Urticaria Induced Basophil Activation


Sunquest Code:UIBASA  
Epic Code:LAB6817Epic Name:Urticaria Basophil Activation
Methodology:Semi-quantitative flow cytometry
CPT Code:88184, 88185 x2
Turnaround Time:Specimens are sent to reference laboratory Mon-Sat; results are reported within 2-5 days.
Compliance:

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.



Collection Instructions

Specimen:Blood
Optimal Volume:2 mL
Minimum\Peds Volume:1.2 mL
Causes for Rejection:Specimens other than serum. Contaminated, grossly hemolyzed or lipemic specimens.


Processing and Shipping

Specimen Processing:Centrifuge and aliquot 1 mL, 0.5 mL minimum within 2 hours of collection. Store frozen.
Shipping Instructions:Ship at frozen temperature. CRITICAL FROZEN. Separate specimens must be submitted when multiple tests are ordered.
Test Performed at or Referral Lab Lab Sendouts  (ARUP)
Referral Lab number:2005416


Interpretive

Reference Range:

27 percent or less

Negative – No basophil activation detected.

28-38 percent

Indeterminate – Borderline basophil activation detected.

39 percent or greater

Positive – Basophil activation detected.

 

 

Use:Determine whether CD203c is upregulated in suspected chronic urticaria if urticaria is felt to be due to autoimmune antibodies to the basophil IgE receptor or to IgE.


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