Colistin: the re-emerging antibiotic for multidrug-resistant Gram-negative bacterial infections
Increasing multidrug resistance in Gram-negative bacteria, in particular Pseudomonas aeruginosa, Acinetobacter baumannii, and Klebsiella pneumoniae, presents a critical problem. Limited therapeutic options have forced infectious disease clinicians and microbiologists to reappraise the clinical appli...
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Veröffentlicht in: | The Lancet infectious diseases 2006-09, Vol.6 (9), p.589-601 |
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creator | Li, Jian Nation, Roger L Turnidge, John D Milne, Robert W Coulthard, Kingsley Rayner, Craig R Paterson, David L |
description | Increasing multidrug resistance in Gram-negative bacteria, in particular
Pseudomonas aeruginosa, Acinetobacter baumannii, and
Klebsiella pneumoniae, presents a critical problem. Limited therapeutic options have forced infectious disease clinicians and microbiologists to reappraise the clinical application of colistin, a polymyxin antibiotic discovered more than 50 years ago. We summarise recent progress in understanding the complex chemistry, pharmacokinetics, and pharmacodynamics of colistin, the interplay between these three aspects, and their effect on the clinical use of this important antibiotic. Recent clinical findings are reviewed, focusing on evaluation of efficacy, emerging resistance, potential toxicities, and combination therapy. In the battle against rapidly emerging bacterial resistance we can no longer rely entirely on the discovery of new antibiotics; we must also pursue rational approaches to the use of older antibiotics such as colistin. |
doi_str_mv | 10.1016/S1473-3099(06)70580-1 |
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Pseudomonas aeruginosa, Acinetobacter baumannii, and
Klebsiella pneumoniae, presents a critical problem. Limited therapeutic options have forced infectious disease clinicians and microbiologists to reappraise the clinical application of colistin, a polymyxin antibiotic discovered more than 50 years ago. We summarise recent progress in understanding the complex chemistry, pharmacokinetics, and pharmacodynamics of colistin, the interplay between these three aspects, and their effect on the clinical use of this important antibiotic. Recent clinical findings are reviewed, focusing on evaluation of efficacy, emerging resistance, potential toxicities, and combination therapy. In the battle against rapidly emerging bacterial resistance we can no longer rely entirely on the discovery of new antibiotics; we must also pursue rational approaches to the use of older antibiotics such as colistin.</description><identifier>ISSN: 1473-3099</identifier><identifier>EISSN: 1474-4457</identifier><identifier>DOI: 10.1016/S1473-3099(06)70580-1</identifier><identifier>PMID: 16931410</identifier><identifier>CODEN: LANCAO</identifier><language>eng</language><publisher>London: Elsevier Ltd</publisher><subject>Anti-Bacterial Agents - therapeutic use ; Antibacterial agents ; Antibiotics ; Antibiotics. Antiinfectious agents. Antiparasitic agents ; Bacteria ; Bacterial diseases ; Biological and medical sciences ; Colistin - administration & dosage ; Colistin - pharmacokinetics ; Colistin - therapeutic use ; Dose-Response Relationship, Drug ; Drug Resistance, Multiple ; Gram-Negative Bacterial Infections - drug therapy ; Humans ; Infectious diseases ; Medical sciences ; Pharmacokinetics ; Pharmacology. Drug treatments</subject><ispartof>The Lancet infectious diseases, 2006-09, Vol.6 (9), p.589-601</ispartof><rights>2006 Elsevier Ltd</rights><rights>2006 INIST-CNRS</rights><rights>Copyright Elsevier Limited Sep 2006</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c563t-9563bad2c0dfdcad4cee60043e2682df38f0398812cd877cfc6bdf4bc4464bc13</citedby><cites>FETCH-LOGICAL-c563t-9563bad2c0dfdcad4cee60043e2682df38f0398812cd877cfc6bdf4bc4464bc13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1473309906705801$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18029680$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16931410$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Jian</creatorcontrib><creatorcontrib>Nation, Roger L</creatorcontrib><creatorcontrib>Turnidge, John D</creatorcontrib><creatorcontrib>Milne, Robert W</creatorcontrib><creatorcontrib>Coulthard, Kingsley</creatorcontrib><creatorcontrib>Rayner, Craig R</creatorcontrib><creatorcontrib>Paterson, David L</creatorcontrib><title>Colistin: the re-emerging antibiotic for multidrug-resistant Gram-negative bacterial infections</title><title>The Lancet infectious diseases</title><addtitle>Lancet Infect Dis</addtitle><description>Increasing multidrug resistance in Gram-negative bacteria, in particular
Pseudomonas aeruginosa, Acinetobacter baumannii, and
Klebsiella pneumoniae, presents a critical problem. Limited therapeutic options have forced infectious disease clinicians and microbiologists to reappraise the clinical application of colistin, a polymyxin antibiotic discovered more than 50 years ago. We summarise recent progress in understanding the complex chemistry, pharmacokinetics, and pharmacodynamics of colistin, the interplay between these three aspects, and their effect on the clinical use of this important antibiotic. Recent clinical findings are reviewed, focusing on evaluation of efficacy, emerging resistance, potential toxicities, and combination therapy. In the battle against rapidly emerging bacterial resistance we can no longer rely entirely on the discovery of new antibiotics; we must also pursue rational approaches to the use of older antibiotics such as colistin.</description><subject>Anti-Bacterial Agents - therapeutic use</subject><subject>Antibacterial agents</subject><subject>Antibiotics</subject><subject>Antibiotics. Antiinfectious agents. Antiparasitic agents</subject><subject>Bacteria</subject><subject>Bacterial diseases</subject><subject>Biological and medical sciences</subject><subject>Colistin - administration & dosage</subject><subject>Colistin - pharmacokinetics</subject><subject>Colistin - therapeutic use</subject><subject>Dose-Response Relationship, Drug</subject><subject>Drug Resistance, Multiple</subject><subject>Gram-Negative Bacterial Infections - drug therapy</subject><subject>Humans</subject><subject>Infectious diseases</subject><subject>Medical sciences</subject><subject>Pharmacokinetics</subject><subject>Pharmacology. 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Antiinfectious agents. Antiparasitic agents</topic><topic>Bacteria</topic><topic>Bacterial diseases</topic><topic>Biological and medical sciences</topic><topic>Colistin - administration & dosage</topic><topic>Colistin - pharmacokinetics</topic><topic>Colistin - therapeutic use</topic><topic>Dose-Response Relationship, Drug</topic><topic>Drug Resistance, Multiple</topic><topic>Gram-Negative Bacterial Infections - drug therapy</topic><topic>Humans</topic><topic>Infectious diseases</topic><topic>Medical sciences</topic><topic>Pharmacokinetics</topic><topic>Pharmacology. 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Pseudomonas aeruginosa, Acinetobacter baumannii, and
Klebsiella pneumoniae, presents a critical problem. Limited therapeutic options have forced infectious disease clinicians and microbiologists to reappraise the clinical application of colistin, a polymyxin antibiotic discovered more than 50 years ago. We summarise recent progress in understanding the complex chemistry, pharmacokinetics, and pharmacodynamics of colistin, the interplay between these three aspects, and their effect on the clinical use of this important antibiotic. Recent clinical findings are reviewed, focusing on evaluation of efficacy, emerging resistance, potential toxicities, and combination therapy. In the battle against rapidly emerging bacterial resistance we can no longer rely entirely on the discovery of new antibiotics; we must also pursue rational approaches to the use of older antibiotics such as colistin.</abstract><cop>London</cop><pub>Elsevier Ltd</pub><pmid>16931410</pmid><doi>10.1016/S1473-3099(06)70580-1</doi><tpages>13</tpages></addata></record> |
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subjects | Anti-Bacterial Agents - therapeutic use Antibacterial agents Antibiotics Antibiotics. Antiinfectious agents. Antiparasitic agents Bacteria Bacterial diseases Biological and medical sciences Colistin - administration & dosage Colistin - pharmacokinetics Colistin - therapeutic use Dose-Response Relationship, Drug Drug Resistance, Multiple Gram-Negative Bacterial Infections - drug therapy Humans Infectious diseases Medical sciences Pharmacokinetics Pharmacology. Drug treatments |
title | Colistin: the re-emerging antibiotic for multidrug-resistant Gram-negative bacterial infections |
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