Colistin in the 21st century

被引:359
作者
Nation, Roger L. [1 ]
Li, Jian [1 ]
机构
[1] Monash Univ, Monash Inst Pharmaceut Sci, Facil Antiinfect Drug Dev & Innovat, Melbourne, Vic, Australia
基金
英国医学研究理事会;
关键词
approaches to optimizing therapy; colistin; Gram-negative infections; MULTIDRUG-RESISTANT GRAM; VENTILATOR-ASSOCIATED PNEUMONIA; IN-VITRO PHARMACODYNAMICS; CRITICALLY-ILL PATIENTS; ACINETOBACTER-BAUMANNII; PSEUDOMONAS-AERUGINOSA; POLYMYXIN-B; INTRAVENOUS COLISTIN; CYSTIC-FIBROSIS; NEGATIVE BACTERIA;
D O I
10.1097/QCO.0b013e328332e672
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Purpose of review Colistin is a 50-year-old antibiotic that is being used increasingly as a 'last-line' therapy to treat infections caused by multidrug-resistant Gram-negative bacteria, when essentially no other options are available. Despite its age, or because of its age, there has been a dearth of knowledge on its pharmacological and microbiological properties. This review focuses on recent studies aimed at optimizing the clinical use of this old antibiotic. Recent findings A number of factors, including the diversity in the pharmaceutical products available, have hindered the optimal use of colistin. Recent advances in understanding of the pharmacokinetics and pharmacodynamics of colistin, and the emerging knowledge on the relationship between the pharmacokinetics and pharmacodynamics, provide a solid base for optimization of dosage regimens. The potential for nephrotoxicity has been a lingering concern, but recent studies provide useful new information on the incidence, severity and reversibility of this adverse effect. Recent approaches to the use of other antibiotics in combination with colistin hold promise for increased antibacterial efficacy with less potential for emergence of resistance. Summary Because few, if any, new antibiotics with activity against multidrug-resistant Gram-negative bacteria will be available within the next several years, it is essential that colistin is used in ways that maximize its antibacterial efficacy and minimize toxicity and development of resistance. Recent developments have improved use of colistin in the 21st century.
引用
收藏
页码:535 / 543
页数:9
相关论文
共 95 条
[11]   A formyltransferase required for polymyxin resistance in Escherichia coli and the modification of lipid a with 4-amino-4-deoxy-L-arabinose -: Identification and function of UDP-4-deoxy-4-formamido-L-arabinose [J].
Breazeale, SD ;
Ribeiro, AA ;
McClerren, AL ;
Raetz, RH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (14) :14154-14167
[12]   Capsule polysaccharide mediates bacterial resistance to antimicrobial peptides [J].
Campos, MA ;
Vargas, MA ;
Regueiro, V ;
Llompart, CM ;
Albertí, S ;
Bengoechea, JA .
INFECTION AND IMMUNITY, 2004, 72 (12) :7107-7114
[13]   Secondary acylation of Klebsiella pneumoniae lipopolysaccharide contributes to sensitivity to antibacterial peptides [J].
Clements, Abigail ;
Tull, Dedreia ;
Jenney, Adam W. ;
Farn, Jacinta L. ;
Kim, Sang-Hyun ;
Bishop, Russell E. ;
McPhee, Joseph B. ;
Hancock, Robert E. W. ;
Hartland, Elizabeth L. ;
Pearse, Martin J. ;
Wijburg, Odilia L. C. ;
Jackson, David C. ;
McConville, Malcolm J. ;
Strugnell, Richard A. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (21) :15569-15577
[14]  
Conway SP, 2000, ANN PHARMACOTHER, V34, P1238
[15]   Pharmacokinetic/pharmacodynamic parameters: Rationale for antibacterial dosing of mice and men [J].
Craig, WA .
CLINICAL INFECTIOUS DISEASES, 1998, 26 (01) :1-10
[16]   Successful treatment of multidrug-resistant Acinetobacter baumanii ventriculitis with intravenous and intraventricular colistin [J].
Dalgic, N. ;
Ceylan, Y. ;
Sancar, M. ;
Telhan, L. ;
Kafadar, I. ;
Cavusoglu, H. ;
Ceylan, O. ;
Hasim, O. .
ANNALS OF TROPICAL PAEDIATRICS, 2009, 29 (02) :141-147
[17]   The crisis of resistance: Identifying drug exposures to suppress amplification of resistant mutant subpopulations [J].
Drusano, GL ;
Louie, A ;
Deziel, M ;
Gumbo, T .
CLINICAL INFECTIOUS DISEASES, 2006, 42 (04) :525-532
[18]  
DUCHANI RV, 2009, 49 INT C ANT AG CHEM
[19]  
DUDHANI RV, 2007, 47 INT C ANT AG CHEM, P1
[20]   Measurement of urinary N-acetyl-b-D-glucosaminidase in adult patients with cystic fibrosis:: Before, during and after treatment with intravenous antibiotics [J].
Etherington, C. ;
Bosomworth, M. ;
Clifton, I. ;
Peckham, D. G. ;
Conway, S. P. .
JOURNAL OF CYSTIC FIBROSIS, 2007, 6 (01) :67-73