CU (CHRONIC URTICARIA) INDEX
test app
Specimen Type:
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Blood |
Container/Tube
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Preferred:
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Gold/Red SST Vacutainer®.
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Acceptable:
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Plain, red-top Vacutainer®.
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Collection Volume:
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4.0 mL (minimum 1.0 mL)
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Patient Preparation:
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Patients taking calcineurin inhibitors should stop medication 72 hour prior to collection.
Patients taking prednisone should be off their medication for 2 weeks prior to collection.
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Sample Rejection:
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Mislabeled or unlabeled specimens.
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Special Instructions:
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None
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Test Availability:
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Daily
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Turnaround Time:
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3-9 days
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Test set-up:
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Monday & Thursday
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Lab Testing Section:
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Send-outs
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Referred to:
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Mayo Medical Laboratories to Viracor-IBT Lab (MMLI) / Test ID: FCUIX
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Reference Range:
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<10.0
The CU Index test is the second generation Functional Anti-FceR test. Patients with a CU Index > or = 10 have basophil reactive factors in their serum which supports an autoimmune basis for disease.
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Critical Values:
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None established
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Limitations:
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NA
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Methodology:
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Ex Vivo Challenge, Cell Culture and Histamine Analysis
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Test Classification:
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This test was developed and its performance characteristics determined by Viracor-Eurofins. It has not been cleared or approved by the U.S. Food and Drug Administration.
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Lab Processing instructions:
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Centrifuge to separate within 2 hours of collection. Aliquot serum into a 5 mL, screw-capped plastic vial for transport.
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Processed Volume:
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2.0 mL (minimum 0.5 mL) serum
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Transport Temperature:
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Ambient
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Analyte Stability:
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Ambient (unprocessed): NA
PROCESSED
Ambient: 14 days
Refrigerated: 14 days
Frozen: 14 days
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Notes:
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NA |
EPIC order name:
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Chronic Urticara Index, Serum (EPIP Test# LAB3041)
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Cerner order name:
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CU Index, Serum
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CPT Codes:
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86343
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LOINC Value:
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63369-3
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Synonyms:
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Chronic Urticaria
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Last Updated: 03/20
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Last Reviewed: 10/24
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