Transcription Mediated Amplification (TMA)
This test is for use under an Emergency Use Authorization only; it is intended for use as described in the CDC ZIKA Diagnostic Testing Guidance and under the Food and Drug Administration's (FDA) Emergency Use Authorization (EUA).
ZIKA,ZIKA RNA QUAL
Specimen requirements | |
|---|---|
| Patient preparation | None Specified |
| Preferred specimen(s) | 3 mL serum |
| Minimum volume | 1.5 mL |
| Collection instructions | Collect blood in a serum separator tube or a standard red-top, allow blood to clot at room temperature. The specimen should be centrifuged as soon as possible, and serum transferred to a new aliquot tube. Transport refrigerated (cold packs) to local Quest Diagnostics accessioning laboratory. Transport frozen (dry ice): If shipping directly to the performing laboratory by an overnight air courier. Specimens must not be left in lock bins. |
| Transport container | Transport tube |
| Transport temperature | Refrigerated (cold packs) |
| Specimen stability | Room temperature: Unacceptable Refrigerated: 7 days Frozen: 30 days |
| Reject criteria | Samples received in original collection container |
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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