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

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FELBA<br />

80782<br />

porphyrins in the stool, is very sensitive, and provides quantitative results.<br />

Useful For: Colorectal cancer screening Screening for gastrointestinal bleeding<br />

Interpretation: This is a quantitative assay but results are reported qualitatively as negative or<br />

positive for the presence of fecal occult blood; the cutoff for positivity is 100 ng/mL hemoglobin. The<br />

following comments will be reported with the qualitative result for patients >17 years: -Positive results;<br />

further testing is recommended if clinically indicated. This test has 97% specificity for detection of<br />

lower gastrointestinal bleeding in colorectal cancer. -Negative results; this test will not detect upper<br />

gastrointestinal bleeding; HQ/9220 HemoQuant, Feces test should be ordered if clinically indicated.<br />

Reference Values:<br />

Negative<br />

This test has not been validated in a pediatric population, results should be interpreted in the context of<br />

the patient's presentation.<br />

Clinical References: 1. Levin B, Lieberman DA, McFarland B, et al: Screening and Surveillance<br />

for the Early Detection of Colorectal Cancer and Adenomatous Polyps, 2008: A Joint Guideline from<br />

the American Cancer Society, the US Multi-Society Task Force on Colorectal Cancer, and the<br />

American College of Radiology. CA Cancer J Clin 2008;58:130 2. Whitlock EP, Lin JS, Liles E, et al:<br />

Screening for colorectal cancer: a targeted, updated systematic review for the U.S. Preventive Services<br />

Task Force. Ann Intern Med 2008;149:638 3. Hol L, Wilschut JA, van Ballegooijen M, et al: Screening<br />

for colorectal cancer: random comparison of guaiac and immunochemical faecal occult blood testing at<br />

different cut-off levels. Br J Cancer 2009;100:1103 4. Levi Z, Rozen P, Hazazi R, et al: A quantitative<br />

immunochemical fecal occult blood test for colorectal neoplasia. Ann Intern Med 2007;146:244 5.<br />

Tannous B, Lee-Lewandrowski E, Sharples C, et al: Comparison of conventional guaiac to four<br />

immunochemical methods for fecal occult blood testing: implications for clinical practice in hospital<br />

and outpatient settings. Clin Chem Acta 2009;400:120-122<br />

Felbamate (Felbatol), Serum<br />

Clinical Information: Felbamate is an anticonvulsant drug approved for treatment of partial<br />

seizures with or without secondary generalization in persons >14 years of age. It is also approved for<br />

Lennox-Gastout syndrome in children >2 years of age. Felbamate is well absorbed (>90%) and is<br />

metabolized by the hepatic cytochrome P450 system. Metabolites lack anticonvulsant activity. The<br />

elimination half-life of felbamate ranges from 13 to 23 hours. Optimal response to felbamate is seen<br />

with serum concentrations between 30 mcg/mL to 60 mcg/mL. Patients who are elderly or have renal<br />

dysfunction may require reduced dosing; felbamate should not be given to individuals with hepatic<br />

disease. Toxicity can be severe, including life-threatening aplastic anemia or liver failure, but no<br />

defined toxic concentration has been established. Coadministration of felbamate increases the<br />

concentration of phenytoin and valproic acid, decreases carbamazepine concentration, and increases<br />

carbamazepine-10,11-epoxide (its active metabolite). Conversely, coadministration of phenytoin or<br />

carbamazepine causes a decrease in felbamate concentration.<br />

Useful For: Determining whether a poor therapeutic response is attributable to noncompliance or<br />

lack of drug effectiveness Monitoring changes in serum concentrations resulting from interactions with<br />

coadministered drugs such as barbiturates and phenytoin<br />

Interpretation: Optimal response to felbamate is associated with serum concentrations of 30<br />

mcg/mL to 60 mcg/mL. Toxic serum concentrations for felbamate have not been established.<br />

Reference Values:<br />

30.0-60.0 mcg/mL<br />

Clinical References: 1. Johannessen, SI, Tomson, T: Pharmacokinetic Variability of Newer<br />

Antiepileptic Drugs: When is Monitoring Needed? Clin Pharmacokinet 2006; 45 (11): 1061-10752.<br />

Schmidt D: Felbamate: successful development of a new compound for the treatment of epilepsy.<br />

Epilepsia 1996;34(Suppl 7):S30-S33 2. Patsalos PN: Antiepileptic drugs--best practice guidelines 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 739

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