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2266. Management of Ertapenem-Resistant, Meropenem-Susceptible Enterobacteriaceae

BACKGROUND: Carbapenemases are the most frequent mechanism of carbapenem resistance in Enterobacteriaceae. However, alternative mechanisms such as loss of porin channels or up-regulation of efflux pumps can cause intermediate- to high-level resistance to ertapenem (ERTA) and possibly reduced suscept...

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Autores principales: Srinivas, Pavithra, Wu, Janet, Neuner, Elizabeth A, Pallotta, Andrea, Richter, Sandra S, Tsigrelis, Constantine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6810591/
http://dx.doi.org/10.1093/ofid/ofz360.1944
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author Srinivas, Pavithra
Wu, Janet
Neuner, Elizabeth A
Pallotta, Andrea
Richter, Sandra S
Tsigrelis, Constantine
author_facet Srinivas, Pavithra
Wu, Janet
Neuner, Elizabeth A
Pallotta, Andrea
Richter, Sandra S
Tsigrelis, Constantine
author_sort Srinivas, Pavithra
collection PubMed
description BACKGROUND: Carbapenemases are the most frequent mechanism of carbapenem resistance in Enterobacteriaceae. However, alternative mechanisms such as loss of porin channels or up-regulation of efflux pumps can cause intermediate- to high-level resistance to ertapenem (ERTA) and possibly reduced susceptibilities to meropenem (MERO) leading to discordant phenotypic profiles. Clinical implications of discordant carbapenem susceptibilities and optimal therapy options are yet unknown. We sought to describe our experience with carbapenem-discordant Enterobacteriaceae (CDE). METHODS: Descriptive study of hospitalized adult patients with a CDE positive culture from December 1/16 - December 1/18. Discordance was defined as Enterobacteriaceae with an ERTA-resistant and MERO-susceptible phenotype. Primary objective was to describe antibiotic use patterns for CDE infections. Secondary outcomes included infectious diseases (ID) involvement and clinical outcomes. Clinical failure was defined as a composite of in-hospital mortality, switch of definitive therapy due to clinical worsening, re-hospitalization within 30 days for re-infection, or failure to achieve blood culture clearance for ≥7 days. RESULTS: A total of 55 patients with CDE were identified. Most common organisms were Enterobacter cloacae complex (72%) and Klebsiella pneumoniae (9%). Of 21 isolates tested, 1 (4.8%) was positive for a carbapenemase. Mean age of patients was 61 ± 16 years, 51% were admitted to a medicine service, and 18% were immunocompromised. ID was involved in 82% of CDE cases. Most common sites were urine (33%), wound/tissue (27%), and respiratory (18%). 43/55 (78%) patients were treated – 17/43 (40%) with MERO, 14/43 (33%) with fluoroquinolones. Ceftazidime/avibactam and tigecycline were used in 4 (9%) patients each. Combination therapy was used in 8 (19%) patients, most commonly with MERO or tigecycline. Clinical failure occurred in 21/43 (49%) patients – 8/43 (19%) were receiving MERO-based therapy, 13/43 (30%) were receiving a non-MERO-based therapy. CONCLUSION: Discordance between ERTA and MERO susceptibility was more common in Enterobacter spp. Majority of isolates tested negative for a carbapenemase. MERO and fluoroquinolones were the most frequently used antibiotics for treatment of CDE infections. DISCLOSURES: All authors: No reported disclosures.
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spelling pubmed-68105912019-10-28 2266. Management of Ertapenem-Resistant, Meropenem-Susceptible Enterobacteriaceae Srinivas, Pavithra Wu, Janet Neuner, Elizabeth A Pallotta, Andrea Richter, Sandra S Tsigrelis, Constantine Open Forum Infect Dis Abstracts BACKGROUND: Carbapenemases are the most frequent mechanism of carbapenem resistance in Enterobacteriaceae. However, alternative mechanisms such as loss of porin channels or up-regulation of efflux pumps can cause intermediate- to high-level resistance to ertapenem (ERTA) and possibly reduced susceptibilities to meropenem (MERO) leading to discordant phenotypic profiles. Clinical implications of discordant carbapenem susceptibilities and optimal therapy options are yet unknown. We sought to describe our experience with carbapenem-discordant Enterobacteriaceae (CDE). METHODS: Descriptive study of hospitalized adult patients with a CDE positive culture from December 1/16 - December 1/18. Discordance was defined as Enterobacteriaceae with an ERTA-resistant and MERO-susceptible phenotype. Primary objective was to describe antibiotic use patterns for CDE infections. Secondary outcomes included infectious diseases (ID) involvement and clinical outcomes. Clinical failure was defined as a composite of in-hospital mortality, switch of definitive therapy due to clinical worsening, re-hospitalization within 30 days for re-infection, or failure to achieve blood culture clearance for ≥7 days. RESULTS: A total of 55 patients with CDE were identified. Most common organisms were Enterobacter cloacae complex (72%) and Klebsiella pneumoniae (9%). Of 21 isolates tested, 1 (4.8%) was positive for a carbapenemase. Mean age of patients was 61 ± 16 years, 51% were admitted to a medicine service, and 18% were immunocompromised. ID was involved in 82% of CDE cases. Most common sites were urine (33%), wound/tissue (27%), and respiratory (18%). 43/55 (78%) patients were treated – 17/43 (40%) with MERO, 14/43 (33%) with fluoroquinolones. Ceftazidime/avibactam and tigecycline were used in 4 (9%) patients each. Combination therapy was used in 8 (19%) patients, most commonly with MERO or tigecycline. Clinical failure occurred in 21/43 (49%) patients – 8/43 (19%) were receiving MERO-based therapy, 13/43 (30%) were receiving a non-MERO-based therapy. CONCLUSION: Discordance between ERTA and MERO susceptibility was more common in Enterobacter spp. Majority of isolates tested negative for a carbapenemase. MERO and fluoroquinolones were the most frequently used antibiotics for treatment of CDE infections. DISCLOSURES: All authors: No reported disclosures. Oxford University Press 2019-10-23 /pmc/articles/PMC6810591/ http://dx.doi.org/10.1093/ofid/ofz360.1944 Text en © The Author(s) 2019. 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 Abstracts
Srinivas, Pavithra
Wu, Janet
Neuner, Elizabeth A
Pallotta, Andrea
Richter, Sandra S
Tsigrelis, Constantine
2266. Management of Ertapenem-Resistant, Meropenem-Susceptible Enterobacteriaceae
title 2266. Management of Ertapenem-Resistant, Meropenem-Susceptible Enterobacteriaceae
title_full 2266. Management of Ertapenem-Resistant, Meropenem-Susceptible Enterobacteriaceae
title_fullStr 2266. Management of Ertapenem-Resistant, Meropenem-Susceptible Enterobacteriaceae
title_full_unstemmed 2266. Management of Ertapenem-Resistant, Meropenem-Susceptible Enterobacteriaceae
title_short 2266. Management of Ertapenem-Resistant, Meropenem-Susceptible Enterobacteriaceae
title_sort 2266. management of ertapenem-resistant, meropenem-susceptible enterobacteriaceae
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6810591/
http://dx.doi.org/10.1093/ofid/ofz360.1944
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