Efficacy and Safety of Colistin in Clinical Practice

Main Article Content

สิริมา สิตะรุโน
วิชัย สันติมาลีวรกุล

Abstract

Colistin (polymyxin E) is an antimicrobial agent in the polymyxins group. Its mechanism of action is like detergent by interfering with the transmission of various substances into cytoplasmic bacteria cells. The drug commonly used for treatment of infection is colistin methanesulfonate (CMS), which is less toxic than colistin sulfate. CMS has been used for treatment of gram-negative bacterial infections especially those caused by multidrug resistant pathogens such as Acinetobacter spp, Pseudomonas aeruginosa, Escherichia coli and Klebsiella pneumonia. At present, these pathogens remain susceptible to colistin for more than 90%. CMS is a non-active prodrug. However, it becomes active substance, colistin, after being hydrolyzed in vivo. Colistin is mainly distributed in blood stream and is poorly distributed to the lung parenchyma and cerebrospinal fluid. CMS is mainly excreted through kidney, while colistin elimination is essentially extrarenal. CMS can be administered by intramuscular, intravenous, inhalation, and intraventricular/intrathecal route. Colistin causes major adverse reactions, including renal toxicity and neurotoxicity. Appropriate dosing and duration of treatment with colistin should be applied to prevent nephrotoxicity and nephrotoxicity.

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