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HelpTest Code FABP2 Allergic Bronchopulmonary Aspergillosis Panel II
Specimen Required
Specimen Type: Serum
Container/Tube: Red or SST
Specimen Volume: 1.5 mL
Collection Instructions: Draw blood in a plain, red-top tube(s) or serum gel tube(s). Spin down and send 1.5 mL of serum refrigerate in a plastic vial.
Method Name
ImmunoCAP 1000
ImmunoCAP FEIA
Enzyme immunoassay (FEIA)
Reporting Name
Allergic Bronchopulmonary Panel IISpecimen Type
SerumSpecimen Minimum Volume
1 mL
Specimen Stability Information
| Specimen Type | Temperature | Time | Special Container |
|---|---|---|---|
| Serum | Refrigerated (preferred) | 28 days | |
| Frozen | 365 days | ||
| Ambient | 7 days |
Reject Due To
| Lipemia | Mild OK; Gross Reject |
Reference Values
Total IgE
Age Related     Reference Range
1-11 months                 0-12
     1 year                    0-15
     2 year                    1-29
     3 year                    4-35
     4 year                    2-33
     5 year                    8-56
     6 year                    3-95
     7 year                    2-88
     8 year                    5-71
     9 year                    3-88
    10 year                    7-110
11-14 year                    7-111
15-19 year                   6-96
20-30 year                   4-59
31-50 year                   5-79
51-80 year                   3-48
Aspergillus fumigatus IgE
Reference Range: <0.35 kU/LÂ Â Â
Aspergillus fumigatus IgG
Reference Range: <46 mcg/mL
Aspergillus fumigatus Mix Gel Diffusion
Reference Range: Negative
Interpretation
Aspergillus fumigatus IgE
Class   IgE (kU/L)        Comment
0Â Â Â Â Â Â Â Â Â <0.10Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Negative
0/1Â Â Â Â Â Â Â 0.10-0.34Â Â Â Â Â Â Â Â Â Â Equivocal/Borderline
1Â Â Â Â Â Â Â Â Â 0.35-0.69Â Â Â Â Â Â Â Â Â Â Low Positive
2Â Â Â Â Â Â Â Â Â 0.70-3.49Â Â Â Â Â Â Â Â Â Â Moderate Positive
3Â Â Â Â Â Â Â Â Â 3.50-17.49Â Â Â Â Â Â Â Â High Positive
4Â Â Â Â Â Â Â Â Â 17.50-49.99Â Â Â Â Â Â Very High Positive
5Â Â Â Â Â Â Â Â Â 50.00-99.99Â Â Â Â Â Â Very High Positive
6Â Â Â Â Â Â Â Â Â >99.99Â Â Â Â Â Â Â Â Â Â Â Â Â Very High Positive
Day(s) Performed
Monday through Friday
Performing Laboratory
Eurofins ViracorTest Classification
Aspergillus fumigatus IgG This test was developed and its performance characteristics determined by Eurofins Viracor. It has not been cleared or approved by the U.S. Food and Drug Administration.CPT Code Information
86331
86001
86003
82785
LOINC Code Information
| Test ID | Test Order Name | Order LOINC Value |
|---|---|---|
| FABP2 | Allergic Bronchopulmonary Panel II | Not Provided |
| Result ID | Test Result Name | Result LOINC Value |
|---|---|---|
| Z3248 | Total IgE | In Process |
| Z3249 | Aspergillus fumigatus IgE | 6025-1 |
| Z3250 | Class | 102153-4 |
| Z3251 | Aspergillus fumigatus IgG | 26954-8 |
| Z3252 | A. fumigatus Mix Gel Diffusion | 23821-2 |
Clinical Information
Aspergillus fumigatus IgG
Antibody levels greater than the reference range indicate that the patient has been immunologically sensitized to the antigen. The significance of eleveated IgG depends on the nature of the antigen and the patient’s clinical history.
Aspergillus fumigatus Mix Gel Diffusion   Â
The gel diffusion method was used to test this patient's serum for the presence of precipitating antibodies (IgG) to the antigens indicated. These antibodies are serological markers for exposure and immunological sensitization. The clinical significance varies, depending on the history and symptoms. This test was developed and its performance characteristics determined by Viracor Eurofins. It has not been cleared or approved by the FDA