2012 ©
             Publication
Journal Publication
Research Title Change in susceptibility to vancomycin of methicillin-resistant Staphylococcus aureus after in vitro vancomycin exposure  
Date of Distribution 12 October 2012 
Conference
     Title of the Conference การประชุมใหญ่วิชาการประจำปี ครั้งที่ 38  
     Organiser สมาคมโรคติดเชื้อแห่งประเทศไทย 
     Conference Place โรงแรมเดอะซายน์ พัทยา นาเกลือ จังหวัดชลบุรี 
     Province/State ชลบุรี 
     Conference Date 11 October 2012 
     To 14 October 2012 
Proceeding Paper
     Volume 29 
     Issue
     Page 162 
     Editors/edition/publisher Somnuek Sungkanuparph 
     Abstract Background: Vancomycin, a glycopeptide, is a drug of choice for the treatment of methicillin-resistant Staphylococcus aureus (MRSA) infections and is used for an empirical treatment covered Gram-positive organisms. Currently, there has been an upward trend of vancomycin minimum inhibitory concentration (MIC) for the MRSA isolates. According to Clinical and Laboratory Standards Institute (CLSI) criteria, isolates with vancomycin MICs of ≥ 16 μg/ml are defined as vancomycin-resistant S. aureus (VRSA), those with MICs of 4-8 μg/ml are vancomycin-intermediate S. aureus (VISA), and those with MICs ≤ 2 μg/ml are defined as vancomycin-susceptible S. aureus (VSSA). In addition, S. aureus isolates, which have vancomycin MICs within susceptible range but contain a resistant population frequency of 1 in 106 or greater and are able to grow in the presence of 4 μg/ml of vancomycin or greater, are defined as heterogeneous vancomycinintermediate S. aureus (hVISA). The aim of this study was to investigate the change of vancomicin MICs for the MRSA isolates when cultured in vancomycin condition. Methods: A total of 55 MRSA isolates from patients in Srinagarind hospital were grown in media containing 2 μg/ml of vancomycin for 1-7 days. An isolate that grew in the media was transferred to additional media with 3, 4, 5, 6, 7 and 8 μg/ml of vancomycin until it was unable to grow. Vancomycin MIC was determined by an agar dilution method and vancomycin resistance was screened by one point analysis (OPA) method. Results: At the beginning, the 55 isolates had vancomycin MICs of 1-2 μg/ml. After vancomycin exposure, 20 (36.4%) could grow in the media containing 3-8 μg/ml of vancomycin. Their vancomycin MICs were 2-8 mg/ml. It was found that 2, 2, 1, 8, 3 and 4 isolates had vancomycin MIC increase in 8, 5, 4, 3, 2 and 0.5 times respectively. The change of vancomycin susceptibility of these isolates was generated between 1-7 days. Screening for vancomycin resistance by OPA revealed that 10 isolates (50%) were VISA and 7 isolates (35%) were hVISA. The hVISA isolates should be confirmed by a population analysis profile with area under the curve method (PAP-AUC) using S. aureus Mu3 strain as reference strain. Conclusion: This in vitro study implied that isolate with reduced susceptibility to vancomycin may occur in patient with prolonged treatment with vancomycin. 
Author
545090027-0 Miss SUJINTANA WONGTHONG [Main Author]
Associated Medical Sciences Master's Degree

Peer Review Status มีผู้ประเมินอิสระ 
Level of Conference ชาติ 
Type of Proceeding Abstract 
Type of Presentation Oral 
Part of thesis true 
Presentation awarding false 
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