4.7 Article

Modifiable Risk Factors for the Emergence of Ceftolozane-tazobactam Resistance

期刊

CLINICAL INFECTIOUS DISEASES
卷 73, 期 11, 页码 E4599-E4606

出版社

OXFORD UNIV PRESS INC
DOI: 10.1093/cid/ciaa1306

关键词

antimicrobial resistance; ceftazidime-avibactam; AmpC; DNA polymerase; PBP3

资金

  1. American Lung Association Research Grant

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The study investigates the emergence of ceftolozane-tazobactam (TOL-TAZ) resistance in patients infected with Pseudomonas aeruginosa. Results suggest that inadequate source control and lack of extended TOL-TAZ infusions may increase the risk of developing TOL-TAZ resistance.
Background. Ceftolozane-tazobactam (TOL-TAZ) affords broad coverage against Pseudomonas aeruginosa. Regrettably, TOL-TAZ resistance has been reported. We sought to identify modifiable risk factors that may reduce the emergence of TOL-TAZ resistance. Methods. Twenty-eight consecutive patients infected with carbapenem-resistant P. aeruginosa isolates susceptible to TOL-TAZ, treated with >= 72 hours of TOL-TAZ, and with P. aeruginosa isolates available both before and after TOL-TAZ exposure between January 2018 and December 2019 in Baltimore, Maryland, were included. Cases were defined as patients with at least a 4-fold increase in P. aeruginosa TOL-TAZ MICs after exposure to TOL-TAZ. Independent risk factors for the emergence of TOL-TAZ resistance comparing cases and controls were investigated using logistic regression. Whole genome sequencing of paired isolates was used to identify mechanisms of resistance that emerged during TOL-TAZ therapy. Results. Fourteen patients (50%) had P. aeruginosa isolates which developed at least a 4-fold increase in TOL-TAZ MICs(ie, cases). Cases were more likely to have inadequate source control (29% vs 0%, P = .04) and were less likely to receive TOL-TAZ as an extended 3-hour infusion (0% vs 29%; P = .04). Eighty-six percent of index isolates susceptible to ceftazidime-avibactam (CAZ-AVI) had subsequent P. aeruginosa isolates with high-level resistance to CAZ-AVI, after TOL-TAZ exposure and without any CAZ-AVI exposure. Common mutations identified in TOL-TAZ resistant isolates involved AmpC, a known binding site for both ceftolozane and ceftazidime, and DNA polymerase. Conclusions. Due to our small sample size, our results remain exploratory but forewarn of the potential emergence of TOL-TAZ resistance during therapy and suggest extending TOL-TAZ infusions may be protective. Larger studies are needed to investigate this association.

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