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本文引用的文献

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Impact of Real-Time Therapeutic Drug Monitoring on the Prescription of Antibiotics in Burn Patients Requiring Admission to the Intensive Care Unit.实时治疗药物监测对入住重症监护病房的烧伤患者抗生素处方的影响。
Antimicrob Agents Chemother. 2018 Feb 23;62(3). doi: 10.1128/AAC.01818-17. Print 2018 Mar.
2
Dramatic Increase of Amoxicillin-Induced Crystal Nephropathy Found in a Cohort Study of French Pharmacovigilance Centers.法国药物警戒中心队列研究发现阿莫西林相关性结晶肾病急剧增加。
Antimicrob Agents Chemother. 2018 Feb 23;62(3). doi: 10.1128/AAC.01630-17. Print 2018 Mar.
3
Non-linear absorption pharmacokinetics of amoxicillin: consequences for dosing regimens and clinical breakpoints.阿莫西林的非线性吸收药代动力学:对给药方案和临床断点的影响
J Antimicrob Chemother. 2016 Oct;71(10):2909-17. doi: 10.1093/jac/dkw226. Epub 2016 Jun 20.
4
Therapeutic drug monitoring of anti-infective agents in critically ill patients.危重症患者抗感染药物的治疗药物监测
Expert Rev Clin Pharmacol. 2016 Jul;9(7):961-79. doi: 10.1586/17512433.2016.1172209. Epub 2016 Apr 15.
5
Amoxicillin Crystalluria, an Emerging Complication with an Old and Well-Known Antibiotic.阿莫西林结晶尿症,一种由一种古老且广为人知的抗生素引发的新出现的并发症。
Antimicrob Agents Chemother. 2016 Apr 22;60(5):3248. doi: 10.1128/AAC.00359-16. Print 2016 May.
6
Stability of amoxicillin and amoxicillin/clavulanic acid reconstituted in isotonic saline.阿莫西林及阿莫西林/克拉维酸在等渗盐水中复溶后的稳定性
J Chemother. 2017 Feb;29(1):54-56. doi: 10.1179/1973947815Y.0000000052. Epub 2016 Jul 22.
7
Impact of the introduction of real-time therapeutic drug monitoring on empirical doses of carbapenems in critically ill burn patients.实时治疗药物监测的引入对重症烧伤患者碳青霉烯类药物经验性剂量的影响。
Burns. 2015 Aug;41(5):956-68. doi: 10.1016/j.burns.2015.01.001. Epub 2015 Feb 10.
8
How do we use therapeutic drug monitoring to improve outcomes from severe infections in critically ill patients?我们如何利用治疗药物监测来改善重症患者严重感染的治疗效果?
BMC Infect Dis. 2014 Nov 28;14:288. doi: 10.1186/1471-2334-14-288.
9
Individualised antibiotic dosing for patients who are critically ill: challenges and potential solutions.个体化抗生素剂量给药用于危重症患者:挑战与潜在解决方案。
Lancet Infect Dis. 2014 Jun;14(6):498-509. doi: 10.1016/S1473-3099(14)70036-2. Epub 2014 Apr 24.
10
An international, multicentre survey of β-lactam antibiotic therapeutic drug monitoring practice in intensive care units.一项关于重症监护病房β-内酰胺类抗生素治疗药物监测实践的国际多中心调查。
J Antimicrob Chemother. 2014 May;69(5):1416-23. doi: 10.1093/jac/dkt523. Epub 2014 Jan 16.

瑞士一家三级烧伤治疗中心的阿莫西林治疗烧伤患者的群体药代动力学研究。

Population Pharmacokinetic Study of Amoxicillin-Treated Burn Patients Hospitalized at a Swiss Tertiary-Care Center.

机构信息

Service of Pharmacy, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland.

School of Pharmaceutical Sciences, University of Geneva, University of Lausanne, Geneva, Switzerland.

出版信息

Antimicrob Agents Chemother. 2018 Aug 27;62(9). doi: 10.1128/AAC.00505-18. Print 2018 Sep.

DOI:10.1128/AAC.00505-18
PMID:29914948
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6125536/
Abstract

The objective of this study was to investigate the population pharmacokinetics (PK) of amoxicillin in ICU burn patients and the optimal dosage regimens. This was a prospective study involving 21 consecutive burn patients receiving amoxicillin. PK data were analyzed using nonlinear mixed-effects modeling. Monte-Carlo simulations assessed the influence of various amoxicillin dosage regimens with identified covariates on the probability to achieve a target (PTA) value of time during which free amoxicillin concentrations in plasma exceeded the MIC (T>MIC). A two-compartment model best described the data. Creatinine clearance (CL) and body weight (BW) influenced amoxicillin CL and central volume of distribution (), respectively. The median CL (Cockcroft-Gault formula) was high (128 ml/min), with 25% of patients having CLs of >150 ml/min. The CL, , and half-life () values at steady state for a patient with a CL of 110 ml/min and BW of 70 kg were 13.6 liters/h, 9.7 liters, and 0.8 h, respectively. Simulations showed that a target T>MIC of ≥50% was achieved (PTA > 90%) with standard amoxicillin dosage regimens (1 to 2 g every 6 to 8 h [q6-8h]) when the MIC was low (<1 mg/liter). However, increased dosages of up to 2 g/4 h were necessary in patients with augmented CLs or higher MICs. Prolonging amoxicillin infusion from 30 min to 2 h had a favorable effect on target attainment. In conclusion, this population analysis shows an increased amoxicillin CL and substantial CL PK variability in burn patients compared to literature data with nonburn patients. Situations of augmented CL and/or high bacterial MIC target values may require dosage increases and longer infusion durations. (This study has been registered at ClinicalTrials.gov under identifier NCT01965340.).

摘要

本研究旨在探讨 ICU 烧伤患者中阿莫西林的群体药代动力学(PK)和最佳剂量方案。这是一项涉及 21 例连续接受阿莫西林治疗的烧伤患者的前瞻性研究。采用非线性混合效应模型分析 PK 数据。蒙特卡罗模拟评估了具有已确定协变量的各种阿莫西林剂量方案对达到目标(PTA)值的影响,即游离阿莫西林在血浆中的浓度超过 MIC(T>MIC)的时间。两室模型最能描述数据。肌酐清除率(CL)和体重(BW)分别影响阿莫西林 CL 和中央分布容积()。按 Cockcroft-Gault 公式计算,中位 CL 较高(128 ml/min),25%的患者 CL>150 ml/min。CL、、和稳态时半衰期()值为 110 ml/min 且 BW 为 70 kg 的患者分别为 13.6 升/小时、9.7 升和 0.8 小时。模拟表明,在 MIC 较低(<1 mg/L)时,标准阿莫西林剂量方案(q6-8h 时每 6-8 小时 1 至 2 g)即可实现目标 T>MIC≥50%(PTA>90%)。然而,在 CL 增加或 MIC 较高的患者中,需要增加至 2 g/4 h 的剂量。将阿莫西林输注时间从 30 分钟延长至 2 小时对目标实现有积极影响。总之,与非烧伤患者的文献数据相比,该群体分析显示烧伤患者的阿莫西林 CL 增加且 CL PK 变异性较大。CL 增加和/或高细菌 MIC 靶值的情况可能需要增加剂量和延长输注时间。(本研究已在 ClinicalTrials.gov 注册,标识符为 NCT01965340。)