Bareggi S R, Tata M R, Guizzaro A, Pirola R, Parisi A, Monza C G
Department of Pharmacology, School of Medicine, University of Milan, Italy.
Int Clin Psychopharmacol. 1994 Spring;9(1):9-16. doi: 10.1097/00004850-199400910-00002.
The pharmacokinetics, tolerability, and efficacy of carbamazepine (CBZ) and the pharmacokinetics of carbamazepine-10, 11-epoxide (CBZE) were studied after chronic administration of a conventional tablet formation or of the controlled-release (CR) formulation of CBZ 400 mg (Tegretol 400) to 20 patients with epilepsy treated with carbamazepine and complaining of intermittent adverse effects. To compare the two formulations at the same doses and dose schedules, the study design had to be open, within-patient, with an initial 4 week period to individually adjust the dosage schedule with conventional CBZ followed by a 4 week period in which the CR formulation was substituted for conventional CBZ at the same daily dose and given by the same schedule. A further 4 week period was also studied to evaluate the same dosage of the CR formulation but given b.i.d. In this latter period six patients required an increase in dosage (200 mg/day). Before the beginning of the study and at the end of each period seizure frequency and tolerability were assessed. Tolerability was estimated with a specifically prepared scale that assesses the main items and with an overall rating scale. At the end of each treatment period, serum levels of CBZ and CBZE were determined at various times over a 10 h period. Peak plasma concentrations (Cmax) of CBZ and the fluctuation index (FI) were significantly lower for the CR CBZ, although minimal and mean plasma concentrations were the same in the three periods of the study.(ABSTRACT TRUNCATED AT 250 WORDS)
对20名服用卡马西平(CBZ)并抱怨有间歇性不良反应的癫痫患者,在长期服用常规片剂或400毫克卡马西平控释(CR)制剂(得理多400)后,研究了卡马西平的药代动力学、耐受性和疗效,以及卡马西平-10,11-环氧化物(CBZE)的药代动力学。为了在相同剂量和给药方案下比较两种制剂,研究设计必须是开放性的、患者自身对照的,最初为期4周,用常规卡马西平单独调整给药方案,随后为期4周,在此期间用相同日剂量的CR制剂替代常规卡马西平,并按相同方案给药。还研究了另外4周,以评估相同剂量的CR制剂但每日两次给药的情况。在这后一阶段,有6名患者需要增加剂量(200毫克/天)。在研究开始前和每个阶段结束时评估癫痫发作频率和耐受性。耐受性用专门编制的评估主要项目的量表和总体评分量表进行评估。在每个治疗阶段结束时,在10小时内的不同时间点测定血清中CBZ和CBZE的水平。CR卡马西平的CBZ峰血浆浓度(Cmax)和波动指数(FI)显著较低,尽管在研究的三个阶段中最低和平均血浆浓度相同。(摘要截短至250字)