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β-内酰胺类与β-内酰胺酶抑制剂联合制剂对尿液分离株中产超广谱β-内酰胺酶肠杆菌科细菌的活性

Activity of beta-lactam beta-lactamase inhibitor combinations against extended spectrum Beta-lactamase producing Enterobacteriaceae in urinary isolates.

作者信息

Afridi Faisal Iqbal, Farooqi Badar Jahan

机构信息

Department of Clinical Microbiology, Dr. Ziauddin University Hospital, Karachi.

出版信息

J Coll Physicians Surg Pak. 2012 Jun;22(6):358-62.

PMID:22630093
Abstract

OBJECTIVE

To determine the susceptibility pattern of beta-lactam beta-lactamase inhibitor combinations against extended-spectrum beta-lactamase (ESBL) producing Enterobacteriaceae in urinary isolates.

STUDY DESIGN

Observational study.

PLACE AND DURATION OF STUDY

Ziauddin University Hospital, Karachi, from February to October 2008.

METHODOLOGY

A total of 190 consecutive non-duplicate isolates of ESBL producing Enterobacteriaceae from urine samples of in-patients were included in the study. Urinary samples from out-patients, repeat samples and non-ESBL producing isolates were excluded. Detection of ESBL was carried out by double disk diffusion technique. Antimicrobial susceptibility testing was performed using modified Kirby Bauer's disk diffusion method according to CLSI guidelines. Statistical analysis was performed by SPSS version 10.

RESULTS

Of the 190 ESBL isolates tested, 88 cases (46.31%) were sensitive and 6 cases (3.15%) were resistant to all three combinations, the rest 96 cases (50.52%) were resistant to at least one of the combinations. Susceptibility pattern of cefoperazone/sulbactam, piperacillin/tazobactam, and amoxicillin/clavulanic acid was 95.26, 92.10, and 44.31 percent respectively.

CONCLUSION

Cefoperazone/sulbactam exhibited the best activity against ESBL producing Enterobacteriaceae followed by piperacillin/tazobactam. Hospital antibiotic policies should be reviewed periodically to reduce the usage of extended spectrum cephalosporins and replace them with beta-lactam beta-lactamase inhibitor combinations agent for treating urinary tract infections.

摘要

目的

确定β-内酰胺类与β-内酰胺酶抑制剂联合用药对泌尿道分离出的产超广谱β-内酰胺酶(ESBL)肠杆菌科细菌的敏感性模式。

研究设计

观察性研究。

研究地点及时间

2008年2月至10月,卡拉奇的齐亚丁大学医院。

方法

本研究纳入了190株来自住院患者尿液样本的产ESBL肠杆菌科细菌的连续非重复分离株。门诊患者的尿液样本、重复样本及非产ESBL分离株被排除。采用双纸片扩散法检测ESBL。根据CLSI指南,使用改良的 Kirby Bauer 纸片扩散法进行药敏试验。采用SPSS 10版进行统计分析。

结果

在检测的190株ESBL分离株中,88例(46.31%)对所有三种联合用药敏感,6例(3.15%)对所有三种联合用药耐药,其余96例(50.52%)对至少一种联合用药耐药。头孢哌酮/舒巴坦、哌拉西林/他唑巴坦和阿莫西林/克拉维酸的敏感率分别为95.26%、92.10%和44.31%。

结论

头孢哌酮/舒巴坦对产ESBL肠杆菌科细菌的活性最佳,其次是哌拉西林/他唑巴坦。应定期审查医院抗生素政策,以减少广谱头孢菌素的使用,并将其替换为β-内酰胺类与β-内酰胺酶抑制剂联合用药来治疗尿路感染。

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