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Infective endocarditis in haemodialysis patients: 16-year experience at one institution

Objectives. To ascertain the characteristics, outcomes and correlates of mortality in chronic haemodialysis patients with confirmed infective endocarditis (IE). Methods. Patients were identified by computerized discharge diagnosis and chart review of admissions to Saint Louis University hospital fro...

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Autores principales: Baroudi, Samir, Qazi, Rizwan A., Lentine, Krista L., Bastani, Bahar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4421220/
https://www.ncbi.nlm.nih.gov/pubmed/25983896
http://dx.doi.org/10.1093/ndtplus/sfn026
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author Baroudi, Samir
Qazi, Rizwan A.
Lentine, Krista L.
Bastani, Bahar
author_facet Baroudi, Samir
Qazi, Rizwan A.
Lentine, Krista L.
Bastani, Bahar
author_sort Baroudi, Samir
collection PubMed
description Objectives. To ascertain the characteristics, outcomes and correlates of mortality in chronic haemodialysis patients with confirmed infective endocarditis (IE). Methods. Patients were identified by computerized discharge diagnosis and chart review of admissions to Saint Louis University hospital from January 1990 through January 2006. Modified Duke Criteria were retrospectively applied to confirm the diagnosis of IE. Survivors and non-survivors were compared to identify clinical correlates of IE mortality. Results. We identified 59 patients with IE who had received dialysis for a mean duration of 52.9 ± 58.0 months prior to IE diagnosis. Dialysis access comprised 28 (47.5%) catheters, 26 (44.1%) arteriovenous grafts, 3 (5.1%) arteriovenous fistulas and 2 (3.4%) life sites. The causative organisms were MRSA in 15 (25%), MSSA 12 (20%), S. Epidermidis 10 (17%), Enterococci 8 (14%), multi-organism 6 (10%), gram negative 2 (3%) and VRE 1 (2%). Valves involved were mitral valve in 37 (63%), aortic valve in 10 (17%), tricuspid valve in 3 (5%) and multiple valves in 8 (13%) cases. Patient mortality was 28.8% (n = 17) during hospitalization, 37.9% (n = 22) at 30 days and 63.1% (n = 36) at 1 year. In multivariable logistic regression, the adjusted odds ratio of in-hospital mortality was 3.6-fold higher in those with IE and arteriovenous grafts (P = 0.04, 95% CI 1.04–12.27) compared to other forms of dialysis access. Conclusion. Mortality of IE remains high, despite the availability of potent antibiotics. Patients with arteriovenous grafts who develop IE may face increased risk for in-hospital mortality, perhaps reflecting difficulty eradicating endovascular infection if a graft is involved.
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spelling pubmed-44212202015-05-15 Infective endocarditis in haemodialysis patients: 16-year experience at one institution Baroudi, Samir Qazi, Rizwan A. Lentine, Krista L. Bastani, Bahar NDT Plus Teaching Point (Section Editor: A. Meyrier) Objectives. To ascertain the characteristics, outcomes and correlates of mortality in chronic haemodialysis patients with confirmed infective endocarditis (IE). Methods. Patients were identified by computerized discharge diagnosis and chart review of admissions to Saint Louis University hospital from January 1990 through January 2006. Modified Duke Criteria were retrospectively applied to confirm the diagnosis of IE. Survivors and non-survivors were compared to identify clinical correlates of IE mortality. Results. We identified 59 patients with IE who had received dialysis for a mean duration of 52.9 ± 58.0 months prior to IE diagnosis. Dialysis access comprised 28 (47.5%) catheters, 26 (44.1%) arteriovenous grafts, 3 (5.1%) arteriovenous fistulas and 2 (3.4%) life sites. The causative organisms were MRSA in 15 (25%), MSSA 12 (20%), S. Epidermidis 10 (17%), Enterococci 8 (14%), multi-organism 6 (10%), gram negative 2 (3%) and VRE 1 (2%). Valves involved were mitral valve in 37 (63%), aortic valve in 10 (17%), tricuspid valve in 3 (5%) and multiple valves in 8 (13%) cases. Patient mortality was 28.8% (n = 17) during hospitalization, 37.9% (n = 22) at 30 days and 63.1% (n = 36) at 1 year. In multivariable logistic regression, the adjusted odds ratio of in-hospital mortality was 3.6-fold higher in those with IE and arteriovenous grafts (P = 0.04, 95% CI 1.04–12.27) compared to other forms of dialysis access. Conclusion. Mortality of IE remains high, despite the availability of potent antibiotics. Patients with arteriovenous grafts who develop IE may face increased risk for in-hospital mortality, perhaps reflecting difficulty eradicating endovascular infection if a graft is involved. Oxford University Press 2008-08 2008-04-10 /pmc/articles/PMC4421220/ /pubmed/25983896 http://dx.doi.org/10.1093/ndtplus/sfn026 Text en © The Author [2008]. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved. For Permissions, please e-mail: journals.permissions@oxfordjournals.org http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Teaching Point (Section Editor: A. Meyrier)
Baroudi, Samir
Qazi, Rizwan A.
Lentine, Krista L.
Bastani, Bahar
Infective endocarditis in haemodialysis patients: 16-year experience at one institution
title Infective endocarditis in haemodialysis patients: 16-year experience at one institution
title_full Infective endocarditis in haemodialysis patients: 16-year experience at one institution
title_fullStr Infective endocarditis in haemodialysis patients: 16-year experience at one institution
title_full_unstemmed Infective endocarditis in haemodialysis patients: 16-year experience at one institution
title_short Infective endocarditis in haemodialysis patients: 16-year experience at one institution
title_sort infective endocarditis in haemodialysis patients: 16-year experience at one institution
topic Teaching Point (Section Editor: A. Meyrier)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4421220/
https://www.ncbi.nlm.nih.gov/pubmed/25983896
http://dx.doi.org/10.1093/ndtplus/sfn026
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