Effect of vigabatrin on the pharmacokinetics of carbamazepine

被引:8
作者
Sánchez-Alcaraz, A
Quintana, B
López, E
Rodríguez, I
Llopis, P
机构
[1] Hosp La Ribera, Serv Farm, Dept Pharm, Valencia 46600, Spain
[2] Lluis Alcanyis Hosp, Valencia, Spain
关键词
carbamazepine; interactions; plasma concentrations; vigabatrine;
D O I
10.1046/j.1365-2710.2002.00441.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Objective: To evaluate a possible interaction between vigabatrin and carbamazepine in epileptic patients. Methods: Steady-state serum concentrations of carbamazepine with and without vigabatrin were compared. The study group consisted of 15 patients (eight females, seven males, and mean age 31 +/- 12 years), with refractory partial epilepsy. They received vigabatrin as add-on therapy. Patients received carbamazepine monotherapy for at least 6 months and the carbamazepine-vigabatrin combination for at least 3 months. Blood samples were obtained in the morning, before the first daily dose and the carbamazepine plasma concentrations were analysed by fluorescence polarization immunoassay (TDx System). Results: No statistically significant differences were found in mean carbamazepine daily dose. Mean trough concentrations were 7 9 +/- 1.4 mug/mL with carbamazepine alone, and 6.5 +/- 2.0 mug mL with carbamazepine-vigabatrin association (P < 0 03). The mean values of pharmacokinetic parameters were: level dose ratio (L/D) = 0.59 +/- 0.20 vs. 0.45 +/- 0.15 (P < 0.05) and plasma clearance (CI) = 78.5 +/- 25.8 vs. 105.8 +/- 38.9 mL/h/kg (P < 0.05), with carbamazepine alone and carbamazepine-vigabatrin combination, respectively. Conclusion: Vigabatrin produced a statistically significant increase in the plasma clearance of carbamazepine when the two drugs were given simultaneously.
引用
收藏
页码:427 / 430
页数:4
相关论文
共 8 条
[1]  
FERRIOLS F, 1996, EUROPEAN HOSP PHARM, V2, P33
[2]   VIGABATRIN-INDUCED DECREASE IN SERUM PHENYTOIN CONCENTRATION DOES NOT INVOLVE A CHANGE IN PHENYTOIN BIOAVAILABILITY [J].
GATTI, G ;
BARTOLI, A ;
MARCHISELLI, R ;
MICHELUCCI, R ;
TASSINARI, CA ;
PISANI, F ;
ZACCARA, G ;
TIMMINGS, P ;
RICHENS, A ;
PERUCCA, E .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1993, 36 (06) :603-606
[3]  
GOLDSMITH P, 1995, ACTA NEUROL SCAND, V92, P35
[4]  
PERUCCA E, 1995, ACTA NEUROL SCAND, V92, P31
[5]   VIGABATRIN - CLINICAL PHARMACOKINETICS [J].
REY, E ;
PONS, G ;
OLIVE, G .
CLINICAL PHARMACOKINETICS, 1992, 23 (04) :267-278
[6]  
REYNOLDS EH, EPILEPSIA, V181, P1
[7]  
RIMMER EM, 1989, BR J CLIN PHARM S1, V27, P27
[8]   Plasma concentrations of vigabatrin in epileptic patients [J].
SanchezAlcaraz, A ;
Quintana, B ;
Rodriguez, I ;
Lopez, E .
JOURNAL OF CLINICAL PHARMACY AND THERAPEUTICS, 1996, 21 (06) :393-398