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BK Virus DNA, Quantitative, Real-Time PCR, Urine
Test Code16581
CPT Codes
87799
Preferred Specimen
0.7 mL random urine submitted in a sterile, leak-proof container - no preservative
Minimum Volume
0.3 mL
Transport Temperature
Frozen
Specimen Stability
Room temperature: 48 hours
Refrigerated: 7 days
Frozen: 30 days
Refrigerated: 7 days
Frozen: 30 days
Methodology
Real-Time Polymerase Chain Reaction
FDA Status
This test was developed and its analytical performance characteristics have been determined by Quest Diagnostics. It has not been cleared or approved by FDA. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.
Setup Schedule
Monday-Sunday Morning
Report available: Next Day
Report available: Next Day
Reference Range
BK Virus DNA,QN RT PCR | Not Detected (copies/mL) |
BK Virus DNA,QN RT PCR | Not Detected (Log copies/mL) |
Clinical Significance
This test is used to determine the presence of BK virus DNA in patients' specimens. Detection of the virus in these specimens may be indicative of an active infection, as PCR detects the presence of the virus, and not the hosts reaction to the virus. Polyomavirus BK DNA detection in urine or plasma is associated with an increased risk of graft rejection in renal recipients. Quantitative testing may indicate change in risk over time. This is a quantitative molecular test, with a linear range of 500-500,000,000 copies/mL.
Performing Laboratory
Quest Diagnostics Nichols Institute
14225 Newbrook Drive
Chantilly, VA 20153