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Post-Transplant, Parvovirus B19 DNA, Quantitative, Real-Time PCR, Serum : 18066
Test CodePTPVPS or 18066
Alias/See Also
PTxplnt, Specialized, Txplnt, Services, Quest Advanced
CPT Codes
87799
Transport Container
1 mL (0.5 mL minimum) serum collected in a red top tube (no gel) or Serum Separator Tube.
Transport Temperature
Refrigerated
Specimen Stability
Room temperature: 48 hours; Refrigerated: 7 days; Frozen: 30 days
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
