Har-Even Ronly, Stepensky David, Britzi Malka, Soback Stefan, Chaim Adina Bar, Brandriss Norit, Goldman Michael, Berkovitch Matitiahu, Kozer Eran
Pediatric Emergency Unit, Clinical Pharmacology & Toxicology Unit and Pediatric Ward B, Assaf Harofeh Medical Center, Zerifin, Israel.
J Clin Pharmacol. 2014 Sep;54(9):1023-30. doi: 10.1002/jcph.307. Epub 2014 Apr 21.
We aimed to determine the relationship between plasma and cerebrospinal fluid (CSF) concentrations of ibuprofen and the antipyretic effect in pediatric patients. A prospective cohort of infants and children aged 3 months to 15 years and treated with ibuprofen was studied. The patients received ibuprofen (via oral route, median dose of 10.0 mg/kg; 3.4-11.4 mg/kg range), samples of blood and CSF were collected, and body temperature was measured. Sequential analysis of the pharmacokinetic and pharmacodynamic data from 28 patients was performed using a population modeling approach. The observed concentration versus time data indicated substantial pharmacokinetic variability in absorption and distribution of ibuprofen between the patients. The pharmacokinetic modeling outcomes indicate that following a ∼25-minute lag time, ibuprofen is rapidly absorbed to the central compartment and rapidly equilibrates with the CSF, resulting in the total ibuprofen concentration in the CSF versus plasma (CCSF /Cplasma ) of 0.011 ± 0.007. The antipyretic effect of ibuprofen was best described by an indirect response PK-PD model incorporating patient baseline body temperature and ibuprofen concentration in the CSF. We conclude that the pharmacokinetic-pharmacodynamic modeling can be used to predict the time course of ibuprofen plasma and CSF concentrations and of the antipyretic effects in individual pediatric patients.
我们旨在确定布洛芬的血浆和脑脊液(CSF)浓度与儿科患者解热作用之间的关系。对一组年龄在3个月至15岁之间且接受布洛芬治疗的婴幼儿和儿童进行了前瞻性队列研究。患者接受布洛芬治疗(经口服途径,中位剂量为10.0 mg/kg;范围为3.4 - 11.4 mg/kg),采集血液和脑脊液样本,并测量体温。使用群体建模方法对28例患者的药代动力学和药效学数据进行了序贯分析。观察到的浓度随时间变化的数据表明,患者之间布洛芬在吸收和分布方面存在显著的药代动力学变异性。药代动力学建模结果表明,经过约25分钟的滞后时间后,布洛芬迅速吸收进入中央室,并迅速与脑脊液达到平衡,导致脑脊液中布洛芬的总浓度与血浆浓度之比(CCSF /Cplasma)为0.011±0.007。布洛芬的解热作用最好用一个间接反应PK-PD模型来描述,该模型纳入了患者的基线体温和脑脊液中布洛芬的浓度。我们得出结论,药代动力学-药效学建模可用于预测个体儿科患者布洛芬血浆和脑脊液浓度的时间进程以及解热作用。