Panebianco Deborah L, Maes Andrea
Merck Research Laboratories, Clinical Pharmacology Statistics, North Wales, PA 19454-1099, USA.
Pharm Stat. 2011 Jan-Feb;10(1):27-33. doi: 10.1002/pst.404.
Unless all of a drug is eliminated during each dosing interval, the plasma concentrations within a dosing interval will increase until the time course of change in plasma concentrations becomes invariant from one dosing interval to the next, resulting in steady state. A simple method for estimating drug concentration time to steady state based on multiple dose area under the plasma concentration-time curve and effective rate of drug accumulation is presented. Several point estimates and confidence intervals for time to 90% of steady state are compared, and a recommendation is made on how to summarize and present the results.
除非在每个给药间隔期内药物全部被清除,否则给药间隔期内的血浆浓度将会升高,直至血浆浓度变化的时间过程在相邻给药间隔期之间保持不变,从而达到稳态。本文提出了一种基于多剂量血浆浓度-时间曲线下面积和药物蓄积有效率来估算药物浓度达到稳态所需时间的简单方法。比较了达到90%稳态所需时间的几个点估计值和置信区间,并就如何总结和呈现结果给出了建议。