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Prediction of Prednisolone Dose Correction Using Machine Learning

Wrong dose, a common prescription error, can cause serious patient harm, especially in the case of high-risk drugs like oral corticosteroids. This study aims to build a machine learning model to predict dose-related prescription modifications for oral prednisolone tablets (i.e., highly imbalanced da...

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Autores principales: Sato, Hiroyasu, Kimura, Yoshinobu, Ohba, Masahiro, Ara, Yoshiaki, Wakabayashi, Susumu, Watanabe, Hiroaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9995628/
https://www.ncbi.nlm.nih.gov/pubmed/36910914
http://dx.doi.org/10.1007/s41666-023-00128-3
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author Sato, Hiroyasu
Kimura, Yoshinobu
Ohba, Masahiro
Ara, Yoshiaki
Wakabayashi, Susumu
Watanabe, Hiroaki
author_facet Sato, Hiroyasu
Kimura, Yoshinobu
Ohba, Masahiro
Ara, Yoshiaki
Wakabayashi, Susumu
Watanabe, Hiroaki
author_sort Sato, Hiroyasu
collection PubMed
description Wrong dose, a common prescription error, can cause serious patient harm, especially in the case of high-risk drugs like oral corticosteroids. This study aims to build a machine learning model to predict dose-related prescription modifications for oral prednisolone tablets (i.e., highly imbalanced data with very few positive cases). Prescription data were obtained from the electronic medical records at a single institute. Cluster analysis classified the clinical departments into six clusters with similar patterns of prednisolone prescription. Two patterns of training datasets were created with/without preprocessing by the SMOTE method. Five ML models (SVM, KNN, GB, RF, and BRF) and logistic regression (LR) models were constructed by Python. The model was internally validated by five-fold stratified cross-validation and was validated with a 30% holdout test dataset. Eighty-two thousand five hundred fifty-three prescribing data for prednisolone tablets containing 135 dose-corrected positive cases were obtained. In the original dataset (without SMOTE), only the BRF model showed a good performance (in test dataset, ROC-AUC:0.917, recall: 0.951). In the training dataset preprocessed by SMOTE, performance was improved on all models. The highest performance models with SMOTE were SVM (in test dataset, ROC-AUC: 0.820, recall: 0.659) and BRF (ROC-AUC: 0.814, recall: 0.634). Although the prescribing data for dose-related collection are highly imbalanced, various techniques such as the following have allowed us to build high-performance prediction models: data preprocessing by SMOTE, stratified cross-validation, and BRF classifier corresponding to imbalanced data. ML is useful in complicated dose audits such as oral prednisolone. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s41666-023-00128-3.
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spelling pubmed-99956282023-03-10 Prediction of Prednisolone Dose Correction Using Machine Learning Sato, Hiroyasu Kimura, Yoshinobu Ohba, Masahiro Ara, Yoshiaki Wakabayashi, Susumu Watanabe, Hiroaki J Healthc Inform Res Research Article Wrong dose, a common prescription error, can cause serious patient harm, especially in the case of high-risk drugs like oral corticosteroids. This study aims to build a machine learning model to predict dose-related prescription modifications for oral prednisolone tablets (i.e., highly imbalanced data with very few positive cases). Prescription data were obtained from the electronic medical records at a single institute. Cluster analysis classified the clinical departments into six clusters with similar patterns of prednisolone prescription. Two patterns of training datasets were created with/without preprocessing by the SMOTE method. Five ML models (SVM, KNN, GB, RF, and BRF) and logistic regression (LR) models were constructed by Python. The model was internally validated by five-fold stratified cross-validation and was validated with a 30% holdout test dataset. Eighty-two thousand five hundred fifty-three prescribing data for prednisolone tablets containing 135 dose-corrected positive cases were obtained. In the original dataset (without SMOTE), only the BRF model showed a good performance (in test dataset, ROC-AUC:0.917, recall: 0.951). In the training dataset preprocessed by SMOTE, performance was improved on all models. The highest performance models with SMOTE were SVM (in test dataset, ROC-AUC: 0.820, recall: 0.659) and BRF (ROC-AUC: 0.814, recall: 0.634). Although the prescribing data for dose-related collection are highly imbalanced, various techniques such as the following have allowed us to build high-performance prediction models: data preprocessing by SMOTE, stratified cross-validation, and BRF classifier corresponding to imbalanced data. ML is useful in complicated dose audits such as oral prednisolone. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s41666-023-00128-3. Springer International Publishing 2023-02-15 /pmc/articles/PMC9995628/ /pubmed/36910914 http://dx.doi.org/10.1007/s41666-023-00128-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Sato, Hiroyasu
Kimura, Yoshinobu
Ohba, Masahiro
Ara, Yoshiaki
Wakabayashi, Susumu
Watanabe, Hiroaki
Prediction of Prednisolone Dose Correction Using Machine Learning
title Prediction of Prednisolone Dose Correction Using Machine Learning
title_full Prediction of Prednisolone Dose Correction Using Machine Learning
title_fullStr Prediction of Prednisolone Dose Correction Using Machine Learning
title_full_unstemmed Prediction of Prednisolone Dose Correction Using Machine Learning
title_short Prediction of Prednisolone Dose Correction Using Machine Learning
title_sort prediction of prednisolone dose correction using machine learning
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9995628/
https://www.ncbi.nlm.nih.gov/pubmed/36910914
http://dx.doi.org/10.1007/s41666-023-00128-3
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