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247. Evaluation of the Efficacy and Safety of Cefazolin in Non-Pneumococci Streptococcal Bacteremia

BACKGROUND: Among the large variation of streptococcal infections, recommended therapies are generally well-defined. There is a lack of efficacy data on alternative therapies, notably in phylogenetic groups that are less studied. The purpose of this study is to quantify the differences in clinical e...

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Autores principales: Wibisono, Arya, Rose, Dusten T T, Jaso, Theresa (Terry)
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10677406/
http://dx.doi.org/10.1093/ofid/ofad500.320
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author Wibisono, Arya
Rose, Dusten T T
Jaso, Theresa (Terry)
author_facet Wibisono, Arya
Rose, Dusten T T
Jaso, Theresa (Terry)
author_sort Wibisono, Arya
collection PubMed
description BACKGROUND: Among the large variation of streptococcal infections, recommended therapies are generally well-defined. There is a lack of efficacy data on alternative therapies, notably in phylogenetic groups that are less studied. The purpose of this study is to quantify the differences in clinical efficacy and safety between recommended antibiotics (penicillins and ceftriaxone) compared to cefazolin for uncomplicated non-pneumococci streptococcal bacteremia. METHODS: This is a multi-center, retrospective cohort study from January 2017 to January 2021. Patients were included if older than 18 years of age and had a non-pneumococci streptococcal isolate recovered on blood cultures. Patients were excluded if they had a polymicrobial bacteremia, diagnosed meningitis or endocarditis, received less than two days of a study drug, or received more than three days of a non-study drug. The primary outcome was treatment failure defined as: 30-day in-hospital all-cause mortality; or the alteration of targeted therapy after at least 48 hours of treatment for (1) concern of clinical failure based on progress notes in the electronic medical record or (2) an adverse drug reaction. Secondary outcomes included 90-day all-cause mortality, intensive care unit length of stay, hospital length of stay, C. difficile infection, adverse events, and 6-month infection related readmissions. [Figure: see text] RESULTS: A total of 230 patients were included: 177 in the penicillins/ceftriaxone group and 53 in the cefazolin group. Baseline demographics were balanced between the two groups in regard to age, sex, comorbidity score, infection severity, and infectious disease consultation. The most commonly identified pathogens were S. pyogenes (30.9%), S. agalactiae (26.5%), and S. mitis/oralis (11.7%). Analysis showed no significant difference between treatment failures with recommended antibiotics (6/177, 3.4%) and cefazolin (1/53, 1.9%), p=1.00. No differences were noted in secondary safety outcomes. [Figure: see text] [Figure: see text] [Figure: see text] CONCLUSION: Rates of treatment failure with cefazolin were not significantly different compared to recommended antibiotics in the treatment of uncomplicated non-pneumococci streptococcal bacteremia. Cefazolin may be a potential option for treatment in these infections. Further studies are warranted. DISCLOSURES: All Authors: No reported disclosures
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spelling pubmed-106774062023-11-27 247. Evaluation of the Efficacy and Safety of Cefazolin in Non-Pneumococci Streptococcal Bacteremia Wibisono, Arya Rose, Dusten T T Jaso, Theresa (Terry) Open Forum Infect Dis Abstract BACKGROUND: Among the large variation of streptococcal infections, recommended therapies are generally well-defined. There is a lack of efficacy data on alternative therapies, notably in phylogenetic groups that are less studied. The purpose of this study is to quantify the differences in clinical efficacy and safety between recommended antibiotics (penicillins and ceftriaxone) compared to cefazolin for uncomplicated non-pneumococci streptococcal bacteremia. METHODS: This is a multi-center, retrospective cohort study from January 2017 to January 2021. Patients were included if older than 18 years of age and had a non-pneumococci streptococcal isolate recovered on blood cultures. Patients were excluded if they had a polymicrobial bacteremia, diagnosed meningitis or endocarditis, received less than two days of a study drug, or received more than three days of a non-study drug. The primary outcome was treatment failure defined as: 30-day in-hospital all-cause mortality; or the alteration of targeted therapy after at least 48 hours of treatment for (1) concern of clinical failure based on progress notes in the electronic medical record or (2) an adverse drug reaction. Secondary outcomes included 90-day all-cause mortality, intensive care unit length of stay, hospital length of stay, C. difficile infection, adverse events, and 6-month infection related readmissions. [Figure: see text] RESULTS: A total of 230 patients were included: 177 in the penicillins/ceftriaxone group and 53 in the cefazolin group. Baseline demographics were balanced between the two groups in regard to age, sex, comorbidity score, infection severity, and infectious disease consultation. The most commonly identified pathogens were S. pyogenes (30.9%), S. agalactiae (26.5%), and S. mitis/oralis (11.7%). Analysis showed no significant difference between treatment failures with recommended antibiotics (6/177, 3.4%) and cefazolin (1/53, 1.9%), p=1.00. No differences were noted in secondary safety outcomes. [Figure: see text] [Figure: see text] [Figure: see text] CONCLUSION: Rates of treatment failure with cefazolin were not significantly different compared to recommended antibiotics in the treatment of uncomplicated non-pneumococci streptococcal bacteremia. Cefazolin may be a potential option for treatment in these infections. Further studies are warranted. DISCLOSURES: All Authors: No reported disclosures Oxford University Press 2023-11-27 /pmc/articles/PMC10677406/ http://dx.doi.org/10.1093/ofid/ofad500.320 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
Wibisono, Arya
Rose, Dusten T T
Jaso, Theresa (Terry)
247. Evaluation of the Efficacy and Safety of Cefazolin in Non-Pneumococci Streptococcal Bacteremia
title 247. Evaluation of the Efficacy and Safety of Cefazolin in Non-Pneumococci Streptococcal Bacteremia
title_full 247. Evaluation of the Efficacy and Safety of Cefazolin in Non-Pneumococci Streptococcal Bacteremia
title_fullStr 247. Evaluation of the Efficacy and Safety of Cefazolin in Non-Pneumococci Streptococcal Bacteremia
title_full_unstemmed 247. Evaluation of the Efficacy and Safety of Cefazolin in Non-Pneumococci Streptococcal Bacteremia
title_short 247. Evaluation of the Efficacy and Safety of Cefazolin in Non-Pneumococci Streptococcal Bacteremia
title_sort 247. evaluation of the efficacy and safety of cefazolin in non-pneumococci streptococcal bacteremia
topic Abstract
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10677406/
http://dx.doi.org/10.1093/ofid/ofad500.320
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