Outcomes of Intravenous Push versus Intermittent Infusion Administration of Cefepime in Critically Ill Patients

Author:

Smith Susan E.1ORCID,Halbig Zachary2ORCID,Fox Nicholas R.3,Bland Christopher M.4ORCID,Branan Trisha N.1ORCID

Affiliation:

1. Department of Clinical and Administrative Pharmacy, University of Georgia College of Pharmacy, Athens, GA 30602, USA

2. Department of Pharmacy, Piedmont Athens Regional, Athens, GA 30606, USA

3. Athens Pulmonary, Piedmont Athens Regional, Athens, GA 30606, USA

4. Department of Clinical and Administrative Pharmacy, University of Georgia College of Pharmacy, Savannah, GA 31405, USA

Abstract

The equivalence of intravenous push (IVP) and piggyback (IVPB) administration has not been evaluated in the critically ill population for most medications, but it is especially relevant for antibiotics, such as cefepime, that exhibit time-dependent bactericidal activity. A single center, retrospective, observational pre/post-protocol change study included critically ill adults who received cefepime as empiric therapy between August 2015 and 2021. The primary outcome was treatment failure, which was defined as a composite of escalation of antibiotic regimen or all-cause mortality. Secondary outcomes included adverse drug events, days of cefepime therapy, total days of antibiotic therapy, and ICU and hospital length of stay. Outcomes were compared using Chi-squared, Mann Whitney U, and binary logistic regression as appropriate. A total of 285 patients were included: 87 IVPB and 198 IVP. Treatment failure occurred in 18% (n = 16) of the IVPB group and 27% (n = 54) of the IVP group (p = 0.109). There were no significant differences in secondary outcomes. Longer duration of antibiotics (odds ratio [OR] 1.057, 95% confidence interval [CI] 1.013–1.103), SOFA score (OR 1.269, 95% CI 1.154–1.397) and IVP administration of cefepime (OR 2.370, 95% CI 1.143–4.914) were independently associated with treatment failure. Critically ill patients who received IVP cefepime were more likely to experience treatment failure in an adjusted analysis. The current practice of IVP cefepime should be reevaluated, as it may not provide similar clinical outcomes in the critically ill population.

Publisher

MDPI AG

Subject

Pharmacology (medical),Infectious Diseases,Microbiology (medical),General Pharmacology, Toxicology and Pharmaceutics,Biochemistry,Microbiology

Reference36 articles.

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2. Surviving sepsis campaign: International guidelines for management of sepsis and septic shock 2021;Evans;Intensive Care Med.,2021

3. Extended-Infusion Cefepime Reduces Mortality in Patients with Pseudomonas aeruginosa Infections;Bauer;Antimicrob. Agents Chemother.,2013

4. Saline Shortages—Many Causes, No Simple Solution;Fox;N. Engl. J. Med.,2018

5. (2023, May 31). ISMP Safe Practice Guidelines for Adult IV Push Medications. A Compilation of Safe Practices from the ISMP Adult I.V. Push Medication Safety Summit. Available online: https://www.ismp.org/sites/default/files/attachments/2017-11/ISMP97-Guidelines-071415-3.%20FINAL.pdf.

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