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Histamine, Plasma
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Aid in evaluation of patient with allergic signs and symptoms, such as anaphylaxis; may assist in diagnosing and monitoring of mast-cell activation disorders.
Quantitative Enzyme-Linked Immunosorbent Assay
Tue, Sat
1-6 days
Lavender (EDTA) or pink (K2EDTA). Collect in a pre-chilled tube and on ice.
Centrifuge refrigerated and separate upper two-thirds of plasma within 20 minutes. Transfer 1 mL plasma to an ARUP Standard Transport Tube and freeze immediately. (Min: 0.5 mL)
CRITICAL FROZEN. Separate specimens must be submitted when multiple tests are ordered.
Lipemic or hemolyzed specimens.
After separation from cells: Ambient: Unacceptable; Refrigerated: 6 hours; Frozen: 6 months
Effective June 13, 2011
0-8 nmol/L
Compliance Statement D: For laboratory tests using a manufactured RUO kit. This test was developed and its performance characteristics determined by ARUP Laboratories. The U. S. Food and Drug Administration has not approved or cleared this test; however, FDA clearance or approval is not currently required for clinical use. The results are not intended to be used as the sole means for clinical diagnosis or patient management decisions.
Hotline History
83088
| Component Test Code* | Component Chart Name | LOINC |
|---|---|---|
| 0070036 | Histamine, Plasma | 34316-0 |
- plasma histamine
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