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Patient similarity analytics for explainable clinical risk prediction

BACKGROUND: Clinical risk prediction models (CRPMs) use patient characteristics to estimate the probability of having or developing a particular disease and/or outcome. While CRPMs are gaining in popularity, they have yet to be widely adopted in clinical practice. The lack of explainability and inte...

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Autores principales: Fang, Hao Sen Andrew, Tan, Ngiap Chuan, Tan, Wei Ying, Oei, Ronald Wihal, Lee, Mong Li, Hsu, Wynne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8247104/
https://www.ncbi.nlm.nih.gov/pubmed/34210320
http://dx.doi.org/10.1186/s12911-021-01566-y
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author Fang, Hao Sen Andrew
Tan, Ngiap Chuan
Tan, Wei Ying
Oei, Ronald Wihal
Lee, Mong Li
Hsu, Wynne
author_facet Fang, Hao Sen Andrew
Tan, Ngiap Chuan
Tan, Wei Ying
Oei, Ronald Wihal
Lee, Mong Li
Hsu, Wynne
author_sort Fang, Hao Sen Andrew
collection PubMed
description BACKGROUND: Clinical risk prediction models (CRPMs) use patient characteristics to estimate the probability of having or developing a particular disease and/or outcome. While CRPMs are gaining in popularity, they have yet to be widely adopted in clinical practice. The lack of explainability and interpretability has limited their utility. Explainability is the extent of which a model’s prediction process can be described. Interpretability is the degree to which a user can understand the predictions made by a model. METHODS: The study aimed to demonstrate utility of patient similarity analytics in developing an explainable and interpretable CRPM. Data was extracted from the electronic medical records of patients with type-2 diabetes mellitus, hypertension and dyslipidaemia in a Singapore public primary care clinic. We used modified K-nearest neighbour which incorporated expert input, to develop a patient similarity model on this real-world training dataset (n = 7,041) and validated it on a testing dataset (n = 3,018). The results were compared using logistic regression, random forest (RF) and support vector machine (SVM) models from the same dataset. The patient similarity model was then implemented in a prototype system to demonstrate the identification, explainability and interpretability of similar patients and the prediction process. RESULTS: The patient similarity model (AUROC = 0.718) was comparable to the logistic regression (AUROC = 0.695), RF (AUROC = 0.764) and SVM models (AUROC = 0.766). We packaged the patient similarity model in a prototype web application. A proof of concept demonstrated how the application provided both quantitative and qualitative information, in the form of patient narratives. This information was used to better inform and influence clinical decision-making, such as getting a patient to agree to start insulin therapy. CONCLUSIONS: Patient similarity analytics is a feasible approach to develop an explainable and interpretable CRPM. While the approach is generalizable, it can be used to develop locally relevant information, based on the database it searches. Ultimately, such an approach can generate a more informative CRPMs which can be deployed as part of clinical decision support tools to better facilitate shared decision-making in clinical practice. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12911-021-01566-y.
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spelling pubmed-82471042021-07-02 Patient similarity analytics for explainable clinical risk prediction Fang, Hao Sen Andrew Tan, Ngiap Chuan Tan, Wei Ying Oei, Ronald Wihal Lee, Mong Li Hsu, Wynne BMC Med Inform Decis Mak Research BACKGROUND: Clinical risk prediction models (CRPMs) use patient characteristics to estimate the probability of having or developing a particular disease and/or outcome. While CRPMs are gaining in popularity, they have yet to be widely adopted in clinical practice. The lack of explainability and interpretability has limited their utility. Explainability is the extent of which a model’s prediction process can be described. Interpretability is the degree to which a user can understand the predictions made by a model. METHODS: The study aimed to demonstrate utility of patient similarity analytics in developing an explainable and interpretable CRPM. Data was extracted from the electronic medical records of patients with type-2 diabetes mellitus, hypertension and dyslipidaemia in a Singapore public primary care clinic. We used modified K-nearest neighbour which incorporated expert input, to develop a patient similarity model on this real-world training dataset (n = 7,041) and validated it on a testing dataset (n = 3,018). The results were compared using logistic regression, random forest (RF) and support vector machine (SVM) models from the same dataset. The patient similarity model was then implemented in a prototype system to demonstrate the identification, explainability and interpretability of similar patients and the prediction process. RESULTS: The patient similarity model (AUROC = 0.718) was comparable to the logistic regression (AUROC = 0.695), RF (AUROC = 0.764) and SVM models (AUROC = 0.766). We packaged the patient similarity model in a prototype web application. A proof of concept demonstrated how the application provided both quantitative and qualitative information, in the form of patient narratives. This information was used to better inform and influence clinical decision-making, such as getting a patient to agree to start insulin therapy. CONCLUSIONS: Patient similarity analytics is a feasible approach to develop an explainable and interpretable CRPM. While the approach is generalizable, it can be used to develop locally relevant information, based on the database it searches. Ultimately, such an approach can generate a more informative CRPMs which can be deployed as part of clinical decision support tools to better facilitate shared decision-making in clinical practice. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12911-021-01566-y. BioMed Central 2021-07-01 /pmc/articles/PMC8247104/ /pubmed/34210320 http://dx.doi.org/10.1186/s12911-021-01566-y Text en © The Author(s) 2021 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Fang, Hao Sen Andrew
Tan, Ngiap Chuan
Tan, Wei Ying
Oei, Ronald Wihal
Lee, Mong Li
Hsu, Wynne
Patient similarity analytics for explainable clinical risk prediction
title Patient similarity analytics for explainable clinical risk prediction
title_full Patient similarity analytics for explainable clinical risk prediction
title_fullStr Patient similarity analytics for explainable clinical risk prediction
title_full_unstemmed Patient similarity analytics for explainable clinical risk prediction
title_short Patient similarity analytics for explainable clinical risk prediction
title_sort patient similarity analytics for explainable clinical risk prediction
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8247104/
https://www.ncbi.nlm.nih.gov/pubmed/34210320
http://dx.doi.org/10.1186/s12911-021-01566-y
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