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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7777937/ http://dx.doi.org/10.1093/ofid/ofaa439.302 |
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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 |
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