Higuchi S, Aoyama T, Horioka M
Department of Hospital Pharmacy, Faculty of Medicine, Kyushu University, Fukuoka, Japan.
J Pharmacobiodyn. 1987 Dec;10(12):703-18. doi: 10.1248/bpb1978.10.703.
PEDA, an integrated program in BASIC for implementation on microcomputers, has been developed for use in clinical practice to assist dosage adjustment for individual patients. A parameter optimization for individual patients is based on the principle of Bayes' theory and Maximum Likelihood Estimation, and utilizes a prior information on the distribution of population pharmacokinetic parameters, means and variances, as well as serum drug concentrations. The program can accommodate a one-compartment open linear model and a non-linear model at steady state (Michaelis-Menten model) and handle both uniform and non-uniform multiple dosage regimens mostly arising from clinical settings. Clinical examples which demonstrate the ability and the flexibility of the program are provided. The program may also be used as an aid for instruction in clinical pharmacokinetics.
PEDA是一个用BASIC语言编写的集成程序,用于在微型计算机上运行,已开发用于临床实践,以协助个体患者的剂量调整。个体患者的参数优化基于贝叶斯理论和最大似然估计原理,并利用关于群体药代动力学参数分布、均值和方差以及血清药物浓度的先验信息。该程序可以采用单室开放线性模型和稳态非线性模型(米氏模型),并处理大多来自临床环境的均匀和非均匀多剂量方案。文中提供了临床实例,展示了该程序的能力和灵活性。该程序还可用作临床药代动力学教学的辅助工具。