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影响抗癫痫药物浓度的因素分析——卡马西平

Analysis of the factors influencing anti-epileptic drug concentrations--carbamazepine.

作者信息

Ichikou N, Ieiri I, Higuchi S, Hirata K, Yamada H, Aoyama T

机构信息

Department of Neuro-Psychiatry, Kyushu University Hospital, Fukuoka, Japan.

出版信息

J Clin Pharm Ther. 1990 Oct;15(5):337-49. doi: 10.1111/j.1365-2710.1990.tb00394.x.

Abstract

The factors that influence carbamazepine (CBZ) serum concentrations and level:dose ratios were evaluated retrospectively on 83 consecutive routine CBZ determinations from chronically treated epileptic patients. The total level:dose ratio was lower when the drug was given in combination with phenytoin or with phenytoin plus other anti-epileptic drugs (AED) than when CBZ was given alone. The free level:dose ratio was also decreased during concomitant treatment with phenytoin. In spite of alterations to both level:dose ratios, the free fraction of CBZ was unaltered when in combination with other AEDs. There were statistically significant correlations between the CBZ dose (mg/kg/day) and the serum levels:total (r = 0.372, P less than 0.001) and free (r = 0.335, P less than 0.005). However, the wide scatter in the CBZ serum levels at each given dose were such that the relationships had no predictive values. Stepwise multivariate regression analysis (MVR) was also performed. A comparison of the normalized regression coefficients indicated that the CBZ dose, PHT dose, the time elapsed from the previous dose, the albumin concentration and the triglyceride levels were important factors which influence the CBZ total serum level. Similar analysis for the CBZ free serum level, gave a multiple correlation coefficient of 0.838, which indicates that 70.3% of the variance was explained by nine independent variables. The major factors that significantly affected the free serum level of CBZ were CBZ dose, PHT dose, the time elapsed from the previous dose and the triglyceride and albumin levels. Our observations indicate that it may be possible to predict reliably the CBZ serum concentrations for individual patients before institution of CBZ therapy.

摘要

我们对83例慢性治疗癫痫患者连续进行的卡马西平(CBZ)常规测定结果进行回顾性分析,以评估影响CBZ血清浓度及血药浓度与剂量比值的因素。与单独使用CBZ相比,当CBZ与苯妥英钠或苯妥英钠加其他抗癫痫药物(AED)联合使用时,总血药浓度与剂量比值较低。在与苯妥英钠联合治疗期间,游离血药浓度与剂量比值也降低。尽管两种血药浓度与剂量比值均发生改变,但CBZ与其他AED联合使用时,其游离分数未发生改变。CBZ剂量(mg/kg/天)与血清总浓度(r = 0.372,P < 0.001)和游离浓度(r = 0.335,P < 0.005)之间存在统计学显著相关性。然而,在每个给定剂量下,CBZ血清浓度的广泛离散使得这些关系没有预测价值。我们还进行了逐步多元回归分析(MVR)。对标准化回归系数的比较表明,CBZ剂量、苯妥英钠剂量、上次给药后的时间、白蛋白浓度和甘油三酯水平是影响CBZ血清总浓度的重要因素。对CBZ游离血清浓度进行类似分析,得到的多重相关系数为0.838,这表明70.3%的变异可由9个独立变量解释。显著影响CBZ游离血清浓度的主要因素是CBZ剂量、苯妥英钠剂量、上次给药后的时间以及甘油三酯和白蛋白水平。我们的观察结果表明,在开始CBZ治疗之前,有可能可靠地预测个体患者的CBZ血清浓度。

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