Extended Infusion β-Lactams for the Treatment of Gram-Negative Bacteremia in Children

Author:

Zembles Tracy N.1,Kuhn Evelyn M.2,Thompson Nathan E.3,Mitchell Michelle L.3

Affiliation:

1. Department of Enterprise Safety (TNZ), Children's Wisconsin, Milwaukee, WI

2. Department of Business Intelligence and Data Warehousing (EMK), Children's Wisconsin, Milwaukee, WI

3. Department of Pediatrics (NET, MLM), Medical College of Wisconsin, Milwaukee, WI

Abstract

OBJECTIVE The pharmacokinetics of β-lactam antibiotics favor administration via an extended infusion. Although literature to support extended infusion β-lactams exists for adults, few data are available in pediatrics, especially among patients with bacteremia. The purpose of this study was to compare clinical outcomes between extended and standard infusions in children with Gram-negative bacteremia. METHODS This retrospective chart analysis included hospitalized patients ages 0 to 18 years who received at least 72 hours of cefepime, meropenem, or piperacillin-tazobactam between January 1, 2013 and July 30, 2021. Clinical outcomes included duration of antibiotic therapy, hospital length of stay, readmission within 30 days, all-cause mortality, time to blood culture clearance, and time to normalization of inflammatory markers. RESULTS A total of 124 patients (51 extended infusion, 73 standard infusion) met criteria for evaluation. Duration of antibiotic therapy was shorter in the extended infusion group (6.6 days versus 10.2 days; p = 0.01). There were no differences in hospital length of stay, readmission rates, all-cause mortality, time to normalization of inflammatory markers, or time to blood culture clearance. CONCLUSIONS Use of extended infusion β-lactam antibiotics in children with Gram-negative bacteremia was associated with shorter durations of therapy and should be the preferred method of administration when feasible.

Publisher

Pediatric Pharmacy Advocacy Group

Subject

Pharmacology (medical),Pediatrics, Perinatology and Child Health

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3. Antibiotic exposure as a risk factor for emergence of resistance: the influence of concentration;Gould,2002

4. Optimizing antibiotic pharmacodynamics for clinical practice;Connors;Pharm Anal Acta,2013

5. Prolonging beta-lactam infusion: a review of the rationale and evidence, and guidance for implementation;MacVane;Int J Antimicrob Agents,2014

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