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Labcorp Oklahoma, Inc.
Test Directory


Index:

Chronic Urticaria PD-BATC

Order Name CU INDEX
Test Number: 5587555
Revision Date 06/03/2025
Test Name Methodology LOINC Code
Chronic Urticaria PD-BATC
Flow cytometry 75023-2 
SPECIMEN REQUIREMENTS
Specimen Specimen Volume (min) Specimen Type Specimen Container Transport Environment
Preferred 1 mL (0.5 mL) Serum Clot Activator (SST or Red No-Gel) Frozen
Instructions Specimen: Serum 1 mL (0.5 mL Minimum Volume: 0.5 mL (Note: This volume does not allow for repeat testing.)
Container: Gel-barrier tube or red-top tube
Collection: Allow to clot then Transfer separated serum to a plastic transport tube and Freeze.
Storage Requirements:Frozen
Stability Requirements: Room temperature 1 day, Refrigerated 14 days, Frozen 2 months (Freeze/thaw cycles Stable x3)
Cause for Rejection: Specimen that are inadequately labeled, lipemic, hemolyzed, cloudy or microbiologically contaminated.
GENERAL INFORMATION
Expected TAT 7 - 10 days 
Clinical Use Chronic Urticaria - Pooled Donor Basophil Activation Testing (PD-BAT) 
CPT Code(s) 86849
Internal Comments 10/17/17 link - JK
3/1/17 tat update - JK
11/13/18 - Test name update; synonyms added - ticket # 650249 (SN)
6/3/25 changed from Chronic Urticaria Index  to Chronic Urticaria - Pooled Donor Basophil Activation Testing (PD-BAT)
Labcorp Test Code: from 820022 to 505800
CPT from 86352 to 86352
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.
Lab Section Reference Lab