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Outcomes of Intravenous Push versus Intermittent Infusion Administration of Cefepime in Critically Ill Patients
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, retrospecti...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10295171/ https://www.ncbi.nlm.nih.gov/pubmed/37370315 http://dx.doi.org/10.3390/antibiotics12060996 |
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author | Smith, Susan E. Halbig, Zachary Fox, Nicholas R. Bland, Christopher M. Branan, Trisha N. |
author_facet | Smith, Susan E. Halbig, Zachary Fox, Nicholas R. Bland, Christopher M. Branan, Trisha N. |
author_sort | Smith, Susan E. |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-10295171 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-102951712023-06-28 Outcomes of Intravenous Push versus Intermittent Infusion Administration of Cefepime in Critically Ill Patients Smith, Susan E. Halbig, Zachary Fox, Nicholas R. Bland, Christopher M. Branan, Trisha N. Antibiotics (Basel) Article 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. MDPI 2023-06-01 /pmc/articles/PMC10295171/ /pubmed/37370315 http://dx.doi.org/10.3390/antibiotics12060996 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Smith, Susan E. Halbig, Zachary Fox, Nicholas R. Bland, Christopher M. Branan, Trisha N. Outcomes of Intravenous Push versus Intermittent Infusion Administration of Cefepime in Critically Ill Patients |
title | Outcomes of Intravenous Push versus Intermittent Infusion Administration of Cefepime in Critically Ill Patients |
title_full | Outcomes of Intravenous Push versus Intermittent Infusion Administration of Cefepime in Critically Ill Patients |
title_fullStr | Outcomes of Intravenous Push versus Intermittent Infusion Administration of Cefepime in Critically Ill Patients |
title_full_unstemmed | Outcomes of Intravenous Push versus Intermittent Infusion Administration of Cefepime in Critically Ill Patients |
title_short | Outcomes of Intravenous Push versus Intermittent Infusion Administration of Cefepime in Critically Ill Patients |
title_sort | outcomes of intravenous push versus intermittent infusion administration of cefepime in critically ill patients |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10295171/ https://www.ncbi.nlm.nih.gov/pubmed/37370315 http://dx.doi.org/10.3390/antibiotics12060996 |
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