Literature DB >> 6850652

Hypermetabolism of phenytoin as a cause of treatment failure.

L H Lebrun, J P Villeneuve.   

Abstract

Hypermetabolism of phenytoin is not frequently recognized as a cause of treatment failure. We report the case of a 37-year-old male in whom detailed pharmacokinetic investigation revealed that hypermetabolism, rather than lack of compliance or poor absorption, was responsible for low plasma levels of phenytoin. An increase of his daily dose of phenytoin to 800 mg resulted in adequate plasma levels and good seizure control. Additional studies with two model drugs metabolized by the liver--aminopyrine and antipyrine--showed that he was also a fast metabolizer for these substrates, suggesting a nonspecific induction of hepatic drug metabolizing enzymes. Low plasma phenytoin levels should not be systematically ascribed to lack of compliance, and increased phenytoin metabolism should be considered as an occasional cause of treatment failure.

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Year:  1983        PMID: 6850652     DOI: 10.1097/00002826-198303000-00008

Source DB:  PubMed          Journal:  Clin Neuropharmacol        ISSN: 0362-5664            Impact factor:   1.592


  3 in total

1.  Accuracy and clinical utility of simplified tests of antipyrine metabolism.

Authors:  G C Farrell; L Zaluzny
Journal:  Br J Clin Pharmacol       Date:  1984-10       Impact factor: 4.335

2.  Treatment goals: response and nonresponse.

Authors:  Jean-Paul Macher; Marc-Antoine Crocq
Journal:  Dialogues Clin Neurosci       Date:  2004-03       Impact factor: 5.986

3.  Effect of plasmapheresis on serum levels of clobazam, levetiracetam and topiramate.

Authors:  To Harmony Hau Man; Chang Richard Shek-Kwan; Chan Angel On-Kei; Chan Phoebe Wing Lam
Journal:  Epilepsy Behav Case Rep       Date:  2017-07-19
  3 in total

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