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哌拉西林/他唑巴坦在新生儿和婴幼儿人群中的群体药代动力学研究。

Population pharmacokinetics of piperacillin/tazobactam in neonates and young infants.

机构信息

Department of Pharmacy, Children's Hospital of Fudan University, Shanghai, China.

出版信息

Eur J Clin Pharmacol. 2013 Jun;69(6):1223-33. doi: 10.1007/s00228-012-1413-4. Epub 2013 Jan 26.

Abstract

OBJECTIVES

To develop population pharmacokinetic (PK) models for piperacillin/tazobactam in neonates and infants of less than 2 months of age in order to determine the appropriate dosing regimen and provide a rational basis for the development of preliminary dosing guidelines suitable for this population.

METHODS

A two-stage, open-label study was conducted in neonates and infants less than 2 months of age in the neonatal intensive care unit (NICU). A total of 207 piperacillin and 204 tazobactam concentration-time data sets from 71 patients were analyzed using a nonlinear mixed-effect modeling approach (NONMEM VII). PK models were developed for piperacillin and tazobactam. The final models were evaluated using both bootstrap and visual predictive checks. External model evaluations were made in 20 additional patients.

RESULTS

For neonates and young infants less than 2 months of age, the median central clearance was 0.133 and 0.149 L/h/kg for piperacillin and tazobactam, respectively. Postmenstrual age (PMA) was identified as the most significant covariate on central clearance of piperacillin and tazobactam. However, the combination of current bodyweight (BW) and postnatal age proved to be superior to PMA alone. BW was the most important covariate for apparent central volume of distribution. Both internal and external evaluations supported the prediction of the final piperacillin and tazobactam PK models. The dosing strategy 44.44/5.56 mg/kg/dose piperacillin/tazobactam every 8 or 12 h evaluated in this study achieved the pharmacodynamic target (free piperacillin concentrations >4 mg/L for more than 50 % of the dosing interval) in about 67 % of infants.

CONCLUSIONS

Population PK models accurately described the PK profiles of piperacillin/tazobactam in infants less than 2 months of age. The results indicated that higher doses or more frequent dosing regimens may be required for controlling infection in this population in NICU.

摘要

目的

建立哌拉西林/他唑巴坦在 2 个月以下新生儿和婴儿中的群体药代动力学(PK)模型,以确定合适的给药方案,并为制定适合该人群的初步给药指南提供合理依据。

方法

在新生儿重症监护病房(NICU)对 2 个月以下的新生儿和婴儿进行了两阶段、开放性研究。采用非线性混合效应建模方法(NONMEM VII)对 71 例患者的 207 个哌拉西林和 204 个他唑巴坦浓度-时间数据集进行分析。为哌拉西林和他唑巴坦建立了 PK 模型。使用 Bootstrap 和可视化预测检查对最终模型进行了评估。在 20 例额外患者中进行了外部模型评估。

结果

对于 2 个月以下的新生儿和婴儿,哌拉西林和他唑巴坦的中位中心清除率分别为 0.133 和 0.149 L/h/kg。胎龄(PMA)被确定为哌拉西林和他唑巴坦中心清除率的最重要协变量。然而,当前体重(BW)和出生后年龄的组合被证明优于 PMA 单独使用。BW 是表观中央分布容积的最重要协变量。内部和外部评估均支持最终哌拉西林和他唑巴坦 PK 模型的预测。本研究评估的 44.44/5.56 mg/kg/dose 哌拉西林/他唑巴坦每 8 或 12 小时给药方案在约 67%的婴儿中达到了药效学目标(游离哌拉西林浓度>4 mg/L 超过给药间隔的 50%)。

结论

群体 PK 模型准确描述了 2 个月以下婴儿中哌拉西林/他唑巴坦的 PK 特征。结果表明,在 NICU 中,该人群可能需要更高的剂量或更频繁的给药方案来控制感染。

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