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Multidrug-resistant, extensively drug-resistant and pandrug-resistant bacteria: an international expert proposal for interim standard definitions for acquired resistance.耐多药、广泛耐药和全耐药细菌:获得性耐药的国际专家临时标准定义建议
Clin Microbiol Infect. 2012 Mar;18(3):268-81. doi: 10.1111/j.1469-0691.2011.03570.x. Epub 2011 Jul 27.
2
Implications of augmented renal clearance in critically ill patients.危重症患者肾清除增强的意义。
Nat Rev Nephrol. 2011 Jul 19;7(9):539-43. doi: 10.1038/nrneph.2011.92.
3
Recommended β-lactam regimens are inadequate in septic patients treated with continuous renal replacement therapy.推荐的β-内酰胺方案在接受连续肾脏替代治疗的脓毒症患者中是不足够的。
Crit Care. 2011;15(3):R137. doi: 10.1186/cc10257. Epub 2011 Jun 6.
4
Multidrug-resistant Gram-negative bacteria: how to treat and for how long.耐多药革兰氏阴性菌:如何治疗及治疗时长。
Int J Antimicrob Agents. 2010 Dec;36 Suppl 2:S50-4. doi: 10.1016/j.ijantimicag.2010.11.014. Epub 2010 Dec 3.
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Insufficient β-lactam concentrations in the early phase of severe sepsis and septic shock.严重脓毒症和脓毒性休克早期β-内酰胺浓度不足。
Crit Care. 2010;14(4):R126. doi: 10.1186/cc9091. Epub 2010 Jul 1.
6
Prospective monitoring of cefepime in intensive care unit adult patients.重症监护病房成年患者头孢吡肟的前瞻性监测。
Crit Care. 2010;14(2):R51. doi: 10.1186/cc8941. Epub 2010 Apr 1.
7
Effect of obesity on the pharmacokinetics of drugs in humans.肥胖对人体药物药代动力学的影响。
Clin Pharmacokinet. 2010;49(2):71-87. doi: 10.2165/11318100-000000000-00000.
8
A systematic review on clinical benefits of continuous administration of beta-lactam antibiotics.关于持续使用β-内酰胺类抗生素临床益处的系统评价。
Crit Care Med. 2009 Jun;37(6):2071-8. doi: 10.1097/CCM.0b013e3181a0054d.
9
Pharmacokinetic issues for antibiotics in the critically ill patient.危重症患者使用抗生素的药代动力学问题。
Crit Care Med. 2009 Mar;37(3):840-51; quiz 859. doi: 10.1097/CCM.0b013e3181961bff.
10
Evaluation of area under the inhibitory curve (AUIC) and time above the minimum inhibitory concentration (T>MIC) as predictors of outcome for cefepime and ceftazidime in serious bacterial infections.评估抑制曲线下面积(AUIC)和高于最低抑菌浓度的时间(T>MIC)作为头孢吡肟和头孢他啶治疗严重细菌感染疗效预测指标的研究
Int J Antimicrob Agents. 2008 Apr;31(4):345-51. doi: 10.1016/j.ijantimicag.2007.12.009. Epub 2008 Mar 4.

治疗多重耐药铜绿假单胞菌败血症性休克的最佳美罗培南浓度。

Optimal meropenem concentrations to treat multidrug-resistant Pseudomonas aeruginosa septic shock.

机构信息

Department of Intensive Care, Hôpital Erasme, Université Libre de Bruxelles, Brussels, Belgium.

出版信息

Antimicrob Agents Chemother. 2012 Apr;56(4):2129-31. doi: 10.1128/AAC.06389-11. Epub 2012 Jan 30.

DOI:10.1128/AAC.06389-11
PMID:22290984
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3318384/
Abstract

A patient with septic shock due to extensively drug resistant (XDR) Pseudomonas aeruginosa was cured by optimizing the meropenem (MEM) regimen to obtain at least 40% of the time between two administrations in which drug levels were four times higher than the MIC of the pathogen. As the standard drug dose did not achieve these optimal concentrations, the MEM regimen was progressively increased up to 12 g/day (3 g every 6 h in a 3-h extended infusion), which eventually resulted in sepsis resolution. High MEM dosage may represent a valuable therapeutic option for infection due to multidrug-resistant (MDR) strains, and drug monitoring would allow rapid regimen adjustment in clinical practice.

摘要

一名患有广泛耐药(XDR)铜绿假单胞菌败血症性休克的患者通过优化美罗培南(MEM)方案得到治愈,该方案使两次给药之间药物浓度高于病原体 MIC 的时间至少达到 40%,从而使药物浓度达到 4 倍。由于标准药物剂量无法达到这些最佳浓度,因此逐渐增加 MEM 方案剂量直至 12 g/天(3 g 每 6 小时延长输注 3 小时),最终导致败血症得到解决。高剂量 MEM 可能代表对多药耐药(MDR)菌株感染的有价值的治疗选择,药物监测可在临床实践中快速调整方案。