1017株临床分离细菌耐药谱及耐药机制分析

Sui-na Geng, Yong-yu Rui, Qian Wang, Cheng-hui Mou, Xiao-hong Zhou, Jie Zhang
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引用次数: 0

摘要

目的:了解临床分离细菌的药敏情况,为合理使用抗生素提供依据。方法:采用BD Phoenix法对临床分离的1017株细菌进行鉴定,并采用K-B法对抗菌药物进行耐药性检测。采用WHONET5进行分析。结果:检出最多的细菌为铜绿假单胞菌(19.37%)、凝固酶阴性葡萄球菌(CNS, 17.70%)、大肠杆菌(13.27%)、金黄色葡萄球菌(SA, 12.09%)、粪肠杆菌(11.8%)、肺炎克雷伯菌(7.57%)。革兰氏阴性菌株对亚胺培南的敏感性为81.5%,对头孢他啶的敏感性为70%以上。大肠杆菌和肺炎克雷伯菌分离株产生广谱β -内酰胺酶(ESBLs)的发生率分别为34.8%和45.5%。革兰氏阳性菌株对万古霉素和替柯planin的敏感性分别为98.8%和100.0%,对呋喃唑酮、亚胺培南、阿米卡星、哌拉西林/他唑巴坦的敏感性均在70%以上。CNS和SA耐药率分别为78.2%和46.8%。结论:1017株临床分离细菌ESBL产率高,耐oxacillin耐药,提示合理使用抗菌药物和采取有效的控制措施对减少耐药和防止多重耐药菌的传播具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Analysis of drug resistance spectrum and its mechanism in 1017 clinical bacterial isolates].

Objective: To investigate the drug susceptibility of the clinical bacterial isolates to provide evidence for more adequate use of antibiotics.

Methods: Altogether 1017 clinical bacterial isolates were identified by BD Phoenix and tested for resistance against antimicrobial agents by K-B method. WHONET5 was applied for the analysis.

Results: The most frequent bacteria detected included P. aeruginosa (19.37%), coagulase-negative Staphylococci (CNS, 17.70%), E. coli (13.27%), S. aureu (SA, 12.09%), E. faecalis (11.8%), and K. pneumoniae (7.57%). In gram-negative isolates, the susceptibility rate of imipenem was 81.5%, and that of ceftazidime was above 70%. The incidences of E.coli and K. pneumoniae isolates producing extended spectrum beta-lactamase (ESBLs) were 34.8% and 45.5% respectively. In gram-positive isolates, the susceptibility rates of vancomycin and Teicoplanin were 98.8% and 100.0% respectively, and those of furazolidone, imipenem, amikacin, piperacillin/ tazobactam were above 70%. The oxacillin resistant rates of CNS and SA were 78.2% and 46.8%.

Conclusion: The 1017 clinical bacterial isolates are characterized by high ratio of ESBL production and oxacillin resistance, suggesting the importance of adequate use of antimicrobial agents and effective control measures for reducing the drug resistance and preventing the spread of multi drug- resistant bacteria.

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