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Test Code HSPP Hypersensitivity Pneumonitis Panel

Reporting Name

Hypersensitivity Pneumonitis Panel

Performing Laboratory

Eurofins Viracor


Specimen Required


Container/Tube:

Preferred: Red top

Acceptable: Serum gel

Collection Instructions: 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 Type

Serum

Specimen Minimum Volume

0.5 mL

Specimen Stability Information

Specimen Type Temperature Time Special Container
Serum Refrigerated (preferred) 28 days
  Frozen  28 days
  Ambient  7 days

Day(s) Performed

Monday through Friday

Report Available

2 to 7 days

Reference Values

Alternaria tenuis/alternata IgG

<12.0 mcg/mL

Aspergillus fumigatus IgG

<46.0 mcg/mL

Aureobasidium pullulans IgG

<18.0 mcg/mL

Laceyella sacchari IgG

<25.0 mcg/mL

Micropolyspora faeni IgG

<5.0 mcg/mL

Penicillium Chrysogenum/notatum IgG

<22.0 mcg/mL

Phoma betae IgG

<8.0 mcg/mL

Trchoderma viride IgG

<10.0 mcg/mL

 

Antibody levels greater than the reference range indicate that the patient has been immunologically sensitized to the antigen. The significance of elevated IgG depends on the nature of the antigen and the patient's clinical history. The test method was the Phadia ImmunoCAP.

Method Name

Immunoassay FEIA

Test Classification

This test was developed and its performance characteristics determined by Eurofins Viracor. It has not been cleared or approved the the U.S. Food and Drug Administration.

CPT Code Information

86001 x 8

LOINC Code Information

Test ID Test Order Name Order LOINC Value
FHSPP Hypersensitivity Pneumonitis Panel Not Provided

 

Result ID Test Result Name Result LOINC Value
Z3166 Alternaria tenuis/alternata IgG 26951-4
Z3167 Aspergillus fumigatus IgG 26954-8
Z3168 Aureobasidium pullulans IgG 26955-5
Z6124 Laceyella sacchari IgG Not Provided
Z3169 Micropolyspora faeni IgG 26948-0
Z3170 Penicillium Chrysogenum IgG 26957-1
Z3171 Phoma betae IgG 35551-1
Z3173 Trichoderma viride IgG 49687-7