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Evaluation of Tigecycline Susceptibility in Multidrug-Resistant Bacteria at the University Hospital of Marrakech (Morocco)

机译:马拉喀什大学医院(摩洛哥)对耐多药细菌中替加环素敏感性的评估

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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.
机译:细菌对抗生素的抗药性现象是主要的公共卫生问题。耐多药细菌的流行迅速增加,在发病率,死亡率和医疗保健费用方面造成严重后果。 Tigecycline是这种细菌的一种新型活性甘氨酰环素,可以作为治疗这些感染的替代疗法。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出的耐多药生物的体外活性。这是对一系列171种耐多药细菌的描述性前瞻性研究,包括102株产生广谱β-内酰胺酶的肠杆菌科细菌(ESBL)临床分离株和85株耐多药鲍曼不动杆菌临床分离株。 Tigecycline的体外活性是通过按照CASFM的建议,使用试纸“ E-test”在琼脂培养基上通过扩散法测定最小抑菌浓度(MIC)来测定的。 71%的鲍曼不动杆菌分离株对Tigecycline敏感,MIC≤1mg/ l,而17.6%的测试菌株对Tigecycline中等敏感度,MIC在1-2 mg / l之间,有11.4%的MIC耐药2毫克/升ESBL肠杆菌菌株大多数(77.5%)的MIC≤1 mg / l。在MIC介于1和2 mg / l之间的分离株中发现15.6%的中等敏感性,但是在MIC> 2 mg / l的肠杆菌分离株中有6.8%对Tigecycline产生抗药性。 Tigecycline是一种有趣的治疗选择,可能在多药耐药性感染的治疗中起重要作用。检测Tigecycline的敏感性状态对于优化其使用并将该分子保存在我们的治疗药库中是必要的。

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