Literature DB >> 24693468

Therapeutic drug concentrations of teicoplanin in clinical settings.

So-Yun Nah1, Jae Hyoung Im1, Jin Yeob Yeo1, Ji-Hyeon Baek1, Cheol-Woo Kim2, Moon-Seok Nam2, Hye-Kyung Lee3, Moon-Hyun Chung1, Jin-Soo Lee1.   

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.

Entities:  

Keywords:  Dosing regimen; Drug monitoring; Loading dose; Teicoplanin

Year:  2014        PMID: 24693468      PMCID: PMC3970309          DOI: 10.3947/ic.2014.46.1.35

Source DB:  PubMed          Journal:  Infect Chemother        ISSN: 1598-8112


  14 in total

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Authors:  A P Wilson
Journal:  Clin Pharmacokinet       Date:  2000-09       Impact factor: 6.447

2.  Teicoplanin therapy for Staphylococcus aureus septicaemia: relationship between pre-dose serum concentrations and outcome.

Authors:  I Harding; A P MacGowan; L O White; E S Darley; V Reed
Journal:  J Antimicrob Chemother       Date:  2000-06       Impact factor: 5.790

3.  Analyses of teicoplanin concentrations from 1994 to 2006 from a UK assay service.

Authors:  C M Tobin; A M Lovering; E Sweeney; A P MacGowan
Journal:  J Antimicrob Chemother       Date:  2010-08-03       Impact factor: 5.790

4.  Simplified dosing regimens of teicoplanin for patient groups stratified by renal function and weight using Monte Carlo simulation.

Authors:  Takaaki Yamada; Toshiharu Nonaka; Takahisa Yano; Toshio Kubota; Nobuaki Egashira; Takehiro Kawashiri; Ryozo Oishi
Journal:  Int J Antimicrob Agents       Date:  2012-07-19       Impact factor: 5.283

Review 5.  Dosage recommendations for teicoplanin.

Authors:  A P Wilson; R N Grüneberg; H Neu
Journal:  J Antimicrob Chemother       Date:  1993-12       Impact factor: 5.790

6.  Significance of individual adjustment of initial loading dosage of teicoplanin based on population pharmacokinetics.

Authors:  Takashi Niwa; Yoshinori Imanishi; Tomofumi Ohmori; Katsuhiko Matsuura; Nobuo Murakami; Yoshinori Itoh
Journal:  Int J Antimicrob Agents       Date:  2010-02-24       Impact factor: 5.283

7.  Treatment of bone, joint, and vascular-access-associated gram-positive bacterial infections with teicoplanin.

Authors:  R N Greenberg
Journal:  Antimicrob Agents Chemother       Date:  1990-12       Impact factor: 5.191

Review 8.  Clinical pharmacokinetics of teicoplanin.

Authors:  M Rowland
Journal:  Clin Pharmacokinet       Date:  1990-03       Impact factor: 6.447

9.  Teicoplanin pharmacokinetics in healthy volunteers after administration of intravenous loading and maintenance doses.

Authors:  W R Outman; C H Nightingale; K R Sweeney; R Quintiliani
Journal:  Antimicrob Agents Chemother       Date:  1990-11       Impact factor: 5.191

10.  The use and therapeutic drug monitoring of teicoplanin in the UK.

Authors:  E S R Darley; A P MacGowan
Journal:  Clin Microbiol Infect       Date:  2004-01       Impact factor: 8.067

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  4 in total

1.  Evaluating the optimal dose of teicoplanin with therapeutic drug monitoring: not too high for adverse event, not too low for treatment efficacy.

Authors:  Si-Ho Kim; Cheol-In Kang; Kyungmin Huh; Sun Young Cho; Doo Ryeon Chung; Soo-Youn Lee; Yae-Jean Kim; Kyong Ran Peck
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2019-08-01       Impact factor: 3.267

2.  Clinical efficacy and safety in patients treated with teicoplanin with a target trough concentration of 20 μg/mL using a regimen of 12 mg/kg for five doses within the initial 3 days.

Authors:  Takashi Ueda; Yoshio Takesue; Kazuhiko Nakajima; Kaoru Ichiki; Kaori Ishikawa; Yoshiko Takai; Kumiko Yamada; Toshie Tsuchida; Naruhito Otani; Yoshiko Takahashi; Mika Ishihara; Shingo Takubo; Hiroki Ikeuchi; Motoi Uchino; Takeshi Kimura
Journal:  BMC Pharmacol Toxicol       Date:  2020-07-08       Impact factor: 2.483

3.  Therapeutic Drug Level Monitoring of Teicoplanin in Korean Pediatric Patients with Normal versus Impaired Renal Function.

Authors:  Joon Sik Choi; Jong Min Kim; Dongsub Kim; Si Ho Kim; Heeyeon Cho; Hyung Doo Park; Soo Youn Lee; Cheol In Kang; Yae Jean Kim
Journal:  J Korean Med Sci       Date:  2020-11-30       Impact factor: 2.153

4.  Is therapeutic drug monitoring of teicoplanin useful?

Authors:  Shin-Woo Kim
Journal:  Infect Chemother       Date:  2014-03
  4 in total

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