Removal of 10-hydroxycarbazepine by plasmapheresis

被引:9
作者
Christensen, J [1 ]
Balslev, T
Villadsen, J
Heinsvig, EM
Dam, M
Poulsen, JH
机构
[1] Aarhus Univ Hosp, Dept Neurol, DK-8000 Aarhus C, Denmark
[2] Aarhus Univ Hosp, Dept Pediat, DK-8000 Aarhus, Denmark
[3] Aarhus Univ Hosp, Dept Clin Immunol, DK-8000 Aarhus C, Denmark
[4] Aarhus Univ Hosp, Dept Clin Biochem, DK-8000 Aarhus C, Denmark
[5] Aarhus Univ, Dept Clin Pharmacol, Aarhus, Denmark
关键词
oxcarbazepine; plasmapheresis; Rasmussen encephalitis;
D O I
10.1097/00007691-200108000-00009
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Removal of the oxcarbazepine metabolite 10-hydroxycarbazepine (MHD) by plasmapheresis was evaluated during a series of six plasmaphereses of a 13-year-old boy with Rasmussen encephalitis. Plasmapheresis was performed after steady-state concentrations of MHD had been achieved with a dose of 2550 mg oxcarbazepine daily. The mean amount of MHD removed per plasmapheresis was 78.9 mg (SD: 6.0 mg), representing 3% to 4% of the daily oxcarbazepine dose and approximately 5% to 6% of body stores of MHD. The mean steady-state trough MHD concentration was 33.3 mg/L (SD: 1.8 mg/L), and this was remarkably stable during the entire plasmapheresis period. The serum concentration of MHD) was only mildly reduced by the procedure. The areas under the concentration curve of MHD) on the first and sixth day of plasmapheresis were, 99%, and 94%, respectively, of the pre-plasmapheresis values. The results are in agreement with studies on other anticonvulsant medications (carbamazepine, valproic acid, phenobarbital, and phenytoin), indicating that minor fractions (2% to 10%) of body stores of these drugs are depleted during plasmapheresis. The authors conclude that it is unnecessary to adjust the oxcarbazepine dosage when performing single-volume plasma exchanges or even multiple exchanges during an extended period. It is further proposed that plasmapheresis is unlikely to be of therapeutic benefit in the treatment of an oxcarbazepine overdose.
引用
收藏
页码:374 / 379
页数:6
相关论文
共 25 条
[1]  
Andrews PI, 1996, CURR OPIN NEUROBIOL, V6, P673
[2]   Plasmapheresis in Rasmussen's encephalitis [J].
Andrews, PI ;
Dichter, MA ;
Berkovic, SF ;
Newton, MR ;
McNamara, JO .
NEUROLOGY, 1996, 46 (01) :242-246
[3]   COMPARATIVE PHARMACOKINETICS OF THE NEWER ANTIEPILEPTIC DRUGS [J].
BIALER, M .
CLINICAL PHARMACOKINETICS, 1993, 24 (06) :441-452
[4]  
Dam Mogens, 1995, P987
[5]  
DICKINSON RG, 1989, EUR J CLIN PHARMACOL, V37, P69
[6]  
Dulac O, 1996, CURR OPIN NEUROL, V9, P75
[7]  
Flesch G, 1999, EUR J PHARM SCI, V8, pxxii
[8]   OXCARBAZEPINE - A REVIEW OF ITS PHARMACOLOGY AND THERAPEUTIC POTENTIAL IN EPILEPSY, TRIGEMINAL NEURALGIA AND AFFECTIVE-DISORDERS [J].
GRANT, SM ;
FAULDS, D .
DRUGS, 1992, 43 (06) :873-888
[9]   EVALUATION OF PLASMAPHERESIS IN THE TREATMENT OF AN ACUTE OVERDOSE OF CARBAMAZEPINE [J].
KALE, PB ;
THOMSON, PA ;
PROVENZANO, R ;
HIGGINS, MJ .
ANNALS OF PHARMACOTHERAPY, 1993, 27 (7-8) :866-870
[10]   USE OF SALIVA FOR MONITORING OXCARBAZEPINE THERAPY IN EPILEPTIC PATIENTS [J].
KLITGAARD, NA ;
KRISTENSEN, O .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 1986, 31 (01) :91-94