Clinical and Laboratory Standards Institute and European Committee on Antimicrobial Susceptibility Testing Position Statements on Polymyxin B and Colistin Clinical Breakpoints

• Published in: Clinical infectious diseases Vol. 71; no. 9; pp. e523 - e529
• Main Authors: Satlin, Michael J, Lewis, James S, Weinstein, Melvin P, Patel, Jean, Humphries, Romney M, Kahlmeter, Gunnar, Giske, Christian G, Turnidge, John
• Format: Journal Article
• Language: English
• Published: US Oxford University Press 03.12.2020
• Subjects: Anti-Bacterial Agents - pharmacology; Colistin - pharmacology; Humans; Laboratories; Medicin och hälsovetenskap; Microbial Sensitivity Tests; Polymyxin B - pharmacology; Reference Standards; CLSI; polymyxin; clinical breakpoints; EUCAST; colistin
• ISSN: 1058-4838; 1537-6591; 1537-6591
• DOI: 10.1093/cid/ciaa121

Abstract Recent data on polymyxin pharmacokinetics, pharmacodynamics, toxicity, and clinical outcomes suggest these agents have limited clinical utility. Pharmacokinetics-pharmacodynamics data show a steady-state concentration of 2 μg/mL is required for killing bacteria with colistin minimum inhibitory concentrations of 2 μg/mL. Less than 50% of patients with normal renal function achieve this exposure, and it is associated with high risk of nephrotoxicity. This exposure does not achieve bacterial stasis in pneumonia models. Randomized and observational studies consistently demonstrate increased mortality for polymyxins compared with alternative agents. The Clinical and Laboratory Standards Institute (CLSI) and European Committee on Antimicrobial Susceptibility Testing (EUCAST) are 2 global organizations that establish interpretive criteria for in vitro susceptibility data. CLSI has recently taken the step to eliminate the “susceptible” interpretive category for the polymyxins, whereas EUCAST maintains this interpretive category. This viewpoint describes the opinions of these organizations and the data that were used to inform their perspectives. Recent pharmacokinetic, pharmacodynamic, microbiological and clinical data demonstrate the polymyxins have limited clinical utility, although they frequently demonstrate in vitro activity against extensively drug resistant Gram negative bacteria. CLSI and EUCAST interpretation of polymyxin MICs are described.