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In Vitro Activity of Polymyxin B in Combination with Various Antibiotics against Extensively Drug-Resistant Enterobacter cloacae with Decreased Susceptibility to Polymyxin B.多粘菌素B与多种抗生素联合对多粘菌素B敏感性降低的广泛耐药阴沟肠杆菌的体外活性
Antimicrob Agents Chemother. 2016 Aug 22;60(9):5238-46. doi: 10.1128/AAC.00270-16. Print 2016 Sep.

本文引用的文献

1
Susceptibility testing of the polymyxins: where are we now?多粘菌素的药敏试验:我们目前处于什么阶段?
Pharmacotherapy. 2015 Jan;35(1):22-7. doi: 10.1002/phar.1505. Epub 2014 Oct 20.
2
Treating infections caused by carbapenemase-producing Enterobacteriaceae.治疗产碳青霉烯酶肠杆菌科细菌感染。
Clin Microbiol Infect. 2014 Sep;20(9):862-72. doi: 10.1111/1469-0691.12697. Epub 2014 Jul 12.
3
In vitro and in vivo activities of tigecycline-colistin combination therapies against carbapenem-resistant Enterobacteriaceae.替加环素-黏菌素联合疗法对耐碳青霉烯类肠杆菌科细菌的体外和体内活性
Antimicrob Agents Chemother. 2014 Jun;58(6):3541-6. doi: 10.1128/AAC.02449-14. Epub 2014 Mar 31.
4
Polymyxins for the treatment of extensively-drug-resistant Gram-negative bacteria: from pharmacokinetics to bedside.用于治疗广泛耐药革兰氏阴性菌的多粘菌素:从药代动力学到临床应用
Expert Rev Anti Infect Ther. 2014 May;12(5):531-3. doi: 10.1586/14787210.2014.902307. Epub 2014 Mar 25.
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Combination therapy for carbapenem-resistant Gram-negative bacteria.碳青霉烯类耐药革兰氏阴性菌的联合治疗。
Expert Rev Anti Infect Ther. 2013 Dec;11(12):1333-53. doi: 10.1586/14787210.2013.845523. Epub 2013 Nov 6.
6
Molecular characterization of Klebsiella pneumoniae carbapenemase-producing isolates in southern Brazil.巴西南部产碳青霉烯酶肺炎克雷伯菌的分子特征。
J Med Microbiol. 2013 Nov;62(Pt 11):1721-1727. doi: 10.1099/jmm.0.062141-0. Epub 2013 Sep 2.
7
Clinical epidemiology of the global expansion of Klebsiella pneumoniae carbapenemases.全球扩展型碳青霉烯酶肺炎克雷伯菌的临床流行病学。
Lancet Infect Dis. 2013 Sep;13(9):785-96. doi: 10.1016/S1473-3099(13)70190-7.
8
Systematic review and meta-analysis of in vitro synergy of polymyxins and carbapenems.系统评价和体外协同作用的多粘菌素和碳青霉烯类抗生素的荟萃分析。
Antimicrob Agents Chemother. 2013 Oct;57(10):5104-11. doi: 10.1128/AAC.01230-13. Epub 2013 Aug 5.
9
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多黏菌素B联合亚胺培南、美罗培南或替加环素对产KPC-2且对这些抗菌药物具有高最低抑菌浓度(MIC)的肠杆菌科细菌的体外活性。

In vitro activity of polymyxin B plus imipenem, meropenem, or tigecycline against KPC-2-producing Enterobacteriaceae with high MICs for these antimicrobials.

作者信息

Barth Natália, Ribeiro Vanessa B, Zavascki Alexandre P

机构信息

Laboratório de Pesquisa em Resistência Bacteriana, LABRESIS, Hospital de Clínicas de Porto Alegre, Porto Alegre, Brazil Programa de Pós-Graduação em Ciências Médicas, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.

Laboratório de Pesquisa em Resistência Bacteriana, LABRESIS, Hospital de Clínicas de Porto Alegre, Porto Alegre, Brazil Universidade Federal do Pampa (Unipampa), Campus Uruguaiana, Uruguaiana, Brazil.

出版信息

Antimicrob Agents Chemother. 2015;59(6):3596-7. doi: 10.1128/AAC.00365-15. Epub 2015 Mar 23.

DOI:10.1128/AAC.00365-15
PMID:25801560
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4432205/
Abstract

We evaluated the in vitro activity of polymyxin B plus imipenem, meropenem, or tigecycline against six KPC-2-producing Enterobacteriaceae strains with high MICs for these antimicrobial agents. Polymyxin B with carbapenems, especially meropenem, were the most active combinations for Klebsiella pneumoniae and Enterobacter cloacae regardless of the polymyxin B concentration used in the time-kill assay. This combination was also synergistic against two Serratia marcescens strains that are intrinsically resistant to polymyxins. Polymyxin B and tigecycline also presented synergistic activity in most experiments.

摘要

我们评估了多粘菌素B联合亚胺培南、美罗培南或替加环素对6株产KPC-2的肠杆菌科菌株的体外活性,这些菌株对这些抗菌药物具有较高的最低抑菌浓度(MIC)。多粘菌素B与碳青霉烯类药物,尤其是美罗培南,无论在时间杀菌试验中使用的多粘菌素B浓度如何,都是对肺炎克雷伯菌和阴沟肠杆菌最具活性的组合。这种组合对两种天然对多粘菌素耐药的粘质沙雷氏菌菌株也具有协同作用。在大多数实验中,多粘菌素B和替加环素也表现出协同活性。