Korman B, Jennings L S, Rigg J R
Department of Anaesthesia, Royal Perth Hospital, Perth, Australia.
J Pharmacokinet Biopharm. 1998 Jun;26(3):319-28. doi: 10.1023/a:1023285426388.
We describe a method of rapidly obtaining a specified steady state plasma concentration of an intravenous drug within precise limits. The technique requires an initial bolus to raise the plasma concentration to the upper limit followed by a series of constant-rate infusions each of which is associated with a minimum plasma concentration equal to the lower limit. The infusion rate is stepped down when the plasma concentration returns to the upper limit. Computer simulation, based on the method, is used to generate plasma concentration-time curves with fluctuations of up to 10% about selected steady state concentrations of amrinone, esmolol, lidocaine, midazolam, propofol, and theophylline. The utility of this general approach to intravenous dosing and potential limitations of the method are discussed.
我们描述了一种在精确限度内快速获得静脉注射药物特定稳态血浆浓度的方法。该技术需要一次初始推注将血浆浓度提高到上限,随后进行一系列恒速输注,每次输注的最低血浆浓度等于下限。当血浆浓度回到上限时,输注速率逐步降低。基于该方法的计算机模拟用于生成关于氨力农、艾司洛尔、利多卡因、咪达唑仑、丙泊酚和茶碱选定稳态浓度波动高达10%的血浆浓度-时间曲线。讨论了这种静脉给药通用方法的实用性和该方法的潜在局限性。