Literature DB >> 17825421

Teicoplanin levels in bone and joint infections: are standard doses subtherapeutic?

Philippa C Matthews1, Alison Taylor, Ivor Byren, Bridget L Atkins.   

Abstract

OBJECTIVES: Previously published data suggest that a trough serum teicoplanin level of > or = 20 mg/l is predictive of improved outcomes in serious staphylococcal infection. We investigated how dose regimen and patient characteristics impact on trough teicoplanin levels in patients with musculoskeletal infection, in order to help standardise teicoplanin use.
METHODS: We prospectively collected data for 141 clinically stable adults with bone and joint infection treated as outpatients with teicoplanin. Patients with end stage renal failure were excluded.
RESULTS: The most frequently used teicoplanin dose regimens were 400 mg or 600 mg i.v. once daily. Trough levels were available for 78% of episodes, of which 51% were > or = 20 mg/l. Unsurprisingly, a level of > or = 20 mg/l occurred more often with a dose of 600 mg than with lower doses (p=0.005). There was no significant relationship between teicoplanin level and age, body weight or creatinine clearance, but male gender was associated with lower trough levels than female gender (p=0.03).
CONCLUSIONS: These data suggest that teicoplanin levels of > or = 20 mg/l for bone and joint infection in stable adult patients are best achieved with a daily dose of at least 600 mg.

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Year:  2007        PMID: 17825421     DOI: 10.1016/j.jinf.2007.07.012

Source DB:  PubMed          Journal:  J Infect        ISSN: 0163-4453            Impact factor:   6.072


  6 in total

1.  Enhanced loading regimen of teicoplanin is necessary to achieve therapeutic pharmacokinetics levels for the improvement of clinical outcomes in patients with renal dysfunction.

Authors:  T Ueda; Y Takesue; K Nakajima; K Ichiki; A Doita; Y Wada; T Tsuchida; Y Takahashi; M Ishihara; H Ikeuchi; M Uchino; T Kimura
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2016-06-09       Impact factor: 3.267

2.  Population pharmacokinetics and pharmacodynamics of teicoplanin in neonates: making better use of C-reactive protein to deliver individualized therapy.

Authors:  V Ramos-Martín; M N Neely; P McGowan; S Siner; K Padmore; M Peak; M W Beresford; M A Turner; S Paulus; W W Hope
Journal:  J Antimicrob Chemother       Date:  2016-08-19       Impact factor: 5.790

Review 3.  Acute infectious osteomyelitis in children: new treatment strategies for an old enemy.

Authors:  Sabrina Congedi; Chiara Minotti; Carlo Giaquinto; Liviana Da Dalt; Daniele Donà
Journal:  World J Pediatr       Date:  2020-05-11       Impact factor: 2.764

4.  Clinical practice guidelines for therapeutic drug monitoring of teicoplanin: a consensus review by the Japanese Society of Chemotherapy and the Japanese Society of Therapeutic Drug Monitoring.

Authors:  Yuki Hanai; Yoshiko Takahashi; Takashi Niwa; Toshihiko Mayumi; Yukihiro Hamada; Toshimi Kimura; Kazuaki Matsumoto; Satoshi Fujii; Yoshio Takesue
Journal:  J Antimicrob Chemother       Date:  2022-03-31       Impact factor: 5.790

5.  Teicoplanin-based antimicrobial therapy in Staphylococcus aureus bone and joint infection: tolerance, efficacy and experience with subcutaneous administration.

Authors:  Olivier Peeters; Tristan Ferry; Florence Ader; André Boibieux; Evelyne Braun; Anissa Bouaziz; Judith Karsenty; Emmanuel Forestier; Frédéric Laurent; Sébastien Lustig; Christian Chidiac; Florent Valour
Journal:  BMC Infect Dis       Date:  2016-11-03       Impact factor: 3.090

6.  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

  6 in total

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