Immunoassay (IA)
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.
Chronic Urticaria
Specimen requirements | |
|---|---|
| Patient preparation | Overnight fasting is preferred |
| Preferred specimen(s) | 0.5 mL serum collected in a red-top tube (no gel) |
| Minimum volume | 0.3 mL |
| Collection instructions | Serum should be separated from the cells as soon as possible after visible clot formation (usually 15-30 minutes after collection) |
| Transport container | Transport tube |
| Transport temperature | Room temperature |
| Specimen stability | Room temperature: 7 days Refrigerated: 7 days Frozen: 28 days |
| Reject criteria | Moderate or gross hemolysis • Grossly lipemic • Grossly icteric • Serum separator tube (SST) |
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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