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Clostridium difficile-associated diarrhea in dialysis patients()
BACKGROUND: Dialysis patients have impaired host defense mechanisms and frequently require antibiotics for various infective complications. In this study, we investigated whether dialysis patients have greater risk for Clostridium difficile-associated diarrhea (CDAD). METHODS: During the 4-year stud...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4716098/ https://www.ncbi.nlm.nih.gov/pubmed/26889434 http://dx.doi.org/10.1016/j.krcp.2012.12.002 |
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author | Eui Oh, Sook Lee, Seung Min Lee, Young-Ki Choi, Sun Ryoung Choi, Myung-Jin Kim, Jwa-Kyung Song, Young Rim Kim, Soo Jin Park, Tae Jin Kim, Sung Gyun Oh, Jieun Suh, Jang Won Yoon, Jong-Woo Koo, Ja-Ryong Jik Kim, Hyung Noh, Jung Woo |
author_facet | Eui Oh, Sook Lee, Seung Min Lee, Young-Ki Choi, Sun Ryoung Choi, Myung-Jin Kim, Jwa-Kyung Song, Young Rim Kim, Soo Jin Park, Tae Jin Kim, Sung Gyun Oh, Jieun Suh, Jang Won Yoon, Jong-Woo Koo, Ja-Ryong Jik Kim, Hyung Noh, Jung Woo |
author_sort | Eui Oh, Sook |
collection | PubMed |
description | BACKGROUND: Dialysis patients have impaired host defense mechanisms and frequently require antibiotics for various infective complications. In this study, we investigated whether dialysis patients have greater risk for Clostridium difficile-associated diarrhea (CDAD). METHODS: During the 4-year study period (2004–2008), 85 patients with CDAD were identified based on a retrospective review of C difficile toxin assay or histology records. Nosocomial diarrheal patients without CDAD were considered as controls (n=403). We assessed the association between renal function and the prevalence and clinical outcomes of CDAD. RESULTS: There was a significant difference in the prevalence rate of chronic kidney disease (CKD) between CDAD and non-CDAD patients (P<0.001). Sixteen patients (18.8%) of the CDAD group were treated with dialysis, whereas 21 patients (5.2%) of the non-CDAD group were treated with dialysis. There was a significant association between renal function and CDAD in patients on dialysis [odds ratio (OR)=4.44, 95% confidence interval (CI) 2.19–8.99, P<0.001], but not in patients with CKD stage 3–5 (OR=1.10, 95% CI 0.63–1.92, P=0.73). In multivariate analysis, CKD stage 5D was an independent risk factor for the development of CDAD (OR=13.36, 95% CI 2.94–60.67, P=0.001). CONCLUSION: Our data indicate that dialysis patients might be at a greater risk of developing CDAD, which suggests that particular attention should be provided to CDAD when antibiotic treatment is administered to dialysis patients. |
format | Online Article Text |
id | pubmed-4716098 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-47160982016-02-17 Clostridium difficile-associated diarrhea in dialysis patients() Eui Oh, Sook Lee, Seung Min Lee, Young-Ki Choi, Sun Ryoung Choi, Myung-Jin Kim, Jwa-Kyung Song, Young Rim Kim, Soo Jin Park, Tae Jin Kim, Sung Gyun Oh, Jieun Suh, Jang Won Yoon, Jong-Woo Koo, Ja-Ryong Jik Kim, Hyung Noh, Jung Woo Kidney Res Clin Pract Original Article BACKGROUND: Dialysis patients have impaired host defense mechanisms and frequently require antibiotics for various infective complications. In this study, we investigated whether dialysis patients have greater risk for Clostridium difficile-associated diarrhea (CDAD). METHODS: During the 4-year study period (2004–2008), 85 patients with CDAD were identified based on a retrospective review of C difficile toxin assay or histology records. Nosocomial diarrheal patients without CDAD were considered as controls (n=403). We assessed the association between renal function and the prevalence and clinical outcomes of CDAD. RESULTS: There was a significant difference in the prevalence rate of chronic kidney disease (CKD) between CDAD and non-CDAD patients (P<0.001). Sixteen patients (18.8%) of the CDAD group were treated with dialysis, whereas 21 patients (5.2%) of the non-CDAD group were treated with dialysis. There was a significant association between renal function and CDAD in patients on dialysis [odds ratio (OR)=4.44, 95% confidence interval (CI) 2.19–8.99, P<0.001], but not in patients with CKD stage 3–5 (OR=1.10, 95% CI 0.63–1.92, P=0.73). In multivariate analysis, CKD stage 5D was an independent risk factor for the development of CDAD (OR=13.36, 95% CI 2.94–60.67, P=0.001). CONCLUSION: Our data indicate that dialysis patients might be at a greater risk of developing CDAD, which suggests that particular attention should be provided to CDAD when antibiotic treatment is administered to dialysis patients. Elsevier 2013-03 2012-12-31 /pmc/articles/PMC4716098/ /pubmed/26889434 http://dx.doi.org/10.1016/j.krcp.2012.12.002 Text en © 2013. The Korean Society of Nephrology. Published by Elsevier. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Eui Oh, Sook Lee, Seung Min Lee, Young-Ki Choi, Sun Ryoung Choi, Myung-Jin Kim, Jwa-Kyung Song, Young Rim Kim, Soo Jin Park, Tae Jin Kim, Sung Gyun Oh, Jieun Suh, Jang Won Yoon, Jong-Woo Koo, Ja-Ryong Jik Kim, Hyung Noh, Jung Woo Clostridium difficile-associated diarrhea in dialysis patients() |
title | Clostridium difficile-associated diarrhea in dialysis patients() |
title_full | Clostridium difficile-associated diarrhea in dialysis patients() |
title_fullStr | Clostridium difficile-associated diarrhea in dialysis patients() |
title_full_unstemmed | Clostridium difficile-associated diarrhea in dialysis patients() |
title_short | Clostridium difficile-associated diarrhea in dialysis patients() |
title_sort | clostridium difficile-associated diarrhea in dialysis patients() |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4716098/ https://www.ncbi.nlm.nih.gov/pubmed/26889434 http://dx.doi.org/10.1016/j.krcp.2012.12.002 |
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