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新型头孢克肟-克拉维酸组合对革兰氏阴性菌的体外评估

In vitro evaluation of a new cefixime-clavulanic acid combination for gram-negative bacteria.

作者信息

Rawat Deepti, Hasan Azra S, Capoor Malini R, Sarma Smita, Nair Deepthi, Deb Monorama, Pillai Parukutty, Aggarwal Pushpa

机构信息

Department of Microbiology, Vardhaman Mahavir Medical College and Safdarjung Hospital, New Delhi, India.

出版信息

Southeast Asian J Trop Med Public Health. 2009 Jan;40(1):131-9.

Abstract

The study was conducted to evaluate a new cefixime-clavulanic acid combination for in vitro susceptibility towards gram-negative bacteria. A total of 220 isolates of Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeroginosa, Acinetobacter spp, Salmonella enterica serovar Typhi and Salmonella enterica serovar Typhimurium were included in the study. The isolates were tested for susceptibility towards the new combination antimicrobial molecule cefixime with clavulanic acid by disk diffusion and Epsilometer strip (E-strip) Minimum Inhibitary Concentration (MIC) method. Of the 101 E. coli and K. pneumoniae isolates, 62.4% were found to be extended spectrum beta-lactamase (ESBL) producers. Almost half of these were from the community and 55.6% were hospital isolates. Of the ESBL isolates, 19% were AmpC (cephalosporinases that are poorly inhibited by beta lactamase inhibitor) producers while the remaining 81% were non AmpC ESBL producers. The AmpC producers were resistant to both cefixime and the combination, while the non-AmpC producers were sensitive to the combination. The addition of clavulanate to cefixime did not improve the sensitivities of P. aeruginosa and Acinetobacter isolates. There were no ESBL isolates among the S. Typhi isolates, all of which were sensitive to cefixime. Of the S. Typhimurium, 88.9% were ESBL producers and all of these were resistant to cefixime but sensitive to the combination. The combination of cefixime with clavulanic acid offers the advantage of oral administration and appears to be a viable option for the treatment of uncomplicated community acquired infections caused by non-AmpC ESBL producing gram-negative bacteria.

摘要

本研究旨在评估一种新的头孢克肟-克拉维酸组合对革兰氏阴性菌的体外敏感性。该研究共纳入了220株大肠杆菌、肺炎克雷伯菌、铜绿假单胞菌、不动杆菌属、伤寒沙门氏菌和鼠伤寒沙门氏菌。通过纸片扩散法和Epsilometer试纸条(E-试纸条)最低抑菌浓度(MIC)法检测这些菌株对新的抗菌分子组合头孢克肟与克拉维酸的敏感性。在101株大肠杆菌和肺炎克雷伯菌分离株中,发现62.4%为超广谱β-内酰胺酶(ESBL)产生菌。其中近一半来自社区,55.6%为医院分离株。在ESBL分离株中,19%为AmpC(β-内酰胺酶抑制剂抑制效果较差的头孢菌素酶)产生菌,其余81%为非AmpC ESBL产生菌。AmpC产生菌对头孢克肟和该组合均耐药,而非AmpC产生菌对该组合敏感。克拉维酸添加到头孢克肟中并未提高铜绿假单胞菌和不动杆菌分离株的敏感性。伤寒沙门氏菌分离株中没有ESBL分离株,所有菌株对头孢克肟均敏感。在鼠伤寒沙门氏菌中,88.9%为ESBL产生菌,所有这些菌株对头孢克肟耐药,但对该组合敏感。头孢克肟与克拉维酸的组合具有口服给药的优势,似乎是治疗由非AmpC ESBL产生的革兰氏阴性菌引起的非复杂性社区获得性感染的可行选择。

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