Pharmacokinetic studies of linezolid and teicoplanin in the critically ill

Research output: Contribution to journalArticle

  • External authors:
  • Tony Whitehouse
  • Jorge A. Cepeda
  • Rob Shulman
  • Ricardo Nalda-Molina
  • Caroline Tobin
  • Alasdair MacGowan
  • Steve Shaw
  • Chris Kibbler
  • Mervyn Singer
  • A. Peter R Wilson

Abstract

Objectives: To determine the pharmacokinetic characteristics of linezolid and teicoplanin in critically ill patients. Patients and methods: Serum was collected frequently during day 0 and then pre- and 1 h post-dose on days 1, 2, 3, 5, 7 and every third day thereafter during treatment. Serum linezolid concentrations were analysed using HPLC. Serum teicoplanin levels were analysed by fluorescence polarization immunoassay. Results: A two-compartment model was required to characterize linezolid pharmacokinetics (n = 28) and account for the accumulation seen after multiple dosing. The estimated clearance was 0.049 ± 0.016 L/h/kg (±S.E.M. of estimate). At steady state (dosing interval 12 h), linezolid serum concentrations exceeded the breakpoint of 4mg/L for 10.88h (95% Cl 10.09-11.66) after a 600 mg dose with an AUC/MIC of 92.4 (95% Cl 57.2-127.7). Teicoplanin was best described by a two-compartment model (n = 26). The clearance was 4.97 ± 1.58 L/h. Serum levels exceeded the breakpoint of 4 mg/L for the entire dosing interval in all subjects (400 mg dose every 12 h) with an AUC/MIC of 399.3 (95% Cl 329.6-469.0). However, only four of 14 exceeded trough serum concentrations of 10 mg/L. For both agents, trough levels were similar in those who survived and those who died. Conclusions: Linezolid dosage at 600 mg every 12 h was adequate in the critically ill without need for adjustment for renal function. For teicoplanin, further study is needed to confirm if a trough of 10 mg/L is associated with a higher rate of cure than 5 mg/L. If so, serum drug assays would be needed to ensure a therapeutic level. © The British Society for Antimicrobial Chemotherapy 2005; all rights reserved.

Bibliographical metadata

Original languageEnglish
Pages (from-to)333-340
Number of pages7
JournalJournal of Antimicrobial Chemotherapy
Volume55
Issue number3
DOIs
Publication statusPublished - Mar 2005