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1009. Venous 1: A Prospective Multicenter Cohort Study of Enterococcal Bacteremia

BACKGROUND: Enterococci often cause hospital-associated bloodstream infections in critically ill and immunocompromised patients. Prospective studies to assess the clinical impact of enterococcal bacteremia (EB) are lacking. We conducted a prospective study to investigate the clinical and microbiolog...

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Autores principales: Contreras, German, Munita, Jose M, Reyes, Katherine C, Sahasrabhojane, Pranoti, Misikir, Helina, Garza, Heather, Zervos, Marcus J, Aitken, Samuel L, Shelburne, Samuel A, Arias, Cesar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254145/
http://dx.doi.org/10.1093/ofid/ofy210.846
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author Contreras, German
Munita, Jose M
Reyes, Katherine C
Sahasrabhojane, Pranoti
Misikir, Helina
Garza, Heather
Zervos, Marcus J
Aitken, Samuel L
Shelburne, Samuel A
Arias, Cesar
author_facet Contreras, German
Munita, Jose M
Reyes, Katherine C
Sahasrabhojane, Pranoti
Misikir, Helina
Garza, Heather
Zervos, Marcus J
Aitken, Samuel L
Shelburne, Samuel A
Arias, Cesar
author_sort Contreras, German
collection PubMed
description BACKGROUND: Enterococci often cause hospital-associated bloodstream infections in critically ill and immunocompromised patients. Prospective studies to assess the clinical impact of enterococcal bacteremia (EB) are lacking. We conducted a prospective study to investigate the clinical and microbiological factors associated with mortality in EB. METHODS: Adults with EB were prospectively followed in three US tertiary hospitals from September 2016 to March 2018. Individuals with EB for whom follow-up blood culture data within 7 days of index culture were available were included. Microbiologic failure (MF) was defined as clearance of bacteremia ≥4 days after the first blood culture. The main outcome was hospital mortality. RESULTS: A total of 282 patients were included with 69 (24%) infected with vancomycin-resistant enterococci (VRE). The majority of patients were male (60%) with a median age of 63 years. Median length of hospitalization for VRE patients was longer (25 d) than non-VRE (13 days, P < 0.001). E. faecium corresponded to 77% of VRE isolates, whereas E. faecalis comprised 72% of non-VRE. The average time to first blood culture was 16 days for VRE vs. 4 days for non-VRE (P < 0.001). Patients with VRE were more likely to have hematological malignancy or bone marrow transplant (P < 0.003), whereas patients infected non-VRE were more likely to have solid tumors (P = 0.02). The most common antibiotic used was daptomycin as monotherapy for both VRE and non-VRE with a median dose of 8 mg/kg for both groups. Overall mortality was 25% (43% vs. 20% in VRE vs. non-VRE patients, respectively; P < 0.0001). Factors significantly associated with mortality in univariate analyses included ICU admission, prolonged hospitalization, hematological malignancy, use of immunosuppressive therapy, hemodialysis, neutropenia (<500 cell/mL), Pitt bacteremia score >3, infection with VRE and MF. ICU admission (RR 3.3; 95% CI 1.7–7.5, neutropenia (RR 4.1; 95% CI 1.3–12.9), Pitt bacteremia score >3 (RR 6.8; 95% CI 2.6–18.0), MF (RR 4.7; 95% CI 2.2–10.3) and infection with VRE (RR 4.1; 95% CI 1.1–16.6) remained significantly associated with mortality in multivariate analyses. CONCLUSION: The presence of VRE in EB and MF are associated with increased mortality. EB represent a major burden of disease in hospital settings. DISCLOSURES: C. Arias, Merck & Co., Inc.: Grant Investigator, Research support. MeMed: Grant Investigator, Research support. Allergan: Grant Investigator, Research support.
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spelling pubmed-62541452018-11-28 1009. Venous 1: A Prospective Multicenter Cohort Study of Enterococcal Bacteremia Contreras, German Munita, Jose M Reyes, Katherine C Sahasrabhojane, Pranoti Misikir, Helina Garza, Heather Zervos, Marcus J Aitken, Samuel L Shelburne, Samuel A Arias, Cesar Open Forum Infect Dis Abstracts BACKGROUND: Enterococci often cause hospital-associated bloodstream infections in critically ill and immunocompromised patients. Prospective studies to assess the clinical impact of enterococcal bacteremia (EB) are lacking. We conducted a prospective study to investigate the clinical and microbiological factors associated with mortality in EB. METHODS: Adults with EB were prospectively followed in three US tertiary hospitals from September 2016 to March 2018. Individuals with EB for whom follow-up blood culture data within 7 days of index culture were available were included. Microbiologic failure (MF) was defined as clearance of bacteremia ≥4 days after the first blood culture. The main outcome was hospital mortality. RESULTS: A total of 282 patients were included with 69 (24%) infected with vancomycin-resistant enterococci (VRE). The majority of patients were male (60%) with a median age of 63 years. Median length of hospitalization for VRE patients was longer (25 d) than non-VRE (13 days, P < 0.001). E. faecium corresponded to 77% of VRE isolates, whereas E. faecalis comprised 72% of non-VRE. The average time to first blood culture was 16 days for VRE vs. 4 days for non-VRE (P < 0.001). Patients with VRE were more likely to have hematological malignancy or bone marrow transplant (P < 0.003), whereas patients infected non-VRE were more likely to have solid tumors (P = 0.02). The most common antibiotic used was daptomycin as monotherapy for both VRE and non-VRE with a median dose of 8 mg/kg for both groups. Overall mortality was 25% (43% vs. 20% in VRE vs. non-VRE patients, respectively; P < 0.0001). Factors significantly associated with mortality in univariate analyses included ICU admission, prolonged hospitalization, hematological malignancy, use of immunosuppressive therapy, hemodialysis, neutropenia (<500 cell/mL), Pitt bacteremia score >3, infection with VRE and MF. ICU admission (RR 3.3; 95% CI 1.7–7.5, neutropenia (RR 4.1; 95% CI 1.3–12.9), Pitt bacteremia score >3 (RR 6.8; 95% CI 2.6–18.0), MF (RR 4.7; 95% CI 2.2–10.3) and infection with VRE (RR 4.1; 95% CI 1.1–16.6) remained significantly associated with mortality in multivariate analyses. CONCLUSION: The presence of VRE in EB and MF are associated with increased mortality. EB represent a major burden of disease in hospital settings. DISCLOSURES: C. Arias, Merck & Co., Inc.: Grant Investigator, Research support. MeMed: Grant Investigator, Research support. Allergan: Grant Investigator, Research support. Oxford University Press 2018-11-26 /pmc/articles/PMC6254145/ http://dx.doi.org/10.1093/ofid/ofy210.846 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
Contreras, German
Munita, Jose M
Reyes, Katherine C
Sahasrabhojane, Pranoti
Misikir, Helina
Garza, Heather
Zervos, Marcus J
Aitken, Samuel L
Shelburne, Samuel A
Arias, Cesar
1009. Venous 1: A Prospective Multicenter Cohort Study of Enterococcal Bacteremia
title 1009. Venous 1: A Prospective Multicenter Cohort Study of Enterococcal Bacteremia
title_full 1009. Venous 1: A Prospective Multicenter Cohort Study of Enterococcal Bacteremia
title_fullStr 1009. Venous 1: A Prospective Multicenter Cohort Study of Enterococcal Bacteremia
title_full_unstemmed 1009. Venous 1: A Prospective Multicenter Cohort Study of Enterococcal Bacteremia
title_short 1009. Venous 1: A Prospective Multicenter Cohort Study of Enterococcal Bacteremia
title_sort 1009. venous 1: a prospective multicenter cohort study of enterococcal bacteremia
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254145/
http://dx.doi.org/10.1093/ofid/ofy210.846
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