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庆大霉素在小儿体外膜肺氧合中的群体药代动力学分析

Population Pharmacokinetic Analysis of Gentamicin in Pediatric Extracorporeal Membrane Oxygenation.

作者信息

Moffett Brady S, Morris Jennifer, Galati Marianne, Munoz Flor M, Arikan Ayse Akcan

机构信息

Department of Pharmacy, Texas Children's Hospital.

Department of Pediatrics, Baylor College of Medicine.

出版信息

Ther Drug Monit. 2018 Oct;40(5):581-588. doi: 10.1097/FTD.0000000000000547.

Abstract

BACKGROUND

Gentamicin pharmacokinetics may be altered in pediatric patients undergoing extracorporeal membrane oxygenation (ECMO). Description of gentamicin pharmacokinetics and relevant variables can improve dosing.

METHODS

A retrospective population pharmacokinetic study was designed, and pediatric patients who received gentamicin while undergoing ECMO therapy over a period of 6 1/2 years were included. Data collection included the following: patient demographics, serum creatinine, albumin, hematocrit, gentamicin dosing and serum concentrations, urine output, and ECMO circuit parameters. Descriptive statistics were used to characterize the patient population. Population pharmacokinetic analysis was performed with NONMEM, and simulation was performed to identify empiric doses to achieve therapeutic serum concentrations.

RESULTS

A total of 37 patients met study criteria (75.7% male patients), with a median age of 0.17 [interquartile range (IQR) 0.12-0.82] years. Primary indications for ECMO included the following: congenital diaphragmatic hernia (n = 17), persistent pulmonary hypertension (n = 5), and septic shock (n = 4). Patients received a total of 117 gentamicin doses [median 1.8 (IQR 1.4-2.9) mg/kg/dose] and had 125 serum concentrations measured at a median of 22.8 (IQR 15.8-25.5) hours after a dose. Population pharmacokinetic analysis identified a 2-compartment model with additive error as the best fit. Covariates included the following: allometrically scaled fat-free mass on clearance, central and peripheral volume of distribution (VDcentral and VDperipheral), and intercompartmental clearance; serum creatinine on clearance; ultrafiltration rate on central volume of distribution. Simulation identified dosage of 4-5 mg/kg/dose every 24 hours for neonates and infants as an acceptable empiric dosing regimen. Children and adolescents had elevated trough concentrations when dosed according to traditional dosing methods.

CONCLUSIONS

Fat-free mass should be used to dose gentamicin in pediatric ECMO patients. Serum creatinine is a marker of gentamicin clearance and should be used to adjust gentamicin dosing in pediatric ECMO patients.

摘要

背景

接受体外膜肺氧合(ECMO)治疗的儿科患者,庆大霉素的药代动力学可能会发生改变。对庆大霉素药代动力学及相关变量的描述有助于优化给药方案。

方法

开展一项回顾性群体药代动力学研究,纳入在6年半时间内接受ECMO治疗期间使用庆大霉素的儿科患者。数据收集内容包括:患者人口统计学信息、血清肌酐、白蛋白、血细胞比容、庆大霉素给药剂量及血清浓度、尿量以及ECMO回路参数。采用描述性统计方法对患者群体进行特征分析。使用NONMEM进行群体药代动力学分析,并进行模拟以确定达到治疗性血清浓度的经验性剂量。

结果

共有37例患者符合研究标准(男性患者占75.7%),中位年龄为0.17岁[四分位间距(IQR)0.12 - 0.82岁]。ECMO的主要适应证包括:先天性膈疝(n = 17)、持续性肺动脉高压(n = 5)和感染性休克(n = 4)。患者共接受117剂庆大霉素[中位剂量1.8(IQR 1.4 - 2.9)mg/kg/剂],并在给药后中位时间22.8(IQR 15.8 - 25.5)小时测定了125次血清浓度。群体药代动力学分析确定二室模型加误差为最佳拟合模型。协变量包括:根据体表面积标化的去脂体重对清除率、中央室和外周室分布容积(VDcentral和VDperipheral)以及室间清除率的影响;血清肌酐对清除率的影响;超滤率对中央室分布容积的影响。模拟确定,对于新生儿和婴儿,每24小时给予4 - 5 mg/kg/剂的剂量是可接受的经验性给药方案。儿童和青少年按照传统给药方法给药时谷浓度升高。

结论

在儿科ECMO患者中,应根据去脂体重来确定庆大霉素的给药剂量。血清肌酐是庆大霉素清除率的标志物,应用于调整儿科ECMO患者的庆大霉素给药剂量。

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