Abstract

Pseudomonas aeruginosa remains an important pathogen. Our purpose was to determine the minimum inhibitory con-centration (MIC) and pharmacodynamic (PD) parameters predicting a positive response to therapy with piperacil-lin-tazobactam. Medical records were retrospectively reviewed at 3 centers. Data were recorded to assess age, type of disease, renal function, weight (body mass), MIC, antimicrobial treatment, and clinical outcome. Success was response to piperacillin-tazobactam alone, or in combination with another active agent; failure was lack of response. Of 78 eva-luable patients, 63 responded (7 UTI; 56 non-UTI) and 15 did not; 26 responding received combination therapy and 37 monotherapy. Piperacillin-tazobactam treatment was successful in 53 of 63 of non-UTI disease with a MIC of ≤64/4 μg/mL, but in only 3 of 7 with a MIC of >64/4 μg/mL (P = 0.023); overall 9 of 10 infections by strains with MICs = 32 - 64 μg/mL had a successful outcome. Piperacillin estimated time above MIC at 20% separated those responding from those that did not (P = 0.019).

Highlights

  • The global plague of antibiotic resistant infections is recognized as a serious threat to world-wide healthcare [1]

  • Our purpose was to determine the minimum inhibitory concentration (MIC) and pharmacodynamic (PD) parameters predicting a positive response to therapy with piperacillin-tazobactam

  • The purpose of this study was to collect data that would determine what susceptibility breakpoint reliably predicts clinical success when piperacillin-tazobactam is used for therapy of P. aeruginosa infection at adequate doses and what pharmacodynamic parameter(s) can guide in predicting human clinical response

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Summary

Introduction

The global plague of antibiotic resistant infections is recognized as a serious threat to world-wide healthcare [1]. This has been accompanied by a steady decline in the research and development of new antimicrobial agents to deal with the challenge. One of the key pathogen groups included in this threat are multidrug-resistant, increasingly pan-resistant, Gram-negative bacilli [1,2]. In this group is Pseudomonas aeruginosa, which remains an important pathogen that is steadily becoming more resistant to antimicrobial agents [3,4]. Therapy of serious infection with P. aeruginosa has been accomplished with a combination of agents owing to the frequent resistance seen in this pathogen [5]

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