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Mayo Test Catalog, (Sorted By Test Name) - Mayo Medical ...

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FRFIT<br />

90330<br />

RASE<br />

82366<br />

sensitization to particular allergens prior to beginning immunotherapy, and to investigate the specificity of<br />

allergic reactions to insect venom allergens, drugs, or chemical allergens.<br />

Interpretation: Detection of IgE antibodies in serum (Class 1 or greater) indicates an increased<br />

likelihood of allergic disease as opposed to other etiologies and defines the allergens that may be<br />

responsible for eliciting signs and symptoms. The level of IgE antibodies in serum varies directly with<br />

the concentration of IgE antibodies expressed as a class score or kU/L.<br />

Reference Values:<br />

Class IgE kU/L Interpretation<br />

0 Negative<br />

1 0.35-0.69 Equivocal<br />

2 0.70-3.49 Positive<br />

3 3.50-17.4 Positive<br />

4 17.5-49.9 Strongly positive<br />

5 50.0-99.9 Strongly positive<br />

6 > or =100 Strongly positive Reference values<br />

apply to all ages.<br />

Clinical References: Homburger HA: Allergic diseases. In Clinical Diagnosis and Management<br />

by Laboratory Methods. 21st edition. Edited by RA McPherson, MR Pincus. New York, WB Saunders<br />

Company, 2007, Chapter 53, Part VI, pp 961-971<br />

Rabies Antibody Endpoint<br />

Interpretation: Qualitative results. For those who want to know if they need a booster of rabies<br />

vaccine. RFFIT stands for Rapid Fluorescent Foci Inhibition <strong>Test</strong>. It is a serum neutralization<br />

(inhibition) test, which means it measures the ability of rabies specific antibodies to neutralize rabies<br />

virus and prevent the virus from infecting cells. The antibodies are called rabies virus neutralizing<br />

antibodies (RVNA).<br />

Reference Values:<br />

Reportable range is 0.1 to 15.0 IU/mL<br />

Less than 0.1 IU/mL: Below detection limit<br />

>15.0 IU/mL or >14.0 IU/mL: Above reportable range<br />

In humans a result of 0.5 IU/mL or higher is considered acceptable according to the World Health<br />

Organization (WHO) guidelines; see WHO and Advisory Committee on Immunization Practices<br />

documents for additional guidance.<br />

<strong>Test</strong> Performed by: RFFIT/K-State Rabies Laboratory<br />

Manhattan/K-State Innovation Center<br />

2005 Research Park Circle<br />

Manhattan, KS 66502<br />

Rape Seed, IgE<br />

Clinical Information: Clinical manifestations of immediate hypersensitivity (allergic) diseases are<br />

caused by the release of proinflammatory mediators (histamine, leukotrienes, and prostaglandins) from<br />

immunoglobulin E (IgE)-sensitized effector cells (mast cells and basophils) when cell-bound IgE<br />

antibodies interact with allergen. In vitro serum testing for IgE antibodies provides an indication of the<br />

immune response to allergen(s) that may be associated with allergic disease. The allergens chosen for<br />

Current as of January 3, 2013 2:22 pm CST 800-533-1710 or 507-266-5700 or <strong>Mayo</strong><strong>Medical</strong>Laboratories.com Page 1531

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