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874. Diagnostic Stewardship of Gastrointestinal Multiplex PCR Panels in Hospitalized Children
BACKGROUND: The introduction of multiplex gastrointestinal panels (GIP) led to increased rates of children with stool testing, high rates of negative results, and no change in clinical outcomes for most children. We aimed to reduce overall stool testing and stool testing with negative results by 20%...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9751538/ http://dx.doi.org/10.1093/ofid/ofac492.067 |
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author | Cotter, Jillian Stokes, Claire Tong, Suhong Dominguez, Samuel R |
author_facet | Cotter, Jillian Stokes, Claire Tong, Suhong Dominguez, Samuel R |
author_sort | Cotter, Jillian |
collection | PubMed |
description | BACKGROUND: The introduction of multiplex gastrointestinal panels (GIP) led to increased rates of children with stool testing, high rates of negative results, and no change in clinical outcomes for most children. We aimed to reduce overall stool testing and stool testing with negative results by 20%. METHODS: We engaged stakeholders and implemented multi-modal interventions including 1) education and development of a clinical pathway to guide testing, and 2) electronic medical record (EMR)-based testing changes including built in stool testing restrictions with optional approval process (Table 1), and quantification of stool caliber in the EMR by nursing using the validated Bristol Stool Scale (BSS). We included all hospitalized children who had stool testing performed at a large children’s hospital over 30 months (2018–2020). Outcomes included the rate of stool tests and negative stool results per 10,000 patient-days. We evaluated rates of BSS documentation and GIPs performed for children hospitalized for > 96 hours as process measures. Balancing measures included the percent of ordered tests that were restricted, and percent of initially restricted tests that were approved. We compared the rate of actionable results (bacteria or parasite identified) between initially restricted but ultimately approved tests and non-restricted tests. [Figure: see text] RESULTS: There were 2,001 tests performed for 1,982 encounters (Table 2). After interventions, we found special cause variation with a 29% sustained decrease in the rate of stool testing and a 28% decrease in the rate of negative stool results (Figures 1,2). The rate of use of BSS was 81% and was sustained. There was a 33% decrease in the number of GIPs performed for children hospitalized for >96 hours. 34% of ordered stool tests per month were restricted, and this did not change over time. 56% of initially restricted tests were ultimately approved with no change over time, and these tests had a lower rate of actionable results compared to non-restricted tests (25 vs 34%, p=0.02). [Figure: see text] [Figure: see text] [Figure: see text] CONCLUSION: Education coupled with EMR-based testing restrictions resulted in reduced rates of overall stool testing and low-value stool testing. Sustained ordering of restricted tests over time suggests that EMR-decision support is needed and likely cannot be removed. DISCLOSURES: Samuel R. Dominguez, MD PhD, BioFire Diagnostics: Advisor/Consultant|BioFire Diagnostics: Grant/Research Support|Karius: Advisor/Consultant|Pfizer: Grant/Research Support. |
format | Online Article Text |
id | pubmed-9751538 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-97515382022-12-16 874. Diagnostic Stewardship of Gastrointestinal Multiplex PCR Panels in Hospitalized Children Cotter, Jillian Stokes, Claire Tong, Suhong Dominguez, Samuel R Open Forum Infect Dis Abstracts BACKGROUND: The introduction of multiplex gastrointestinal panels (GIP) led to increased rates of children with stool testing, high rates of negative results, and no change in clinical outcomes for most children. We aimed to reduce overall stool testing and stool testing with negative results by 20%. METHODS: We engaged stakeholders and implemented multi-modal interventions including 1) education and development of a clinical pathway to guide testing, and 2) electronic medical record (EMR)-based testing changes including built in stool testing restrictions with optional approval process (Table 1), and quantification of stool caliber in the EMR by nursing using the validated Bristol Stool Scale (BSS). We included all hospitalized children who had stool testing performed at a large children’s hospital over 30 months (2018–2020). Outcomes included the rate of stool tests and negative stool results per 10,000 patient-days. We evaluated rates of BSS documentation and GIPs performed for children hospitalized for > 96 hours as process measures. Balancing measures included the percent of ordered tests that were restricted, and percent of initially restricted tests that were approved. We compared the rate of actionable results (bacteria or parasite identified) between initially restricted but ultimately approved tests and non-restricted tests. [Figure: see text] RESULTS: There were 2,001 tests performed for 1,982 encounters (Table 2). After interventions, we found special cause variation with a 29% sustained decrease in the rate of stool testing and a 28% decrease in the rate of negative stool results (Figures 1,2). The rate of use of BSS was 81% and was sustained. There was a 33% decrease in the number of GIPs performed for children hospitalized for >96 hours. 34% of ordered stool tests per month were restricted, and this did not change over time. 56% of initially restricted tests were ultimately approved with no change over time, and these tests had a lower rate of actionable results compared to non-restricted tests (25 vs 34%, p=0.02). [Figure: see text] [Figure: see text] [Figure: see text] CONCLUSION: Education coupled with EMR-based testing restrictions resulted in reduced rates of overall stool testing and low-value stool testing. Sustained ordering of restricted tests over time suggests that EMR-decision support is needed and likely cannot be removed. DISCLOSURES: Samuel R. Dominguez, MD PhD, BioFire Diagnostics: Advisor/Consultant|BioFire Diagnostics: Grant/Research Support|Karius: Advisor/Consultant|Pfizer: Grant/Research Support. Oxford University Press 2022-12-15 /pmc/articles/PMC9751538/ http://dx.doi.org/10.1093/ofid/ofac492.067 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Abstracts Cotter, Jillian Stokes, Claire Tong, Suhong Dominguez, Samuel R 874. Diagnostic Stewardship of Gastrointestinal Multiplex PCR Panels in Hospitalized Children |
title | 874. Diagnostic Stewardship of Gastrointestinal Multiplex PCR Panels in Hospitalized Children |
title_full | 874. Diagnostic Stewardship of Gastrointestinal Multiplex PCR Panels in Hospitalized Children |
title_fullStr | 874. Diagnostic Stewardship of Gastrointestinal Multiplex PCR Panels in Hospitalized Children |
title_full_unstemmed | 874. Diagnostic Stewardship of Gastrointestinal Multiplex PCR Panels in Hospitalized Children |
title_short | 874. Diagnostic Stewardship of Gastrointestinal Multiplex PCR Panels in Hospitalized Children |
title_sort | 874. diagnostic stewardship of gastrointestinal multiplex pcr panels in hospitalized children |
topic | Abstracts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9751538/ http://dx.doi.org/10.1093/ofid/ofac492.067 |
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