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Improving Appropriate Diagnosis of Clostridioides difficile Infection Through an Enteric Pathogen Order Set With Computerized Clinical Decision Support: An Interrupted Time Series Analysis
BACKGROUND: Inappropriate testing for Clostridioides difficile leads to overdiagnosis of C difficile infection (CDI). We determined the effect of a computerized clinical decision support (CCDS) order set on C difficile polymerase chain reaction (PCR) test utilization and clinical outcomes. METHODS:...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7566360/ https://www.ncbi.nlm.nih.gov/pubmed/33094113 http://dx.doi.org/10.1093/ofid/ofaa366 |
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author | Liu, Catherine Lan, Kristine Krantz, Elizabeth M Kim, H Nina Zier, Jacqlynn Bryson-Cahn, Chloe Chan, Jeannie D Jain, Rupali Lynch, John B Pergam, Steven A Pottinger, Paul S Sweet, Ania Whimbey, Estella Bryan, Andrew |
author_facet | Liu, Catherine Lan, Kristine Krantz, Elizabeth M Kim, H Nina Zier, Jacqlynn Bryson-Cahn, Chloe Chan, Jeannie D Jain, Rupali Lynch, John B Pergam, Steven A Pottinger, Paul S Sweet, Ania Whimbey, Estella Bryan, Andrew |
author_sort | Liu, Catherine |
collection | PubMed |
description | BACKGROUND: Inappropriate testing for Clostridioides difficile leads to overdiagnosis of C difficile infection (CDI). We determined the effect of a computerized clinical decision support (CCDS) order set on C difficile polymerase chain reaction (PCR) test utilization and clinical outcomes. METHODS: This study is an interrupted time series analysis comparing C difficile PCR test utilization, hospital-onset CDI (HO-CDI) rates, and clinical outcomes before and after implementation of a CCDS order set at 2 academic medical centers: University of Washington Medical Center (UWMC) and Harborview Medical Center (HMC). RESULTS: Compared with the 20-month preintervention period, during the 12-month postimplementation of the CCDS order set, there was an immediate and sustained reduction in C difficile PCR test utilization rates at both hospitals (HMC, −28.2% [95% confidence interval {CI}, −43.0% to −9.4%], P = .005; UWMC, −27.4%, [95% CI, −37.5% to −15.6%], P < .001). There was a significant reduction in rates of C difficile tests ordered in the setting of laxatives (HMC, −60.8% [95% CI, −74.3% to −40.1%], P < .001; UWMC, −37.3%, [95% CI, −58.2% to −5.9%], P = .02). The intervention was associated with an increase in the C difficile test positivity rate at HMC (P = .01). There were no significant differences in HO-CDI rates or in the proportion of patients with HO-CDI who developed severe CDI or CDI-associated complications including intensive care unit transfer, extended length of stay, 30-day mortality, and toxic megacolon. CONCLUSIONS: Computerized clinical decision support tools can improve C difficile diagnostic test stewardship without causing harm. Additional studies are needed to identify key elements of CCDS tools to further optimize C difficile testing and assess their effect on adverse clinical outcomes. |
format | Online Article Text |
id | pubmed-7566360 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-75663602020-10-21 Improving Appropriate Diagnosis of Clostridioides difficile Infection Through an Enteric Pathogen Order Set With Computerized Clinical Decision Support: An Interrupted Time Series Analysis Liu, Catherine Lan, Kristine Krantz, Elizabeth M Kim, H Nina Zier, Jacqlynn Bryson-Cahn, Chloe Chan, Jeannie D Jain, Rupali Lynch, John B Pergam, Steven A Pottinger, Paul S Sweet, Ania Whimbey, Estella Bryan, Andrew Open Forum Infect Dis Major Articles BACKGROUND: Inappropriate testing for Clostridioides difficile leads to overdiagnosis of C difficile infection (CDI). We determined the effect of a computerized clinical decision support (CCDS) order set on C difficile polymerase chain reaction (PCR) test utilization and clinical outcomes. METHODS: This study is an interrupted time series analysis comparing C difficile PCR test utilization, hospital-onset CDI (HO-CDI) rates, and clinical outcomes before and after implementation of a CCDS order set at 2 academic medical centers: University of Washington Medical Center (UWMC) and Harborview Medical Center (HMC). RESULTS: Compared with the 20-month preintervention period, during the 12-month postimplementation of the CCDS order set, there was an immediate and sustained reduction in C difficile PCR test utilization rates at both hospitals (HMC, −28.2% [95% confidence interval {CI}, −43.0% to −9.4%], P = .005; UWMC, −27.4%, [95% CI, −37.5% to −15.6%], P < .001). There was a significant reduction in rates of C difficile tests ordered in the setting of laxatives (HMC, −60.8% [95% CI, −74.3% to −40.1%], P < .001; UWMC, −37.3%, [95% CI, −58.2% to −5.9%], P = .02). The intervention was associated with an increase in the C difficile test positivity rate at HMC (P = .01). There were no significant differences in HO-CDI rates or in the proportion of patients with HO-CDI who developed severe CDI or CDI-associated complications including intensive care unit transfer, extended length of stay, 30-day mortality, and toxic megacolon. CONCLUSIONS: Computerized clinical decision support tools can improve C difficile diagnostic test stewardship without causing harm. Additional studies are needed to identify key elements of CCDS tools to further optimize C difficile testing and assess their effect on adverse clinical outcomes. Oxford University Press 2020-08-21 /pmc/articles/PMC7566360/ /pubmed/33094113 http://dx.doi.org/10.1093/ofid/ofaa366 Text en © The Author(s) 2020. 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 | Major Articles Liu, Catherine Lan, Kristine Krantz, Elizabeth M Kim, H Nina Zier, Jacqlynn Bryson-Cahn, Chloe Chan, Jeannie D Jain, Rupali Lynch, John B Pergam, Steven A Pottinger, Paul S Sweet, Ania Whimbey, Estella Bryan, Andrew Improving Appropriate Diagnosis of Clostridioides difficile Infection Through an Enteric Pathogen Order Set With Computerized Clinical Decision Support: An Interrupted Time Series Analysis |
title | Improving Appropriate Diagnosis of Clostridioides difficile Infection Through an Enteric Pathogen Order Set With Computerized Clinical Decision Support: An Interrupted Time Series Analysis |
title_full | Improving Appropriate Diagnosis of Clostridioides difficile Infection Through an Enteric Pathogen Order Set With Computerized Clinical Decision Support: An Interrupted Time Series Analysis |
title_fullStr | Improving Appropriate Diagnosis of Clostridioides difficile Infection Through an Enteric Pathogen Order Set With Computerized Clinical Decision Support: An Interrupted Time Series Analysis |
title_full_unstemmed | Improving Appropriate Diagnosis of Clostridioides difficile Infection Through an Enteric Pathogen Order Set With Computerized Clinical Decision Support: An Interrupted Time Series Analysis |
title_short | Improving Appropriate Diagnosis of Clostridioides difficile Infection Through an Enteric Pathogen Order Set With Computerized Clinical Decision Support: An Interrupted Time Series Analysis |
title_sort | improving appropriate diagnosis of clostridioides difficile infection through an enteric pathogen order set with computerized clinical decision support: an interrupted time series analysis |
topic | Major Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7566360/ https://www.ncbi.nlm.nih.gov/pubmed/33094113 http://dx.doi.org/10.1093/ofid/ofaa366 |
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