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Herpes Simplex Virus, Type 1 and 2 DNA, Quantitative, Real-Time PCR : 19502
Test CodeHSVPQT or 19502
CPT Codes
87530x2
Transport Container
1 mL (0.3 mL min) CSF, vitreous, pericardial, pleural, or amniotic fluid collected in a sterile, leakproof container OR
1 mL (0.3 mL min) serum OR
1 mL (0.3 mL min) plasma collected in an EDTA (lavender-top) tube
1 mL (0.3mL min) whole blood collected in an EDTA (lavender-top) tube
Alternative Specimen(s)
1 mL (0.3 mL) bronchoalveolar lavage or bronchial wash collected in a sterile leak-proof container
Note: Do not freeze whole blood.
1 mL (0.3 mL min) serum OR
1 mL (0.3 mL min) plasma collected in an EDTA (lavender-top) tube
1 mL (0.3mL min) whole blood collected in an EDTA (lavender-top) tube
Alternative Specimen(s)
1 mL (0.3 mL) bronchoalveolar lavage or bronchial wash collected in a sterile leak-proof container
Note: Do not freeze whole blood.
Transport Temperature
Whole blood: Refrigerated
All other specimen types: Frozen
All other specimen types: Frozen
Specimen Stability
Room temperature: 48 hours; Refrigerated 7 days; Frozen: 30 days; Whole blood: Unacceptable frozen
Reject Criteria (Eg, hemolysis? Lipemia? Thaw/Other?)
Whole blood received frozen
Methodology
Real-Time Polymerase Chain Reaction
Setup Schedule
Daily
Report Available
1 day (From receipt in the performing Lab)
Limitations
Laboratory test results should always be considered in the context of clinical observations. This test was developed, and its performance characteristics determined by Quest Diagnostics. 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
The detection of HSV-1 and HSV-2 DNA is based upon the real-time amplification, detection and differentiation of specific HSV-1 and HSV-2 genomic DNA sequences by PCR from total DNA extracted from the specimen.
The quantitative range of this assay is 100-2,000,000 copies/mL.
The quantitative range of this assay is 100-2,000,000 copies/mL.
Performing Laboratory
Quest Diagnostics