Borrelia burgdorferi DNA, Qualitative Real-Time PCR, Miscellaneous
Test code
CPT code(s)*
Test resources
Test FAQ
Details
Methodology
Real-Time Polymerase Chain Reaction
Assay category
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.
Alternative name(s)
Lyme,Tick borne
Specimen requirements | |
|---|---|
| Patient preparation | None Specified |
| Preferred specimen(s) | 3 mL whole blood collected in an EDTA (lavender-top) tube or 3 mL CSF or synovial fluid collected in a sterile plastic leak-proof container |
| Alternative specimen(s) | Whole blood collected in: ACD (yellow-top) tube |
| Minimum volume | 0.5 mL |
| Transport container | Whole blood: EDTA (lavender-top) tube CSF or synovial fluid: Sterile leak-proof container |
| Transport temperature | Refrigerated (cold packs) |
| Specimen stability | Whole blood CSF or synovial fluid |
| Reject criteria | Lithium heparin (green-top) tube • Sodium heparin (green-top) tube |
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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