Li Jian, Nation Roger L, Turnidge John D, Milne Robert W, Coulthard Kingsley, Rayner Craig R, Paterson David L
Facility for Anti-infective Drug Development and Innovation, Victorian College of Pharmacy, Monash University, Parkville, Victoria, Australia.
Lancet Infect Dis. 2006 Sep;6(9):589-601. doi: 10.1016/S1473-3099(06)70580-1.
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.
革兰氏阴性菌,尤其是铜绿假单胞菌、鲍曼不动杆菌和肺炎克雷伯菌中日益增加的多重耐药性是一个关键问题。有限的治疗选择迫使传染病临床医生和微生物学家重新评估多黏菌素的临床应用,多黏菌素是一种50多年前发现的多黏菌素类抗生素。我们总结了在理解多黏菌素复杂的化学性质、药代动力学和药效学方面的最新进展,这三个方面之间的相互作用,以及它们对这种重要抗生素临床应用的影响。本文回顾了近期的临床研究结果,重点评估了疗效、新出现的耐药性、潜在毒性和联合治疗。在对抗迅速出现的细菌耐药性的斗争中,我们不能再完全依赖新抗生素的发现;我们还必须寻求合理使用多黏菌素等老抗生素的方法。