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2441. Outcomes of Patients With Vancomycin-Resistant Enterococcus Blood Stream Infections (BSI) Treated With Daptomycin
BACKGROUND: Reports of poor outcomes in patients (patients) infected with VRE strains with daptomycin (DAP) minimum inhibitory concentrations (MIC) near the susceptible breakpoint (<=4 μg/ml) are noted in the literature. We assessed the relationship of clinical outcomes for patients treated with...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254510/ http://dx.doi.org/10.1093/ofid/ofy210.2094 |
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author | Shimose, Luis A Rios, Maria X Bueno Athans, Vasilios Bass, Stephanie Li, Manshi Wang, Xiaofeng Otiso, Joshua Duggal, Abhijit Richter, Sandra S Kovacs, and Christopher |
author_facet | Shimose, Luis A Rios, Maria X Bueno Athans, Vasilios Bass, Stephanie Li, Manshi Wang, Xiaofeng Otiso, Joshua Duggal, Abhijit Richter, Sandra S Kovacs, and Christopher |
author_sort | Shimose, Luis A |
collection | PubMed |
description | BACKGROUND: Reports of poor outcomes in patients (patients) infected with VRE strains with daptomycin (DAP) minimum inhibitory concentrations (MIC) near the susceptible breakpoint (<=4 μg/ml) are noted in the literature. We assessed the relationship of clinical outcomes for patients treated with DAP to the initial MIC. METHODS: Retrospective study of consecutive adult patients with VRE BSI treated with DAP for at least 48 hours (November 2011–January 2015) in a tertiary hospital in Cleveland, OH. Patients were grouped based on the initial DAP MIC (MIC ≤ 2 μg/mL and MIC = 4 μg/mL) determined by a commercial broth microdilution method (Sensititre). Demographic and clinical data were extracted via EMR. Outcomes for all-cause mortality at 30 days (30-D mortality) and 90 days (90-D mortality), 30-day mortality attributed directly to VRE BSI (30-D mortality VRE) and microbiological failure (MF) were measured. MF was defined as duration of bacteremia ≥4 days after at least 48 hours of DAP use and achievement of source control when possible. We also assessed the impact of concomitant β-lactam use on MF. RESULTS: A total of 192 patients were identified. Baseline characteristics are shown in Table 1. Outcomes for MF, 30-D mortality VRE, 30-D mortality and 90-D mortality are shown in Table 2. Impact of concomitant β-lactam use on MF is shown in Figure 1. CONCLUSION: In this retrospective study, MF and mortality were not significantly higher for BSI caused by VRE with DAP MICs of 4 μg/ml, regardless of concomitant β-lactam use. [Image: see text] [Image: see text] [Image: see text] DISCLOSURES: S. S. Richter, bioMerieux: Grant Investigator, Research grant. BD Diagnostics: Grant Investigator, Research grant. Roche: Grant Investigator, Research grant. Hologic: Grant Investigator, Research grant. Diasorin: Grant Investigator, Research grant. Accelerate: Grant Investigator, Research grant. Biofire: Grant Investigator, Research grant. |
format | Online Article Text |
id | pubmed-6254510 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-62545102018-11-28 2441. Outcomes of Patients With Vancomycin-Resistant Enterococcus Blood Stream Infections (BSI) Treated With Daptomycin Shimose, Luis A Rios, Maria X Bueno Athans, Vasilios Bass, Stephanie Li, Manshi Wang, Xiaofeng Otiso, Joshua Duggal, Abhijit Richter, Sandra S Kovacs, and Christopher Open Forum Infect Dis Abstracts BACKGROUND: Reports of poor outcomes in patients (patients) infected with VRE strains with daptomycin (DAP) minimum inhibitory concentrations (MIC) near the susceptible breakpoint (<=4 μg/ml) are noted in the literature. We assessed the relationship of clinical outcomes for patients treated with DAP to the initial MIC. METHODS: Retrospective study of consecutive adult patients with VRE BSI treated with DAP for at least 48 hours (November 2011–January 2015) in a tertiary hospital in Cleveland, OH. Patients were grouped based on the initial DAP MIC (MIC ≤ 2 μg/mL and MIC = 4 μg/mL) determined by a commercial broth microdilution method (Sensititre). Demographic and clinical data were extracted via EMR. Outcomes for all-cause mortality at 30 days (30-D mortality) and 90 days (90-D mortality), 30-day mortality attributed directly to VRE BSI (30-D mortality VRE) and microbiological failure (MF) were measured. MF was defined as duration of bacteremia ≥4 days after at least 48 hours of DAP use and achievement of source control when possible. We also assessed the impact of concomitant β-lactam use on MF. RESULTS: A total of 192 patients were identified. Baseline characteristics are shown in Table 1. Outcomes for MF, 30-D mortality VRE, 30-D mortality and 90-D mortality are shown in Table 2. Impact of concomitant β-lactam use on MF is shown in Figure 1. CONCLUSION: In this retrospective study, MF and mortality were not significantly higher for BSI caused by VRE with DAP MICs of 4 μg/ml, regardless of concomitant β-lactam use. [Image: see text] [Image: see text] [Image: see text] DISCLOSURES: S. S. Richter, bioMerieux: Grant Investigator, Research grant. BD Diagnostics: Grant Investigator, Research grant. Roche: Grant Investigator, Research grant. Hologic: Grant Investigator, Research grant. Diasorin: Grant Investigator, Research grant. Accelerate: Grant Investigator, Research grant. Biofire: Grant Investigator, Research grant. Oxford University Press 2018-11-26 /pmc/articles/PMC6254510/ http://dx.doi.org/10.1093/ofid/ofy210.2094 Text en © The Author(s) 2018. 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 Shimose, Luis A Rios, Maria X Bueno Athans, Vasilios Bass, Stephanie Li, Manshi Wang, Xiaofeng Otiso, Joshua Duggal, Abhijit Richter, Sandra S Kovacs, and Christopher 2441. Outcomes of Patients With Vancomycin-Resistant Enterococcus Blood Stream Infections (BSI) Treated With Daptomycin |
title | 2441. Outcomes of Patients With Vancomycin-Resistant Enterococcus Blood Stream Infections (BSI) Treated With Daptomycin |
title_full | 2441. Outcomes of Patients With Vancomycin-Resistant Enterococcus Blood Stream Infections (BSI) Treated With Daptomycin |
title_fullStr | 2441. Outcomes of Patients With Vancomycin-Resistant Enterococcus Blood Stream Infections (BSI) Treated With Daptomycin |
title_full_unstemmed | 2441. Outcomes of Patients With Vancomycin-Resistant Enterococcus Blood Stream Infections (BSI) Treated With Daptomycin |
title_short | 2441. Outcomes of Patients With Vancomycin-Resistant Enterococcus Blood Stream Infections (BSI) Treated With Daptomycin |
title_sort | 2441. outcomes of patients with vancomycin-resistant enterococcus blood stream infections (bsi) treated with daptomycin |
topic | Abstracts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254510/ http://dx.doi.org/10.1093/ofid/ofy210.2094 |
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