The Clinical Significance of Vancomycin Minimum Inhibitory Concentration in Staphylococcus aureus Infections: A Systematic Review and Meta-analysis

被引:398
作者
van Hal, S. J. [1 ,2 ]
Lodise, T. P. [3 ]
Paterson, D. L. [4 ]
机构
[1] Liverpool Hosp, Dept Microbiol & Infect Dis, Sydney SW Pathol Serv Liverpool, S Western Sydney Local Hlth Network, Sydney, NSW 1087, Australia
[2] Univ Western Australia, Sch Med, Microbiol & Infect Dis Unit, Antibiot Resistance & Mobile Elements Grp, Nedlands, WA 6009, Australia
[3] Albany Coll Pharm & Hlth Sci, New York, NY USA
[4] Univ Queensland, Clin Res Ctr, Royal Brisbane & Womens Hosp Campus, Brisbane, Qld 4072, Australia
关键词
RISK-FACTORS; BACTERICIDAL ACTIVITY; RESISTANT; BACTEREMIA; INTERMEDIATE; PERSISTENT; SUSCEPTIBILITY; MORTALITY; EFFICACY; OUTCOMES;
D O I
10.1093/cid/cir935
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Emerging data suggest that vancomycin may be less effective against serious methicillin-resistant Staphylococcus aureus (MRSA) infections with minimum inhibitory concentration (MIC) values at the higher end of the susceptibility range. The purpose of this review is to examine the strength of these associations. Methods. All relevant studies pertaining to treatment outcomes or mortality associated with vancomycin MIC were retrieved from the medical literature from January 1996 through August 2011 and analyzed according to Cochrane guidelines. Results. Of the 270 studies identified, 48 studies were reviewed, with 22 studies included in the final metaanalysis. Vancomycin MIC was significantly associated with mortality for MRSA infection irrespective of the source of infection or MIC methodology (odds ratio [OR], 1.64; 95% confidence interval [CI], 1.14-2.37; P < .01). This mortality association was predominantly driven by bloodstream infections (BSIs; OR, 1.58; 95% CI, 1.06-2.37; P = .03) and isolates with a vancomycin MIC of 2 mu g/mL by Etest (OR, 1.72; 95% CI, 1.34-2.21; P < .01). Vancomycin MIC was significantly associated with treatment failure irrespective of source of infection or MIC methodology (OR, 2.69; 95% CI, 1.60-4.51; P < .01). Conclusion. High vancomycin MIC was associated with a higher mortality rate in MRSA BSI. Thus, institutions should consider conducting Etest MICs on all MRSA BSI isolates. Although these data highlight concerns about vancomycin, currently, there are no data to support better survival rates with alternative antibiotics. Data are sorely needed to determine whether other agents can remedy these outcomes observed with vancomycin for MRSA infections with elevated vancomycin MIC values.
引用
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页码:755 / 771
页数:17
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