Post-Transplant, Parvovirus B19 DNA, Quantitative, Real-Time PCR, Plasma : 18068

Test Code
PTPVPP or 18068


Alias/See Also
PTxplnt, Specialized, Txplnt, Services, Quest Advanced


CPT Codes
87799

Transport Container
1 mL (0.5 mL minimum) plasma collected in an EDTA (lavender-top) tube.


Transport Temperature
Refrigerated


Specimen Stability
Room temperature: 48 hours; Refrigerated: 7 days; Frozen: Unacceptable


Reject Criteria (Eg, hemolysis? Lipemia? Thaw/Other?)
Received frozen


Methodology
Real-Time Polymerase Chain Reaction

Setup Schedule
Sunday - Saturday


Report Available
1 day


Limitations
Laboratory test results should always be considered in the context of clinical observations. This test was developed, and its performance characteristics determined by med fusion. It has not been cleared or approved by the U.S. Food and Drug Administration (FDA). The FDA has determined that such clearance or approval is not necessary. This test is used for clinical purposes. It should not be regarded as investigational for research. This laboratory is certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA) as qualified to perform high complexity clinical laboratory testing.


Reference Range
Not Detected


Clinical Significance
Parvovirus B19 infection has a wide variety of disease manifestations, including Fifth disease, transient aplastic crisis, persistent anemia and congenital hydrops fetalis. Quantification of parvovirus B19 genomic DNA is based upon Real-Time PCR amplification and detection. Reportable range is 100 to 100,000,000 copies/mL (2.00 to 8.00 Log copies/mL).


Performing Laboratory
med fusion



The CPT Codes provided in this document are based on AMA guidelines and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payor being billed. Any Profile/panel component may be ordered separately. Reflex tests are performed at an additional charge.