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A Review of the Clinical Pharmacokinetics of Polymyxin B
Polymyxin B remains an antibiotic of last resort because of its toxicities. Although newer therapies are becoming available, it is anticipated that resistance to these agents will continue to emerge, and understanding the safest and most efficacious manner to deliver polymyxin B will remain highly i...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6466567/ https://www.ncbi.nlm.nih.gov/pubmed/30909507 http://dx.doi.org/10.3390/antibiotics8010031 |
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author | Avedissian, Sean N. Liu, Jiajun Rhodes, Nathaniel J. Lee, Andrew Pais, Gwendolyn M. Hauser, Alan R. Scheetz, Marc H. |
author_facet | Avedissian, Sean N. Liu, Jiajun Rhodes, Nathaniel J. Lee, Andrew Pais, Gwendolyn M. Hauser, Alan R. Scheetz, Marc H. |
author_sort | Avedissian, Sean N. |
collection | PubMed |
description | Polymyxin B remains an antibiotic of last resort because of its toxicities. Although newer therapies are becoming available, it is anticipated that resistance to these agents will continue to emerge, and understanding the safest and most efficacious manner to deliver polymyxin B will remain highly important. Recent data have demonstrated that polymyxin B may be less nephrotoxic than colistin. Pharmacokinetically, polymyxin B is primarily eliminated via non-renal pathways, and most do not recommend adjusting the dose for renal impairment. However, some recent studies suggest a weak relationship between polymyxin B clearance and patient creatinine clearance. This review article will describe the clinical pharmacokinetics of polymyxin B and address relevant issues in chemistry and assays available. |
format | Online Article Text |
id | pubmed-6466567 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-64665672019-04-18 A Review of the Clinical Pharmacokinetics of Polymyxin B Avedissian, Sean N. Liu, Jiajun Rhodes, Nathaniel J. Lee, Andrew Pais, Gwendolyn M. Hauser, Alan R. Scheetz, Marc H. Antibiotics (Basel) Review Polymyxin B remains an antibiotic of last resort because of its toxicities. Although newer therapies are becoming available, it is anticipated that resistance to these agents will continue to emerge, and understanding the safest and most efficacious manner to deliver polymyxin B will remain highly important. Recent data have demonstrated that polymyxin B may be less nephrotoxic than colistin. Pharmacokinetically, polymyxin B is primarily eliminated via non-renal pathways, and most do not recommend adjusting the dose for renal impairment. However, some recent studies suggest a weak relationship between polymyxin B clearance and patient creatinine clearance. This review article will describe the clinical pharmacokinetics of polymyxin B and address relevant issues in chemistry and assays available. MDPI 2019-03-22 /pmc/articles/PMC6466567/ /pubmed/30909507 http://dx.doi.org/10.3390/antibiotics8010031 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Avedissian, Sean N. Liu, Jiajun Rhodes, Nathaniel J. Lee, Andrew Pais, Gwendolyn M. Hauser, Alan R. Scheetz, Marc H. A Review of the Clinical Pharmacokinetics of Polymyxin B |
title | A Review of the Clinical Pharmacokinetics of Polymyxin B |
title_full | A Review of the Clinical Pharmacokinetics of Polymyxin B |
title_fullStr | A Review of the Clinical Pharmacokinetics of Polymyxin B |
title_full_unstemmed | A Review of the Clinical Pharmacokinetics of Polymyxin B |
title_short | A Review of the Clinical Pharmacokinetics of Polymyxin B |
title_sort | review of the clinical pharmacokinetics of polymyxin b |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6466567/ https://www.ncbi.nlm.nih.gov/pubmed/30909507 http://dx.doi.org/10.3390/antibiotics8010031 |
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