Relationship between Vancomycin-Resistant Staphylococcus aureus, Vancomycin-Intermediate S. aureus, High Vancomycin MIC, and Outcome in Serious S. aureus Infections

被引:76
作者
Holmes, Natasha E. [1 ,3 ]
Johnson, Paul D. R. [1 ,3 ]
Howden, Benjamin P. [1 ,2 ,4 ,5 ]
机构
[1] Austin Hlth, Dept Infect Dis, ACIR, Heidelberg, Vic, Australia
[2] Austin Hlth, Dept Microbiol, Heidelberg, Vic, Australia
[3] Univ Melbourne, Dept Med, Parkville, Vic 3052, Australia
[4] Monash Univ, Dept Microbiol, Clayton, Vic 3168, Australia
[5] Univ Melbourne, Dept Microbiol & Immunol, Parkville, Vic 3052, Australia
关键词
MINIMUM INHIBITORY CONCENTRATION; REDUCED SUSCEPTIBILITY; CLINICAL-FEATURES; BACTEREMIA; STRAINS; VALUES; MRSA;
D O I
10.1128/JCM.00775-12
中图分类号
Q93 [微生物学];
学科分类号
071005 [微生物学];
摘要
Vancomycin has been used successfully for over 50 years for the treatment of Staphylococcus aureus infections, particularly those involving methicillin-resistant S. aureus. It has proven remarkably reliable, but its efficacy is now being questioned with the emergence of strains of S. aureus that display heteroresistance, intermediate resistance, and, occasionally, complete vancomycin resistance. More recently, an association has been established between poor outcome and infections with strains of S. aureus with an elevated vancomycin MIC within the susceptible range. This minireview summarizes the definitions, mechanisms, clinical impact, and laboratory identification of reduced vancomycin susceptibility in S. aureus and discusses practical issues for the diagnostic laboratory in testing and interpreting vancomycin susceptibility for S. aureus infections.
引用
收藏
页码:2548 / 2552
页数:5
相关论文
共 34 条
[1]
British Society for Antimicrobial Chemotherapy (BSAC), 2011, BSAC METH ANT SUSC T
[2]
Clinical features associated with bacteremia due to heterogeneous vancomycin-intermediate Staphylococcus aureus [J].
Charles, PGP ;
Ward, PB ;
Johnson, PDR ;
Howden, BP ;
Grayson, ML .
CLINICAL INFECTIOUS DISEASES, 2004, 38 (03) :448-451
[3]
Clinical and Laboratory Standards Institute, 2006, M07A7 CLSI
[4]
Contribution of a thickened cell wall and its glutamine nonamidated component to the vancomycin resistance expressed by Staphylococcus aureus Mu50 [J].
Cui, LZ ;
Murakami, H ;
Kuwahara-Arai, K ;
Hanaki, H ;
Hiramatsu, K .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (09) :2276-2285
[5]
Resistance to teicoplanin developing during treatment of methicillin-resistant Staphylococcus aureus infection [J].
Elsaghier, AAF ;
Aucken, HM ;
Hamilton-Miller, JM ;
Shaw, S ;
Kibbler, CC .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2002, 49 (02) :423-424
[6]
European Committee on Antimicrobial Susceptibility Testing (EUCAST), 2011, MIC INH ZON DIAM DIS
[7]
Hiramatsu K, 2001, Lancet Infect Dis, V1, P147, DOI 10.1016/S1473-3099(01)00091-3
[8]
Dissemination in Japanese hospitals of strains of Staphylococcus aureus heterogeneously resistant to vancomycin [J].
Hiramatsu, K ;
Aritaka, N ;
Hanaki, H ;
Kawasaki, S ;
Hosoda, Y ;
Hori, S ;
Fukuchi, Y ;
Kobayashi, I .
LANCET, 1997, 350 (9092) :1670-1673
[9]
Vancomycin Minimum Inhibitory Concentration and Outcome in Patients With Staphylococcus aureus Bacteremia: Pearl or Pellet? [J].
Holland, Thomas L. ;
Fowler, Vance G., Jr. .
JOURNAL OF INFECTIOUS DISEASES, 2011, 204 (03) :329-331
[10]
Antibiotic Choice May Not Explain Poorer Outcomes in Patients With Staphylococcus aureus Bacteremia and High Vancomycin Minimum Inhibitory Concentrations [J].
Holmes, Natasha E. ;
Turnidge, John D. ;
Munckhof, Wendy J. ;
Robinson, James O. ;
Korman, Tony M. ;
O'Sullivan, Matthew V. N. ;
Anderson, Tara L. ;
Roberts, Sally A. ;
Gao, Wei ;
Christiansen, Keryn J. ;
Coombs, Geoffrey W. ;
Johnson, Paul D. R. ;
Howden, Benjamin P. .
JOURNAL OF INFECTIOUS DISEASES, 2011, 204 (03) :340-347