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Sorted By Test Name - Mayo Medical Laboratories

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FENTU<br />

89655<br />

testing often depend upon the age of the patient, history of allergen exposure, season of the year, and<br />

clinical manifestations. In individuals predisposed to develop allergic disease(s), the sequence of<br />

sensitization and clinical manifestations proceed as follows: eczema and respiratory disease (rhinitis and<br />

bronchospasm) in infants and children less than 5 years due to food sensitivity (milk, egg, soy, and wheat<br />

proteins) followed by respiratory disease (rhinitis and asthma) in older children and adults due to<br />

sensitivity to inhalant allergens (dust mite, mold, and pollen inhalants).<br />

Useful For: <strong>Test</strong>ing for IgE antibodies may be useful to establish the diagnosis of an allergic disease<br />

and to define the allergens responsible for eliciting signs and symptoms. <strong>Test</strong>ing also may be useful to<br />

identify allergens which may be responsible for allergic disease and/or anaphylactic episode, to confirm<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 the<br />

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 by<br />

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 />

Fentanyl Confirmation, Urine<br />

Clinical Information: Fentanyl is an extremely fast acting synthetic opioid related to the<br />

phenylpiperidiens.(1,2) It is available in injectable as well as transdermal formulations.(1) The analgesic<br />

effects of fentanyl is similar to those of morphine and other opioids(1): it interacts predominantly with the<br />

opioid mu-receptor. These mu-binding sites are discretely distributed in the human brain, spinal cord, and<br />

other tissue.(1,3) Fentanyl is approximately 80% to 85% protein bound. In plasma, the protein binding<br />

capacity of fentanyl decreases with increasing ionization of the drug. Alterations in pH may affect its<br />

distribution between plasma and the central nervous system (CNS). The average volume of distribution<br />

for fentanyl is 6 L/kg (range 3-8).(3,4) In humans, the drug appears to be metabolized primarily by<br />

oxidative N-dealkylation to norfentanyl and other inactive metabolites that do not contribute materially to<br />

the observed activity of the drug. Within 72 hours of intravenous (IV) administration, approximately 75%<br />

of the dose is excreted in urine, mostly as metabolites with

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