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Antimicrob Agents Chemother. 2016 Nov 21;60(12):7527-7529. doi: 10.1128/AAC.01208-16. Print 2016 Dec.
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Impact of blaNDM-1 on fitness and pathogenicity of Escherichia coli and Klebsiella pneumoniae.blaNDM-1 对大肠杆菌和肺炎克雷伯菌的适应性和致病性的影响。
Int J Antimicrob Agents. 2016 Jun;47(6):430-5. doi: 10.1016/j.ijantimicag.2016.02.019. Epub 2016 Apr 26.
2
The Pandemic H30 Subclone of Escherichia coli Sequence Type 131 Is Associated With Persistent Infections and Adverse Outcomes Independent From Its Multidrug Resistance and Associations With Compromised Hosts.大肠杆菌序列型131的大流行H30亚克隆与持续性感染及不良结局相关,与其多重耐药性以及与宿主免疫功能受损的关联无关。
Clin Infect Dis. 2016 Jun 15;62(12):1529-1536. doi: 10.1093/cid/ciw193. Epub 2016 Mar 29.
3
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Clin Ther. 2015 Jul 1;37(7):1564-71. doi: 10.1016/j.clinthera.2015.05.501. Epub 2015 Jun 15.
4
Activities of ceftazidime and avibactam against β-lactamase-producing Enterobacteriaceae in a hollow-fiber pharmacodynamic model.在中空纤维药效学模型中头孢他啶和阿维巴坦对产β-内酰胺酶肠杆菌科细菌的活性
Antimicrob Agents Chemother. 2014 Jun;58(6):3366-72. doi: 10.1128/AAC.00080-14. Epub 2014 Mar 31.
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Antibiotic prescription patterns in the empiric therapy of severe sepsis: combination of antimicrobials with different mechanisms of action reduces mortality.严重脓毒症经验性治疗中的抗生素处方模式:联合使用具有不同作用机制的抗菌药物可降低死亡率。
Crit Care. 2012 Nov 18;16(6):R223. doi: 10.1186/cc11869.
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Antimicrob Agents Chemother. 2012 Dec;56(12):6137-46. doi: 10.1128/AAC.00851-12. Epub 2012 Sep 17.
7
In vivo comparison of CXA-101 (FR264205) with and without tazobactam versus piperacillin-tazobactam using human simulated exposures against phenotypically diverse gram-negative organisms.在体内比较 CXA-101(FR264205)与他唑巴坦联用和不联用哌拉西林-他唑巴坦对表型多样的革兰氏阴性菌的模拟人体暴露效果。
Antimicrob Agents Chemother. 2012 Jan;56(1):544-9. doi: 10.1128/AAC.01752-10. Epub 2011 Nov 7.
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Double-carbapenem therapy for carbapenemase-producing Klebsiella pneumoniae.产碳青霉烯酶肺炎克雷伯菌的双重碳青霉烯类治疗。
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In vivo efficacy of simulated human dosing regimens of prolonged-infusion doripenem against carbapenemase- producing Klebsiella pneumoniae.模拟人体延长输注美罗培南给药方案对产碳青霉烯酶肺炎克雷伯菌的体内疗效。
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人源化哌拉西林-他唑巴坦暴露量与哌拉西林-他唑巴坦耐药/泛β-内酰胺敏感大肠埃希菌的体外-体内不一致性

In Vitro-In Vivo Discordance with Humanized Piperacillin-Tazobactam Exposures against Piperacillin-Tazobactam-Resistant/Pan-β-Lactam-Susceptible Escherichia coli.

作者信息

Monogue M L, Nicolau D P

机构信息

Center for Anti-Infective Research and Development, Hartford Hospital, Hartford, Connecticut, USA.

Center for Anti-Infective Research and Development, Hartford Hospital, Hartford, Connecticut, USA

出版信息

Antimicrob Agents Chemother. 2016 Nov 21;60(12):7527-7529. doi: 10.1128/AAC.01208-16. Print 2016 Dec.

DOI:10.1128/AAC.01208-16
PMID:27799205
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5119043/
Abstract

Recent findings have identified Escherichia coli strains that are pan-β-lactam susceptible (PBL-S) but piperacillin-tazobactam resistant (TZP-R) in vitro We assessed the in vivo significance of this resistance profile in a neutropenic murine pneumonia model using humanized exposures of TZP with 18 clinical E. coli isolates, 8 TZP-S/PBL-S and 10 genotypically confirmed TZP-R/PBL-S. Despite phenotypically and genotypically defined resistance, TZP displayed efficacy against these isolates. Additional studies are required to define the clinical implications of these TZP-R/PBL-S strains.

摘要

最近的研究发现,在体外存在对所有β-内酰胺类药物敏感(PBL-S)但对哌拉西林-他唑巴坦耐药(TZP-R)的大肠杆菌菌株。我们在中性粒细胞减少的小鼠肺炎模型中,使用人源化的哌拉西林-他唑巴坦暴露剂量,对18株临床分离的大肠杆菌进行了评估,其中8株为TZP敏感/PBL敏感,10株经基因分型确认为TZP耐药/PBL敏感。尽管这些菌株在表型和基因型上都表现出耐药性,但哌拉西林-他唑巴坦对它们仍有疗效。需要进一步的研究来明确这些TZP耐药/PBL敏感菌株的临床意义。