Therapeutic Drug Concentrations of Teicoplanin in Clinical Settings.
- Author:
So Yun NAH
1
;
Jae Hyoung IM
;
Jin Yeob YEO
;
Ji Hyeon BAEK
;
Cheol Woo KIM
;
Moon Seok NAM
;
Hye Kyung LEE
;
Moon Hyun CHUNG
;
Jin Soo LEE
Author Information
- Publication Type:Original Article
- Keywords: Teicoplanin; Drug monitoring; Loading dose; Dosing regimen
- MeSH: Drug Monitoring; Gram-Positive Bacteria; Hospitals, Teaching; Humans; Plasma; Retrospective Studies; Teicoplanin*
- From:Infection and Chemotherapy 2014;46(1):35-41
- CountryRepublic of Korea
- Language:English
- Abstract: 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.
