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St. John Health System
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Index:

Chronic Urticaria Index

Order Name CU INDEX
Test Number: 5587555
Revision Date 12/12/2022
Test Name Methodology LOINC Code
Chronic Urticaria Index
Ex-Vivo challenge and cell culture/Histamine analysis  
SPECIMEN REQUIREMENTS
Specimen Specimen Volume (min) Specimen Type Specimen Container Transport Environment
Preferred 1.5 mL (0.15 mL) Serum Clot Activator (SST or Red No-Gel) Room Temperature
Instructions Specimen Type: Red-top tube or gel-barrier tube
Specimen Storage: Maintain specimen at room temperature Stability: Room temperature up to 1 week Frozen up to 1 year
Specimen Collection: Serum should be separated from cells within two hours of venipuncture. Send serum in a plastic transport tube.
Special Instructions: Testing referred to Eurofins Viracor LLC TC 2103
Specimen Stability: Ambient: Not Available, Refrigerated : Not Available, Frozen: Not Available
GENERAL INFORMATION
Expected TAT 6 - 11 days  
Clinical Use Patients with a chronic form of urticaria who are positive (> 10) with the CU index® have an autoimmune basis for their disease. A positive result does not indicate which autoantibody (anti-IgE, anti-FceRI or anti-FceRII) is present.
Ex-Vivo Challenge and cell culture: Donor blood cells are incubated with patient serum, a negative control and a positive control. Following the ex-vivo challenge, the cells are centrifuged and the supernatant is recovered for assay of histamine released. Histamine Analysis: Using a quantitative enzyme immunoassay, the histamine released into the supernatant is measured and compared to the total histamine in the basophils. This test has not been cleared or approved for diagnostic use by the U.S. Food and Drug Administration. 
Notes Labcorp Test Code: 820022
CPT Code(s) 86352
Service Provided By Labcorp Oklahoma, Inc.
Lab Section Reference Lab