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老年急性护理患者皮下芬太尼的群体药代动力学模型。

Population pharmacokinetic model of subcutaneous fentanyl in older acute care patients.

机构信息

UniSA: Clinical and Health Sciences, University of South Australia, Adelaide, Australia.

Basil Hetzel Institute for Translational Research, The Queen Elizabeth Hospital, Woodville, Australia.

出版信息

Eur J Clin Pharmacol. 2021 Sep;77(9):1357-1368. doi: 10.1007/s00228-021-03126-9. Epub 2021 Apr 3.

Abstract

PURPOSE

Subcutaneous fentanyl injection is commonly prescribed to manage acute pain in older patients; however, there is a gap in the literature describing the pharmacokinetic parameters for this route of administration in this population. The aim of this study was to develop and evaluate a population pharmacokinetic model for subcutaneous fentanyl injection in older patients.

METHODS

Twenty-one patients who received subcutaneous fentanyl injections (50 to 75 μg) were recruited. Fentanyl concentrations were determined using a validated liquid chromatography/tandem mass spectrometry method. A population pharmacokinetic model was developed using non-linear mixed-effects modelling. A base model was selected based on the Akaike information criterion. Age, sex, body weight, number of previous fentanyl doses, number of prescribed medications, creatinine clearance, Charlson Comorbidity Index, Identification of Seniors at Risk score and concurrent use of CYP3A4 inhibitors were covariates considered for inclusion. A p value of < 0.05 was considered statistically significant for inclusion of covariates in the final model by stepwise addition. The simulation performance of the model was assessed by visual predictive check.

RESULTS

A one-compartment, first-order absorption with lag time and linear elimination model was the best to fit to the fentanyl concentration data. The absorption rate constant was 0.136 h (between subject variability (BSV), 46%), lag time 0.66 h (BSV 51%), apparent volume of distribution 6.28 L (BSV 30%), and apparent clearance 16.3 L.h (BSV 54%). The Charlson Comorbidity Index was the only covariate included in the final model, where a higher value of the index increased fentanyl exposure and C.

CONCLUSION

This is the first report of subcutaneous fentanyl population pharmacokinetic model to evaluate fentanyl pharmacokinetic in older patients. The between subject variability in clearance and subcutaneous absorption rate was relatively high, and some patients recorded high fentanyl concentrations in the context of their titration to effect.

摘要

目的

皮下注射芬太尼常用于治疗老年患者的急性疼痛;然而,文献中对于该人群中该给药途径的药代动力学参数存在空白。本研究旨在建立和评估老年患者皮下注射芬太尼的群体药代动力学模型。

方法

招募了 21 名接受皮下芬太尼注射(50-75μg)的患者。使用经过验证的液相色谱/串联质谱法测定芬太尼浓度。使用非线性混合效应模型建立群体药代动力学模型。根据赤池信息量准则选择基础模型。年龄、性别、体重、芬太尼剂量、处方药物数量、肌酐清除率、Charlson 合并症指数、老年人风险识别评分和同时使用 CYP3A4 抑制剂等为潜在的协变量。协变量纳入最终模型的统计学意义标准为逐步添加时 P 值<0.05。通过可视化预测检查评估模型的模拟性能。

结果

最适合拟合芬太尼浓度数据的是一室、一级吸收、有滞后时间和线性消除模型。吸收速率常数为 0.136 h(个体间变异度(BSV)46%),滞后时间为 0.66 h(BSV 51%),表观分布容积为 6.28 L(BSV 30%),表观清除率为 16.3 L.h(BSV 54%)。Charlson 合并症指数是唯一纳入最终模型的协变量,该指数越高,芬太尼的暴露量和 C 越大。

结论

这是首例评估老年患者皮下芬太尼群体药代动力学模型的报告。清除率和皮下吸收速率的个体间变异度相对较高,一些患者在滴定至有效剂量时记录到了较高的芬太尼浓度。

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