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治疗对耐万古霉素肠球菌医院感染的影响。

Impact of Therapy on Nosocomial Acquisition of Vancomycin-Resistant Enterococci.

作者信息

Correa-Martínez Carlos L, Hagemeier Niklas C J, Froböse Neele J, Kampmeier Stefanie

机构信息

Institute of Hygiene, University Hospital Münster, Robert-Koch-Straße 41, 48149 Münster, Germany.

Institute of Medical Microbiology, University Hospital Münster, Domagkstraße 10, 48149 Münster, Germany.

出版信息

Pharmaceuticals (Basel). 2021 Oct 21;14(11):1066. doi: 10.3390/ph14111066.

Abstract

Vancomycin is frequently used for the treatment of infections (CDI). There are concerns that this might increase the risk of selecting vancomycin resistant enterococci (VRE). Here, we evaluated whether there is an increased risk of VRE acquisition following vancomycin for CDI specific treatment. Patients with CDI, metronidazole, or oral vancomycin treatment and without preexisting VRE were monitored for VRE acquisition. VRE isolates from patients with acquired and preexisting colonization were collected and subjected to whole genome sequencing. In total, 281 patients (median age 56 years, 54% of the male sex) presented with toxin positive . Of them, 170 patients met the inclusion criteria, comprising 37 patients treated with metronidazole and 133 treated with oral vancomycin. In total, 14 patients meeting the inclusion criteria acquired VRE (vancomycin: = 11; metronidazole: = 3). Statistical analysis revealed no significant differences between both VRE acquisition rates. Genetic comparison of detected VRE isolates resulted in eight clusters of closely related genotypes comprising acquired and preexisting strains. Our results suggest that vancomycin and metronidazole likewise increase the risk of VRE acquisition. Genetic comparison indicates that VRE acquisition is a result of both antibiotic selection and pathogen transmission.

摘要

万古霉素常用于治疗艰难梭菌感染(CDI)。人们担心这可能会增加选择耐万古霉素肠球菌(VRE)的风险。在此,我们评估了针对CDI进行特异性治疗使用万古霉素后VRE获得风险是否增加。对患有CDI、接受甲硝唑或口服万古霉素治疗且无既往VRE感染的患者进行VRE获得情况监测。收集获得性定植和既往定植患者的VRE分离株并进行全基因组测序。共有281例患者(中位年龄56岁,男性占54%)出现毒素阳性。其中,170例患者符合纳入标准,包括37例接受甲硝唑治疗的患者和133例接受口服万古霉素治疗的患者。共有14例符合纳入标准的患者获得了VRE(万古霉素组:n = 11;甲硝唑组:n = 3)。统计分析显示两组VRE获得率之间无显著差异。对检测到的VRE分离株进行基因比较,结果发现有8个由获得性菌株和既往菌株组成的密切相关基因型簇。我们的结果表明,万古霉素和甲硝唑同样会增加VRE获得的风险。基因比较表明,VRE获得是抗生素选择和病原体传播共同作用的结果。

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