaturePeriod
Room temperature24 hours (stability provided by manufacturer or literature reference)
Refrigerated6 days (stability provided by manufacturer or literature reference)
Frozen6 weeks (stability provided by manufacturer or literature reference)
Freeze/thaw cyclesStable x4 (stability provided by manufacturer or literature reference)

Storage Instructions

Freeze (preferred) or refrigerate.

Causes for Rejection

Incorrect anticoagulant; PPT™ not centrifuged

References

Yao JD, Young S, Heilek GM, et al. Diagnosis and monitoring of HCV infection using the cobas® HCV test for use on the cobas® 6800/8800 systems. J Clin Virol. 2018 May;102:63-69.29518694

LOINC® Map

Order Code Order Code Name Order Loinc Result Code Result Code Name UofM Result LOINC
550080 HCV RT-PCR, Quant (Non-Graph) 11011-4 550266 Hepatitis C Quantitation IU/mL 11011-4
550080 HCV RT-PCR, Quant (Non-Graph) 11011-4 550259 HCV log10 log10 IU/mL 38180-6
550080 HCV RT-PCR, Quant (Non-Graph) 11011-4 550307 Test Information: 19147-8
Order Code550080
Order Code NameHCV RT-PCR, Quant (Non-Graph)
Order Loinc11011-4
Result Code550266
Result Code NameHepatitis C Quantitation
UofMIU/mL
Result LOINC11011-4
Order Code550080
Order Code NameHCV RT-PCR, Quant (Non-Graph)
Order Loinc11011-4
Result Code550259
Result Code NameHCV log10
UofMlog10 IU/mL
Result LOINC38180-6
Order Code550080
Order Code NameHCV RT-PCR, Quant (Non-Graph)
Order Loinc11011-4
Result Code550307
Result Code NameTest Information:
UofM
Result LOINC19147-8
Reflex Table for Hepatitis C Quantitation
Order Code Order Name Result Code Result Name UofM Result LOINC
Reflex 1 550265 HCV RNA (International Units) 550263 HCV RNA (International Units) IU/mL 11011-4
Reflex 1
Order Code550265
Order NameHCV RNA (International Units)
Result Code550263
Result NameHCV RNA (International Units)
UofMIU/mL
Result LOINC11011-4
Reflex Table for Hepatitis C Quantitation
Order Code Order Name Result Code Result Name UofM Result LOINC
Reflex 1 550265 HCV RNA (International Units) 550264 HCV log10 log10 IU/mL 38180-6
Reflex 1
Order Code550265
Order NameHCV RNA (International Units)
Result Code550264
Result NameHCV log10
UofMlog10 IU/mL
Result LOINC38180-6