急诊阿米卡星剂量优化:人群药代动力学模拟研究。

IF 2.8 4区 医学 Q2 MEDICAL LABORATORY TECHNOLOGY
Nada Dia, Sabrina De Winter, Matthias Gijsen, Stefanie Desmet, Peter Vanbrabant, Willy Peetermans, Isabel Spriet, Erwin Dreesen
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引用次数: 0

摘要

背景:在急诊住院的成年脓毒症或感染性休克患者中,单次静脉注射15mg /kg阿米卡星剂量不足以达到当地报告的最低抑制浓度(MIC) 2mg /L和欧洲抗微生物药敏试验委员会肠杆菌临床断点8mg /L的药代动力学-药效学目标。目的:为所有患者提供具有临床可接受的目标实现概率(PTA)的阿米卡星给药策略。方法:采用双室群体药代动力学模型(NONMEM 7.5)进行随机模拟。根据慢性肾脏病流行病学协作方程(eGFRCKD-EPI),在当地报道的MIC为2mg /L和临床断点为8mg /L时,评估了PTA在虚拟患者体重、体重指数、血清总蛋白、血清钠、体液平衡和肾小球滤过率的各种给药策略。药动药效学指标分别为浓度-时间曲线下24小时面积(AUC24h)/MIC≥80和给药后24小时浓度(C24h) < 3mg /L。结果:8mg /L的临床突破点PTA为:结论:相对于体重给药,建议采用平给药。然而,选择1500 mg或3500 mg的剂量可能会损害疗效(MIC为2 mg/L)或安全性(临床断点为8 mg/L),造成两难境地。临床验证是必要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dose Optimization of Amikacin in the Emergency Department: A Population Pharmacokinetics Simulation Study.

Background: In adult patients with sepsis or septic shock admitted to the emergency department, a single intravenous 15 mg/kg amikacin dose provides inadequate pharmacokinetic-pharmacodynamic target attainment at the locally reported minimum inhibitory concentration (MIC) of 2 mg/L and the European Committee on Antimicrobial Susceptibility Testing clinical breakpoint for Enterobacterales of 8 mg/L.

Objectives: To provide an amikacin dosing strategy with a clinically acceptable probability of target attainment (PTA) for all patients.

Methods: Stochastic simulations were performed using a two-compartment population pharmacokinetics model of amikacin (NONMEM 7.5). PTA was evaluated for various dosing strategies across a range of virtual patients' body weight, body mass index, serum total protein, serum sodium, fluid balance, and estimated glomerular filtration rate according to the Chronic Kidney Disease Epidemiology Collaboration equation (eGFRCKD-EPI), at the locally reported MIC of 2 mg/L and the clinical breakpoint of 8 mg/L. The pharmacokinetic-pharmacodynamic targets were a 24-hour area under the concentration-time curve (AUC24h)/MIC of ≥80 and a 24-hour postdose concentration (C24h) of < 3 mg/L for efficacy and safety, respectively.

Results: The PTA for the clinical breakpoint of 8 mg/L was <90% with standard 15 mg/kg dosing, across all patient characteristics. A flat 1500-mg dose achieved ≥90% PTA for the entire population at a MIC of 2 mg/L. However, at the clinical breakpoint of 8 mg/L, a flat 3500-mg dose provided ≥90% PTA only when the eGFRCKD-EPI was <96 mL/min/1.73 m2. The C24h was similar for 1500 mg and 15 mg/kg dosing, whereas 3500 mg resulted in a higher C24h.

Conclusions: A flat dose is recommended over weight-based dosing. However, selecting a 1500-mg or 3500-mg dose may compromise either efficacy (MIC 2 mg/L) or safety (clinical breakpoint 8 mg/L), posing a dilemma. Clinical validation is warranted.

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来源期刊
Therapeutic Drug Monitoring
Therapeutic Drug Monitoring 医学-毒理学
CiteScore
5.00
自引率
8.00%
发文量
213
审稿时长
4-8 weeks
期刊介绍: Therapeutic Drug Monitoring is a peer-reviewed, multidisciplinary journal directed to an audience of pharmacologists, clinical chemists, laboratorians, pharmacists, drug researchers and toxicologists. It fosters the exchange of knowledge among the various disciplines–clinical pharmacology, pathology, toxicology, analytical chemistry–that share a common interest in Therapeutic Drug Monitoring. The journal presents studies detailing the various factors that affect the rate and extent drugs are absorbed, metabolized, and excreted. Regular features include review articles on specific classes of drugs, original articles, case reports, technical notes, and continuing education articles.
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