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915. Global 2018 Surveillance of Eravacycline Against Gram-positive Pathogens, Including Resistant Isolates
BACKGROUND: Eravacycline (ERV) is a fully-synthetic, fluorocycline antibacterial approved by the FDA and EMA for the treatment of complicated intra-abdominal infections (cIAI) in patients ≥18 years of age. The purpose of this study was to further monitor the in vitro activity of ERV against Gram-pos...
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/PMC7776539/ http://dx.doi.org/10.1093/ofid/ofaa439.1103 |
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author | Morgan, Steven Hwang, Sara Efimova, Ekaterina Hawser, Stephen Morrissey, Ian Lijfrock, Virgil |
author_facet | Morgan, Steven Hwang, Sara Efimova, Ekaterina Hawser, Stephen Morrissey, Ian Lijfrock, Virgil |
author_sort | Morgan, Steven |
collection | PubMed |
description | BACKGROUND: Eravacycline (ERV) is a fully-synthetic, fluorocycline antibacterial approved by the FDA and EMA for the treatment of complicated intra-abdominal infections (cIAI) in patients ≥18 years of age. The purpose of this study was to further monitor the in vitro activity of ERV against Gram-positive pathogens, such as Staphylococcus aureus (including methicillin-resistant S. aureus, MRSA), Enterococcus spp. (including vancomycin-resistant Enterococcus, VRE) and Streptococcus spp. METHODS: Isolates were collected globally during 2018 from various body sites. Minimum inhibitory concentrations (MICs) were determined by CLSI broth microdilution. Antibiotic susceptibility was determined using the most recent CLSI breakpoints (30(th) ed CLSI M100 document), except for ERV and tigecycline (TGC) where FDA breakpoints from 2018 and 2005, respectively, were applied. RESULTS: Summary MIC data for ERV and select comparators are shown in the Table. ERV MIC(50/90) for Enterococcus spp were 0.06/0.12 μg/mL and were not affected by the presence of vancomycin resistant mechanisms. The MIC(90) of ERV against VRE was 2-fold lower than TGC, at a value of 0.12 μg/mL. ERV MIC(90) values for methicillin-susceptible S. aureus (MSSA) was 0.12 μg/mL and for MRSA was 0.25 μg/mL. Generally, for all pathogens, ERV MIC(90) values were 2- to 4-fold lower than TGC. Table [Image: see text] CONCLUSION: ERV in vitro activity was demonstrated for clinically important Gram-positive pathogens, including resistant isolates. Overall, ERV demonstrated lower MIC(90) values than comparators for all organisms. This 2018 global surveillance highlights ERV’s utility against Gram-positive organisms and further underscores its role in cIAI, where these pathogens play a causative role. DISCLOSURES: Steven Morgan, PharMD, Tetraphase Pharmaceuticals (Employee) Sara Hwang, PharMD, Tetraphase Pharmaceuticals (Employee) Ekaterina Efimova, PharMD, Tetraphase Pharmaceuticals (Employee) Stephen Hawser, PhD, Tetraphase Pharmaceuticals (Scientific Research Study Investigator) Virgil Lijfrock, PharMD, Tetraphase (Employee) |
format | Online Article Text |
id | pubmed-7776539 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-77765392021-01-07 915. Global 2018 Surveillance of Eravacycline Against Gram-positive Pathogens, Including Resistant Isolates Morgan, Steven Hwang, Sara Efimova, Ekaterina Hawser, Stephen Morrissey, Ian Lijfrock, Virgil Open Forum Infect Dis Poster Abstracts BACKGROUND: Eravacycline (ERV) is a fully-synthetic, fluorocycline antibacterial approved by the FDA and EMA for the treatment of complicated intra-abdominal infections (cIAI) in patients ≥18 years of age. The purpose of this study was to further monitor the in vitro activity of ERV against Gram-positive pathogens, such as Staphylococcus aureus (including methicillin-resistant S. aureus, MRSA), Enterococcus spp. (including vancomycin-resistant Enterococcus, VRE) and Streptococcus spp. METHODS: Isolates were collected globally during 2018 from various body sites. Minimum inhibitory concentrations (MICs) were determined by CLSI broth microdilution. Antibiotic susceptibility was determined using the most recent CLSI breakpoints (30(th) ed CLSI M100 document), except for ERV and tigecycline (TGC) where FDA breakpoints from 2018 and 2005, respectively, were applied. RESULTS: Summary MIC data for ERV and select comparators are shown in the Table. ERV MIC(50/90) for Enterococcus spp were 0.06/0.12 μg/mL and were not affected by the presence of vancomycin resistant mechanisms. The MIC(90) of ERV against VRE was 2-fold lower than TGC, at a value of 0.12 μg/mL. ERV MIC(90) values for methicillin-susceptible S. aureus (MSSA) was 0.12 μg/mL and for MRSA was 0.25 μg/mL. Generally, for all pathogens, ERV MIC(90) values were 2- to 4-fold lower than TGC. Table [Image: see text] CONCLUSION: ERV in vitro activity was demonstrated for clinically important Gram-positive pathogens, including resistant isolates. Overall, ERV demonstrated lower MIC(90) values than comparators for all organisms. This 2018 global surveillance highlights ERV’s utility against Gram-positive organisms and further underscores its role in cIAI, where these pathogens play a causative role. DISCLOSURES: Steven Morgan, PharMD, Tetraphase Pharmaceuticals (Employee) Sara Hwang, PharMD, Tetraphase Pharmaceuticals (Employee) Ekaterina Efimova, PharMD, Tetraphase Pharmaceuticals (Employee) Stephen Hawser, PhD, Tetraphase Pharmaceuticals (Scientific Research Study Investigator) Virgil Lijfrock, PharMD, Tetraphase (Employee) Oxford University Press 2020-12-31 /pmc/articles/PMC7776539/ http://dx.doi.org/10.1093/ofid/ofaa439.1103 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 Morgan, Steven Hwang, Sara Efimova, Ekaterina Hawser, Stephen Morrissey, Ian Lijfrock, Virgil 915. Global 2018 Surveillance of Eravacycline Against Gram-positive Pathogens, Including Resistant Isolates |
title | 915. Global 2018 Surveillance of Eravacycline Against Gram-positive Pathogens, Including Resistant Isolates |
title_full | 915. Global 2018 Surveillance of Eravacycline Against Gram-positive Pathogens, Including Resistant Isolates |
title_fullStr | 915. Global 2018 Surveillance of Eravacycline Against Gram-positive Pathogens, Including Resistant Isolates |
title_full_unstemmed | 915. Global 2018 Surveillance of Eravacycline Against Gram-positive Pathogens, Including Resistant Isolates |
title_short | 915. Global 2018 Surveillance of Eravacycline Against Gram-positive Pathogens, Including Resistant Isolates |
title_sort | 915. global 2018 surveillance of eravacycline against gram-positive pathogens, including resistant isolates |
topic | Poster Abstracts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7776539/ http://dx.doi.org/10.1093/ofid/ofaa439.1103 |
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