Level of Evidence for Therapeutic Drug Monitoring of Vancomycin

被引:7
作者
Jelassi, Mohamed Larbi
Benlmouden, Amine
Lefeuvre, Sandrine [2 ]
Mainardi, Jean-Luc [2 ,3 ,4 ,5 ]
Billaud, Eliane M. [1 ,2 ]
机构
[1] Hop Europeen Georges Pompidou, AP HP, Serv Pharmacol Toxicol, F-75015 Paris, France
[2] Univ Paris 05, Paris, France
[3] Hop Europeen Georges Pompidou, AP HP, Unite Mobile Microbil Clin, Lab Rech Mol Antibiot,Serv Microbiol, F-75015 Paris, France
[4] Ctr Rech Cordeliers, INSERM, Equipe 12, UMR S 872, Paris, France
[5] Univ Paris 06, Paris, France
来源
THERAPIE | 2011年 / 66卷 / 01期
关键词
vancomycin; therapeutic drug monitoring; RESISTANT STAPHYLOCOCCUS-AUREUS; MINIMUM INHIBITORY CONCENTRATION; ADMINISTRATION REGIMENS; COST-EFFECTIVENESS; MISSISSIPPI MUD; INTENSIVE-CARE; PHARMACOKINETICS; NEPHROTOXICITY; INFECTIONS; OUTCOMES;
D O I
10.2515/therapie/2011005
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Level of Evidence for Therapeutic Drug Monitoring of Vancomycin. Vancomycin is an antibiotic for exclusive hospital use administrated in intravenous infusion to treat systemic infections. It is mainly eliminated by kidneys and potentially nephrotoxic. Data available show that Therapeutic Drug Monitoring (TDM) of vancomycin is highly recommended. It aims to ensure efficacy and avoid resistance by maintaining trough plasma concentrations above the MIC. Secondary, vancomycine TDM may be indicated to prevent nephrotoxicity in high risk patients. TDM is often underwent at steady state (48 to 72 h after the treatment initiation) unless in case of renal impairment (24 h). While compared with intermittent administration, continuous infusion did not result in prognosis improvement; however it resulted in lower pharmacokinetic variability and better cost-efficiency. Targeted trough concentrations for intermittent infusion are between 15 and 20 mg/L (up to 25-30 mg/L for GISA). In case of continuous infusion, targets are higher (25 to 40 mg/L).
引用
收藏
页码:29 / 37
页数:9
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