替加环素对尼泊尔三级医院血流感染的多重耐药肠杆菌科细菌的体外活性

Ajay Yadav, B. Khanal, A. K. Patel, Alina Karna
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引用次数: 0

摘要

背景:扩展谱β -内酰胺酶(ESBL)和金属β -内酰胺酶(MBL)等多重耐药肠杆菌科细菌是引起血流感染的病原体。为了克服这一点,需要使用适当的抗生素准确诊断耐多药模式。替加环素是一种广谱抗生素,对耐多药肠杆菌科具有较强的抗药活性。本研究旨在发现替加环素体外对肠杆菌科细菌的耐药模式,如ESBL和MBL。方法:2014年9月1日至2015年8月31日在B.P.柯伊拉腊卫生科学研究所微生物学系进行描述性横断面研究。根据临床和实验室标准协会(CLSI)的建议进行ESBL的确认,并通过双盘协同试验检测MBL的产生。采用Kirby-Bauer圆盘扩散法进行替加环素药敏试验。结果:共分离肠杆菌192株(1.70%)。其中ESBL 94株(49%),碳青霉烯酶51株(26.5%),MBL产生菌22株(11.5%)。64株(33.4%)为耐多药菌株。所有分离株对替加环素均无耐药。结论:替加环素对BSI产的耐多药肠杆菌科细菌具有良好的体外活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Invitro Activity of Tigecycline against Multidrug-Resistant Enterobacteriaceae from Blood Stream Infection in a Tertiary Care Hospital of Nepal
Background: Multidrug resistant (MDR) enterobacteriaceae like extended spectrum beta lactamase (ESBL) and metallo-beta lactamase (MBL) are being encountered as the causative agents of blood stream infection. To overcome this, accurate diagnosis of MDR pattern with appropriate antibiotics is required. Tigecycline is a broad spectrum antibiotic which exhibit strong activity against MDR enterobacteriaceae. This study is aimed to find out resistance pattern like ESBL and MBL with invitro activity of tigecycline against enterobacteriaceae. Methods: A descriptive cross-sectional study was conducted in the Department of Microbiology, B.P. Koirala Institute of Health Sciences, from 1st September 2014 to 31st August 2015. Confirmation for ESBL was done as recommended by Clinical and Laboratory Standard Institute (CLSI) and MBL production was detected by double disk synergy test. Antibiotic sensitivity test against tigecycline was done by Kirby-Bauer disk diffusion method. Results: 192 (1.70%) enterobacteriaceae were isolated throughout the study. Among them, 94 (49%) were ESBL, 51 (26.5%) were carbapenemase and 22 (11.5%) were MBL producers. A total of 64 (33.4%) isolates were found to be MDR. None of the isolates was resistant against tigecycline. Conclusion: Tigecycline is found to have excellent invitro activity against MDR enterobacteriaceae from BSI.
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