Test Code FHZCP Hazelnut Component Panel
Specimen Required
Specimen Type: Serum
Container/Tube: Red or SST
Specimen Volume: 1 mL
Collection Instructions: Draw blood in a plain red-top tube(s), serum gel tube(s) is acceptable. Spin down and send 1 mL of serum refrigerated in a plastic vial.
Method Name
ImmunoCAP FEIA
Reporting Name
Hazelnut Component PanelSpecimen Type
SerumSpecimen Minimum Volume
0.5 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Serum | Refrigerated (preferred) | 28 days | |
Frozen | 365 days | ||
Ambient | 28 days |
Reject Due To
Hemolysis | Mild OK; Gross reject |
Lipemia | Mild OK; Gross reject |
Icterus | Mild OK; Gross reject |
Other | NA |
Clinical Information
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 Values
Class IgE |
(kU/L) |
Comment |
0 |
<0.10 |
Negative |
0/1 |
0.10-0.34 |
Equivocal/Borderline |
1 |
0.35-0.69 |
Low Positive |
2 |
0.70-3.49 |
Moderate Positive |
3 |
3.50-17.49 |
High Positive |
4 |
17.50-49.99 |
Very High Positive |
5 |
50.00-99.99 |
Very High Positive |
6 |
>99.99 |
Very High Positive |
Day(s) Performed
Monday through Friday
Report Available
1 to 7 daysPerforming Laboratory
Eurofins ViracorTest Classification
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.CPT Code Information
86008 x 4