Test Code HV2QU HIV-2 RNA Detection and Quantification, Real-Time qRT-PCR, Plasma
Ordering Guidance
This test is indicated for either 1) confirmatory qualitative detection of HIV-2 RNA in individuals with indeterminate or positive HIV-2-specific antibody but negative HIV-1-specific antibody test results; or 2) baseline or serial monitoring of HIV-2 viral load in those with confirmed HIV-2 infection with or without antiretroviral therapy.
Shipping Instructions
Ship specimen frozen on dry ice. If shipment will be delayed for more than 24 hours, freeze specimen at -20 to -80° C (up to 35 days) before shipment and then transport on dry ice.
Specimen Required
Supplies: Sarstedt Aliquot Tube, 5 mL (T914)
Collection Container/Tube: Lavender top (EDTA)
Submission Container/Tube: Plastic vial
Specimen Volume: 2.1 mL Plasma
Collection Instructions: Centrifuge and aliquot plasma into a plastic vial.
Secondary ID
623478Useful For
Confirmatory detection of human immunodeficiency virus type 2 (HIV-2) RNA in clinical plasma specimens for the diagnosis of acute or established HIV-2 infection
Quantifying plasma HIV-2 RNA levels (viral load) in individuals living with HIV-2:
-Before initiating antiretroviral therapy to obtain baseline viral load
-For monitoring HIV-2 disease progression with or without antiretroviral therapy
Testing Algorithm
The following algorithms are available:
-HIV Prenatal Testing Algorithm, Including Follow-up of Reactive Rapid Serologic Test Results
Special Instructions
Method Name
Reverse Transcription Real-time Polymerase Chain Reaction (RT-qPCR)
Reporting Name
HIV-2 RNA Detect / Quant, PSpecimen Type
Plasma EDTASpecimen Minimum Volume
Plasma: 1.1 mL
Specimen Stability Information
| Specimen Type | Temperature | Time | Special Container |
|---|---|---|---|
| Plasma EDTA | Frozen (preferred) | 60 days | ALIQUOT TUBE |
| Refrigerated | 6 days | ALIQUOT TUBE |
Reject Due To
| Gross hemolysis | OK |
| Gross lipemia | OK |
| Gross icterus | OK |
Reference Values
Undetected
Day(s) Performed
Varies (once per week)
Report Available
1 to 14 daysPerforming Laboratory
Mayo Clinic Laboratories in Rochester
Test Classification
This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. It has not been cleared or approved by the US Food and Drug Administration.CPT Code Information
87539
LOINC Code Information
| Test ID | Test Order Name | Order LOINC Value |
|---|---|---|
| HV2QU | HIV-2 RNA Detect / Quant, P | 69354-9 |
| Result ID | Test Result Name | Result LOINC Value |
|---|---|---|
| 623478 | HIV-2 RNA Detect / Quant, P | 69354-9 |