DNA Sequencing • Reverse Transcriptase Polymerase Chain Reaction (RT-PCR)
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) | 2 mL plasma collected in an EDTA (lavender-top) tube or PPT (white-top) tube |
| Alternative specimen(s) | 2 mL CSF collected in a sterile leak-proof container |
| Minimum volume | 0.6 mL plasma • 0.6 mL CSF |
| Collection instructions | Do not freeze whole blood or any samples stored in primary tube. Freshly drawn specimens (whole blood) may be stored at 2-25° C for up to 24 hours prior to centrifugation. Separate plasma from cells within 24 hours of collection by centrifugation. If shipping frozen, transfer plasma to a leak-proof transport tube, then freeze prior to shipment. Follow manufacturer's instructions for collection tube handling. CSF: Collect CSF using standard procedures. Transfer to a sterile, leak-proof container. Ship frozen. |
| Transport container | Transport tube |
| Transport temperature | Frozen |
| Specimen stability | Room temperature: 24 hours Refrigerated: 6 days Frozen: 42 days |
| Reject criteria | Plasma received frozen in the plasma preparation tube (PPT) • Serum • Whole blood >24 hours old • Frozen whole blood |
The Result and LOINC® information listed below should not be used for electronic interface maintenance with Quest Diagnostics. Please contact the Quest Diagnostics Connectivity Help Desk for more information at 800-697-9302.
NOTE: The codes listed in the table are not orderable Test Codes
Result code | Result name | LOINC code | Component name |
|---|---|---|---|
| 86007864 | HIV 1 GENOTYPE | 48558-1 | HIV genotype |
| Quest Diagnostics Nichols Institute-San Juan Capistrano, CA |
| 33608 Ortega Highway |
| San Juan Capistrano, CA 92675-2042 |
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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