An investigation of vancomycin minimum inhibitory concentration creep among methicillin-resistant Staphylococcus aureus strains isolated from pediatric patients and healthy children in Northern Taiwan

Abstract Background and purpose The phenomenon of vancomycin minimum inhibitory concentration (MIC) creep is an increasingly serious problem in the treatment of methicillin-resistant Staphylococcus aureus (MRSA) infections. In this study, we investigated the vancomycin and daptomycin MIC values of M...

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Veröffentlicht in:Journal of microbiology, immunology and infection immunology and infection, 2017-06, Vol.50 (3), p.362-369
Hauptverfasser: Chang, Chia-Ning, Lo, Wen-Tsung, Chan, Ming-Chin, Yu, Ching-Mei, Wang, Chih-Chien
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Sprache:eng
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Zusammenfassung:Abstract Background and purpose The phenomenon of vancomycin minimum inhibitory concentration (MIC) creep is an increasingly serious problem in the treatment of methicillin-resistant Staphylococcus aureus (MRSA) infections. In this study, we investigated the vancomycin and daptomycin MIC values of MRSA strains isolated from pediatric patients and MRSA colonized healthy children. Then, we assessed whether there was evidence of clonal dissemination for strains with an MIC to vancomycin of ≥ 1.5 μg/mL. Methods We collected clinical MRSA isolates from pediatric patients and from healthy children colonized with MRSA during 2008–2012 at a tertiary medical center in northern Taiwan and obtained vancomycin and daptomycin MIC values using the Etest method. Pulse-field gel electrophoresis (PFGE) and staphylococcal cassette chromosome (SCC mec ) typing were used to assess clonal dissemination for strains with an MIC to vancomycin of ≥ 1.5 μg/mL. Results A total 195 MRSA strains were included in this study; 87 were isolated patients with a clinical MRSA infection, and the other 108 strains from nasally colonized healthy children. Vancomycin MIC ≥ 1.5 μg/mL was seen in more clinical isolates (60/87, 69%) than colonized isolates (32/108, 29.6%), p  
ISSN:1684-1182
1995-9133
DOI:10.1016/j.jmii.2015.05.013