Test Overview
Test Methodology
Fluorescent Enzyme Immunoassay (FEIA)
Test Usage
This assay is used to detect allergen specific-IgE using the ImmunoCAP® FEIA method. In vitro allergy testing is the primary testing mode for allergy diagnosis.
Reference Range *
Class 0: <0.10 kU/L=Negative; Class 0/1: 0.10-0.34 kU/L=Equivocal/Borderline; Class 1: 0.35-0.69 kU/L=Low Positive; Class 2: 0.70-3.49 kU/L=Moderate Positive; Class 3: 3.50-17.49 kU/L= High Positive; Class 4: 17.50-49.99 kU/L=Very High Positive; Class 5: 50.00-99.99 kU/L= Very High Positive; Class 6: >99.99 kU/L=Very High Positive
Test Details
Days Set Up
Monday - Saturday
Analytic Time
2 - 4 days
Soft Order Code
VTILA
MiChart Code
VTILA
Laboratory
Sendout
Reference Laboratory
Viracor Eurofins (38010E)
Section
Special Testing
Specimen Requirements
Collection Instructions
Collect specimen in SST or red top tube. Spin and aliquot into screw capped plastic tube. Send to Specimen Processing ambient.
Normal Volume
0.5 mL serum
Minimum Volume
0.3 ml serum
Additional Information
Test performed by Viracor Eurofins
Billing
CPT Code
86003
Fee Code
AA568
NY State Approved
No