共 50 条
Impact of area under the concentration-time curve to minimum inhibitory concentration ratio on vancomycin treatment outcomes in methicillin-resistant Staphylococcus aureus bacteraemia
被引:42
|作者:
Song, Kyoung-Ho
[1
]
Kim, Hong Bin
[1
]
Kim, Hyung-sook
[2
]
Lee, Myung Jin
[1
]
Jung, Younghee
[1
,3
]
Kim, Gayeon
[1
]
Hwang, Jeong-Hwan
[1
]
Kim, Nak-Hyun
[4
]
Kim, Moonsuk
[1
]
Kim, Chung-Jong
[1
]
Choe, Pyoeng Gyun
[4
]
Chung, Jae-Yong
[5
]
Park, Wan Beom
[4
]
Kim, Eu Suk
[1
]
Park, Kyoung Un
[6
]
Kim, Nam Joong
[4
]
Kim, Eui-Chong
[7
]
Oh, Myoung-don
[4
]
机构:
[1] Seoul Natl Univ, Bundang Hosp, Dept Internal Med, 166 Gumi Ro, Songnam 463707, South Korea
[2] Seoul Natl Univ, Bundang Hosp, Dept Pharm, Songnam 463707, South Korea
[3] Konyang Univ Hosp, Dept Internal Med, Daejeon, South Korea
[4] Seoul Natl Univ Hosp, Dept Internal Med, Seoul 110744, South Korea
[5] Seoul Natl Univ, Bundang Hosp, Dept Clin Pharmacol & Therapeut, Songnam 463707, South Korea
[6] Seoul Natl Univ, Bundang Hosp, Dept Lab Med, Songnam 463707, South Korea
[7] Seoul Natl Univ Hosp, Dept Lab Med, Seoul 110744, South Korea
关键词:
Vancomycin;
Staphylococcus aureus;
Methicillin-resistant;
Area under the concentration time curve;
Minimum inhibitory concentration;
Pharmacokinetics;
BLOOD-STREAM INFECTIONS;
MORTALITY;
PHARMACODYNAMICS;
ASSOCIATION;
PREDICTORS;
EXPOSURE;
FAILURE;
ADULTS;
KOREA;
D O I:
10.1016/j.ijantimicag.2015.09.010
中图分类号:
R51 [传染病];
学科分类号:
100401 ;
摘要:
There have been few clinical studies on the association between the vancomycin 24-h area under the concentration-time curve (AUC(24)) to minimum inhibitory concentration (MIC) ratio and vancomycin treatment outcomes in methicillin-resistant Staphylococcus aureus (MRSA) infections. To examine this association and to establish a suitable cut-off value for AUC(24)/MIC, a multicentre prospective observational study was conducted in patients with MRSA bacteraemia. Data were collected on all patients aged >= 18 years with MRSA bacteraemia treated with vancomycin for >= 72 h without dialysis. The MIC was determined by broth microdilution (BMD) and Etest. Treatment failure was defined as (i) 30-day mortality, (ii) persistent bacteraemia (>= 7 days) and (iii) recurrence (<= 30 days after completion of therapy). AUC(24) was estimated by a Bayesian approach based on individual vancomycin concentrations. The AUC(24)/MIC cut-off value for differentiating treatment success and failure was calculated by Classification and Regression Tree (CART) analysis. In total, 117 patients were enrolled, among which vancomycin treatment failure occurred in 38 (32.5%). In univariate analysis, high vancomycin MIC and low trough levels were unrelated to treatment outcomes. In the CART analysis, low vancomycin AUC(24)/MIC [<392.7 (BMD) and <397.2 (Etest)] was associated with treatment failure. In multivariate analysis, low AUC24/MIC was a risk factor for treatment failure [adjusted odds ratio (aOR) = 3.50, 95% confidence interval (CI) 1.39-8.82 by BMD; aOR = 5.61, 95% CI 2.07-15.24 by Etest]. AUC(24)/MIC is associated with vancomycin treatment outcomes in MRSA bacteraemia, and seeking individualised AUC(24)/MIC ratios above target (>400) may improve treatment outcomes. (C) 2015 Elsevier B.V. and the International Society of Chemotherapy. All rights reserved.
引用
收藏
页码:689 / 695
页数:7
相关论文