摩洛哥马拉喀什大学医院多药耐药菌对替加环素的敏感性评价

Zemrani Yassin, Ahroui Yassine, Ait Zirri Khadija, Eddyb Saadia, Soraa Nabila
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摘要

细菌对抗生素的耐药现象是一个重大的公共卫生问题。耐多药细菌的流行正在迅速增加,在发病率和死亡率以及保健费用方面造成严重后果。替加环素是一种针对这种细菌的新型活性甘环素,可能是治疗这些感染的一种替代方法。这项工作的目的是评估替加环素对马拉喀什穆罕默德六世医院分离的多药耐药生物的体外活性。本研究对171种多重耐药细菌进行了描述性前瞻性研究,其中包括102株产β-内酰胺酶肠杆菌科(ESBL)临床分离株和85株多重耐药鲍曼不动杆菌临床分离株。替加环素体外活性采用琼脂培养基上扩散法测定最低抑菌浓度(MIC),采用试纸“e -试验”法,按照CASFM的建议进行测定。Tigecycline 71%的鲍曼不动杆菌分离株敏感的麦克风≤1 mg / l,而17.6%的测试菌株之间有中间Tigecycline敏感性麦克风1和2 mg / l, 11日,4%是耐药与麦克风> 2 mg / l。ESBL enterobacterial菌株大多是用麦克风(77年5%)≤1 mg / l。中间敏感性被发现在15.6%的隔离与麦克风之间的1和2 mg / l,然而,MIC> 2 mg /l的分离肠杆菌中有6.8%对替加环素耐药。替加环素是一种有趣的治疗选择,可能在治疗多重耐药感染方面发挥重要作用。检测替加环素的敏感性状态对于优化其使用和保存该分子在我们的治疗武器库中是必要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of Tigecycline Susceptibility in Multidrug-Resistant Bacteria at the University Hospital of Marrakech (Morocco)
The phenomenon of bacterial resistance to antibiotics is a major public health problem. The prevalence of multidrug-resistant bacteria is rapidly increasing with heavy consequences in terms of morbidity and mortality and health care costs. Tigecycline is a new active glycylcycline on this type of germ and could be a therapeutic alternative for the management of these infections. The aim of this work is to evaluate the in vitro activity of Tigecycline against multidrug-resistant organisms isolated at Mohammed VI hospital in Marrakech. It is a descriptive prospective study of a series of 171 multidrug-resistant bacteria including 102 clinical isolates of extended-spectrum β-lactamase-producing Enterobacteriaceae (ESBL) and 85 clinical isolates of multidrug-resistant Acinetobacter baumannii. The in vitro activity of Tigecycline was measured by the determination of the minimum inhibitory concentration (MIC) by diffusion method on agar medium using the strips "E-test" according to the recommendations of the CASFM. 71% of Acinetobacter baumannii isolates were sensitive to Tigecycline of with MIC ≤1mg / l, while 17.6% of tested strains had intermediate sensitivity to Tigecycline with a MIC between 1 and 2 mg / l, 11,4% were resistant with a MIC> 2 mg / l. ESBL enterobacterial strains were mostly (77,5%) with a MIC ≤ 1 mg / l. Intermediate sensitivity was found in 15.6% of the isolates with a MIC between 1 and 2 mg / l, however, resistance to Tigecycline was found in 6.8% of enterobacterial isolates with a MIC> 2 mg /l. Tigecycline is an interesting therapeutic option and may have an important role in the treatment of multidrug-resistant infections. Detection of the sensitivity status of Tigecycline is necessary to optimize its use and preserve this molecule in our therapeutic arsenal.
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