Test ID FHYPP Hypersensitivity Pneumonitis Extended Panel (Farmer's Lung Panel)
Method Name
Qualitative Immunodiffusion/Quantitative ImmunoCAP Fluorescent Enzyme Immunoassay
Reporting Name
Hypersensitivity Pneumo Ext PanelSpecimen Type
SerumDraw blood in a plain red-top tube(s), serum gel tube is acceptable. Spin down and send 5 mL of serum refrigerated in a plastic vial.
Specimen Minimum Volume
2 mL
Specimen Stability Information
Specimen Type | Temperature | Time |
---|---|---|
Serum | Refrigerated (preferred) | 14 days |
Frozen | 365 days | |
Ambient | 48 hours |
Reference Values
Procedure Units Ref Internal
A. fumigatus #1 Ab, Precipitin |
|
None Detected |
A. fumigatus #6 Ab, Precipitin |
|
None Detected |
A. pullulans Ab, Precipitin |
|
None Detected |
Pigeon Serum, Ab, Precipitin |
|
None Detected |
M. faeni Ab, Precipitin |
|
None Detected |
T. vulgaris #1 Ab, Precipitin |
|
None Detected |
A. flavus Ab, Precipitin |
|
None Detected |
A. fumigatus #2 Ab, Precipitin |
|
None Detected |
A. fumigatus #3 Ab, Precipitin |
|
None Detected |
S. viridis Ab, Precipitin |
|
None Detected |
T. candidus Ab, Precipitin |
|
None Detected |
T. sacchari Ab, Precipitin |
|
None Detected |
Allergen, Animal, Feather Mix IgE |
kU/L |
Negative |
Allergen, Food, Beef IgE |
kU/L |
≤0.34 |
Allergen, Food, Pork IgE |
kU/L |
≤0.34 |
Allergen, Fungi/Mold, Phoma betae IgE |
kU/L |
≤0.34 |
Allergen, Interp, Immunocap Score IgE |
|
See Reference, Interval: Allergen, Interpretation |
A. Pullulans Ab, Precipitin:
Testing includes antibodies directed at Aureobasidium pullulans, Aspergillus flavus, Aspergillus fumigatus #1, Aspergillus fumigatus #2, Aspergillus fumigatus #3, Aspergillus fumigatus #6, Micropolyspora faeni, Saccharomonospora viridis, Thermoactinomyces candidus, Thermoactinomyces vulgaris #1, and Thermoactinomyces vulgaris #1, and Thermoactinomyces sacchari.
Allergen, Interp, Immunocap Score IgE:
Reference Interval: Allergen, Interpretation
Less than 0.10 kU/L No significant level detected
0.10-0.34 kU/L Clinical relevance undetermined
0.35-0.70 kU/L Low
0.71-3.50 kU/L Moderate
3.51-17.50 kU/L High
17.51 or Greater kU/L Very High
Allergen results of 0.10-0.34 kU/L are intended for specialist use as the clinical relevance is undetermined. Even though increasing ranges are reflective of increasing concentrations of allergen-specific IgE, these concentrations may not correlate with the degree of clinical response of skin testing results when challenged with a specific allergen. The correlation of allergy laboratory results with clinical history and in vivo reactivity to specific allergens is essential. A negative test may not rule out clinical allergy or even anaphylaxis.
Day(s) Performed
Sunday through Saturday
Report Available
3 - 7 daysPerforming Laboratory
ARUP LaboratoriesTest Classification
Analyte specific reagents (ASR) are used in many laboratory tests necessary for standard medical care and generally do not require U.S. Food and Drug Administration (FDA) approval or clearance. This test was developed and its performance characteristics determined by ARUP Laboratories. The U.S. Food and Drug Administration has not approved or cleared this test; however, FDA clearance or approval is not currently required for diagnosis or patient management decisions. This test should not be regarded as investigational or for research use.CPT Code Information
86003 x 3
86005
86331 x 7
86606 x 5