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Effects of co-infection on the clinical outcomes of Clostridium difficile infection

BACKGROUND: Clostridium difficile (C. difficile) is a spore-forming, Gram-positive rod that is known to be associated with antibiotic use. It is one of the leading causes of nosocomial diarrhea in the industrialized world and therefore warrants further study of its nature. It isn’t clear if co-infec...

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Autores principales: Shafiq, Muhammad, Alturkmani, Hani, Zafar, Yousaf, Mittal, Vishal, Lodhi, Hafsa, Ullah, Waqas, Brewer, Joseph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7041107/
https://www.ncbi.nlm.nih.gov/pubmed/32123545
http://dx.doi.org/10.1186/s13099-020-00348-7
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author Shafiq, Muhammad
Alturkmani, Hani
Zafar, Yousaf
Mittal, Vishal
Lodhi, Hafsa
Ullah, Waqas
Brewer, Joseph
author_facet Shafiq, Muhammad
Alturkmani, Hani
Zafar, Yousaf
Mittal, Vishal
Lodhi, Hafsa
Ullah, Waqas
Brewer, Joseph
author_sort Shafiq, Muhammad
collection PubMed
description BACKGROUND: Clostridium difficile (C. difficile) is a spore-forming, Gram-positive rod that is known to be associated with antibiotic use. It is one of the leading causes of nosocomial diarrhea in the industrialized world and therefore warrants further study of its nature. It isn’t clear if co-infection by other organisms can affect the outcome of C. difficile infection (CDI). METHODS: A single center retrospective study was done and it used inclusion criteria of 18 years of age and being tested positive for CDI on FilmArray® multiplex gastro-intestinal (GI) panel. Exclusion criteria were a GI panel performed on an outpatient basis, recurrent CDI, and the presence of end-stage renal disease, cirrhosis, or a non-GI infection. The stool sample for all patients were collected within 48 h of presentation to the hospital. There were 235 of 2576 GI panels selected for a retrospective chart review based on the above criteria. Among these 235 patients, 38 had a co-infection (CDI+ another GI infection = group A or cases) and the rest had only CDI (group B or controls). Group A was compared with group B for CDI severity, its response to treatment, recurrence, and length of the hospital stay, using 0.05 as the alpha criterion. RESULTS: Most patients with CDI were female and above the age of 60 years. Co infection did not increase the severity of CDI based both on the American College of Gastroenterology criteria (p 0.16) as well as Infectious Disease Society of America criteria (p 0.77). Co infection group also didn’t have significantly different CDI related treatment failure rate (p 0.23), or CDI recurrence rate (p 0.49). Co-infection was also not associated with lengthier hospital stay (p 0.41). CONCLUSION: Our study suggests that co-infection doesn’t affect the severity of CDI or can cause treatment failures. Additionally, there was no significant increase in hospital stay, or increase in CDI recurrence associated with co-infection. Therefore, if CDI is the leading clinical diagnosis and a patient is tested positive for co-infection in addition to CDI on FilmArray® multiplex GI panel, this co-infection shouldn’t change the management for CDI. Limitations of this study (including retrospective nature of the study, small sample size, single site study, not including all microbiome and non-inclusion of race) should also be taken into account, while considering the applicability of the results of this study.
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spelling pubmed-70411072020-03-02 Effects of co-infection on the clinical outcomes of Clostridium difficile infection Shafiq, Muhammad Alturkmani, Hani Zafar, Yousaf Mittal, Vishal Lodhi, Hafsa Ullah, Waqas Brewer, Joseph Gut Pathog Research BACKGROUND: Clostridium difficile (C. difficile) is a spore-forming, Gram-positive rod that is known to be associated with antibiotic use. It is one of the leading causes of nosocomial diarrhea in the industrialized world and therefore warrants further study of its nature. It isn’t clear if co-infection by other organisms can affect the outcome of C. difficile infection (CDI). METHODS: A single center retrospective study was done and it used inclusion criteria of 18 years of age and being tested positive for CDI on FilmArray® multiplex gastro-intestinal (GI) panel. Exclusion criteria were a GI panel performed on an outpatient basis, recurrent CDI, and the presence of end-stage renal disease, cirrhosis, or a non-GI infection. The stool sample for all patients were collected within 48 h of presentation to the hospital. There were 235 of 2576 GI panels selected for a retrospective chart review based on the above criteria. Among these 235 patients, 38 had a co-infection (CDI+ another GI infection = group A or cases) and the rest had only CDI (group B or controls). Group A was compared with group B for CDI severity, its response to treatment, recurrence, and length of the hospital stay, using 0.05 as the alpha criterion. RESULTS: Most patients with CDI were female and above the age of 60 years. Co infection did not increase the severity of CDI based both on the American College of Gastroenterology criteria (p 0.16) as well as Infectious Disease Society of America criteria (p 0.77). Co infection group also didn’t have significantly different CDI related treatment failure rate (p 0.23), or CDI recurrence rate (p 0.49). Co-infection was also not associated with lengthier hospital stay (p 0.41). CONCLUSION: Our study suggests that co-infection doesn’t affect the severity of CDI or can cause treatment failures. Additionally, there was no significant increase in hospital stay, or increase in CDI recurrence associated with co-infection. Therefore, if CDI is the leading clinical diagnosis and a patient is tested positive for co-infection in addition to CDI on FilmArray® multiplex GI panel, this co-infection shouldn’t change the management for CDI. Limitations of this study (including retrospective nature of the study, small sample size, single site study, not including all microbiome and non-inclusion of race) should also be taken into account, while considering the applicability of the results of this study. BioMed Central 2020-02-25 /pmc/articles/PMC7041107/ /pubmed/32123545 http://dx.doi.org/10.1186/s13099-020-00348-7 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Shafiq, Muhammad
Alturkmani, Hani
Zafar, Yousaf
Mittal, Vishal
Lodhi, Hafsa
Ullah, Waqas
Brewer, Joseph
Effects of co-infection on the clinical outcomes of Clostridium difficile infection
title Effects of co-infection on the clinical outcomes of Clostridium difficile infection
title_full Effects of co-infection on the clinical outcomes of Clostridium difficile infection
title_fullStr Effects of co-infection on the clinical outcomes of Clostridium difficile infection
title_full_unstemmed Effects of co-infection on the clinical outcomes of Clostridium difficile infection
title_short Effects of co-infection on the clinical outcomes of Clostridium difficile infection
title_sort effects of co-infection on the clinical outcomes of clostridium difficile infection
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7041107/
https://www.ncbi.nlm.nih.gov/pubmed/32123545
http://dx.doi.org/10.1186/s13099-020-00348-7
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