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External validation of clinical scores to predict complications of Clostridium difficile infection
BACKGROUND: Clostridium difficile infection (CDI) is the most common cause of nosocomial diarrhea. About one in 5 patients with CDI (median 18%) develop a complication (cCDI), including mortality. Many predictive scores have been published to identify patients at risk of cCDI but none is currently r...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5631488/ http://dx.doi.org/10.1093/ofid/ofx163.1005 |
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author | Beauregard-Paultre, Catherine Chakra, Claire Nour Abou Mcgeer, Allison Labbé, Annie-Claude Simor, Andrew E Gold, Wayne Muller, Matthew P Powis, Jeff Katz, Kevin Cadarette, Suzanne Pépin, Jacques Garneau, Julian R Valiquette, Louis |
author_facet | Beauregard-Paultre, Catherine Chakra, Claire Nour Abou Mcgeer, Allison Labbé, Annie-Claude Simor, Andrew E Gold, Wayne Muller, Matthew P Powis, Jeff Katz, Kevin Cadarette, Suzanne Pépin, Jacques Garneau, Julian R Valiquette, Louis |
author_sort | Beauregard-Paultre, Catherine |
collection | PubMed |
description | BACKGROUND: Clostridium difficile infection (CDI) is the most common cause of nosocomial diarrhea. About one in 5 patients with CDI (median 18%) develop a complication (cCDI), including mortality. Many predictive scores have been published to identify patients at risk of cCDI but none is currently recommended for clinical use and few were validated. We conducted an external validation study of predictive tools for cCDI. METHODS: Predictive tools were identified through a systematic review. We included those reporting at least an internal validation process. We performed the external validation on a multicenter prospective cohort of 1380 Canadian adults with confirmed CDI. Most cases were elderly (median age 71), had a healthcare facility-associated CDI (90%), and cCDI occurred in 8%. NAP1 strain was found in 52%. The performance of each scoring system was analyzed using individual outcomes. Modifications in predictors were made to match available data in the validation cohort. RESULTS: We assessed 3 predictive scores and one predictive model. The performance (95% CI) of higher thresholds are shown in the Table. All scores had a low sensitivity and PPV, and moderate specificity and NPV. The model of Shivashankar 2013 (age, WBC> 15, narcotic use, antacids use, creatinine ratio > 1.5) predicted 25% probability of cCDI. All showed similar AUC (0.63–0.67). CONCLUSION: The predictive tools included in our study showed moderate performance in a validation cohort with a low rate of cCDI and high proportion of NAP1 strains. Further research is needed to develop an accurate predictive tool to guide clinicians in the management of CDI. DISCLOSURES: J. Powis, Merck: Grant Investigator, Research grant; GSK: Grant Investigator, Research grant; Roche: Grant Investigator, Research grant; Synthetic Biologicals: Investigator, Research grant |
format | Online Article Text |
id | pubmed-5631488 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-56314882017-11-07 External validation of clinical scores to predict complications of Clostridium difficile infection Beauregard-Paultre, Catherine Chakra, Claire Nour Abou Mcgeer, Allison Labbé, Annie-Claude Simor, Andrew E Gold, Wayne Muller, Matthew P Powis, Jeff Katz, Kevin Cadarette, Suzanne Pépin, Jacques Garneau, Julian R Valiquette, Louis Open Forum Infect Dis Abstracts BACKGROUND: Clostridium difficile infection (CDI) is the most common cause of nosocomial diarrhea. About one in 5 patients with CDI (median 18%) develop a complication (cCDI), including mortality. Many predictive scores have been published to identify patients at risk of cCDI but none is currently recommended for clinical use and few were validated. We conducted an external validation study of predictive tools for cCDI. METHODS: Predictive tools were identified through a systematic review. We included those reporting at least an internal validation process. We performed the external validation on a multicenter prospective cohort of 1380 Canadian adults with confirmed CDI. Most cases were elderly (median age 71), had a healthcare facility-associated CDI (90%), and cCDI occurred in 8%. NAP1 strain was found in 52%. The performance of each scoring system was analyzed using individual outcomes. Modifications in predictors were made to match available data in the validation cohort. RESULTS: We assessed 3 predictive scores and one predictive model. The performance (95% CI) of higher thresholds are shown in the Table. All scores had a low sensitivity and PPV, and moderate specificity and NPV. The model of Shivashankar 2013 (age, WBC> 15, narcotic use, antacids use, creatinine ratio > 1.5) predicted 25% probability of cCDI. All showed similar AUC (0.63–0.67). CONCLUSION: The predictive tools included in our study showed moderate performance in a validation cohort with a low rate of cCDI and high proportion of NAP1 strains. Further research is needed to develop an accurate predictive tool to guide clinicians in the management of CDI. DISCLOSURES: J. Powis, Merck: Grant Investigator, Research grant; GSK: Grant Investigator, Research grant; Roche: Grant Investigator, Research grant; Synthetic Biologicals: Investigator, Research grant Oxford University Press 2017-10-04 /pmc/articles/PMC5631488/ http://dx.doi.org/10.1093/ofid/ofx163.1005 Text en © The Author 2017. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Abstracts Beauregard-Paultre, Catherine Chakra, Claire Nour Abou Mcgeer, Allison Labbé, Annie-Claude Simor, Andrew E Gold, Wayne Muller, Matthew P Powis, Jeff Katz, Kevin Cadarette, Suzanne Pépin, Jacques Garneau, Julian R Valiquette, Louis External validation of clinical scores to predict complications of Clostridium difficile infection |
title | External validation of clinical scores to predict complications of Clostridium difficile infection |
title_full | External validation of clinical scores to predict complications of Clostridium difficile infection |
title_fullStr | External validation of clinical scores to predict complications of Clostridium difficile infection |
title_full_unstemmed | External validation of clinical scores to predict complications of Clostridium difficile infection |
title_short | External validation of clinical scores to predict complications of Clostridium difficile infection |
title_sort | external validation of clinical scores to predict complications of clostridium difficile infection |
topic | Abstracts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5631488/ http://dx.doi.org/10.1093/ofid/ofx163.1005 |
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