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Application of deep learning algorithm to detect and visualize vertebral fractures on plain frontal radiographs
BACKGROUND: Identification of vertebral fractures (VFs) is critical for effective secondary fracture prevention owing to their association with the increasing risks of future fractures. Plain abdominal frontal radiographs (PARs) are a common investigation method performed for a variety of clinical i...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7842883/ https://www.ncbi.nlm.nih.gov/pubmed/33507982 http://dx.doi.org/10.1371/journal.pone.0245992 |
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author | Chen, Hsuan-Yu Hsu, Benny Wei-Yun Yin, Yu-Kai Lin, Feng-Huei Yang, Tsung-Han Yang, Rong-Sen Lee, Chih-Kuo Tseng, Vincent S. |
author_facet | Chen, Hsuan-Yu Hsu, Benny Wei-Yun Yin, Yu-Kai Lin, Feng-Huei Yang, Tsung-Han Yang, Rong-Sen Lee, Chih-Kuo Tseng, Vincent S. |
author_sort | Chen, Hsuan-Yu |
collection | PubMed |
description | BACKGROUND: Identification of vertebral fractures (VFs) is critical for effective secondary fracture prevention owing to their association with the increasing risks of future fractures. Plain abdominal frontal radiographs (PARs) are a common investigation method performed for a variety of clinical indications and provide an ideal platform for the opportunistic identification of VF. This study uses a deep convolutional neural network (DCNN) to identify the feasibility for the screening, detection, and localization of VFs using PARs. METHODS: A DCNN was pretrained using ImageNet and retrained with 1306 images from the PARs database obtained between August 2015 and December 2018. The accuracy, sensitivity, specificity, and area under the receiver operating characteristic curve (AUC) were evaluated. The visualization algorithm gradient-weighted class activation mapping (Grad-CAM) was used for model interpretation. RESULTS: Only 46.6% (204/438) of the VFs were diagnosed in the original PARs reports. The algorithm achieved 73.59% accuracy, 73.81% sensitivity, 73.02% specificity, and an AUC of 0.72 in the VF identification. CONCLUSION: Computer driven solutions integrated with the DCNN have the potential to identify VFs with good accuracy when used opportunistically on PARs taken for a variety of clinical purposes. The proposed model can help clinicians become more efficient and economical in the current clinical pathway of fragile fracture treatment. |
format | Online Article Text |
id | pubmed-7842883 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-78428832021-02-02 Application of deep learning algorithm to detect and visualize vertebral fractures on plain frontal radiographs Chen, Hsuan-Yu Hsu, Benny Wei-Yun Yin, Yu-Kai Lin, Feng-Huei Yang, Tsung-Han Yang, Rong-Sen Lee, Chih-Kuo Tseng, Vincent S. PLoS One Research Article BACKGROUND: Identification of vertebral fractures (VFs) is critical for effective secondary fracture prevention owing to their association with the increasing risks of future fractures. Plain abdominal frontal radiographs (PARs) are a common investigation method performed for a variety of clinical indications and provide an ideal platform for the opportunistic identification of VF. This study uses a deep convolutional neural network (DCNN) to identify the feasibility for the screening, detection, and localization of VFs using PARs. METHODS: A DCNN was pretrained using ImageNet and retrained with 1306 images from the PARs database obtained between August 2015 and December 2018. The accuracy, sensitivity, specificity, and area under the receiver operating characteristic curve (AUC) were evaluated. The visualization algorithm gradient-weighted class activation mapping (Grad-CAM) was used for model interpretation. RESULTS: Only 46.6% (204/438) of the VFs were diagnosed in the original PARs reports. The algorithm achieved 73.59% accuracy, 73.81% sensitivity, 73.02% specificity, and an AUC of 0.72 in the VF identification. CONCLUSION: Computer driven solutions integrated with the DCNN have the potential to identify VFs with good accuracy when used opportunistically on PARs taken for a variety of clinical purposes. The proposed model can help clinicians become more efficient and economical in the current clinical pathway of fragile fracture treatment. Public Library of Science 2021-01-28 /pmc/articles/PMC7842883/ /pubmed/33507982 http://dx.doi.org/10.1371/journal.pone.0245992 Text en © 2021 Chen et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Chen, Hsuan-Yu Hsu, Benny Wei-Yun Yin, Yu-Kai Lin, Feng-Huei Yang, Tsung-Han Yang, Rong-Sen Lee, Chih-Kuo Tseng, Vincent S. Application of deep learning algorithm to detect and visualize vertebral fractures on plain frontal radiographs |
title | Application of deep learning algorithm to detect and visualize vertebral fractures on plain frontal radiographs |
title_full | Application of deep learning algorithm to detect and visualize vertebral fractures on plain frontal radiographs |
title_fullStr | Application of deep learning algorithm to detect and visualize vertebral fractures on plain frontal radiographs |
title_full_unstemmed | Application of deep learning algorithm to detect and visualize vertebral fractures on plain frontal radiographs |
title_short | Application of deep learning algorithm to detect and visualize vertebral fractures on plain frontal radiographs |
title_sort | application of deep learning algorithm to detect and visualize vertebral fractures on plain frontal radiographs |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7842883/ https://www.ncbi.nlm.nih.gov/pubmed/33507982 http://dx.doi.org/10.1371/journal.pone.0245992 |
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