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首页> 外文期刊>The Journal of Clinical Pharmacology: Official Journal of the American College of Clinical Pharmacology >Estimation and comparison of carbamazepine population pharmacokinetics using dried blood spot and plasma concentrations from people with epilepsy: The clinical implication Sing Teang Kong, BPharm1
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Estimation and comparison of carbamazepine population pharmacokinetics using dried blood spot and plasma concentrations from people with epilepsy: The clinical implication Sing Teang Kong, BPharm1

机译:用癫痫干燥血液斑和血浆浓度估算和比较癫痫患者的血液斑点和血浆浓度:临床意义唱歌Teang Kong,BPharm1

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摘要

To establish using dried blood spot (DBS) as a surrogate to plasma for therapeutic drug monitoring (TDM) of carbamazepine (CBZ), we compared the population pharmacokinetic (PPK) estimates from concurrent DBS and plasma levels. The dose-concentration relationship, estimated parameter and variability were determined. A total of 98 observations from 97 people with epilepsy (PWE) were included in this study. Data was split into 3:1 ratio for the respective index group and validation group. Non-linear mixed effects regression with one compartment, first order absorption and elimination model was utilized. Covariates were screened for inclusion into final model via forward stepwise addition and backward elimination method. Predictive performances of the final models were assessed for bias and precision. The typical clearance for CBZ was estimated to be 5.85 and 5.68 L/h from plasma and DBS concentrations, respectively. The final models for clearance estimates obtained from plasma concentrations (Cplasma) included total daily CBZ dose per unit weight (DD) and sex while from DBS concentrations (Cdbs) included only DD. The final models were both precise and non-bias. The developed PPK models had comparable estimates, errors and predictive performances. Our findings suggest that Cplasma and Cdbs could be used interchangeably for pharmacokinetic studies of CBZ.
机译:为了建立使用干血斑(DBS)作为血浆的替代物用于血浆(CBZ)的治疗药物监测(TDM),我们将群体药代动力学(PPK)与同时DB和血浆水平进行比较。确定剂量浓度关系,估计参数和可变性。这项研究中包括98人从97名癫痫(PWE)的68人观察。数据被分成了相应索引组和验证组的3:1的比例。利用非线性混合效应回归一个隔室,第一阶吸收和消除模型进行了回归。通过向前逐步添加和向后消除方法筛选可协变量以将其纳入最终模型。评估最终模型的预测性能,用于偏差和精度。 CBZ的典型间隙估计为5.85和5.68L / h,分别来自血浆和DBS浓度。从血浆浓度(CPLASMA)获得的间隙估计的最终模型包括每单位重量(DD)的总每日CBZ剂量,并且来自DBS浓度(CDB)仅包括DD。最终模型既精确又非偏见。开发的PPK模型具有可比的估计,错误和预测性能。我们的研究结果表明,Cplasma和CDB可以互换用于CBZ的药代动力学研究。

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