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TOPI<br />

81546<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 />

Topiramate, Serum<br />

Clinical Information: Topiramate is a broad spectrum, anti-epileptic drug used to for various types of<br />

seizures, Lennox-Gastaut syndrome (a type of childhood onset epilepsy), and migraine prophylaxis.<br />

Topiramate blocks sodium channels, potentiates gamma-aminobutyric acid (GABA) activity, and inhibits<br />

potentiation of the glutamate receptor, allowing the drug to block seizure spread. Topiramate shows<br />

favorable pharmacokinetics, with good absorption, low protein binding, and minimal metabolism.<br />

Elimination is predominantly renal as unaltered topiramate, with an elimination half-life of 20 to 30<br />

hours. Serum concentrations of other anticonvulsant drugs are not significantly affected by the concurrent<br />

administration of topiramate, with exception in individual patients on phenytoin exhibiting increased<br />

phenytoin plasma concentrations after addition of topiramate. Coadministration of phenytoin or<br />

carbamazepine decreases topiramate serum concentrations. Changes in co-therapy with phenytoin or<br />

carbamazepine for patients stabilized on topiramate therapy may require dose adjustment due to these<br />

instructions; therapeutic drug monitoring can assist this. As with other renally eliminated anticonvulsant<br />

drugs, patients with impaired renal function exhibit decreased topiramate clearance.<br />

Useful For: Monitoring serum concentrations of topiramate, particularly in patients with renal disease<br />

or those coadministered phenytoin or carbamazepine Assessing compliance Assessing potential toxicity<br />

Interpretation: Most individuals display optimal response to topiramate with serum levels 2.0<br />

mcg/mL to 20.0 mcg/mL. Some individuals may respond well outside of this range, or may display<br />

toxicity within the therapeutic range, thus interpretation should include clinical evaluation. Toxic levels<br />

have not been well established. Therapeutic ranges are based on specimens drawn at trough (ie,<br />

immediately before the next dose).<br />

Reference Values:<br />

2.0-20.0 mcg/mL<br />

Clinical References: 1. Patslos PN, Berry DJ, Bourgeois BF, et al: Antiepileptic drugs-best practice<br />

guidelines for therapeutic drug monitoring: a position paper by the subcommission on therapeutic drug<br />

monitoring, ILAE Commission on Therapeutic Strategies. Epilepsia 2008 Jul;49(7):1239-1276 2.<br />

Johannessen SI, Tomsom T: Pharmacokinetic variablility of newer antiepileptic drugs: when is<br />

monitoring needed? Clin Pharmacokinet 2006;45(11):1061-1075 3. Snozek CL, Rollins LA, Peterson<br />

PW, Langman LJ: Comparison of a new serum topiramate immunoassay to fluorescence polarization<br />

immunoassay. Ther Drug Monit 2010 Feb;32(1):107-111<br />

Current as of January 4, 2013 7:15 pm CST 800-533-1710 or 507-266-5700 or <strong>Mayo</strong><strong>Medical</strong><strong>Laboratories</strong>.com Page 1766

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