A Single-Center Evaluation of Extended Infusion Piperacillin/Tazobactam for Empiric Treatment in the Intensive Care

Kendall Tucker1, Molly Benning2, Keenan Ryan2

  • 1Oregon State University/Oregon Health & Science University, Portland, OR, USA.

Insights

Piperacillin/tazobactam extended infusion may not adequately treat Gram-negative infections in ICUs. Factors like dialysis and prior antibiotic use are linked to resistance, suggesting current dosing needs review for optimal patient care.

Area of Science:

  • Infectious Diseases
  • Critical Care Medicine
  • Pharmacology

Background:

  • Piperacillin/tazobactam extended infusion (PTZ EI) is a common empirical treatment in intensive care units (ICUs).
  • Gram-negative (GN) organisms with high piperacillin/tazobactam minimum inhibitory concentrations (MICs) indicate potential resistance.
  • Assessing PTZ EI appropriateness is crucial for effective empirical antimicrobial therapy in critically ill patients.

Purpose of the Study:

  • To evaluate the minimum inhibitory concentrations (MICs) of Gram-negative (GN) isolates from ICU patients.
  • To determine if the hospital's protocol for piperacillin/tazobactam (PTZ) 3.375 g extended infusion (EI) over 4 hours every 8 hours is appropriate for empirical use.
  • To identify patient-specific risk factors associated with elevated PTZ MICs in the ICU setting.

Main Methods:

  • Retrospective chart review of ICU patients admitted in 2017 with confirmed GN organisms from non-urinary sources.
  • Exclusion criteria included cystic fibrosis or cultures obtained more than 48 hours before ICU admission.
  • Data collected: demographics, GN organism, culture source, risk factors for resistance, susceptibility profiles, comorbidities, and creatinine clearance.

Main Results:

  • 231 patients were included; the most common organism was *Pseudomonas aeruginosa* (41%).
  • 28% of Gram-negative isolates exhibited piperacillin/tazobactam MICs >16/4 µg/mL, exceeding the susceptibility threshold.
  • Risk factors associated with elevated MICs included dialysis (P=.01), recent intravenous antibiotic use (P<.001), and wounds/trauma (P=.01).

Conclusions:

  • Current piperacillin/tazobactam extended infusion (3.375 g) dosing may not ensure adequate empirical coverage for all Gram-negative organisms in ICU patients.
  • Patients on dialysis, with a history of recent intravenous antibiotic exposure, or with wounds/trauma are at higher risk for infections with less susceptible organisms.
  • Re-evaluation of empirical PTZ EI regimens in ICUs is warranted to optimize treatment outcomes and combat antimicrobial resistance.

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