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Test ID FVEGG Vegetables Panel IgG

Method Name

Enzyme Immunoassay (FEIA)

Reporting Name

Vegetables Panel IgG

Specimen Type

Serum

Draw blood in a plain red-top tube(s), serum gel tube(s) is acceptable. Spin down and send 2 mL of serum refrigerated in a plastic vial.

Specimen Minimum Volume

2 mL

Specimen Stability Information

Specimen Type Temperature Time
Serum Refrigerated (preferred) 28 days
  Frozen  365 days
  Ambient  7 days

Reference Values

Alfalfa (Medicago sativa) IgG

<21.0 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.

 

Asparagus IgG

<2.0 mcg/mL

Avocado IgG

<2.0 mcg/mL

Beet Root IgG

<2.0 mcg/mL

Broccoli IgG

<2.0 mcg/mL

Cabbage IgG

<2.0 mcg/mL

Carrot IgG

<2.0 mcg/mL

Celery IgG

<2.0 mcg/mL

Cucumber IgG

<2.0 mcg/mL

Garlic IgG

<2.0 mcg/mL

Pepper Bell/Paprika (C.annuum) IgG

<2.0 mcg/mL

Lettuce IgG

<2.0 mcg/mL

Mushroom IgG

<2.0 mcg/mL

Olive Black IgG

<2.0 mcg/mL

Onion IgG

<2.0 mcg/mL

Pea Green IgG

<2.0 mcg/mL

Potato Sweet IgG

<2.0 mcg/mL

Potato White IgG

<2.0 mcg/mL

Spinach IgG

<2.0 mcg/mL

Bean Green/String IgG

<2.0 mcg/mL

Tomato IgG

<2.0 mcg/mL

 

The reference range listed on the report is the lower limit of quantitation for the assay. The clinical utility of food-specific IgG tests has not been established. These tests can be used in special clinical situation to select foods for evaluation by diet elimination and challenge in patients who have food-related complaints. It should be recognized that the presence of food-specific IgG alone cannot be taken as evidence of food allergy and only indicated immunologic sensitization to the food allergen in question. This test should only be ordered by physicians who recognize the limitations of the test.

Day(s) Performed

Monday through Friday

Report Available

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 U.S. Food and Drug Administration.

CPT Code Information

86001 x 21

NY State Approved

No