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美罗培南在韩国重症患者中的群体药代动力学及体外膜肺氧合的影响

Population Pharmacokinetics of Meropenem in Critically Ill Korean Patients and Effects of Extracorporeal Membrane Oxygenation.

作者信息

Lee Dong-Hwan, Kim Hyoung-Soo, Park Sunghoon, Kim Hwan-Il, Lee Sun-Hee, Kim Yong-Kyun

机构信息

Department of Clinical Pharmacology, Hallym University Sacred Heart Hospital, Hallym University College of Medicine, Anyang 14066, Korea.

Department of Thoracic and Cardiovascular Surgery, Hallym University Sacred Heart Hospital, Hallym University College of Medicine, Anyang 14066, Korea.

出版信息

Pharmaceutics. 2021 Nov 4;13(11):1861. doi: 10.3390/pharmaceutics13111861.

Abstract

Limited studies have investigated population pharmacokinetic (PK) models and optimal dosage regimens of meropenem for critically ill adult patients using the probability of target attainment, including patients receiving extracorporeal membrane oxygenation (ECMO). A population PK analysis was conducted using non-linear mixed-effect modeling. Monte Carlo simulation was used to determine for how long the free drug concentration was above the minimum inhibitory concentration (MIC) at steady state conditions in patients with various degrees of renal function. Meropenem PK in critically ill patients was described using a two-compartment model, in which glomerular filtration rate was identified as a covariate for clearance. ECMO did not affect meropenem PK. The simulation results showed that the current meropenem dosing regimen would be sufficient for attaining 40%T for at MIC ≤ 4 mg/L. Prolonged infusion over 3 h or a high-dosage regimen of 2 g/8 h was needed for MIC > 2 mg/L or in patients with augmented renal clearance, for a target of 100%T or 100%T. Our study suggests that clinicians should consider prolonged infusion or a high-dosage regimen of meropenem, particularly when treating critically ill patients with augmented renal clearance or those infected with pathogens with decreased in vitro susceptibility, regardless of ECMO support.

摘要

仅有有限的研究使用达标概率研究了美罗培南在重症成年患者中的群体药代动力学(PK)模型和最佳给药方案,其中包括接受体外膜肺氧合(ECMO)的患者。采用非线性混合效应模型进行群体PK分析。使用蒙特卡罗模拟来确定不同程度肾功能患者在稳态条件下游离药物浓度高于最低抑菌浓度(MIC)的持续时间。使用二室模型描述重症患者的美罗培南PK,其中肾小球滤过率被确定为清除率的协变量。ECMO不影响美罗培南的PK。模拟结果表明,对于MIC≤4 mg/L的情况,当前美罗培南给药方案足以达到40%T>MIC。对于MIC>2 mg/L的情况或肾清除率增加的患者,为达到100%T>MIC或100%fT>MIC的目标,需要3小时以上的延长输注或2 g/8 h的高剂量方案。我们的研究表明,临床医生应考虑美罗培南的延长输注或高剂量方案,特别是在治疗肾清除率增加的重症患者或感染体外敏感性降低病原体的患者时,无论是否有ECMO支持。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcd7/8625191/177695e6447c/pharmaceutics-13-01861-g001.jpg

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