Touw D J, Vinks A A, Neef C
Academic Hospital Vrije Universiteit, Department of Pharmacy, Amsterdam, The Netherlands.
Pharm World Sci. 1997 Jun;19(3):142-51. doi: 10.1023/a:1008633526772.
The availability of personal computer programs for individualizing drug dosage regimens has stimulated the interest in modelling population pharmacokinetics. Data from 82 adolescent and adult patients with cystic fibrosis (CF) who were treated with intravenous tobramycin because of an exacerbation of their pulmonary infection were analysed with a non-parametric expectation maximization (NPEM) algorithm. This algorithm estimates the entire discrete joint probability density of the pharmacokinetic parameters. It also provides traditional parametric statistics such as the means, standard deviation, median, covariances and correlations among the various parameters. It also provides graphic-2- and 3-dimensional representations of the marginal densities of the parameters investigated. Several models for intravenous tobramycin in adolescent and adult patients with CF were compared. Covariates were total body weight (for the volume of distribution) and creatinine clearance (for the total body clearance and elimination rate). Because of lack of data on patients with poor renal function, restricted models with non-renal clearance and the non-renal elimination rate constant fixed at literature values of 0.15 L/h and 0.01 h-1 were also included. In this population, intravenous tobramycin could be best described by median (+/-dispersion factor) volume of distribution per unit of total body weight of 0.28 +/- 0.05 L/kg, elimination rate constant of 0.25 +/- 0.10 h-1 and elimination rate constant per unit of creatinine clearance of 0.0008 +/- 0.0009 h-1/(ml/min/1.73 m2). Analysis of populations of increasing size showed that using a restricted model with a non-renal elimination rate constant fixed at 0.01 h-1, a model based on a population of only 10 to 20 patients, contained parameter values similar to those of the entire population and, using the full model, a larger population (at least 40 patients) was needed.
用于个体化药物剂量方案的个人计算机程序的出现激发了人们对群体药代动力学建模的兴趣。对82例因肺部感染加重而接受静脉注射妥布霉素治疗的青少年和成年囊性纤维化(CF)患者的数据,采用非参数期望最大化(NPEM)算法进行分析。该算法可估计药代动力学参数的整个离散联合概率密度。它还提供传统的参数统计量,如各种参数的均值、标准差、中位数、协方差和相关性。它还提供所研究参数边际密度的二维和三维图形表示。比较了CF青少年和成年患者静脉注射妥布霉素的几种模型。协变量为总体重(用于分布容积)和肌酐清除率(用于总体清除率和消除速率)。由于缺乏肾功能不全患者的数据,还纳入了非肾清除率和非肾消除速率常数固定为文献值0.15 L/h和0.01 h-1的受限模型。在该群体中,静脉注射妥布霉素的最佳描述为每单位总体重的分布容积中位数(±离散因子)为0.28±0.05 L/kg,消除速率常数为0.25±0.10 h-1,每单位肌酐清除率的消除速率常数为0.0008±0.0009 h-1/(ml/min/1.73 m2)。对规模不断增加的群体进行分析表明,使用非肾消除速率常数固定为0.01 h-1的受限模型时,仅基于10至20例患者的群体模型所包含的参数值与整个群体的参数值相似;而使用完整模型时,则需要更大的群体(至少40例患者)。