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Incidence and Clinical Outcomes of Clostridium difficile Infection after Treatment with Tuberculosis Medication

BACKGROUND/AIMS: To determine the incidence and clinical characteristics of tuberculosis (TB) medication-associated Clostridium difficile infection. METHODS: This multicenter study included patients from eight tertiary hospitals enrolled from 2008 to 2013. A retrospective analysis was conducted to i...

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Autores principales: Lee, Yu Mi, Huh, Kyu Chan, Yoon, Soon Man, Jang, Byung Ik, Shin, Jeong Eun, Koo, Hoon Sup, Jung, Yunho, Kim, Sae Hee, Moon, Hee Seok, Lee, Seung Woo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial Office of Gut and Liver 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4780455/
https://www.ncbi.nlm.nih.gov/pubmed/26260753
http://dx.doi.org/10.5009/gnl14435
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author Lee, Yu Mi
Huh, Kyu Chan
Yoon, Soon Man
Jang, Byung Ik
Shin, Jeong Eun
Koo, Hoon Sup
Jung, Yunho
Kim, Sae Hee
Moon, Hee Seok
Lee, Seung Woo
author_facet Lee, Yu Mi
Huh, Kyu Chan
Yoon, Soon Man
Jang, Byung Ik
Shin, Jeong Eun
Koo, Hoon Sup
Jung, Yunho
Kim, Sae Hee
Moon, Hee Seok
Lee, Seung Woo
author_sort Lee, Yu Mi
collection PubMed
description BACKGROUND/AIMS: To determine the incidence and clinical characteristics of tuberculosis (TB) medication-associated Clostridium difficile infection. METHODS: This multicenter study included patients from eight tertiary hospitals enrolled from 2008 to 2013. A retrospective analysis was conducted to identify the clinical features of C. difficile infection in patients who received TB medication. RESULTS: C. difficile infection developed in 54 of the 19,080 patients prescribed TB medication, representing a total incidence of infection of 2.83 cases per 1,000 adults. Fifty-one of the 54 patients (94.4%) were treated with rifampin. The patients were usually treated with oral metronidazole, which produced improvement in 47 of the 54 patients (87%). Twenty-three patients clinically improved with continuous rifampin therapy for C. difficile infection. There were no significant differences in improvement between patients treated continuously (n=21) and patients in whom treatment was discontinued (n=26). CONCLUSIONS: The incidence of C. difficile infection after TB medication was not low considering the relatively low TB medication dosage compared to other antibiotics. It may not be always necessary to discontinue TB medication. Instead, decisions concerning discontinuation of TB medication should be based on TB status.
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spelling pubmed-47804552016-03-14 Incidence and Clinical Outcomes of Clostridium difficile Infection after Treatment with Tuberculosis Medication Lee, Yu Mi Huh, Kyu Chan Yoon, Soon Man Jang, Byung Ik Shin, Jeong Eun Koo, Hoon Sup Jung, Yunho Kim, Sae Hee Moon, Hee Seok Lee, Seung Woo Gut Liver Original Article BACKGROUND/AIMS: To determine the incidence and clinical characteristics of tuberculosis (TB) medication-associated Clostridium difficile infection. METHODS: This multicenter study included patients from eight tertiary hospitals enrolled from 2008 to 2013. A retrospective analysis was conducted to identify the clinical features of C. difficile infection in patients who received TB medication. RESULTS: C. difficile infection developed in 54 of the 19,080 patients prescribed TB medication, representing a total incidence of infection of 2.83 cases per 1,000 adults. Fifty-one of the 54 patients (94.4%) were treated with rifampin. The patients were usually treated with oral metronidazole, which produced improvement in 47 of the 54 patients (87%). Twenty-three patients clinically improved with continuous rifampin therapy for C. difficile infection. There were no significant differences in improvement between patients treated continuously (n=21) and patients in whom treatment was discontinued (n=26). CONCLUSIONS: The incidence of C. difficile infection after TB medication was not low considering the relatively low TB medication dosage compared to other antibiotics. It may not be always necessary to discontinue TB medication. Instead, decisions concerning discontinuation of TB medication should be based on TB status. Editorial Office of Gut and Liver 2016-03 2015-08-11 /pmc/articles/PMC4780455/ /pubmed/26260753 http://dx.doi.org/10.5009/gnl14435 Text en Copyright © 2016 by The Korean Society of Gastroenterology, the Korean Society of Gastrointestinal Endoscopy, the Korean Society of Neurogastroenterology and Motility, Korean College of Helicobacter and Upper Gastrointestinal Research, Korean Association the Study of Intestinal Diseases, the Korean Association for the Study of the Liver, Korean Pancreatobiliary Association, and Korean Society of Gastrointestinal Cancer. 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 unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Lee, Yu Mi
Huh, Kyu Chan
Yoon, Soon Man
Jang, Byung Ik
Shin, Jeong Eun
Koo, Hoon Sup
Jung, Yunho
Kim, Sae Hee
Moon, Hee Seok
Lee, Seung Woo
Incidence and Clinical Outcomes of Clostridium difficile Infection after Treatment with Tuberculosis Medication
title Incidence and Clinical Outcomes of Clostridium difficile Infection after Treatment with Tuberculosis Medication
title_full Incidence and Clinical Outcomes of Clostridium difficile Infection after Treatment with Tuberculosis Medication
title_fullStr Incidence and Clinical Outcomes of Clostridium difficile Infection after Treatment with Tuberculosis Medication
title_full_unstemmed Incidence and Clinical Outcomes of Clostridium difficile Infection after Treatment with Tuberculosis Medication
title_short Incidence and Clinical Outcomes of Clostridium difficile Infection after Treatment with Tuberculosis Medication
title_sort incidence and clinical outcomes of clostridium difficile infection after treatment with tuberculosis medication
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4780455/
https://www.ncbi.nlm.nih.gov/pubmed/26260753
http://dx.doi.org/10.5009/gnl14435
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