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169. Development of a Real Time Electronic Algorithm to Identify Hospitalized Patients with Community-Acquired Pneumonia

BACKGROUND: Syndrome-based antibiotic stewardship can be limited by difficulty in finding cases for evaluation. We developed an electronic extraction algorithm to prospectively identify CAP patients. METHODS: We included non-oncology patients ≥18 years old admitted to The Johns Hopkins Hospital from...

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Autores principales: Fabre, Valeria, Jones, George, Amoah, Joe, Klein, Eili, Leeman, Hannah, Milstone, Aaron, Smith, Aria, Levin, Scott, Cosgrove, Sara E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7778024/
http://dx.doi.org/10.1093/ofid/ofaa439.213
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author Fabre, Valeria
Fabre, Valeria
Jones, George
Amoah, Joe
Klein, Eili
Leeman, Hannah
Milstone, Aaron
Milstone, Aaron
Smith, Aria
Levin, Scott
Cosgrove, Sara E
author_facet Fabre, Valeria
Fabre, Valeria
Jones, George
Amoah, Joe
Klein, Eili
Leeman, Hannah
Milstone, Aaron
Milstone, Aaron
Smith, Aria
Levin, Scott
Cosgrove, Sara E
author_sort Fabre, Valeria
collection PubMed
description BACKGROUND: Syndrome-based antibiotic stewardship can be limited by difficulty in finding cases for evaluation. We developed an electronic extraction algorithm to prospectively identify CAP patients. METHODS: We included non-oncology patients ≥18 years old admitted to The Johns Hopkins Hospital from 12/2018 to 3/2019 who 1) received common CAP antibiotics for ≥48 hours after admission and 2) had a bacterial urinary antigen and chest imaging ordered within 48 hours of admission that was not for assessment of endotracheal tube or central line placement. Charts of patients meeting these criteria were reviewed by 2 authors to identify true cases of CAP based on IDSA guidelines. Cases identified in 12/2018 (n=111) were used to explore potential indicators of CAP, and cases identified 1–3/2019 (n=173) were used to evaluate combinations of indicators that could identify patients treated for CAP who did have CAP (true CAP) and did not have CAP (false CAP). This cohort was divided into a training and a validation set (2/3 and 1/3, respectively). Potential indicators included vitals signs, laboratory data and free text extracted via natural language processing (NLP). Predictive performance of composite indicators for true CAP were assessed using receiver-operating characteristics (ROC) curves. The Hosmer-Lemeshow goodness fit test was used to test model fit and the Akaike Information Criteria was used to determine model selection. RESULTS: True CAP was observed in 41% (71/173) of cases and 14 potential individual indicators were identified (Table). These were combined to make 45 potential composite indicators. ROC curves for selected composite indicators are shown in the Figure. Models without use of NLP-derived variables had poor discriminative ability. The best model included fever, hypoxemia, leukocytosis, and “consolidation” on imaging with a sensitivity and positive predictive value 78.7% and specificity and negative predictive value of 85.7%. Table. Indicators evaluated to identify patients with CAP [Image: see text] Figure. ROC curves for composite indicators [Image: see text] CONCLUSION: Patients with CAP can be identified using electronic data but use of NLP-derived radiographic criteria is required. These data can be linked with data on antibiotic use and duration to develop reports for clinicians regarding appropriate CAP diagnosis and treatment. DISCLOSURES: All Authors: No reported disclosures
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spelling pubmed-77780242021-01-07 169. Development of a Real Time Electronic Algorithm to Identify Hospitalized Patients with Community-Acquired Pneumonia Fabre, Valeria Fabre, Valeria Jones, George Amoah, Joe Klein, Eili Leeman, Hannah Milstone, Aaron Milstone, Aaron Smith, Aria Levin, Scott Cosgrove, Sara E Open Forum Infect Dis Poster Abstracts BACKGROUND: Syndrome-based antibiotic stewardship can be limited by difficulty in finding cases for evaluation. We developed an electronic extraction algorithm to prospectively identify CAP patients. METHODS: We included non-oncology patients ≥18 years old admitted to The Johns Hopkins Hospital from 12/2018 to 3/2019 who 1) received common CAP antibiotics for ≥48 hours after admission and 2) had a bacterial urinary antigen and chest imaging ordered within 48 hours of admission that was not for assessment of endotracheal tube or central line placement. Charts of patients meeting these criteria were reviewed by 2 authors to identify true cases of CAP based on IDSA guidelines. Cases identified in 12/2018 (n=111) were used to explore potential indicators of CAP, and cases identified 1–3/2019 (n=173) were used to evaluate combinations of indicators that could identify patients treated for CAP who did have CAP (true CAP) and did not have CAP (false CAP). This cohort was divided into a training and a validation set (2/3 and 1/3, respectively). Potential indicators included vitals signs, laboratory data and free text extracted via natural language processing (NLP). Predictive performance of composite indicators for true CAP were assessed using receiver-operating characteristics (ROC) curves. The Hosmer-Lemeshow goodness fit test was used to test model fit and the Akaike Information Criteria was used to determine model selection. RESULTS: True CAP was observed in 41% (71/173) of cases and 14 potential individual indicators were identified (Table). These were combined to make 45 potential composite indicators. ROC curves for selected composite indicators are shown in the Figure. Models without use of NLP-derived variables had poor discriminative ability. The best model included fever, hypoxemia, leukocytosis, and “consolidation” on imaging with a sensitivity and positive predictive value 78.7% and specificity and negative predictive value of 85.7%. Table. Indicators evaluated to identify patients with CAP [Image: see text] Figure. ROC curves for composite indicators [Image: see text] CONCLUSION: Patients with CAP can be identified using electronic data but use of NLP-derived radiographic criteria is required. These data can be linked with data on antibiotic use and duration to develop reports for clinicians regarding appropriate CAP diagnosis and treatment. DISCLOSURES: All Authors: No reported disclosures Oxford University Press 2020-12-31 /pmc/articles/PMC7778024/ http://dx.doi.org/10.1093/ofid/ofaa439.213 Text en © The Author 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 Poster Abstracts
Fabre, Valeria
Fabre, Valeria
Jones, George
Amoah, Joe
Klein, Eili
Leeman, Hannah
Milstone, Aaron
Milstone, Aaron
Smith, Aria
Levin, Scott
Cosgrove, Sara E
169. Development of a Real Time Electronic Algorithm to Identify Hospitalized Patients with Community-Acquired Pneumonia
title 169. Development of a Real Time Electronic Algorithm to Identify Hospitalized Patients with Community-Acquired Pneumonia
title_full 169. Development of a Real Time Electronic Algorithm to Identify Hospitalized Patients with Community-Acquired Pneumonia
title_fullStr 169. Development of a Real Time Electronic Algorithm to Identify Hospitalized Patients with Community-Acquired Pneumonia
title_full_unstemmed 169. Development of a Real Time Electronic Algorithm to Identify Hospitalized Patients with Community-Acquired Pneumonia
title_short 169. Development of a Real Time Electronic Algorithm to Identify Hospitalized Patients with Community-Acquired Pneumonia
title_sort 169. development of a real time electronic algorithm to identify hospitalized patients with community-acquired pneumonia
topic Poster Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7778024/
http://dx.doi.org/10.1093/ofid/ofaa439.213
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