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Test Code MAP ALLERGEN PANEL, MOLDS, SERUM

Additional Codes

Software Test Code
Label Text MAP
EPIC LAB10908

Performing Laboratory

NorDx Laboratories

Useful For

Panel includes: Aspergillus fumigatus (M3C), Alterneria alternata (M6C), Cladosporium herbarum (M2C), Candida albicans (M5), and Mucor racemosus (M4C).

 

The multiallergen IgE antibody test, combined with measurement of IgE, Total in serum, is a very sensitive first-order test for allergic disease. Positive results indicate a high probability of allergic disease induced by one or more allergens present in the multiallergen panel. Negative results effectively rule out allergy, except in rare cases of allergic disease induced by exposure to a single allergen.

 

If an IgE, Total is desired, please order individually IGET.

Method Name

ImmunoCAP® Fluorescence Enzyme Immunoassay (FEIA)

Reference Values

< 0.10 kU/L – Undetectable (Normal)

0.10 – 0.34 kU/L – For specialist use only: Clinical Relevance Undetermined

0.35 – 0.69 kU/L – Low level of allergy, indicative of ongoing sensitization

0.70 – 3.49 kU/L – Moderate level of allergy, indicative of stronger ongoing sensitization

3.5 – 17.49 kU/L – High level of allergy, indicative of high level sensitization

17.5 – 49.9 kU/L – Very high level of allergy, indicative of very high level sensitization

50 – 99.9 kU/L – Very high level of allergy, indicative of very high level sensitization

≥100 kU/L – Very high level of allergy, indicative of very high sensitization

 

CONCENTRATION (kU/L) RESULTS EQUIVALENT TO ALTERNATIVE SCORING METHOD:

CLASS 0: <0.22

CLASS 0/1: 0.22-0.31

CLASS 1: 0.31-0.55

CLASS 2: 0.55-1.4

CLASS 3: 1.4-3.9

CLASS 4: 3.9-19

CLASS 5: 19-100

CLASS 6: >100

When an “R” precedes the test name to a specific allergen, it indicates that the test was developed and its performance characteristics determined by NorDx.

It has not been cleared or approved by the FDA.

Days and Times Test Performed

Monday through Friday

Report Available

1 Day

Profile Information

Individual Test Description

ALTERNARIA ALTERNATA (ALSO KNOWN AS ALTERNARIA TENUIS) IGE
ASPERGILLUS FUMIGATUS IGE
CANDIDA ALBICANS IGE
CLADOSPORIUM HERBARUM IGE
MUCOR RACEMOSUS IGE

Specimen Type

Serum

Preferred Container

Serum Separator Tube (SST)

Preferred Volume

Serum: 2 mL (Serum Separator Tube (SST))

Minimum Volume

Serum: 1.5 mL (Serum Separator Tube (SST))

Specimen Collection and Handling

Spin specimen, separate from clot and send refrigerated.

Specimen Stability Information

Specimen Type: Serum

Frozen: 3 Months

Refrigerated: 7 Days

Must be spun/separated within: 2 Hours

Add On Capable

Yes

Advance Beneficiary Notice Requirements

This test, when ordered on Medicare patients, is subject to the National Coverage Determination (NCD) policies. Please verify that the diagnosis code (ICD code) you have chosen demonstrates medical necessity for the test as documented in the physician’s patient record. The CMS web site is available to assist you with this verification. A properly executed Advance Beneficiary Notice (ABN) must be submitted with the specimen if medical necessity is not demonstrated by the ICD code chosen.

CPT Code Information

CPT Code

CPT Description

CPT Disclaimer

86003 x5 Allergen Specific IgE, Quantitative or Semiquantitative, Crude Allergen Extract, Each  

Performing Laboratory Location

NorDx Laboratories

Acceptable Alternative Container(s)

Red Top Tube