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Microbiological etiology in prosthetic valve endocarditis: A nationwide registry study

BACKGROUND: Prosthetic valve endocarditis (PVE) is a feared complication after heart valve surgery. Studies on differences in bacteriology in various types of PVE are limited. OBJECTIVES: This study aimed to investigate the microbiology of PVE depending on the type of prosthetic valve and timing of...

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Autores principales: Berisha, Blerand, Ragnarsson, Sigurdur, Olaison, Lars, Rasmussen, Magnus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9541636/
https://www.ncbi.nlm.nih.gov/pubmed/35373870
http://dx.doi.org/10.1111/joim.13491
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author Berisha, Blerand
Ragnarsson, Sigurdur
Olaison, Lars
Rasmussen, Magnus
author_facet Berisha, Blerand
Ragnarsson, Sigurdur
Olaison, Lars
Rasmussen, Magnus
author_sort Berisha, Blerand
collection PubMed
description BACKGROUND: Prosthetic valve endocarditis (PVE) is a feared complication after heart valve surgery. Studies on differences in bacteriology in various types of PVE are limited. OBJECTIVES: This study aimed to investigate the microbiology of PVE depending on the type of prosthetic valve and timing of diagnosis. METHODS: A retrospective study based on the Swedish Registry on Infective Endocarditis focusing on PVE was conducted. The cohort was divided into mechanical and bioprosthetic valves; into endocarditis localization in the aortic, mitral, or tricuspid valve; and into early and late PVE. The microbiology in these groups was compared. Predictors of Staphylococcus aureus as the cause of PVE were examined by multivariable logistic regression. RESULTS: A total of 780 episodes of PVE in 749 patients were compared regarding the distribution of causative microbiological agents. The most common agents included alpha‐hemolytic streptococci (29%), S. aureus (22%), enterococci (14%), coagulase‐negative staphylococci (CoNS) (12%), and Cutibacterium acnes (6%). S. aureus was more commonly found on mechanical valves compared to bioprosthetic ones (36% vs. 17%, p < 0.001) whereas alpha‐hemolytic streptococci, enterococci, and CoNS were more common on bioprosthetic valves. There were no significant differences in the microbiology of PVE affecting mitral or aortic valves or in cases of early and late PVE. Predictors for S. aureus as the cause of PVE were end‐stage renal disease, intravenous drug use, mechanical valve, and tricuspid localization of endocarditis. CONCLUSIONS: The type of prosthetic heart valve is associated with the causative pathogen. Patients with mechanical valves are more likely to have PVE caused by S. aureus.
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spelling pubmed-95416362022-10-14 Microbiological etiology in prosthetic valve endocarditis: A nationwide registry study Berisha, Blerand Ragnarsson, Sigurdur Olaison, Lars Rasmussen, Magnus J Intern Med Original Articles BACKGROUND: Prosthetic valve endocarditis (PVE) is a feared complication after heart valve surgery. Studies on differences in bacteriology in various types of PVE are limited. OBJECTIVES: This study aimed to investigate the microbiology of PVE depending on the type of prosthetic valve and timing of diagnosis. METHODS: A retrospective study based on the Swedish Registry on Infective Endocarditis focusing on PVE was conducted. The cohort was divided into mechanical and bioprosthetic valves; into endocarditis localization in the aortic, mitral, or tricuspid valve; and into early and late PVE. The microbiology in these groups was compared. Predictors of Staphylococcus aureus as the cause of PVE were examined by multivariable logistic regression. RESULTS: A total of 780 episodes of PVE in 749 patients were compared regarding the distribution of causative microbiological agents. The most common agents included alpha‐hemolytic streptococci (29%), S. aureus (22%), enterococci (14%), coagulase‐negative staphylococci (CoNS) (12%), and Cutibacterium acnes (6%). S. aureus was more commonly found on mechanical valves compared to bioprosthetic ones (36% vs. 17%, p < 0.001) whereas alpha‐hemolytic streptococci, enterococci, and CoNS were more common on bioprosthetic valves. There were no significant differences in the microbiology of PVE affecting mitral or aortic valves or in cases of early and late PVE. Predictors for S. aureus as the cause of PVE were end‐stage renal disease, intravenous drug use, mechanical valve, and tricuspid localization of endocarditis. CONCLUSIONS: The type of prosthetic heart valve is associated with the causative pathogen. Patients with mechanical valves are more likely to have PVE caused by S. aureus. John Wiley and Sons Inc. 2022-04-19 2022-09 /pmc/articles/PMC9541636/ /pubmed/35373870 http://dx.doi.org/10.1111/joim.13491 Text en © 2022 The Authors. Journal of Internal Medicine published by John Wiley & Sons Ltd on behalf of Association for Publication of The Journal of Internal Medicine. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Berisha, Blerand
Ragnarsson, Sigurdur
Olaison, Lars
Rasmussen, Magnus
Microbiological etiology in prosthetic valve endocarditis: A nationwide registry study
title Microbiological etiology in prosthetic valve endocarditis: A nationwide registry study
title_full Microbiological etiology in prosthetic valve endocarditis: A nationwide registry study
title_fullStr Microbiological etiology in prosthetic valve endocarditis: A nationwide registry study
title_full_unstemmed Microbiological etiology in prosthetic valve endocarditis: A nationwide registry study
title_short Microbiological etiology in prosthetic valve endocarditis: A nationwide registry study
title_sort microbiological etiology in prosthetic valve endocarditis: a nationwide registry study
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9541636/
https://www.ncbi.nlm.nih.gov/pubmed/35373870
http://dx.doi.org/10.1111/joim.13491
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