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Optimizing Polymyxin Combinations Against Resistant Gram-Negative Bacteria

  • Phillip J. Bergen
  • , Zackery P. Bulman
  • , Cornelia B. Landersdorfer
  • , Nicholas Smith
  • , Justin R. Lenhard
  • , Jürgen B. Bulitta
  • , Roger L. Nation
  • , Jian Li
  • , Brian T. Tsuji
  • Monash University
  • SUNY Buffalo
  • University of Florida

Research output: Contribution to journalReview articlepeer-review

43 Scopus citations

Abstract

Polymyxin combination therapy is increasingly used clinically. However, systematic investigations of such combinations are a relatively recent phenomenon. The emerging pharmacodynamic (PD) and pharmacokinetic (PK) data on CMS/colistin and polymyxin B suggest that caution is required with monotherapy. Given this situation, polymyxin combination therapy has been suggested as a possible way to increase bacterial killing and reduce the development of resistance. Considerable in vitro data have been generated in support of this view, particularly recent studies utilizing dynamic models. However, most existing animal data are of poor quality with major shortcomings in study design, while clinical data are generally limited to retrospective analysis and small, low-power, prospective studies. This article provides an overview of clinical and preclinical investigations of CMS/colistin and polymyxin B combination therapy.

Original languageEnglish
Pages (from-to)391-415
Number of pages25
JournalInfectious Diseases and Therapy
Volume4
Issue number4
DOIs
StatePublished - Dec 1 2015

Keywords

  • Colistin
  • Colistin methanesulfonate
  • Combination
  • Pharmacodynamic
  • Polymyxin B
  • Polymyxins

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