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Clostridium difficile--a moving target

Clostridium difficile has been recognized as a pathogen in humans for over 40 years, but in the past decade the incidence has increased and, more importantly, the clinical presentation and consequences have become more serious, with increased morbidity and mortality. The emergence of a new, more pat...

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Detalles Bibliográficos
Autores principales: Tillotson, Glenn S., Tillotson, Joni
Formato: Texto
Lenguaje:English
Publicado: Faculty of 1000 Ltd 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3096886/
https://www.ncbi.nlm.nih.gov/pubmed/21654927
http://dx.doi.org/10.3410/M3-6
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author Tillotson, Glenn S.
Tillotson, Joni
author_facet Tillotson, Glenn S.
Tillotson, Joni
author_sort Tillotson, Glenn S.
collection PubMed
description Clostridium difficile has been recognized as a pathogen in humans for over 40 years, but in the past decade the incidence has increased and, more importantly, the clinical presentation and consequences have become more serious, with increased morbidity and mortality. The emergence of a new, more pathogenic strain, BI/NAP1/027, has driven these shifts. Treatment of this disease has been with two antibiotics, metronidazole and vancomycin, but increasing recurrence, not uncommon with C. difficile infections, has prompted research into several alternative therapies. These include a new class of antibiotic (fidaxomicin), a monoclonal antibody, a vaccine, and most recently a biotherapeutic (which, in this case, is a nontoxin-producing strain of C. difficile). The future management of C. difficile infection will probably require a combination of these approaches once we have the data from ongoing studies.
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spelling pubmed-30968862011-06-08 Clostridium difficile--a moving target Tillotson, Glenn S. Tillotson, Joni F1000 Med Rep Review Article Clostridium difficile has been recognized as a pathogen in humans for over 40 years, but in the past decade the incidence has increased and, more importantly, the clinical presentation and consequences have become more serious, with increased morbidity and mortality. The emergence of a new, more pathogenic strain, BI/NAP1/027, has driven these shifts. Treatment of this disease has been with two antibiotics, metronidazole and vancomycin, but increasing recurrence, not uncommon with C. difficile infections, has prompted research into several alternative therapies. These include a new class of antibiotic (fidaxomicin), a monoclonal antibody, a vaccine, and most recently a biotherapeutic (which, in this case, is a nontoxin-producing strain of C. difficile). The future management of C. difficile infection will probably require a combination of these approaches once we have the data from ongoing studies. Faculty of 1000 Ltd 2011-03-01 /pmc/articles/PMC3096886/ /pubmed/21654927 http://dx.doi.org/10.3410/M3-6 Text en © 2011 Faculty of 1000 Ltd http://creativecommons.org/licenses/by-nc/3.0/legalcode This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. You may not use this work for commercial purposes
spellingShingle Review Article
Tillotson, Glenn S.
Tillotson, Joni
Clostridium difficile--a moving target
title Clostridium difficile--a moving target
title_full Clostridium difficile--a moving target
title_fullStr Clostridium difficile--a moving target
title_full_unstemmed Clostridium difficile--a moving target
title_short Clostridium difficile--a moving target
title_sort clostridium difficile--a moving target
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3096886/
https://www.ncbi.nlm.nih.gov/pubmed/21654927
http://dx.doi.org/10.3410/M3-6
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