Acute phenytoin toxicity followed by seizure breakthrough from a ticlopidine-phenytoin interaction

被引:13
作者
Privitera, M
Welty, TE
机构
[1] UNIV CINCINNATI,COLL MED,DEPT NEUROL,CINCINNATI,OH
[2] UNIV CINCINNATI,COLL PHARM,DIV PHARMACOTHERAPY,CINCINNATI,OH 45267
关键词
D O I
10.1001/archneur.1996.00550110143027
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: To review a case of a drug-drug interaction between phenytoin sodium and ticlopidine hydrochloride that resulted in acute phenytoin toxicity and permanent memory loss. Case Report: A 63-year-old man who was maintained with a stable dose of phenytoin for treatment of seizures began treatment with ticlopidine following percutaneous transluminal angioplasty and stent placement. Within 3 weeks of beginning treatment with ticlopidine, he experienced acute clinical toxic effects of phenytoin with a maximum measured phenytoin concentration of 162.4 mu mol/L. Phenytoin concentration decreased to 36 mu mol/L after discontinuing treatment with ticlopidine and reducing the phenytoin dose. Subsequently, the patient developed probable complex partial status epilepticus. Conclusions: Ticlopidine is a metabolic inhibitor of several drugs. Because of the potential for acute and permanent adverse effects from a drug-drug interaction, phenytoin concentrations should be carefully monitored when beginning or ending ticlopidine therapy.
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页码:1191 / 1192
页数:2
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