Test Code HCVG Hepatitis C Virus Genotype, Serum
Shipping Instructions
Ship specimen frozen on dry ice only. If shipment will be delayed for more than 3 days, freeze serum at -20° C or colder (up to 42 days) until shipment on dry ice.
Specimen Required
Supplies: Sarstedt Aliquot Tube, 5 mL (T914)
Collection Container/Tube: Serum gel (red-top tubes are not acceptable)
Submission Container/Tube: Plastic vial
Specimen Volume: 5 mL
Collection Instructions:
Within 2 hours of collection, centrifuge and aliquot serum into a plastic vial.
Additional Information:
1. This test requires a minimum hepatitis C virus viral load of 500 IU/mL within the 30 days preceding collection.
2. Serum specimens previously submitted to other laboratories for non-microbiology tests are not acceptable for add-on test requests due to possible sample-to-sample carryover from automation used for those tests.
CMH COLLECTION: 4 mL in red gel vacutainer
Specimen Minimum Volume
1.5 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Serum SST | Frozen (preferred) | 42 days | ALIQUOT TUBE |
Refrigerated | 72 hours | ALIQUOT TUBE |
Testing Algorithm
Specimens either generating indeterminate genotype results, results with multiple or mixed hepatitis C virus genotypes (eg, 1, 5; 1, 2; or 1, 5), or those containing genotype 1 with no subtype will be automatically evaluated with by genotype resolution at an additional charge.
The following algorithms are available:
-Chronic Hepatitis C Treatment and Monitoring Algorithm: Direct Antiviral Antigen (DAA) Combination
Reflex Tests
Test ID | Reporting Name | Available Separately | Always Performed |
---|---|---|---|
HCVGR | HCV Genotype Resolution, S | No | No |
Useful For
Determining hepatitis C virus (HCV) genotype (1 to 5) to guide antiviral therapy in patients with chronic hepatitis C
Differentiating between HCV subtypes 1a and 1b
This assay should not be used as a screening test for HCV infection. It should be performed only on specimens obtained from patients confirmed to have HCV RNA levels in serum of 500 IU/mL or higher.
Reject Due To
Gross hemolysis | OK |
Gross lipemia | OK |
Day(s) Performed
Monday through Friday
Report Available
1 to 6 daysReporting Name
HCV Genotype, SReference Values
Undetected
Method Name
Reverse Transcriptase Polymerase Chain Reaction (RT-PCR) followed by Hybridization with Sequence-Specific, Fluorescent-Labeled Oligonucleotide Probes
Performing Laboratory
Mayo Clinic Laboratories in RochesterCPT Code Information
87902