[Linezolid-resistant enterococci].

Q3 Medicine
Tomáš Kraus
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引用次数: 0

Abstract

Aim of the work: To assess the occurrence of linezolid-resistant enterococci (E. faecalis and E. faecium) in patients hospitalized at the centers and clinics of the Institute for Clinical and Experimental Medicine (IKEM).

Material and methods: For the period from 1. 1. 2017 to 31. 12. 2022, isolates of E. faecalis and E. faecium, which were tested for sensitivity to antibiotics, were retrospectively evaluated. Microbiological data were obtained from the laboratory information system ENVIS LIMS, and clinical data from the hospital information system IKEM. Enterococci were identified using a MALDI-TOF mass spectrometer. Susceptibility testing was performed using the disc diffusion method according to EUCAST criteria. Minimum inhibitory concentrations were determined by the Vitek automated system using the P592 card. Verification of resistance to linezolid and determination of the resistance mechanism took place at the National Reference Laboratory for Antibiotics of the National Institute of Public Health in Prague.

Results: In the monitored period, the sensitivity of 6900 strains of E. feacalis (67,0 %) and 3356 strains of E. faecium (33,0 %) was examined. A total of 14 linezolid-resistant enterococci (LRE) were identified - 5x E. faecalis (35,7 %) and 9x E. faecium (64,3 %). The most common mechanism of resistance to linezolid was the presence of the optrA gene in E. faecalis, and 23S rRNA mutation in E. faecium. The material with the largest LRE capture was urine (35,7 %) and secrets or punctates (28,6 %). Only in the species E. faecium, resistance to vancomycin and teicoplanin (LVRE) occurred at the same time. Three patients (21,4 %) developed an LRE infection requiring antibiotic treatment, the remaining eleven patients (78,6 %) were colonized.

Conclusion: The proportion of linezolid-resistant enterococci was in the mentioned period low - 0,14 %. Linezolid therefore remains a safe therapeutic alternative for enterococcal infections when first-line drugs cannot be used.

[Linezolid-resistant enterococci]。
目的:评估临床与实验医学研究所(IKEM)中心和诊所住院患者中耐利奈唑胺肠球菌(粪肠球菌和屎肠球菌)的发生情况。材料和方法:从1。1. 2017 - 31年。12. 2022年,对分离的粪肠球菌和粪肠球菌进行了抗生素敏感性测试,并对其进行了回顾性评估。微生物学数据来自实验室信息系统ENVIS LIMS,临床数据来自医院信息系统IKEM。采用MALDI-TOF质谱仪鉴定肠球菌。药敏试验采用盘片扩散法,按EUCAST标准进行。最低抑菌浓度由Vitek自动系统使用P592卡测定。在布拉格国家公共卫生研究所的国家抗生素参考实验室进行了对利奈唑胺耐药性的核查和耐药性机制的确定。结果:监测期间共检出粪肠杆菌6900株(67.0%)和粪肠杆菌3356株(33.0%)。共检出耐利奈唑胺肠球菌(LRE) 14株,其中粪肠球菌5株(35.7%),粪肠球菌9株(64.3%)。对利奈唑胺耐药最常见的机制是在粪肠杆菌中存在optrA基因,在粪肠杆菌中存在23S rRNA突变。LRE捕获最多的物质是尿液(35.7%)和秘密或点状物(28.6%)。只有粪肠球菌(E. faecium)对万古霉素和替可普宁(LVRE)同时耐药。3例患者(21.4%)发生LRE感染,需要抗生素治疗,其余11例患者(78.6%)定植。结论:该时期耐利奈唑胺肠球菌比例较低,为0.14%。因此,当不能使用一线药物时,利奈唑胺仍然是肠球菌感染的安全治疗选择。
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来源期刊
Klinicka mikrobiologie a infekcni lekarstvi
Klinicka mikrobiologie a infekcni lekarstvi Medicine-Infectious Diseases
CiteScore
0.40
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0.00%
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