Real-Time Polymerase Chain Reaction
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.
Specimen requirements | |
|---|---|
| Patient preparation | None Specified |
| Preferred specimen(s) | 1 mL CSF, pericardial, pleural, or amniotic fluid collected in a sterile leak-proof container or 1 mL serum or 1 mL whole blood or plasma collected in an EDTA (lavender-top) tube |
| Alternative specimen(s) | 1 mL bronchoalveolar lavage or bronchial wash collected in a sterile plastic leak-proof container |
| Minimum volume | 0.3 mL |
| Collection instructions | Note: Do not freeze whole blood |
| Transport container | Sterile plastic leak-proof container |
| Transport temperature | Whole blood: Refrigerated (cold packs) All other specimen types: Frozen |
| Specimen stability | Whole blood Room temperature: 48 hours Refrigerated: 7 days Frozen: Unacceptable All other specimens Room temperature: 48 hours Refrigerated: 7 days Frozen: 30 days |
| HSV 1, DNA, QN, PCR | Not Detected |
| HSV 2, DNA, QN, PCR | Not Detected |
Reference ranges are provided as general guidance only. To interpret test results use the reference range in the laboratory report.
*The CPT codes provided are based on AMA guidance and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payer being billed.
This material contains content from LOINC® (http://loinc.org). The LOINC Table, LOINC Table Core are copyright © 1995-2019, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee and is available at no cost under the license at http://loinc.org/license.
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