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头孢哌酮-舒巴坦合剂对革兰氏阴性杆菌的体外活性

In vitro activity of cefoperazone-sulbactam combination against gram negative bacilli.

作者信息

Poudyal N, Gyawali N, Gurung R, Bhattarai N R, Baral R, Khanal B, Shrestha S, Amatya R, Bhattacharya S K

机构信息

Department of Microbiology, BP Koirala Institute of Health Sciences, Dharan, Nepal.

出版信息

Nepal Med Coll J. 2012 Mar;14(1):5-8.

Abstract

Cefoperazone is a â-lactam antimicrobial and Sulbactam is an irreversible â-lactamase inhibitor. The objective of this study was to know the susceptibility pattern of gram negative bacilli (GNB) towards cefoperazone-sulbactum. All GNB isolated from different clinical samples during the period of May, 2010 to Aug, 2010 were tested for susceptibility to cefoperazone-sulbactum, meropenem, ceftazidime, cefotaxime, ceftriaxone, chloromphenicol, cotrimoxazole, ampicillin, amikacin, nalidixic acid, ciprofloxacin, carbenicillin and piperacillin using standard Kirby-Bauer disc diffusion antimicrobial susceptibility testing method. The susceptibilities were recorded according to CLSI guidelines. A total of 406 GNB were isolated (urine: 66.7%, pus: 19.2%, and blood: 7.9%). Escherichia coli (54.4%) was most frequently isolated organisms followed by Acinetobacter species (17.7%), Klebsiella pneumoniae (9.1%) and Pseudomonas species (6.1%). Overall, 11.8% of isolates showed resistance to cefoperazone-sulbactam. Frequencies of isolates showing resistance to meropenem and amikacin were 14.7% and 26.25% respectively. Only 3.9% of Escherichia coli isolates showed resistance to cefoperazone-sulbactam. For other organisms, their lowest frequency ranging from 0-20%, exhibited resistance to meropenem. In Pseudomonas spp, in-vitro activity of amikacin was also better as only 11.1% isolates showed resistance to it. This study demonstrated the in-vitro synergistic effect of cefoperazonerazone-sulbactam and meropenem having good activity against GNB compared to the activity of other commonly tested antimicrobials. Cefoperazone-sulbactam can be recommended for the clinical practice against GNB exhibiting resistant to other antimicrobials as it is cheaper alternative to meropenem. Our results also focused on the continuous surveillance of the trends and features of resistance of common antimicrobials.

摘要

头孢哌酮是一种β-内酰胺类抗菌药物,舒巴坦是一种不可逆的β-内酰胺酶抑制剂。本研究的目的是了解革兰氏阴性杆菌(GNB)对头孢哌酮-舒巴坦的药敏模式。对2010年5月至2010年8月期间从不同临床样本中分离出的所有GNB进行了头孢哌酮-舒巴坦、美罗培南、头孢他啶、头孢噻肟、头孢曲松、氯霉素、复方新诺明、氨苄西林、阿米卡星、萘啶酸、环丙沙星、羧苄西林和哌拉西林的药敏试验,采用标准的 Kirby-Bauer 纸片扩散法进行抗菌药敏试验。根据CLSI指南记录药敏结果。共分离出406株GNB(尿液:66.7%,脓液:19.2%,血液:7.9%)。大肠埃希菌(54.4%)是最常分离出的菌株,其次是不动杆菌属(17.7%)、肺炎克雷伯菌(9.1%)和假单胞菌属(6.1%)。总体而言,11.8%的分离株对头孢哌酮-舒巴坦耐药。对美罗培南和阿米卡星耐药的分离株频率分别为14.7%和26.25%。只有3.9%的大肠埃希菌分离株对头孢哌酮-舒巴坦耐药。对于其他菌株,其对美罗培南耐药的频率最低,在0-20%之间。在假单胞菌属中,阿米卡星的体外活性也较好,只有11.1%的分离株对其耐药。本研究证明了头孢哌酮-舒巴坦和美罗培南的体外协同作用,与其他常用抗菌药物相比,它们对GNB具有良好的活性。头孢哌酮-舒巴坦可作为一种比美罗培南更便宜的替代品,推荐用于临床治疗对其他抗菌药物耐药的GNB。我们的结果还强调了对常见抗菌药物耐药趋势和特征的持续监测。

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