STEADY-STATE PHARMACOKINETICS OF CONVENTIONAL VERSUS CONTROLLED-RELEASE CARBAMAZEPINE IN PATIENTS WITH EPILEPSY

被引:12
作者
BONNETON, J
ILIADIS, A
GENTON, P
DRAVET, C
VIALLAT, D
MESDJIAN, E
机构
[1] FAC PHARM MARSEILLE,INSERM,U278,27 BLVD JEAN MOULIN,F-13385 MARSEILLE 5,FRANCE
[2] CTR ST PAUL,MARSEILLE,FRANCE
关键词
CONVENTIONAL CARBAMAZEPINE; CONTROLLED-RELEASE CARBAMAZEPINE; PHARMACOKINETICS; (EPILEPSY);
D O I
10.1016/0920-1211(93)90050-H
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The purpose of the present study was to compare the pharmacokinetic parameters of two carbamazepine (CBZ) tablet formulations (conventional (CBZ-CO) and controlled-release (CBZ-CR)) in patients with epilepsy receiving the drug as monotherapy or polytherapy. The absorption rate constant (K(a)), steady-state volume of distribution (V(dss)) and total clearance (CL) were computed with the APIS software using 31 blood level profiles from 23 patients who were divided into four groups: patients receiving CBZ-CO in polytherapy, the same patients switched to CBZ-CR in the same polytherapy conditions, patients receiving CBZ-CO in monotherapy and patients receiving CBZ-CR in monotherapy. The four groups were compared in order to assess the significance of differences in K(a), V(dss), CL and diurnal fluctuations of plasma CBZ concentration. The results show a significant decrease of the K(a) in the CBZ-CR groups compared to the CBZ-CO groups, both on monotherapy and on polytherapy. The comparison between the monotherapy and polytherapy groups shows increases of V(dss) and CL, both in CBZ-CO and CBZ-CR polytherapy groups. Dispersion of pharmacokinetic data was higher in patients on CBZ-CO; among patients on CBZ-CR, dispersion was lowest in the monotherapy group. Clinical improvement was found in four of eight patients switched from CBZ-CO to CBZ-CR. CBZ-CR is therefore a valuable alternative to CBZ-CO.
引用
收藏
页码:257 / 263
页数:7
相关论文
共 27 条
[1]   CONTROLLED RELEASE CARBAMAZEPINE - COGNITIVE SIDE-EFFECTS IN PATIENTS WITH EPILEPSY [J].
ALDENKAMP, AP ;
ALPHERTS, WCJ ;
MOERLAND, MC ;
OTTEVANGER, N ;
VANPARYS, JAP .
EPILEPSIA, 1987, 28 (05) :507-514
[2]   CLINICAL PHARMACOKINETICS AND PHARMACOLOGICAL EFFECTS OF CARBAMAZEPINE AND CARBAMAZEPINE-10,11-EPOXIDE - AN UPDATE [J].
BERTILSSON, L ;
TOMSON, T .
CLINICAL PHARMACOKINETICS, 1986, 11 (03) :177-198
[3]   CLINICAL PHARMACOKINETICS OF CARBAMAZEPINE [J].
BERTILSSON, L .
CLINICAL PHARMACOKINETICS, 1978, 3 (02) :128-143
[4]  
BINELLI S, 1987, 17TH EP INT C JER
[5]  
CANGER R, 1988, B LEGA IT EPIL, V62, P419
[6]  
DAHLSTROM G, 1987, 17TH EP INT C JER
[7]   A COMPARISON OF THE EFFICACY AND TOLERABILITY OF CONTROLLED-RELEASE CARBAMAZEPINE WITH CONVENTIONAL CARBAMAZEPINE [J].
DHALLA, Z ;
BRUNI, J ;
SUTTON, J .
CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES, 1991, 18 (01) :66-68
[8]   ROUTINE MONITORING OF CARBAMAZEPINE AND CARBAMAZEPINE-10,11-EPOXIDE IN PLASMA BY HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY USING 10-METHOXYCARBAMAZEPINE AS INTERNAL STANDARD [J].
ELYAS, AA ;
RATNARAJ, N ;
GOLDBERG, VD ;
LASCELLES, PT .
JOURNAL OF CHROMATOGRAPHY, 1982, 231 (01) :93-101
[9]  
FAIGLE JW, 1982, ANTIEPILEPTIC DRUGS, P483
[10]  
FICHSEL H, 1988, EPILEPSIA, V29, P342