Cargando…

196. Does Cefepime Provide an Advantage over Ceftriaxone in the Treatment of Bloodstream Infections due to Escherichia coli, Klebsiella pneumoniae group, Klebsiella oxytoca, and Proteus spp. if CTX-M is not Detected by Rapid Molecular Testing?

BACKGROUND: The BIOFIRE® Blood Culture Identification 2 (BCID2) Panel (bioMérieux) allows for rapid detection of pathogens and antibiotic resistance genes in bloodstream infections (BSIs), including CTX-M, an Extended Spectrum Beta-Lactamase. Atrium Health’s treatment algorithm recommends cefepime (...

Descripción completa

Detalles Bibliográficos
Autores principales: Lynn Hammer, Katie, Hamm, Alyssa, Welch, Stephanie N, Smith, Jordan R, Ann Medaris, Leigh, Boger, Michael S, Williamson, Julie E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10677336/
http://dx.doi.org/10.1093/ofid/ofad500.269
_version_ 1785150105532235776
author Lynn Hammer, Katie
Hamm, Alyssa
Welch, Stephanie N
Smith, Jordan R
Ann Medaris, Leigh
Boger, Michael S
Boger, Michael S
Williamson, Julie E
author_facet Lynn Hammer, Katie
Hamm, Alyssa
Welch, Stephanie N
Smith, Jordan R
Ann Medaris, Leigh
Boger, Michael S
Boger, Michael S
Williamson, Julie E
author_sort Lynn Hammer, Katie
collection PubMed
description BACKGROUND: The BIOFIRE® Blood Culture Identification 2 (BCID2) Panel (bioMérieux) allows for rapid detection of pathogens and antibiotic resistance genes in bloodstream infections (BSIs), including CTX-M, an Extended Spectrum Beta-Lactamase. Atrium Health’s treatment algorithm recommends cefepime (FEP) over ceftriaxone (CRO) for BSI due to non-CTX-M Escherichia coli, Klebsiella pneumoniae group, Klebsiella oxytoca, or Proteus spp. in critically ill patients. It is unclear if use of FEP improves outcomes over CRO in this setting. METHODS: This was a multisite, retrospective cohort study of adults with BSI due to E. coli, K. pneumoniae group, K. oxytoca, and Proteus spp. without CTX-M detected by BCID2 from April 4, 2022 – February 12, 2023. The primary outcome was a composite of in-hospital mortality and length of stay (LOS) more than 14 days in patients who received FEP vs CRO. Secondary outcomes included in-hospital mortality, hospital LOS, intensive care unit (ICU) LOS, rates of mechanical ventilation, and rates of CRO and FEP resistance. RESULTS: Three hundred patients were enrolled: 150 in each group. Patients in the FEP group were more severely ill at baseline by ICU status and PITT bacteremia score and were less likely to have a urinary source of BSI (Table 1). The composite primary outcome of in-hospital mortality or extended LOS occurred in 54/150 (36%) in the FEP group vs 24/150 (16%) in the CRO group; (p < 0.001). In-hospital mortality, hospital LOS, rates of mechanical ventilation and CRO resistance were higher in the FEP 5/158 (3%) vs. 2/150 (1%) in the CRO group. ICU LOS, in-hospital mortality and rates of FEP resistance were similar (Figures 1 and 2). Of note, of the 7/308 isolates with CRO resistance there was no in-hospital mortality or extended LOS in the CRO group and 5/7 were Proteus spp. There was no FEP resistance. [Figure: see text] [Figure: see text] [Figure: see text] CONCLUSION: Though CRO resistance was relatively low, it was most common among Proteus spp. Treatment with FEP was not associated with improved clinical or microbiological outcomes overall compared to CRO. These results highlight potential overuse of FEP in BSIs due to E.coli, K. pneumoniae group, or K. oxytoca and may have implications on the selection of empiric therapy. DISCLOSURES: All Authors: No reported disclosures
format Online
Article
Text
id pubmed-10677336
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-106773362023-11-27 196. Does Cefepime Provide an Advantage over Ceftriaxone in the Treatment of Bloodstream Infections due to Escherichia coli, Klebsiella pneumoniae group, Klebsiella oxytoca, and Proteus spp. if CTX-M is not Detected by Rapid Molecular Testing? Lynn Hammer, Katie Hamm, Alyssa Welch, Stephanie N Smith, Jordan R Ann Medaris, Leigh Boger, Michael S Boger, Michael S Williamson, Julie E Open Forum Infect Dis Abstract BACKGROUND: The BIOFIRE® Blood Culture Identification 2 (BCID2) Panel (bioMérieux) allows for rapid detection of pathogens and antibiotic resistance genes in bloodstream infections (BSIs), including CTX-M, an Extended Spectrum Beta-Lactamase. Atrium Health’s treatment algorithm recommends cefepime (FEP) over ceftriaxone (CRO) for BSI due to non-CTX-M Escherichia coli, Klebsiella pneumoniae group, Klebsiella oxytoca, or Proteus spp. in critically ill patients. It is unclear if use of FEP improves outcomes over CRO in this setting. METHODS: This was a multisite, retrospective cohort study of adults with BSI due to E. coli, K. pneumoniae group, K. oxytoca, and Proteus spp. without CTX-M detected by BCID2 from April 4, 2022 – February 12, 2023. The primary outcome was a composite of in-hospital mortality and length of stay (LOS) more than 14 days in patients who received FEP vs CRO. Secondary outcomes included in-hospital mortality, hospital LOS, intensive care unit (ICU) LOS, rates of mechanical ventilation, and rates of CRO and FEP resistance. RESULTS: Three hundred patients were enrolled: 150 in each group. Patients in the FEP group were more severely ill at baseline by ICU status and PITT bacteremia score and were less likely to have a urinary source of BSI (Table 1). The composite primary outcome of in-hospital mortality or extended LOS occurred in 54/150 (36%) in the FEP group vs 24/150 (16%) in the CRO group; (p < 0.001). In-hospital mortality, hospital LOS, rates of mechanical ventilation and CRO resistance were higher in the FEP 5/158 (3%) vs. 2/150 (1%) in the CRO group. ICU LOS, in-hospital mortality and rates of FEP resistance were similar (Figures 1 and 2). Of note, of the 7/308 isolates with CRO resistance there was no in-hospital mortality or extended LOS in the CRO group and 5/7 were Proteus spp. There was no FEP resistance. [Figure: see text] [Figure: see text] [Figure: see text] CONCLUSION: Though CRO resistance was relatively low, it was most common among Proteus spp. Treatment with FEP was not associated with improved clinical or microbiological outcomes overall compared to CRO. These results highlight potential overuse of FEP in BSIs due to E.coli, K. pneumoniae group, or K. oxytoca and may have implications on the selection of empiric therapy. DISCLOSURES: All Authors: No reported disclosures Oxford University Press 2023-11-27 /pmc/articles/PMC10677336/ http://dx.doi.org/10.1093/ofid/ofad500.269 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Abstract
Lynn Hammer, Katie
Hamm, Alyssa
Welch, Stephanie N
Smith, Jordan R
Ann Medaris, Leigh
Boger, Michael S
Boger, Michael S
Williamson, Julie E
196. Does Cefepime Provide an Advantage over Ceftriaxone in the Treatment of Bloodstream Infections due to Escherichia coli, Klebsiella pneumoniae group, Klebsiella oxytoca, and Proteus spp. if CTX-M is not Detected by Rapid Molecular Testing?
title 196. Does Cefepime Provide an Advantage over Ceftriaxone in the Treatment of Bloodstream Infections due to Escherichia coli, Klebsiella pneumoniae group, Klebsiella oxytoca, and Proteus spp. if CTX-M is not Detected by Rapid Molecular Testing?
title_full 196. Does Cefepime Provide an Advantage over Ceftriaxone in the Treatment of Bloodstream Infections due to Escherichia coli, Klebsiella pneumoniae group, Klebsiella oxytoca, and Proteus spp. if CTX-M is not Detected by Rapid Molecular Testing?
title_fullStr 196. Does Cefepime Provide an Advantage over Ceftriaxone in the Treatment of Bloodstream Infections due to Escherichia coli, Klebsiella pneumoniae group, Klebsiella oxytoca, and Proteus spp. if CTX-M is not Detected by Rapid Molecular Testing?
title_full_unstemmed 196. Does Cefepime Provide an Advantage over Ceftriaxone in the Treatment of Bloodstream Infections due to Escherichia coli, Klebsiella pneumoniae group, Klebsiella oxytoca, and Proteus spp. if CTX-M is not Detected by Rapid Molecular Testing?
title_short 196. Does Cefepime Provide an Advantage over Ceftriaxone in the Treatment of Bloodstream Infections due to Escherichia coli, Klebsiella pneumoniae group, Klebsiella oxytoca, and Proteus spp. if CTX-M is not Detected by Rapid Molecular Testing?
title_sort 196. does cefepime provide an advantage over ceftriaxone in the treatment of bloodstream infections due to escherichia coli, klebsiella pneumoniae group, klebsiella oxytoca, and proteus spp. if ctx-m is not detected by rapid molecular testing?
topic Abstract
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10677336/
http://dx.doi.org/10.1093/ofid/ofad500.269
work_keys_str_mv AT lynnhammerkatie 196doescefepimeprovideanadvantageoverceftriaxoneinthetreatmentofbloodstreaminfectionsduetoescherichiacoliklebsiellapneumoniaegroupklebsiellaoxytocaandproteussppifctxmisnotdetectedbyrapidmoleculartesting
AT hammalyssa 196doescefepimeprovideanadvantageoverceftriaxoneinthetreatmentofbloodstreaminfectionsduetoescherichiacoliklebsiellapneumoniaegroupklebsiellaoxytocaandproteussppifctxmisnotdetectedbyrapidmoleculartesting
AT welchstephanien 196doescefepimeprovideanadvantageoverceftriaxoneinthetreatmentofbloodstreaminfectionsduetoescherichiacoliklebsiellapneumoniaegroupklebsiellaoxytocaandproteussppifctxmisnotdetectedbyrapidmoleculartesting
AT smithjordanr 196doescefepimeprovideanadvantageoverceftriaxoneinthetreatmentofbloodstreaminfectionsduetoescherichiacoliklebsiellapneumoniaegroupklebsiellaoxytocaandproteussppifctxmisnotdetectedbyrapidmoleculartesting
AT annmedarisleigh 196doescefepimeprovideanadvantageoverceftriaxoneinthetreatmentofbloodstreaminfectionsduetoescherichiacoliklebsiellapneumoniaegroupklebsiellaoxytocaandproteussppifctxmisnotdetectedbyrapidmoleculartesting
AT bogermichaels 196doescefepimeprovideanadvantageoverceftriaxoneinthetreatmentofbloodstreaminfectionsduetoescherichiacoliklebsiellapneumoniaegroupklebsiellaoxytocaandproteussppifctxmisnotdetectedbyrapidmoleculartesting
AT bogermichaels 196doescefepimeprovideanadvantageoverceftriaxoneinthetreatmentofbloodstreaminfectionsduetoescherichiacoliklebsiellapneumoniaegroupklebsiellaoxytocaandproteussppifctxmisnotdetectedbyrapidmoleculartesting
AT williamsonjuliee 196doescefepimeprovideanadvantageoverceftriaxoneinthetreatmentofbloodstreaminfectionsduetoescherichiacoliklebsiellapneumoniaegroupklebsiellaoxytocaandproteussppifctxmisnotdetectedbyrapidmoleculartesting