Characterisation of a Staphylococcus aureus strain with progressive loss of susceptibility to vancomycin and daptomycin during therapy

被引:58
作者
Tenover, Fred C. [2 ]
Sinner, Scott W. [3 ]
Segal, Robert E. [3 ]
Huang, Vanthida [4 ]
Alexandre, Shandline S. [5 ]
McGowan, John E., Jr. [1 ]
Weinstein, Melvin P. [3 ,5 ]
机构
[1] Emory Univ, Dept Epidemiol, Rollins Sch Publ Hlth, Atlanta, GA 30322 USA
[2] Ctr Dis Control & Prevent, Div Healthcare Qual Promot, Atlanta, GA 30333 USA
[3] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Div Infect Dis Allergy & Immunol, New Brunswick, NJ 08901 USA
[4] Mercer Univ, Dept Pharm Practice, Coll Pharm & Hlth Sci, Atlanta, GA 30341 USA
[5] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Microbiol Lab, Robert Wood Johnson Univ Hosp, New Brunswick, NJ 08901 USA
关键词
Staphylococci; Vancomycin; Teicoplanin; Heteroresistance; REDUCED SUSCEPTIBILITY; RESISTANT; GLYCOPEPTIDES; ENDOCARDITIS; HETERO;
D O I
10.1016/j.ijantimicag.2008.12.010
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Following an initial response to vancomycin therapy, a patient with meticillin-resistant Staphylococcus aureus (MRSA) bacteraemia developed endocarditis, failed a second course of vancomycin and then failed daptomycin therapy. An increase in the vancomycin minimum inhibitory concentrations of four consecutive MRSA blood isolates from 2 mu g/mL to 8 mu g/mL was shown by Etest. Population analysis of four successive blood culture isolates recovered over the 10-week period showed that the MRSA strain became progressively less susceptible to both vancomycin and daptomycin. Retrospectively, the macro Etest method using teicoplanin indicated a decrease in vancomycin susceptibility in the second blood isolate. The patient improved after treatment with various courses of trimethoprim/sulfamethoxazole, quinupristin/dalfopristin and linezolid. Early detection of vancomycin-heteroresistant S. aureus isolates, which appeared to have clinical significance in this case, continues to be a challenge for the clinical laboratory. Development of suitable practical methods for this should be given priority. Concurrent development of resistance to vancomycin and daptomycin, whilst rare, must be considered in a patient who is unresponsive to daptomycin following vancomycin therapy. (C) 2009 Elsevier B.V. and the International Society of Chemotherapy. All rights reserved.
引用
收藏
页码:564 / 568
页数:5
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