BK Virus by Quantitative NAAT, Plasma
Also known as: BKQ P
Use
This test is used to detect and quantify BK virus in plasma. It is primarily utilized to monitor viral load in transplant patients, where BK virus reactivation can contribute to nephropathy and other complications. Quantification helps in tailoring antiviral treatment and immunosuppressive therapy to prevent organ rejection.
Special Instructions
For this test, it is important to separate plasma from cells within 24 hours of collection. The plasma should then be transferred to an ARUP standard transport tube. This test is approved for use in New York State.
Limitations
The quantitative range of this assay is 1.33 to 8.00 log IU/mL (21.5 to 100,000,000 IU/mL). An interpretation of 'Not Detected' does not exclude the presence of inhibitors or BK virus DNA concentration below the detection limit of the assay. Variations in assay results may occur due to standardization discrepancies across laboratories.
New York Approved
Methodology
PCR-based (qPCR)
Biomarkers
LOINC Codes
- 32284-2
- 32362-6
- 44805-0
- 32284-2
- 44805-0
- 32362-6
Result Turnaround Time
1-3 days
Related Documents
For more information, please review the documents below
Specimen
Plasma
Volume
2mL
Minimum Volume
1mL
Container
ARUP standard transport tube
Collection Instructions
Separate from cells within 24 hours of collection. Transfer to an ARUP standard transport tube.
Causes for Rejection
Heparinized specimens, whole blood, serum. Urine (refer to BK Virus by Quantitative NAAT, Urine, ARUP test code 3006075).
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | 24 hrs |
| Refrigerated | 6 days |
| Frozen | 6 months |