Cargando…

1494. Clinical Factors Associated with a Positive C. difficile PCR Test

BACKGROUND: C. difficile infection (CDI) remains a significant cause of morbidity and mortality. The most appropriate clinical scenario for CDI testing is unclear. The IDSA/SHEA guideline recommends testing patients with unexplained new-onset ≥3 stools in 24 hours. This study sought to evaluate clin...

Descripción completa

Detalles Bibliográficos
Autores principales: Cushman, Teresa, Barron, Michelle, Arbet, Jaron, Weber, Rachel, Zhuang, Yaxu, Jeffers, Alexiss, Huang, Misha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6810002/
http://dx.doi.org/10.1093/ofid/ofz360.1358
_version_ 1783462140006367232
author Cushman, Teresa
Barron, Michelle
Arbet, Jaron
Weber, Rachel
Zhuang, Yaxu
Jeffers, Alexiss
Huang, Misha
author_facet Cushman, Teresa
Barron, Michelle
Arbet, Jaron
Weber, Rachel
Zhuang, Yaxu
Jeffers, Alexiss
Huang, Misha
author_sort Cushman, Teresa
collection PubMed
description BACKGROUND: C. difficile infection (CDI) remains a significant cause of morbidity and mortality. The most appropriate clinical scenario for CDI testing is unclear. The IDSA/SHEA guideline recommends testing patients with unexplained new-onset ≥3 stools in 24 hours. This study sought to evaluate clinical factors associated with a positive C. difficile PCR test. METHODS: We conducted a retrospective cohort study of adults (age >18 years old) admitted to the University of Colorado Hospital for whom a C. difficile PCR, either as a standalone test or part of the Biofire® Filmarray® Gastrointestinal Panel (GI Panel), was ordered between October 1, 2015 and August 31, 2017. Data collected included time since admission to test order, hospital length of stay, history of CDI, antibiotic use in the past 90 days, clinical presentation in the 24 hours preceding test order (fever, leukocytosis, number of stools), and laxative or antibiotic administration within 24 hours of test order. Multivariate logistic regression was used to evaluate the association of the above variables with having a positive C. difficile PCR test. If multiple tests were ordered during a single hospital encounter, only the first test was included in our analysis. RESULTS: 3,070 tests were performed; of these, 72% were ordered in the first 72 hours of admission. Overall, 19% of tests were positive. After adjusting for clinical variables, patients with a prior history of C. difficile or who had received antibiotics in the past 24 hours were significantly more likely to have a positive test [OR 2.2 95% CI (1.54, 3.18) P < 0.0001] and [OR 16 95% CI (8.22, 31.41) P < 0.0001], respectively. Patients who used laxatives were significantly less likely to have a positive test [OR 0.75 95% CI (0.61, 0.91) P = 0.004]. The number of stools and presence of fever or leukocytosis were not significantly associated with a positive test. CONCLUSION: Prior history of C. difficile and antibiotics use was highly associated with a positive C. difficile test, while laxatives use was associated with a negative test. The number of stools was not significantly associated with a positive C. difficile test, suggesting this may be less important clinical factor than previously believed; however, restricting testing in patients receiving laxatives is likely warranted. DISCLOSURES: All authors: No reported disclosures.
format Online
Article
Text
id pubmed-6810002
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-68100022019-10-28 1494. Clinical Factors Associated with a Positive C. difficile PCR Test Cushman, Teresa Barron, Michelle Arbet, Jaron Weber, Rachel Zhuang, Yaxu Jeffers, Alexiss Huang, Misha Open Forum Infect Dis Abstracts BACKGROUND: C. difficile infection (CDI) remains a significant cause of morbidity and mortality. The most appropriate clinical scenario for CDI testing is unclear. The IDSA/SHEA guideline recommends testing patients with unexplained new-onset ≥3 stools in 24 hours. This study sought to evaluate clinical factors associated with a positive C. difficile PCR test. METHODS: We conducted a retrospective cohort study of adults (age >18 years old) admitted to the University of Colorado Hospital for whom a C. difficile PCR, either as a standalone test or part of the Biofire® Filmarray® Gastrointestinal Panel (GI Panel), was ordered between October 1, 2015 and August 31, 2017. Data collected included time since admission to test order, hospital length of stay, history of CDI, antibiotic use in the past 90 days, clinical presentation in the 24 hours preceding test order (fever, leukocytosis, number of stools), and laxative or antibiotic administration within 24 hours of test order. Multivariate logistic regression was used to evaluate the association of the above variables with having a positive C. difficile PCR test. If multiple tests were ordered during a single hospital encounter, only the first test was included in our analysis. RESULTS: 3,070 tests were performed; of these, 72% were ordered in the first 72 hours of admission. Overall, 19% of tests were positive. After adjusting for clinical variables, patients with a prior history of C. difficile or who had received antibiotics in the past 24 hours were significantly more likely to have a positive test [OR 2.2 95% CI (1.54, 3.18) P < 0.0001] and [OR 16 95% CI (8.22, 31.41) P < 0.0001], respectively. Patients who used laxatives were significantly less likely to have a positive test [OR 0.75 95% CI (0.61, 0.91) P = 0.004]. The number of stools and presence of fever or leukocytosis were not significantly associated with a positive test. CONCLUSION: Prior history of C. difficile and antibiotics use was highly associated with a positive C. difficile test, while laxatives use was associated with a negative test. The number of stools was not significantly associated with a positive C. difficile test, suggesting this may be less important clinical factor than previously believed; however, restricting testing in patients receiving laxatives is likely warranted. DISCLOSURES: All authors: No reported disclosures. Oxford University Press 2019-10-23 /pmc/articles/PMC6810002/ http://dx.doi.org/10.1093/ofid/ofz360.1358 Text en © The Author(s) 2019. 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
Cushman, Teresa
Barron, Michelle
Arbet, Jaron
Weber, Rachel
Zhuang, Yaxu
Jeffers, Alexiss
Huang, Misha
1494. Clinical Factors Associated with a Positive C. difficile PCR Test
title 1494. Clinical Factors Associated with a Positive C. difficile PCR Test
title_full 1494. Clinical Factors Associated with a Positive C. difficile PCR Test
title_fullStr 1494. Clinical Factors Associated with a Positive C. difficile PCR Test
title_full_unstemmed 1494. Clinical Factors Associated with a Positive C. difficile PCR Test
title_short 1494. Clinical Factors Associated with a Positive C. difficile PCR Test
title_sort 1494. clinical factors associated with a positive c. difficile pcr test
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6810002/
http://dx.doi.org/10.1093/ofid/ofz360.1358
work_keys_str_mv AT cushmanteresa 1494clinicalfactorsassociatedwithapositivecdifficilepcrtest
AT barronmichelle 1494clinicalfactorsassociatedwithapositivecdifficilepcrtest
AT arbetjaron 1494clinicalfactorsassociatedwithapositivecdifficilepcrtest
AT weberrachel 1494clinicalfactorsassociatedwithapositivecdifficilepcrtest
AT zhuangyaxu 1494clinicalfactorsassociatedwithapositivecdifficilepcrtest
AT jeffersalexiss 1494clinicalfactorsassociatedwithapositivecdifficilepcrtest
AT huangmisha 1494clinicalfactorsassociatedwithapositivecdifficilepcrtest