Test Code HCVDR Hepatitis C Virus Genotypic Antiviral Drug Resistance, Serum
Ordering Guidance
This test is intended for detection of preexisting antiviral drug resistance-associated substitutions in individuals known to be infected with hepatitis C virus (HCV) genotype 1a, 1b, or 3 (any subtype) and being considered for HCV NS3, NS5A, and NS5B inhibitor combination therapy.
Additional Testing Requirements
Prior to requesting this test, patients must have a confirmed serum or plasma hepatitis C virus (HCV) RNA level of 5000 IU/mL or higher within the preceding 30 days and a known HCV genotype result of 1a, 1b, or 3 (any subtype). The following tests are available to provide these prerequisite results:
-HCVQG / Hepatitis C Virus (HCV) RNA Quantification with Reflex to HCV Genotype, Serum
-HCVQN / Hepatitis C Virus (HCV) RNA Detection and Quantification by Real-Time Reverse Transcription-PCR, Serum
-HCVG / Hepatitis C Virus Genotype, Serum
Shipping Instructions
1. Ship specimen frozen on dry ice only.
2. If shipment will be delayed for more than 24 hours, freeze serum at -20 to -80° C before shipment, and transport on dry ice.
Necessary Information
The following 2 questions must be answered at the time of test ordering (if not ordering electronically, note the answers on the test request):
1. What Is the Hepatitis C Virus (HCV) RNA level in IU/mL within the last 30 days? Provide an answer using the following ranges:
- <5000
- 5000 to 1,000,000
- 1,000,001 to 10,000,000
- 10,000,001 to 100,000,000
- >100,000,000
Note: If the answer to this question is not answered or is “Unknown," testing will be canceled.
2. Does the patient have a known hepatitis C genotype of 1a, 1b, or 3 (any subtype)? Yes or No.
Note: If the answer to this question is "No," testing will be canceled.
Specimen Required
Supplies: Sarstedt Aliquot Tube, 5 mL (T914)
Collection Container/Tube: Serum gel
Submission Container/Tube: Plastic vial
Specimen Volume: 2.5 mL
Collection Instructions:
1. Centrifuge blood collection tube per manufacturer's instructions (eg, centrifuge and aliquot within 2 hours of collection for BD Vacutainer tubes).
2. Aliquot serum into a plastic vial.
Specimen Type
Serum SSTSpecimen Minimum Volume
1.6 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Serum SST | Frozen (preferred) | 60 days | ALIQUOT TUBE |
Refrigerated | 7 days | ALIQUOT TUBE |
Reject Due To
Gross hemolysis | OK |
Gross lipemia | OK |
Gross icterus | OK |
Reference Values
An interpretive report will be provided.
Day(s) Performed
Once per week
Report Available
4 to 14 daysSpecimen Retention Time
60 daysPerforming Laboratory
Mayo Clinic Laboratories in RochesterCPT Code Information
87900
87902
87999 (if appropriate for government payers)