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2163. Risk Factors for Carbapenem-Resistant Gram-Negative Bloodstream Infections (BSI) in U.S. Hospitals (2010–2015)

BACKGROUND: Carbapenem-resistant (CR) Gram-negative (GN) infections are associated with higher mortality and extended hospital stays. Time to effective antibiotic treatment is important for patient survival. Classifying the risk factors for CR GN BSI before identification and susceptibility results...

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Autores principales: Cai, Bin, Echols, Roger, Rudin, Deborah, Morgan, Gareth, Nagata, Tsutae
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253812/
http://dx.doi.org/10.1093/ofid/ofy210.1819
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author Cai, Bin
Echols, Roger
Rudin, Deborah
Morgan, Gareth
Nagata, Tsutae
author_facet Cai, Bin
Echols, Roger
Rudin, Deborah
Morgan, Gareth
Nagata, Tsutae
author_sort Cai, Bin
collection PubMed
description BACKGROUND: Carbapenem-resistant (CR) Gram-negative (GN) infections are associated with higher mortality and extended hospital stays. Time to effective antibiotic treatment is important for patient survival. Classifying the risk factors for CR GN BSI before identification and susceptibility results are known is critical; this study explores the risk factors associated with CR GN BSI in U.S. hospitals. METHODS: BSI caused by 11 of the most common GN pathogens were identified from 181 acute care hospitals that contributed microbiology and susceptibility test data to the Premier Healthcare Database 2010–2015. We used univariate analyses to select potential risk factors and a multivariate logistic regression model to predict CR BSI with these risk factors. RESULTS: Among 46,199 patients with GN BSI, 1,592 (3.6%) had CR pathogens. From univariate analyses, the significant factors (P-value <0.05) when comparing CR vs. carbapenem susceptible (CS) infections were age, race, gender, geographic location, admission source, Charlson Comorbidity Index, having BSI while in the ICU or after having stayed in the ICU, and index culture day. Adjusted odds ratios (OR) from multiple logistic regression are shown below. CONCLUSION: Patients with CR GN BSIs were more likely to be of a younger age group, transferred from a health care facility, stayed in ICU, and had positive BSI culture more than 48 hours after admission. Risk of CR BSI increased for patients with congestive heart failure, peripheral vascular disease, dementia, renal disease, and any malignancy. DISCLOSURES: All authors: No reported disclosures.
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spelling pubmed-62538122018-11-28 2163. Risk Factors for Carbapenem-Resistant Gram-Negative Bloodstream Infections (BSI) in U.S. Hospitals (2010–2015) Cai, Bin Echols, Roger Rudin, Deborah Morgan, Gareth Nagata, Tsutae Open Forum Infect Dis Abstracts BACKGROUND: Carbapenem-resistant (CR) Gram-negative (GN) infections are associated with higher mortality and extended hospital stays. Time to effective antibiotic treatment is important for patient survival. Classifying the risk factors for CR GN BSI before identification and susceptibility results are known is critical; this study explores the risk factors associated with CR GN BSI in U.S. hospitals. METHODS: BSI caused by 11 of the most common GN pathogens were identified from 181 acute care hospitals that contributed microbiology and susceptibility test data to the Premier Healthcare Database 2010–2015. We used univariate analyses to select potential risk factors and a multivariate logistic regression model to predict CR BSI with these risk factors. RESULTS: Among 46,199 patients with GN BSI, 1,592 (3.6%) had CR pathogens. From univariate analyses, the significant factors (P-value <0.05) when comparing CR vs. carbapenem susceptible (CS) infections were age, race, gender, geographic location, admission source, Charlson Comorbidity Index, having BSI while in the ICU or after having stayed in the ICU, and index culture day. Adjusted odds ratios (OR) from multiple logistic regression are shown below. CONCLUSION: Patients with CR GN BSIs were more likely to be of a younger age group, transferred from a health care facility, stayed in ICU, and had positive BSI culture more than 48 hours after admission. Risk of CR BSI increased for patients with congestive heart failure, peripheral vascular disease, dementia, renal disease, and any malignancy. DISCLOSURES: All authors: No reported disclosures. Oxford University Press 2018-11-26 /pmc/articles/PMC6253812/ http://dx.doi.org/10.1093/ofid/ofy210.1819 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
Cai, Bin
Echols, Roger
Rudin, Deborah
Morgan, Gareth
Nagata, Tsutae
2163. Risk Factors for Carbapenem-Resistant Gram-Negative Bloodstream Infections (BSI) in U.S. Hospitals (2010–2015)
title 2163. Risk Factors for Carbapenem-Resistant Gram-Negative Bloodstream Infections (BSI) in U.S. Hospitals (2010–2015)
title_full 2163. Risk Factors for Carbapenem-Resistant Gram-Negative Bloodstream Infections (BSI) in U.S. Hospitals (2010–2015)
title_fullStr 2163. Risk Factors for Carbapenem-Resistant Gram-Negative Bloodstream Infections (BSI) in U.S. Hospitals (2010–2015)
title_full_unstemmed 2163. Risk Factors for Carbapenem-Resistant Gram-Negative Bloodstream Infections (BSI) in U.S. Hospitals (2010–2015)
title_short 2163. Risk Factors for Carbapenem-Resistant Gram-Negative Bloodstream Infections (BSI) in U.S. Hospitals (2010–2015)
title_sort 2163. risk factors for carbapenem-resistant gram-negative bloodstream infections (bsi) in u.s. hospitals (2010–2015)
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253812/
http://dx.doi.org/10.1093/ofid/ofy210.1819
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