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Clinical Severity of Clostridium difficile PCR Ribotype 027: A Case-Case Study

BACKGROUND: Clostridium difficile is a leading infectious cause of health care associated diarrhoea. Several industrialised countries have reported increased C. difficile infections and outbreaks, which have been attributed to the emergent PCR ribotype 027 strain. METHODS AND FINDINGS: We conducted...

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Autores principales: Morgan, Oliver W., Rodrigues, Boaventura, Elston, Tony, Verlander, Neville Q., Brown, Derek F. J., Brazier, Jonathan, Reacher, Mark
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2265541/
https://www.ncbi.nlm.nih.gov/pubmed/18350149
http://dx.doi.org/10.1371/journal.pone.0001812
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author Morgan, Oliver W.
Rodrigues, Boaventura
Elston, Tony
Verlander, Neville Q.
Brown, Derek F. J.
Brazier, Jonathan
Reacher, Mark
author_facet Morgan, Oliver W.
Rodrigues, Boaventura
Elston, Tony
Verlander, Neville Q.
Brown, Derek F. J.
Brazier, Jonathan
Reacher, Mark
author_sort Morgan, Oliver W.
collection PubMed
description BACKGROUND: Clostridium difficile is a leading infectious cause of health care associated diarrhoea. Several industrialised countries have reported increased C. difficile infections and outbreaks, which have been attributed to the emergent PCR ribotype 027 strain. METHODS AND FINDINGS: We conducted a case-case study to compare severity of C. difficile disease for patients with 027 versus non-027 ribotypes. We retrospectively collected clinical information about 123/136 patients with C. difficile infections admitted to hospitals in the East of England region in 2006 and from whom stool isolates were cultured and ribotyped as part of an earlier national survey. We defined severe C. difficile disease as having one or more of shock, paralytic ileus, pseudo membranous colitis or toxic megacolon. Patient median age was 83 years old (range 3 to 98, interquartile range 75 to 89), 86% were prescribed antibiotics in the eight weeks before illness onset, 41% had ribotype 027 and 30-day all cause mortality during hospital admission was 21%. Severe disease occurred in 24% (95%CI 13% to 37%) and 17% (95%CI 9% to 27%) of patients with PCR ribotype 027 and non-027 ribotypes respectively. In a multivariable model, ribotype 027 was not associated with severe disease after adjusting for sex, discharge from hospital prior to 60 days of current admission, gastroenteritis on admission, number of initiator antibiotics for C. difficile disease, and hospital where the patient was admitted. CONCLUSIONS: Our study found no evidence to support previous assertions that ribotype 027 is more virulent than other PCR ribotypes. This finding raises questions about the contribution of this strain to the recent increase in C. difficile disease throughout North America and Europe.
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spelling pubmed-22655412008-03-19 Clinical Severity of Clostridium difficile PCR Ribotype 027: A Case-Case Study Morgan, Oliver W. Rodrigues, Boaventura Elston, Tony Verlander, Neville Q. Brown, Derek F. J. Brazier, Jonathan Reacher, Mark PLoS One Research Article BACKGROUND: Clostridium difficile is a leading infectious cause of health care associated diarrhoea. Several industrialised countries have reported increased C. difficile infections and outbreaks, which have been attributed to the emergent PCR ribotype 027 strain. METHODS AND FINDINGS: We conducted a case-case study to compare severity of C. difficile disease for patients with 027 versus non-027 ribotypes. We retrospectively collected clinical information about 123/136 patients with C. difficile infections admitted to hospitals in the East of England region in 2006 and from whom stool isolates were cultured and ribotyped as part of an earlier national survey. We defined severe C. difficile disease as having one or more of shock, paralytic ileus, pseudo membranous colitis or toxic megacolon. Patient median age was 83 years old (range 3 to 98, interquartile range 75 to 89), 86% were prescribed antibiotics in the eight weeks before illness onset, 41% had ribotype 027 and 30-day all cause mortality during hospital admission was 21%. Severe disease occurred in 24% (95%CI 13% to 37%) and 17% (95%CI 9% to 27%) of patients with PCR ribotype 027 and non-027 ribotypes respectively. In a multivariable model, ribotype 027 was not associated with severe disease after adjusting for sex, discharge from hospital prior to 60 days of current admission, gastroenteritis on admission, number of initiator antibiotics for C. difficile disease, and hospital where the patient was admitted. CONCLUSIONS: Our study found no evidence to support previous assertions that ribotype 027 is more virulent than other PCR ribotypes. This finding raises questions about the contribution of this strain to the recent increase in C. difficile disease throughout North America and Europe. Public Library of Science 2008-03-19 /pmc/articles/PMC2265541/ /pubmed/18350149 http://dx.doi.org/10.1371/journal.pone.0001812 Text en Morgan et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Morgan, Oliver W.
Rodrigues, Boaventura
Elston, Tony
Verlander, Neville Q.
Brown, Derek F. J.
Brazier, Jonathan
Reacher, Mark
Clinical Severity of Clostridium difficile PCR Ribotype 027: A Case-Case Study
title Clinical Severity of Clostridium difficile PCR Ribotype 027: A Case-Case Study
title_full Clinical Severity of Clostridium difficile PCR Ribotype 027: A Case-Case Study
title_fullStr Clinical Severity of Clostridium difficile PCR Ribotype 027: A Case-Case Study
title_full_unstemmed Clinical Severity of Clostridium difficile PCR Ribotype 027: A Case-Case Study
title_short Clinical Severity of Clostridium difficile PCR Ribotype 027: A Case-Case Study
title_sort clinical severity of clostridium difficile pcr ribotype 027: a case-case study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2265541/
https://www.ncbi.nlm.nih.gov/pubmed/18350149
http://dx.doi.org/10.1371/journal.pone.0001812
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