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癫痫患者中,缓释型卡马西平每日一次给药与每日两次给药的双模拟对照研究。

Double dummy comparison between once and twice daily dosing with modified-release carbamazepine in epileptic patients.

作者信息

McKee P J, Blacklaw J, Carswell A, Gillham R A, Brodie M J

机构信息

University Department of Medicine and Therapeutics, Western Infirmary, Glasgow.

出版信息

Br J Clin Pharmacol. 1993 Sep;36(3):257-61. doi: 10.1111/j.1365-2125.1993.tb04226.x.

Abstract
  1. Fourteen patients with refractory epilepsy on a twice daily regimen of modified-release carbamazepine (CBZ-MR. Tegretol Retard. Ciba Pharmaceuticals) completed a balanced, double-blind, double dummy, random order, crossover comparison of 8 weeks treatment with once (o.d.) and twice daily (b.d.) dosing. In order to obtain a profile of serum CBZ concentrations over 24 h on once daily dosing, patients were randomised to taking it in the morning (o.d. a.m.) or evening (o.d. p.m.) for 4 weeks. Each treatment was taken with a placebo of the other and total tablet numbers were matched. Blood sampling was undertaken 0, 2, 4, 6, 8, 10, 12 and 24 h after the morning tablets at the end of each 4 week treatment period. 2. Overall, trough serum drug concentrations (Cmin) were lower with once daily dosing (Cmin: b.d. 7.5 mg l-1, o.d. 6.5 mg l-1, P < 0.05, 95% CI of the difference -1.3 to -0.1), but no significant differences were found in average (Cav) or peak (Cmax) concentrations, AUC values or fluctuations in CBZ concentrations. 3. Pharmacokinetic parameters for CBZ 10.11 epoxide, the active metabolite of CBZ did not differ significantly between the dosage schedules. 4. Seizure control was similar during once and twice daily dosing with CBZ-MR (median seizures/month (range): b.d. 1 (0-14.5), o.d. 0.5 (0-11), NS, 95% CI of the difference -1.8 to + 0.25). 5. There were no differences in psychomotor performance between the treatment periods. 6. More patients (n = 11) preferred treatment (P < 0.05) with once daily than twice daily dosing (n = 3) with CBZ-MR. 7. Once daily dosing with CBZ-MR should be possible in the majority of patients receiving the drug as monotherapy.
摘要
  1. 14例难治性癫痫患者接受缓释卡马西平(CBZ-MR,商品名:得理多缓释片,汽巴制药公司生产)每日两次的治疗方案,完成了一项为期8周的平衡、双盲、双模拟、随机顺序、交叉对照试验,比较每日一次(o.d.)和每日两次(b.d.)给药的效果。为了获取每日一次给药时24小时内血清CBZ浓度的情况,患者被随机分为早晨(o.d. a.m.)或晚上(o.d. p.m.)服用4周。每种治疗均搭配另一种的安慰剂,且片剂总数相同。在每个4周治疗期结束时,于早晨服药后0、2、4、6、8、10、12和24小时进行采血。2. 总体而言,每日一次给药时的谷值血清药物浓度(Cmin)较低(Cmin:b.d. 7.5 mg/L,o.d. 6.5 mg/L,P<0.05,差值的95%置信区间为-1.3至-0.1),但平均(Cav)或峰值(Cmax)浓度、AUC值或CBZ浓度波动方面未发现显著差异。3. CBZ的活性代谢产物CBZ 10,11环氧化物的药代动力学参数在两种给药方案间无显著差异。4. 使用CBZ-MR每日一次和每日两次给药时的癫痫控制情况相似(每月癫痫发作中位数(范围):b.d. 1(0-14.5),o.d. 0.5(0-11),无显著性差异,差值的95%置信区间为-1.8至+0.25)。5. 各治疗期之间的精神运动表现无差异。6. 更多患者(n = 11)更喜欢CBZ-MR每日一次给药的治疗方式(P<0.05),而非每日两次给药(n = 3)。7. 大多数接受该药物单药治疗的患者应可以每日一次服用CBZ-MR。

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Comparative bioavailability of carbamazepine from two slow-release preparations.
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本文引用的文献

6
Interdosage fluctuations in plasma carbamazepine concentration determine intermittent side effects.
Arch Neurol. 1984 Aug;41(8):830-4. doi: 10.1001/archneur.1984.04050190036011.
10
Reduction of dosing frequency of carbamazepine with a slow-release preparation.
Epilepsy Res. 1988 Jan-Feb;2(1):32-6. doi: 10.1016/0920-1211(88)90007-1.

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