KMID : 1144320140460010035
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°¨¿°°ú ÈÇпä¹ý 2014 Volume.46 No. 1 p.35 ~ p.41
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Therapeutic Drug Concentrations of Teicoplanin in Clinical Settings
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Nah So-Yun
Im Jae-Hyoung Yeo Jin-Yeob Baek Ji-Hyeon Kim Cheol-Woo Nam Moon-Seok Lee Hye-Kyung Chung Moon-Hyun Lee Jin-Soo
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Abstract
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Background:Teicoplanin is a glycopeptide antibiotic that is widely used in clinical practice for the treatment of infections caused by drug-resistant Gram-positive bacteria. The aim of this study was to analyze plasma teicoplanin concentrations to determine the percentage of patients in whom therapeutic concentrations of teicoplanin were achieved in clinical practice.
Materials and Methods:The plasma teicoplanin concentrations of hospitalized patients receiving treatment at a teaching hospital were retrospectively analyzed. The target level was defined as a plasma teicoplanin concentration of 10 mg/L or greater, since this was generally regarded as the lower limit of the optimal concentration range required for the effective treatment of a majority of infections.
Results:Patients with sub-optimal (< 10 mg/L) plasma teicoplanin concentrations constituted nearly half of the total study population. The majority of these patients received the recommended loading dose, which were three 400 mg doses administered every 12 hours. Sub-group analysis showed a trend that the group receiving loading dose was more likely to reach the optimal teicoplanin concentration.
Conclusions:The data revealed that a significant proportion of patients in clinical practice achieved only sub-optimal teicoplanin concentrations, which emphasizes the importance of the mandatory use of loading dose and routine therapeutic drug monitoring. Treatment reassessment and simulation of individual dose regimens may also be necessary to achieve optimal drug concentrations.
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KEYWORD
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Teicoplanin, Drug monitoring, Loading dose, Dosing regimen
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