Cargando…

258. A Comparison of Cefprozil and Fluoroquinolones for Gram-Negative Bacteremia

BACKGROUND: Beta lactams and fluoroquinolones (FQ) have been evaluated as step-down therapy options for Gram-negative bacteremia (GNB), but the preferred oral step-down antibiotic remains unclear. METHODS: This retrospective, non-inferiority, cohort study included adult patients who received oral st...

Descripción completa

Detalles Bibliográficos
Autores principales: Nolen, Rebecca C, Shor, Emily M, Lucido, Anthony, Hodges, Georgeanne, Metzger, Alex, Wu, Julia, Unverferth, James, Busch, Lauren
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7777937/
http://dx.doi.org/10.1093/ofid/ofaa439.302
_version_ 1783631020198723584
author Nolen, Rebecca C
Shor, Emily M
Lucido, Anthony
Hodges, Georgeanne
Metzger, Alex
Wu, Julia
Unverferth, James
Busch, Lauren
author_facet Nolen, Rebecca C
Shor, Emily M
Lucido, Anthony
Hodges, Georgeanne
Metzger, Alex
Wu, Julia
Unverferth, James
Busch, Lauren
author_sort Nolen, Rebecca C
collection PubMed
description BACKGROUND: Beta lactams and fluoroquinolones (FQ) have been evaluated as step-down therapy options for Gram-negative bacteremia (GNB), but the preferred oral step-down antibiotic remains unclear. METHODS: This retrospective, non-inferiority, cohort study included adult patients who received oral step-down therapy with cefprozil or FQ (ciprofloxacin, levofloxacin) for GNB caused by Proteus spp, Klebsiella spp, or E. coli at SSM Health St. Louis between 1/1/2016 and 2/28/2020. The primary outcome was treatment failure, defined as all-cause mortality or recurrent infection within 30 days of initial bacteremia episode. Assuming an 85% success rate, to achieve 80% power with a noninferiority margin of 15%, 71 patients were required in each arm. Multivariate logistic regression was used to evaluate factors for treatment failure. Factors evaluated for inclusion in the multivariate model were oral antibiotic, age >65 years, urinary source, Pitt bacteremia score >2, ICU admission, and IV antibiotics for >5 days prior to step-down. RESULTS: A total of 174 patients were included— 103 received cefprozil and 71 received FQ. Most baseline characteristics were similar between groups. Patients in the cefprozil group had more ICU admissions (21.3% vs. 7%; p=0.01), had a higher mean Pitt bacteremia score (1.6 vs 0.7; p< 0.001), and received a longer duration (days) of IV antibiotics prior to step-down therapy (5.2 vs 4.1; p< 0.001). Mean total treatment duration (days) was similar between groups (13.1 vs 13.2; p=0.75). Cefprozil 500 mg PO BID was administered in 84.5% of cefprozil patients. Treatment failure occurred in 3.88% (4/103) of cefprozil patients compared to 1.41% (1/71) of FQ patients (mean difference -2.47%; 95% CI -7.52% to 2.58%). The rate of adverse drug reactions was significantly higher in the FQ arm (2.9% vs 12.6%; p=0.016). In the univariate model, E. coli bacteremia, Pitt bacteremia score >2, and IV antibiotic duration >5 days met pre-defined criteria (p< 0.2) for inclusion in the multivariate model. In the multivariate analysis, these factors were not found to be significant. CONCLUSION: Cefprozil was non-inferior to FQ in regard to treatment failure. Cefprozil is an efficacious alternative to FQ for oral step-down treatment of GNB and was associated with significantly fewer adverse effects. DISCLOSURES: All Authors: No reported disclosures
format Online
Article
Text
id pubmed-7777937
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-77779372021-01-07 258. A Comparison of Cefprozil and Fluoroquinolones for Gram-Negative Bacteremia Nolen, Rebecca C Shor, Emily M Lucido, Anthony Hodges, Georgeanne Metzger, Alex Wu, Julia Unverferth, James Busch, Lauren Open Forum Infect Dis Poster Abstracts BACKGROUND: Beta lactams and fluoroquinolones (FQ) have been evaluated as step-down therapy options for Gram-negative bacteremia (GNB), but the preferred oral step-down antibiotic remains unclear. METHODS: This retrospective, non-inferiority, cohort study included adult patients who received oral step-down therapy with cefprozil or FQ (ciprofloxacin, levofloxacin) for GNB caused by Proteus spp, Klebsiella spp, or E. coli at SSM Health St. Louis between 1/1/2016 and 2/28/2020. The primary outcome was treatment failure, defined as all-cause mortality or recurrent infection within 30 days of initial bacteremia episode. Assuming an 85% success rate, to achieve 80% power with a noninferiority margin of 15%, 71 patients were required in each arm. Multivariate logistic regression was used to evaluate factors for treatment failure. Factors evaluated for inclusion in the multivariate model were oral antibiotic, age >65 years, urinary source, Pitt bacteremia score >2, ICU admission, and IV antibiotics for >5 days prior to step-down. RESULTS: A total of 174 patients were included— 103 received cefprozil and 71 received FQ. Most baseline characteristics were similar between groups. Patients in the cefprozil group had more ICU admissions (21.3% vs. 7%; p=0.01), had a higher mean Pitt bacteremia score (1.6 vs 0.7; p< 0.001), and received a longer duration (days) of IV antibiotics prior to step-down therapy (5.2 vs 4.1; p< 0.001). Mean total treatment duration (days) was similar between groups (13.1 vs 13.2; p=0.75). Cefprozil 500 mg PO BID was administered in 84.5% of cefprozil patients. Treatment failure occurred in 3.88% (4/103) of cefprozil patients compared to 1.41% (1/71) of FQ patients (mean difference -2.47%; 95% CI -7.52% to 2.58%). The rate of adverse drug reactions was significantly higher in the FQ arm (2.9% vs 12.6%; p=0.016). In the univariate model, E. coli bacteremia, Pitt bacteremia score >2, and IV antibiotic duration >5 days met pre-defined criteria (p< 0.2) for inclusion in the multivariate model. In the multivariate analysis, these factors were not found to be significant. CONCLUSION: Cefprozil was non-inferior to FQ in regard to treatment failure. Cefprozil is an efficacious alternative to FQ for oral step-down treatment of GNB and was associated with significantly fewer adverse effects. DISCLOSURES: All Authors: No reported disclosures Oxford University Press 2020-12-31 /pmc/articles/PMC7777937/ http://dx.doi.org/10.1093/ofid/ofaa439.302 Text en © The Author 2020. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Poster Abstracts
Nolen, Rebecca C
Shor, Emily M
Lucido, Anthony
Hodges, Georgeanne
Metzger, Alex
Wu, Julia
Unverferth, James
Busch, Lauren
258. A Comparison of Cefprozil and Fluoroquinolones for Gram-Negative Bacteremia
title 258. A Comparison of Cefprozil and Fluoroquinolones for Gram-Negative Bacteremia
title_full 258. A Comparison of Cefprozil and Fluoroquinolones for Gram-Negative Bacteremia
title_fullStr 258. A Comparison of Cefprozil and Fluoroquinolones for Gram-Negative Bacteremia
title_full_unstemmed 258. A Comparison of Cefprozil and Fluoroquinolones for Gram-Negative Bacteremia
title_short 258. A Comparison of Cefprozil and Fluoroquinolones for Gram-Negative Bacteremia
title_sort 258. a comparison of cefprozil and fluoroquinolones for gram-negative bacteremia
topic Poster Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7777937/
http://dx.doi.org/10.1093/ofid/ofaa439.302
work_keys_str_mv AT nolenrebeccac 258acomparisonofcefprozilandfluoroquinolonesforgramnegativebacteremia
AT shoremilym 258acomparisonofcefprozilandfluoroquinolonesforgramnegativebacteremia
AT lucidoanthony 258acomparisonofcefprozilandfluoroquinolonesforgramnegativebacteremia
AT hodgesgeorgeanne 258acomparisonofcefprozilandfluoroquinolonesforgramnegativebacteremia
AT metzgeralex 258acomparisonofcefprozilandfluoroquinolonesforgramnegativebacteremia
AT wujulia 258acomparisonofcefprozilandfluoroquinolonesforgramnegativebacteremia
AT unverferthjames 258acomparisonofcefprozilandfluoroquinolonesforgramnegativebacteremia
AT buschlauren 258acomparisonofcefprozilandfluoroquinolonesforgramnegativebacteremia