Isbister G K, Friberg L E, Hackett L P, Duffull S B
Department of Clinical Toxicology and Pharmacology, Newcastle Mater Hospital, Newcastle and Tropical Toxinology Unit, Menzies School of Health Research, Charles Darwin University, Darwin, Northern Territory, Australia.
Clin Pharmacol Ther. 2007 Jun;81(6):821-7. doi: 10.1038/sj.clpt.6100193. Epub 2007 Apr 4.
The aim of the study was to investigate the pharmacokinetics of quetiapine overdose and the effect of charcoal. The data set included 204 concentration-time points from 54 quetiapine overdose events (median dose 2,700 mg (300-24,000 mg)). Charcoal was administered 0.5-6 h after 19 overdoses. A fully Bayesian methodology for population pharmacokinetic analysis was used and data were modelled using WinBUGS. Uncertainty in the dose history was considered in model building by estimating dose amount and dose time within a possible range. Inclusion of informative priors stabilized the model and population parameter values could be estimated well. A one-compartment model with first-order input and first-order elimination described the data. The final model included uncertainty in dose time. The median and interquartile range of the half-life for individual patients was 6.6 h (4.9-8.4 h). Charcoal was estimated to reduce fraction absorbed by 35%. Co-ingested CYP3A4 inhibitors appeared to decrease clearance and CYP3A4 inducers increase clearance. Charcoal administration may be beneficial after quetiapine overdose.
该研究的目的是调查喹硫平过量用药的药代动力学及活性炭的作用。数据集包括来自54例喹硫平过量事件(中位剂量2700毫克(300 - 24000毫克))的204个浓度-时间点。19例过量用药事件在0.5 - 6小时后给予活性炭。采用全贝叶斯方法进行群体药代动力学分析,并使用WinBUGS对数据进行建模。在模型构建过程中,通过在可能范围内估计剂量和给药时间来考虑剂量历史的不确定性。纳入信息先验稳定了模型,且群体参数值能够得到很好的估计。一个具有一级输入和一级消除的单室模型描述了这些数据。最终模型纳入了给药时间的不确定性。个体患者半衰期的中位数和四分位间距为6.6小时(4.9 - 8.4小时)。据估计,活性炭可使吸收分数降低35%。同时摄入的CYP3A4抑制剂似乎会降低清除率,而CYP3A4诱导剂则会增加清除率。喹硫平过量用药后给予活性炭可能有益。