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Optimizing Polymyxin Combinations Against Resistant Gram-Negative Bacteria
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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Healthcare
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4675771/ https://www.ncbi.nlm.nih.gov/pubmed/26645096 http://dx.doi.org/10.1007/s40121-015-0093-7 |
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author | Bergen, Phillip J. Bulman, Zackery P. Landersdorfer, Cornelia B. Smith, Nicholas Lenhard, Justin R. Bulitta, Jürgen B. Nation, Roger L. Li, Jian Tsuji, Brian T. |
author_facet | Bergen, Phillip J. Bulman, Zackery P. Landersdorfer, Cornelia B. Smith, Nicholas Lenhard, Justin R. Bulitta, Jürgen B. Nation, Roger L. Li, Jian Tsuji, Brian T. |
author_sort | Bergen, Phillip J. |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-4675771 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Springer Healthcare |
record_format | MEDLINE/PubMed |
spelling | pubmed-46757712015-12-19 Optimizing Polymyxin Combinations Against Resistant Gram-Negative Bacteria Bergen, Phillip J. Bulman, Zackery P. Landersdorfer, Cornelia B. Smith, Nicholas Lenhard, Justin R. Bulitta, Jürgen B. Nation, Roger L. Li, Jian Tsuji, Brian T. Infect Dis Ther Review 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. Springer Healthcare 2015-12-08 2015-12 /pmc/articles/PMC4675771/ /pubmed/26645096 http://dx.doi.org/10.1007/s40121-015-0093-7 Text en © The Author(s) 2015 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits any noncommercial use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Review Bergen, Phillip J. Bulman, Zackery P. Landersdorfer, Cornelia B. Smith, Nicholas Lenhard, Justin R. Bulitta, Jürgen B. Nation, Roger L. Li, Jian Tsuji, Brian T. Optimizing Polymyxin Combinations Against Resistant Gram-Negative Bacteria |
title | Optimizing Polymyxin Combinations Against Resistant Gram-Negative Bacteria |
title_full | Optimizing Polymyxin Combinations Against Resistant Gram-Negative Bacteria |
title_fullStr | Optimizing Polymyxin Combinations Against Resistant Gram-Negative Bacteria |
title_full_unstemmed | Optimizing Polymyxin Combinations Against Resistant Gram-Negative Bacteria |
title_short | Optimizing Polymyxin Combinations Against Resistant Gram-Negative Bacteria |
title_sort | optimizing polymyxin combinations against resistant gram-negative bacteria |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4675771/ https://www.ncbi.nlm.nih.gov/pubmed/26645096 http://dx.doi.org/10.1007/s40121-015-0093-7 |
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