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Mayo Clinic Laboratories

Test ID FHPP2 Hypersensitivity Pneumonitis FEIA Panel II

Method Name

Immunoassay FEIA

Reporting Name

Hypersensitivity Pneumonitis Panel

Specimen Type

Serum

Draw blood in a plain red-top tube(s), serum gel tube(s) is acceptable. Spin down and send 0.6 mL of serum refrigerated in a plastic vial.

Specimen Minimum Volume

0.5 mL

Specimen Stability Information

Specimen Type Temperature Time
Serum Refrigerated (preferred)
  Ambient 
  Frozen 

Reference Values

Alternaria tenuis/alternata IgG                 <12 mcg/mL

Aspergillus fumigatus IgG                      <46 mcg/mL

Aureobasidium pullulans IgG                  <18 mcg/mL

Micropolyspora faeni IgG                      <5 mcg/mL

Penicillium Chrysogenum/notatum IgG    <22 mcg/mL

Phoma betae IgG                                  <8 mcg/mL

Thermoactinomyces vulgaris IgG            <13 mcg/mL

Trichoderma viride IgG                           <10 mcg/mL

Day(s) Performed

Monday through Friday

Report Available

2 - 3 days

Performing Laboratory

Viracor-IBT Laboratories

Test Classification

This test was developed and its performance characteristics determined by Viracor-IBT Laboratories. It has not been cleared or approved by the FDA.

CPT Code Information

86001 x 8

NY State Approved

No