Piperacillin/tazobactam versus cefepime or carbapenems for cefoxitin-non-susceptibleEnterobacter cloacae,Klebsiella aerogenes,Citrobacter freundii,Serratia marcescensandMorganella morganiibacteraemia in immunocompromised patients

Author:

Lu Brian1ORCID,Wong Miranda1,Ha David23,Bounthavong Mark4,Banaei Niaz35,Deresinski Stanley23,Diep Calvin1

Affiliation:

1. Department of Pharmacy, Stanford Health Care , 300 Pasteur Drive, Stanford, CA 94305 , USA

2. Department of Quality, Patient Safety and Effectiveness, Stanford Health Care , Stanford, CA , USA

3. Division of Infectious Diseases and Geographic Medicine, Stanford University School of Medicine , Stanford, CA , USA

4. Division of Clinical Pharmacy, UCSD Skaggs School of Pharmacy & Pharmaceutical Sciences , La Jolla, CA , USA

5. Division of Clinical Pathology, Stanford University School of Medicine , Stanford, CA , USA

Abstract

AbstractBackgroundThe role of piperacillin/tazobactam for treatment of serious infections due to AmpC-producing organisms remains debatable, particularly in immunocompromised patients.MethodsThis was a retrospective cohort study in immunocompromised patients that investigated the effect of definitive treatment with either piperacillin/tazobactam versus cefepime or carbapenems for bacteraemia caused by cefoxitin-non-susceptible Enterobacterales. The primary endpoint was a composite of clinical and microbiological failure. A logistic regression model was constructed to assess the impact of definitive treatment choice on the primary endpoint.ResultsA total of 81 immunocompromised patients with blood cultures positive for cefoxitin-non-susceptible Enterobacterales were included for analysis. There was more microbiological failure in the piperacillin/tazobactam arm compared with the cefepime/carbapenem arm (11.4% versus 0.0%, P = 0.019). Definitive treatment with cefepime or a carbapenem was associated with a decreased odds of clinical or microbiological failure (OR 0.303, 95% CI 0.093–0.991, P = 0.048) when controlling for baseline characteristics.ConclusionsIn immunocompromised patients with bacteraemia due to cefoxitin-non-susceptible Enterobacterales, definitive treatment with piperacillin/tazobactam was associated with an increased risk of microbiological failure and higher odds of clinical or microbiological failure compared with cefepime or carbapenems.

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology,Microbiology (medical)

Reference26 articles.

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3. Molecular basis of AmpC hyperproduction in clinical isolates of Escherichia coli;Nelson;Antimicrob Agents Chemother,1999

4. Beyond susceptible and resistant. Part I: treatment of infections due to gram-negative organisms with inducible β-lactamases;MacDougall;J Pediatr Pharmacol Ther,2011

5. Beyond piperacillin-tazobactam: cefepime and AAI101 as a potent β-lactam−β-lactamase inhibitor combination;Papp-Wallace;Antimicrob Agents Chemother,2019

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