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A Machine Learning Approach to Predict Deep Venous Thrombosis Among Hospitalized Patients
Deep venous thrombosis (DVT) is associated with significant morbidity, mortality, and increased healthcare costs. Standard scoring systems for DVT risk stratification often provide insufficient stratification of hospitalized patients and are unable to accurately predict which inpatients are most lik...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7907939/ https://www.ncbi.nlm.nih.gov/pubmed/33625875 http://dx.doi.org/10.1177/1076029621991185 |
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author | Ryan, Logan Mataraso, Samson Siefkas, Anna Pellegrini, Emily Barnes, Gina Green-Saxena, Abigail Hoffman, Jana Calvert, Jacob Das, Ritankar |
author_facet | Ryan, Logan Mataraso, Samson Siefkas, Anna Pellegrini, Emily Barnes, Gina Green-Saxena, Abigail Hoffman, Jana Calvert, Jacob Das, Ritankar |
author_sort | Ryan, Logan |
collection | PubMed |
description | Deep venous thrombosis (DVT) is associated with significant morbidity, mortality, and increased healthcare costs. Standard scoring systems for DVT risk stratification often provide insufficient stratification of hospitalized patients and are unable to accurately predict which inpatients are most likely to present with DVT. There is a continued need for tools which can predict DVT in hospitalized patients. We performed a retrospective study on a database collected from a large academic hospital, comprised of 99,237 total general ward or ICU patients, 2,378 of whom experienced a DVT during their hospital stay. Gradient boosted machine learning algorithms were developed to predict a patient’s risk of developing DVT at 12- and 24-hour windows prior to onset. The primary outcome of interest was diagnosis of in-hospital DVT. The machine learning predictors obtained AUROCs of 0.83 and 0.85 for DVT risk prediction on hospitalized patients at 12- and 24-hour windows, respectively. At both 12 and 24 hours before DVT onset, the most important features for prediction of DVT were cancer history, VTE history, and internal normalized ratio (INR). Improved risk stratification may prevent unnecessary invasive testing in patients for whom DVT cannot be ruled out using existing methods. Improved risk stratification may also allow for more targeted use of prophylactic anticoagulants, as well as earlier diagnosis and treatment, preventing the development of pulmonary emboli and other sequelae of DVT. |
format | Online Article Text |
id | pubmed-7907939 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-79079392021-03-10 A Machine Learning Approach to Predict Deep Venous Thrombosis Among Hospitalized Patients Ryan, Logan Mataraso, Samson Siefkas, Anna Pellegrini, Emily Barnes, Gina Green-Saxena, Abigail Hoffman, Jana Calvert, Jacob Das, Ritankar Clin Appl Thromb Hemost Original Article Deep venous thrombosis (DVT) is associated with significant morbidity, mortality, and increased healthcare costs. Standard scoring systems for DVT risk stratification often provide insufficient stratification of hospitalized patients and are unable to accurately predict which inpatients are most likely to present with DVT. There is a continued need for tools which can predict DVT in hospitalized patients. We performed a retrospective study on a database collected from a large academic hospital, comprised of 99,237 total general ward or ICU patients, 2,378 of whom experienced a DVT during their hospital stay. Gradient boosted machine learning algorithms were developed to predict a patient’s risk of developing DVT at 12- and 24-hour windows prior to onset. The primary outcome of interest was diagnosis of in-hospital DVT. The machine learning predictors obtained AUROCs of 0.83 and 0.85 for DVT risk prediction on hospitalized patients at 12- and 24-hour windows, respectively. At both 12 and 24 hours before DVT onset, the most important features for prediction of DVT were cancer history, VTE history, and internal normalized ratio (INR). Improved risk stratification may prevent unnecessary invasive testing in patients for whom DVT cannot be ruled out using existing methods. Improved risk stratification may also allow for more targeted use of prophylactic anticoagulants, as well as earlier diagnosis and treatment, preventing the development of pulmonary emboli and other sequelae of DVT. SAGE Publications 2021-02-24 /pmc/articles/PMC7907939/ /pubmed/33625875 http://dx.doi.org/10.1177/1076029621991185 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Article Ryan, Logan Mataraso, Samson Siefkas, Anna Pellegrini, Emily Barnes, Gina Green-Saxena, Abigail Hoffman, Jana Calvert, Jacob Das, Ritankar A Machine Learning Approach to Predict Deep Venous Thrombosis Among Hospitalized Patients |
title | A Machine Learning Approach to Predict Deep Venous Thrombosis Among
Hospitalized Patients |
title_full | A Machine Learning Approach to Predict Deep Venous Thrombosis Among
Hospitalized Patients |
title_fullStr | A Machine Learning Approach to Predict Deep Venous Thrombosis Among
Hospitalized Patients |
title_full_unstemmed | A Machine Learning Approach to Predict Deep Venous Thrombosis Among
Hospitalized Patients |
title_short | A Machine Learning Approach to Predict Deep Venous Thrombosis Among
Hospitalized Patients |
title_sort | machine learning approach to predict deep venous thrombosis among
hospitalized patients |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7907939/ https://www.ncbi.nlm.nih.gov/pubmed/33625875 http://dx.doi.org/10.1177/1076029621991185 |
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