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氟喹诺酮类和口服β-内酰胺类抗生素对大肠埃希菌临床分离株的体外活性

[In vitro activity of fluoroquinolones and oral beta lactam antibiotics against clinical isolates of Escherichia coli].

作者信息

Gómez-Martínez J, Marco F, Mensa J, Espasa M, Martínez J A, Jiménez de Anta M T

机构信息

Servicio de Microbiología, Institut d'Investigacions Biomèdiques August Pí i Sunyer (IDIBAPS), Hospital Clínic, Barcelona.

出版信息

Rev Esp Quimioter. 1999 Mar;12(1):54-7.

Abstract

We studied the in vitro activity of amoxicillin-clavulanic acid, cefprozil, cefuroxime, cefpodoxime, ceftibuten, cefixime, ciprofloxacin and sparfloxacin against 400 strains of Escherichia coli. The strains were obtained from urine cultures from patients with community acquired urinary tract infection who were treated in our hospital in 1997 and 1998. Among the six betalactams, ceftibuten and cefixime were the most active in vitro with MIC90 of 0.5 mg/l. Both antimicrobials were 2- and 16-fold more active than cefpodoxime (MIC90 1 mg/l) and cefprozil (MIC90 8 mg/l), respectively. However, overall, the four cephalosporins inhibited between 95% and 99% of isolates. Cefuroxime and amoxicillin-clavulanic acid showed less activity with a MIC90 of 16 mg/l. The percentage of fluoroquinolone-resistant strains was 24% with a similar activity to ciprofloxacin (MIC90 32 mg/l) and sparfloxacin (MIC90 64 mg/l).

摘要

我们研究了阿莫西林-克拉维酸、头孢丙烯、头孢呋辛、头孢泊肟、头孢布烯、头孢克肟、环丙沙星和司帕沙星对400株大肠杆菌的体外活性。这些菌株取自1997年和1998年在我院接受治疗的社区获得性尿路感染患者的尿培养物。在六种β-内酰胺类药物中,头孢布烯和头孢克肟体外活性最强,MIC90为0.5mg/l。这两种抗菌药物的活性分别比头孢泊肟(MIC90为1mg/l)和头孢丙烯(MIC90为8mg/l)高2倍和16倍。然而,总体而言,这四种头孢菌素对95%至99%的分离株有抑制作用。头孢呋辛和阿莫西林-克拉维酸活性较低,MIC90为16mg/l。耐氟喹诺酮菌株的比例为24%,对环丙沙星(MIC90为32mg/l)和司帕沙星(MIC90为64mg/l)的活性相似。

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