Literature DB >> 21750101

Methicillin-resistant Staphylococcus aureus vancomycin susceptibility testing: methodology correlations, temporal trends and clonal patterns.

Sebastiaan J van Hal1, Thelma Barbagiannakos, Mark Jones, Michael C Wehrhahn, Joanne Mercer, Dehua Chen, David L Paterson, Iain B Gosbell.   

Abstract

OBJECTIVES: To determine the correlation between various vancomycin MIC testing methodologies and explore the phenomenon of MIC creep.
METHODS: A total of 417 consecutive non-duplicate methicillin-resistant Staphylococcus aureus (MRSA) bloodstream isolates from Liverpool Hospital between 1997 and 2008 were retrieved. All isolates were classified using PFGE and underwent susceptibility testing for vancomycin using a standard Etest (AB bioMérieux, Solna, Sweden), Vitek2(®) (AST-P612; bioMérieux, Inc., Durham, NC, USA) and broth microdilution (BMD) performed as per the CLSI method.
RESULTS: Over the 12 years, 78% (n = 326) of the isolates were multiresistant MRSA (ST239-like by PFGE, where ST stands for sequence type). The correlation between MIC testing methods was moderate with Spearman's correlation coefficients of 0.50 for BMD versus Etest (P < 0.001), 0.33 for BMD versus Vitek2(®) (P < 0.001) and 0.42 for Etest versus Vitek2(®) (P < 0.001). In general, Etest results were 1 dilution higher while the Vitek2(®) results were 1 dilution lower than the BMD MIC result. MIC creep was dependent on the MIC testing method and the measurement used for analysis (geometric mean MIC versus modal MIC versus frequency analysis), with creep detected for Etest regression analysis only. In contrast, the proportion of isolates with a BMD MIC ≥2 mg/L decreased from 16% to 9% in the latter half of the study. Modal MIC was stable over the 12 years at 1 mg/L irrespective of MIC method used.
CONCLUSIONS: Correlation between vancomycin MIC methodologies remains suboptimal. Temporal MIC trends should be interpreted with caution as these are dependent on the testing methodology and the measurement used for analysis.

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Year:  2011        PMID: 21750101     DOI: 10.1093/jac/dkr280

Source DB:  PubMed          Journal:  J Antimicrob Chemother        ISSN: 0305-7453            Impact factor:   5.790


  21 in total

1.  Carriage of an ACME II variant may have contributed to methicillin-resistant Staphylococcus aureus sequence type 239-like strain replacement in Liverpool Hospital, Sydney, Australia.

Authors:  B A Espedido; J A Steen; T Barbagiannakos; J Mercer; D L Paterson; S M Grimmond; M A Cooper; I B Gosbell; S J van Hal; S O Jensen
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3.  Correlation of methicillin-resistant Staphylococcus aureus vancomycin minimal inhibitory concentration results by Etest and broth microdilution methods with population analysis profile: lack of Etest overestimation of the MIC.

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6.  Precision of vancomycin and daptomycin MICs for methicillin-resistant Staphylococcus aureus and effect of subculture and storage.

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7.  Evaluation of Target Attainment of Vancomycin Area Under the Curve in Children With Methicillin-Resistant Staphylococcus Aureus Bacteremia.

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9.  Vancomycin AUC/MIC ratio and 30-day mortality in patients with Staphylococcus aureus bacteremia.

Authors:  Natasha E Holmes; John D Turnidge; Wendy J Munckhof; J Owen Robinson; Tony M Korman; Matthew V N O'Sullivan; Tara L Anderson; Sally A Roberts; Sanchia J C Warren; Wei Gao; Benjamin P Howden; Paul D R Johnson
Journal:  Antimicrob Agents Chemother       Date:  2013-01-18       Impact factor: 5.191

10.  Impact of Vancomycin MIC on Treatment Outcomes in Invasive Staphylococcus aureus Infections.

Authors:  Kyoung-Ho Song; Moonsuk Kim; Chung Jong Kim; Jeong Eun Cho; Yun Jung Choi; Jeong Su Park; Soyeon Ahn; Hee-Chang Jang; Kyung-Hwa Park; Sook-In Jung; Nara Yoon; Dong-Min Kim; Jeong-Hwan Hwang; Chang Seop Lee; Jae Hoon Lee; Yee Gyung Kwak; Eu Suk Kim; Seong Yeon Park; Yoonseon Park; Kkot Sil Lee; Yeong-Seon Lee; Hong Bin Kim
Journal:  Antimicrob Agents Chemother       Date:  2017-02-23       Impact factor: 5.191

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