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对新生儿和婴儿庆大霉素暴露情况的定量分析对其目前的推荐剂量提出了质疑。

Quantitative Analysis of Gentamicin Exposure in Neonates and Infants Calls into Question Its Current Dosing Recommendations.

机构信息

Paediatric Pharmacology and Pharmacometrics Research, University of Basel Children's Hospital, Basel, Switzerland.

Quantitative Solutions, a Certara Company, London, United Kingdom.

出版信息

Antimicrob Agents Chemother. 2018 Mar 27;62(4). doi: 10.1128/AAC.02004-17. Print 2018 Apr.

Abstract

Optimal dosing of gentamicin in neonates is still a matter of debate despite its common use. We identified gentamicin dosing regimens from eight international guidelines and seven Swiss neonatal intensive care units. The dose per administration, the dosing interval, the total daily dose, and the demographic characteristics between guidelines were compared. There was considerable variability with respect to dose (4 to 6 mg/kg), dosing interval (24 h to 48 h), total daily dose (2.5 to 6 mg/kg/day), and patient demographic characteristics that were used to calculate individualized dosing regimens. A model-based simulation study in 1071 neonates was performed to determine the achievement of efficacious peak gentamicin concentrations according to predefined MICs (/MIC ≥ 10) and safe trough concentrations ( ≤ 2 mg/liter) with recommended dosing regimens. MIC targets of 0.5 and 1 mg/liter were used. Dosing optimization was performed giving priority to the first day of treatment and with the goal of simplifying dosing. Current gentamicin neonatal guidelines allow to achieve effective peak concentrations for MICs ≤ 0.5 mg/liter but not higher. Model-based simulations indicate that to attain peak gentamicin concentrations of ≥10 mg/liter, a dose of 7.5 mg/kg should be administered using an extended dosing interval regimen. Trough concentrations of ≤2 mg/liter can be maintained with a dosing interval of 36 to 48 h in neonates according to gestational and postnatal age. For treatment beyond 3 days, therapeutic drug monitoring is advised to maintain adequate serum concentrations.

摘要

尽管庆大霉素被广泛应用,但在新生儿中的最佳剂量仍存在争议。我们从八项国际指南和七家瑞士新生儿重症监护病房中确定了庆大霉素的给药方案。比较了每次给药剂量、给药间隔、总日剂量以及指南之间的人口统计学特征。在剂量(4 至 6mg/kg)、给药间隔(24 小时至 48 小时)、总日剂量(2.5 至 6mg/kg/天)和用于计算个体化给药方案的患者人口统计学特征方面存在相当大的差异。在 1071 名新生儿中进行了基于模型的模拟研究,以确定根据预定 MIC(/MIC≥10)和安全谷浓度(≤2mg/L)以及推荐的给药方案实现有效庆大霉素峰值浓度的情况。使用了 0.5 和 1mg/L 的 MIC 目标。优先考虑治疗的第一天进行剂量优化,并以简化给药为目标。目前的新生儿庆大霉素指南可以实现 MIC≤0.5mg/L 的有效峰值浓度,但不能更高。基于模型的模拟表明,要达到≥10mg/L 的庆大霉素峰值浓度,应使用延长的给药间隔方案给予 7.5mg/kg 的剂量。根据胎龄和出生后年龄,36 至 48 小时的给药间隔可维持≤2mg/L 的谷浓度。对于 3 天以上的治疗,建议进行治疗药物监测以维持足够的血清浓度。

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