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Cat Component rFel d 1

Test Code: 185810
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Clinical Utility

This assay is used to detect allergen specific-IgE using the ImmunoCAP® FEIA method. In vitro allergy testing is the primary testing mode for allergy diagnosis.

Procedure

The ImmunoCAP® FEIA method uses as the solid phase a flexible, hydrophobic cellulosic polymer to which allergen has been covalently linked. The advantage of this system is that it has a very high antigen binding capacity when compared to other systems and it has minimal non-specific binding with high total IgE. Viracor Eurofins provides an optional low range calibrator at 0.1 kU/L and a 0/1 class. This test has been cleared or approved for diagnostic use by the U.S. Food and Drug Administration.

1-2 business days from receipt of specimen

Specimen Type Order Code CPT Code NY Approved Volume Assay Range Special Instructions
serum 185810 86003 Yes 0.5 mL See Scoring Guide
  • Collect 1-2 mL whole blood in red top tube.
  • Centrifuge and transfer 0.5 mL serum into a transfer tube.
  • Ship at ambient or frozen temperature Monday through Friday.

ImmunoCAP® Quantitative Scoring Guide:

Class IgE (kU/L) Comment
0 <0.10 Negative
0/1 0.10-0.34 Equivocal/Borderline
1 0.35-0.69 Low Positive
2 0.70-3.49 Moderate Positive
3 3.50-17.49 High Positive
4 17.50-49.99 Very High Positive
5 50.00-99.99 Very High Positive
6 >99.99 Very High Positive

Note that Viracor Eurofins includes an extra calibrator at 0.10 kU/L and uses it to
define an optional equivocal class.

Shipping

Ship Monday through Friday. Friday shipments must be labeled for Saturday delivery. All specimens must be labeled with patient's name and collection date. A Viracor Eurofins test requisition form must accompany each specimen. Multiple tests can be run on one specimen. Ship specimens FedEx Priority Overnight® to: Viracor Eurofins, 1001 NW Technology Dr, Lee's Summit, MO 64086.

Causes for Rejection

Lipemic samples may lead to rejection.

Specimens are approved for testing in New York only when indicated in the Specimen Information field above. The CPT codes provided are based onViracor Eurofins' interpretation of the American Medical Association's Current Procedural Terminology (CPT) codes and are provided for informational purposes only. CPT coding is the sole responsibility of the billing party. Questions regarding coding should be addressed to your local Medicare carrier. Viracor Eurofins assumes no responsibility for billing errors due to reliance on the CPT codes illustrated in this material.

References

http://www.phadia.com/en/Products/Allergy-testing-products/ImmunoCAP-Allergen-Information/Epidermals-and-Animal-Proteins/Allergen-Components/rFel-d-1-Cat/

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