Association between piperacillin/tazobactam MIC and survival among hospitalized patients with Enterobacterales infections: retrospective cohort analysis of electronic health records from 161 US hospitals

Author:

Strich Jeffrey R1,Lawandi Alexander1ORCID,Warner Sarah1,Demirkale Cumhur Y1,Sarzynski Sadia1,Babiker Ahmed2ORCID,Dekker John P3,Kadri Sameer S1ORCID

Affiliation:

1. Critical Care Medicine Department, Clinical Center, National Institutes of Health , 10 Center Drive B10, 2C145, Bethesda, MD 20892 , USA

2. Department of Pathology and Laboratory Medicine, Emory University School of Medicine , Atlanta, GA , USA

3. Bacterial Pathogenesis and Antimicrobial Resistance Unit, Laboratory of Clinical Immunology and Microbiology, National Institute of Allergy and Infectious Diseases , Bethesda, MD , USA

Abstract

AbstractIntroductionA recent randomized trial has suggested an increased risk of mortality for ceftriaxone-non-susceptible Enterobacterales infections treated with piperacillin/tazobactam compared with meropenem despite MICs within the susceptible range.MethodsWe conducted a retrospective cohort study of clinical encounters within the Cerner Health Facts database to identify all encounters between 2001 and 2017 in which Enterobacterales infections were treated empirically with piperacillin/tazobactam and for which MICs to the drug were available. Multivariate regression analysis was performed to enable partitioning of MICs into discrete strata based on statistically significant difference in mortality risk.ResultsDuring the study period, 10 101 inpatient encounters were identified meeting inclusion criteria. The crude in-hospital mortality for the entire cohort was 16.5%. Partitioning analysis identified a breakpoint of ≤16/4 mg/L that dichotomized encounters into lower versus higher mortality risk strata in the primary cohort of overall infections. This finding persisted in sequentially granular subsets where specific MICs ≤8/4 mg/L were reported (in lieu of ranges) as well as in the high-reliability subset with bloodstream infections. A higher clinical breakpoint of ≥128/4 mg/L dichotomized encounters with respiratory tract infection. No breakpoint was identified when restricting to encounters with urinary tract infections, ICU admits or upon restricting analysis to encounters with ceftriaxone-resistant isolates.ConclusionsClinical data suggest improved outcomes when piperacillin/tazobactam is prescribed for Enterobacterales infections with an MIC of ≤16/4 mg/L compared with ≥32/4 mg/L.

Funder

Center for Drug Evaluation and Research of the US Food and Drug Administration

National Institutes of Health Clinical Center

National Institute of Allergy and Infectious Diseases

Publisher

Oxford University Press (OUP)

Subject

Microbiology (medical),Infectious Diseases,Immunology and Allergy,Microbiology,Immunology

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