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This Class 1B drug is used to suppress premature ventricular arrhythmias and may be as effective as quinidine or procainamide for this purpose. Mexiletine is less effective in patients with recurrent refractory ventricular tachycardia and fibrillation, and extracardiac side effects may limit its long-term usefulness. Approximately 45% of all patients experience side effects within the commonly accepted therapeutic range of 0.5−2.0 μg/mL.1 Concurrent administration of a Class 1A antiarrhythmic drug (eg, quinidine, disopyramide) or propranolol may provide better control of the arrhythmia and permit a reduction in the dose of mexiletine, thus reducing side effects. Supraventricular arrhythmias are not controlled by mexiletine.
High-pressure liquid chromatography (HPLC)
Therapeutic: 0.75−2.00 μg/mL
Mexiletine is a racemic mixture with equal parts of the (R) and (S) enantiomers, but will be present in plasma in unequal parts due to stereoselective hepatic metabolism. The ratio of the two enantiomers is genetically determined and differs between individuals.1 Toxic effects include dizziness, vomiting, confusion, tremor, bradycardia, and hypotension. Metabolism of mexiletine is accelerated by rifampin, phenobarbital, and phenytoin and retarded by cimetidine and ketoconazole. Half-life is 8 to 17 hours and is urine pH dependent. Acidic urine accelerates elimination.
Serum or plasma
Transfer separated serum or plasma to a plastic transport tube.
Causes for Rejection
|Order Code||Order Code Name||Order Loinc||Result Code||Result Code Name||UofM||Result LOINC|
|716076||Mexiletine (Mexitil), Serum||3819-0||716077||Mexiletine, Serum||ug/mL||3819-0|