Pospisil J, Pelclová D
Department of Clinical Pharmacology, Charles University of Prague, Czech Republic.
Int J Clin Pharmacol Ther. 1994 Mar;32(3):122-5.
The graphical nomogram method to estimate the phenytoin free concentration at any selected total serum phenytoin and/or albumin concentrations was applied using Scatchard binding equation. The binding parameters were calculated by the non-linear least-squares regression analysis of the binding data collected from 96 outpatients on common anticonvulsant therapy. Free phenytoin concentration was measured by the Amicon multi-micro ultrafiltration system. The mean values of N and Kapp were found to be: N = 1.03, and Kapp = 18,500 (M-1). Correlation coefficient for relationship between measured and predicted free phenytoin concentrations was very good (r = 0.94), but the results of prediction-error analysis (MPE = 0.153, and RMSE = 0.296) show that the nomogram method overpredicts the measured free phenytoin (PHT) concentration approximately about 10% higher (15-30 mg/l) than serum phenytoin levels.
使用Scatchard结合方程应用图形列线图法,以估计在任何选定的总血清苯妥英和/或白蛋白浓度下的游离苯妥英浓度。结合参数通过对96名接受常用抗惊厥治疗的门诊患者收集的结合数据进行非线性最小二乘回归分析来计算。游离苯妥英浓度通过Amicon多微超滤系统测量。发现N和Kapp的平均值为:N = 1.03,Kapp = 18,500(M-1)。测量的和预测的游离苯妥英浓度之间关系的相关系数非常好(r = 0.94),但预测误差分析结果(平均预测误差 = 0.153,均方根误差 = 0.296)表明,列线图法预测的游离苯妥英(PHT)浓度比血清苯妥英水平大约高10%(15 - 30 mg/l)。