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HelpHypersensitivity Pneumonitis Panel
Additional Codes
Orderable Codes:
| Epic Code | Atlas Code | Mayo Test ID | Order LOINC |
| LAB17824 | LAB17824 | FHSPP | N/A |
Result Component(s):
| Reporting Name | Epic Code | Atlas Code | Mayo Test ID | Result LOINC |
| Alternaria tenuis/alternata IgG | 12301020962 | MZ3166 | Z3166 | 26951-4 |
| Aspergillus fumigatus IgG | 12301020963 | MZ3167 | Z3167 | 26954-8 |
| Aureobasidium pullulans IgG | 12301020964 | MZ3168 | Z3168 | 26955-5 |
| Laceyella sacchari IgG | 12301020965 | MZ6124 | Z6124 | N/A |
| Micropolyspora faeni IgG | 12301020966 | MZ3169 | Z3169 | 26948-0 |
| Penicillium Chrysogenum IgG | 12301020967 | MZ3170 | Z3170 | 26957-1 |
| Phoma betae IgG | 12301020968 | MZ3171 | Z3171 | 35551-1 |
| Trichoderma viride IgG | 12301020969 | MZ3173 | Z3173 | 49687-7 |
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.
Method Name
Immunoassay FEIA
Reporting Name
Hypersensitivity Pneumonitis PanelSpecimen Type
SerumSpecimen Minimum Volume
0.5 mL
Specimen Stability Information
| Specimen Type | Temperature | Time |
|---|---|---|
| Serum | Refrigerated (preferred) | 28 days |
| Frozen | 28 days | |
| Ambient | 7 days |
Reject Due To
| Hemolysis: | Gross reject |
| Thawing: | Warm OK; Cold OK |
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.
Day(s) Performed
Monday through Friday
Report Available
2 to 7 daysPerforming Laboratory
Eurofins ViracorTest 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 |