Mac-Kay M V, Sanchez Burson J, Martinez-Lanao J, Dominguez-Gil A
Department of Pharmacy and Pharmaceutical Technology, Faculty of Pharmacy, University of Seville, Spain.
Clin Pharmacokinet. 1993 Sep;25(3):243-57. doi: 10.2165/00003088-199325030-00007.
Drug dosage in end-stage renal disease (ESRD) patients undergoing haemodialysis is a very complex problem because of numerous variables relating to the patient, the type of drug administered and the type of dialysis and dialyser. We carried out a multifactorial study of these parameters using a microcomputer program written in BASIC. Three sets of data were fed into the computer: those relating to the biophysical characteristics of the patient, the type of dialysis and dialyser to be used, and others relating to the chemical and pharmacokinetic characteristics of the drug. From these, a predictive intravenous dosage regimen (bolus and infusion) was compiled for each ESRD patient. To check the program we used 2 drugs (tobramycin and vancomycin) and several types of dialyser. The findings were that, with tobramycin, an ESRD patient should be given different postdialytic doses, depending on the type of dialyser used. The maintenance doses calculated by the program were similar to those usually administered to patients receiving clinical treatment with this drug. In the case of vancomycin, the program calculated the clearance value in vivo through the 'Hemoflow F60' dialyser with a polysulphone membrane. The computer program calculated the maintenance dosage of vancomycin that should be given after each dialysis cycle so that its concentration did not fall below its minimum therapeutic concentration.
对于接受血液透析的终末期肾病(ESRD)患者,药物剂量是一个非常复杂的问题,因为涉及众多与患者、所用药物类型以及透析和透析器类型相关的变量。我们使用用BASIC编写的微机程序对这些参数进行了多因素研究。三组数据被输入计算机:与患者生物物理特征相关的数据、拟使用的透析和透析器类型的数据,以及与药物化学和药代动力学特征相关的其他数据。据此,为每位ESRD患者编制了预测性静脉给药方案(推注和输注)。为了检验该程序,我们使用了2种药物(妥布霉素和万古霉素)以及几种类型的透析器。结果发现,对于妥布霉素,ESRD患者应根据所用透析器类型给予不同的透析后剂量。该程序计算出的维持剂量与通常给予接受该药物临床治疗患者的剂量相似。对于万古霉素,该程序通过带有聚砜膜的“Hemoflow F60”透析器计算体内清除率值。计算机程序计算出每次透析周期后应给予的万古霉素维持剂量,以便其浓度不低于最低治疗浓度。