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Deep learning-based detection and segmentation of diffusion abnormalities in acute ischemic stroke
BACKGROUND: Accessible tools to efficiently detect and segment diffusion abnormalities in acute strokes are highly anticipated by the clinical and research communities. METHODS: We developed a tool with deep learning networks trained and tested on a large dataset of 2,348 clinical diffusion weighted...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9053217/ https://www.ncbi.nlm.nih.gov/pubmed/35602200 http://dx.doi.org/10.1038/s43856-021-00062-8 |
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author | Liu, Chin-Fu Hsu, Johnny Xu, Xin Ramachandran, Sandhya Wang, Victor Miller, Michael I. Hillis, Argye E. Faria, Andreia V. |
author_facet | Liu, Chin-Fu Hsu, Johnny Xu, Xin Ramachandran, Sandhya Wang, Victor Miller, Michael I. Hillis, Argye E. Faria, Andreia V. |
author_sort | Liu, Chin-Fu |
collection | PubMed |
description | BACKGROUND: Accessible tools to efficiently detect and segment diffusion abnormalities in acute strokes are highly anticipated by the clinical and research communities. METHODS: We developed a tool with deep learning networks trained and tested on a large dataset of 2,348 clinical diffusion weighted MRIs of patients with acute and sub-acute ischemic strokes, and further tested for generalization on 280 MRIs of an external dataset (STIR). RESULTS: Our proposed model outperforms generic networks and DeepMedic, particularly in small lesions, with lower false positive rate, balanced precision and sensitivity, and robustness to data perturbs (e.g., artefacts, low resolution, technical heterogeneity). The agreement with human delineation rivals the inter-evaluator agreement; the automated lesion quantification of volume and contrast has virtually total agreement with human quantification. CONCLUSION: Our tool is fast, public, accessible to non-experts, with minimal computational requirements, to detect and segment lesions via a single command line. Therefore, it fulfills the conditions to perform large scale, reliable and reproducible clinical and translational research. |
format | Online Article Text |
id | pubmed-9053217 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-90532172022-05-20 Deep learning-based detection and segmentation of diffusion abnormalities in acute ischemic stroke Liu, Chin-Fu Hsu, Johnny Xu, Xin Ramachandran, Sandhya Wang, Victor Miller, Michael I. Hillis, Argye E. Faria, Andreia V. Commun Med (Lond) Article BACKGROUND: Accessible tools to efficiently detect and segment diffusion abnormalities in acute strokes are highly anticipated by the clinical and research communities. METHODS: We developed a tool with deep learning networks trained and tested on a large dataset of 2,348 clinical diffusion weighted MRIs of patients with acute and sub-acute ischemic strokes, and further tested for generalization on 280 MRIs of an external dataset (STIR). RESULTS: Our proposed model outperforms generic networks and DeepMedic, particularly in small lesions, with lower false positive rate, balanced precision and sensitivity, and robustness to data perturbs (e.g., artefacts, low resolution, technical heterogeneity). The agreement with human delineation rivals the inter-evaluator agreement; the automated lesion quantification of volume and contrast has virtually total agreement with human quantification. CONCLUSION: Our tool is fast, public, accessible to non-experts, with minimal computational requirements, to detect and segment lesions via a single command line. Therefore, it fulfills the conditions to perform large scale, reliable and reproducible clinical and translational research. Nature Publishing Group UK 2021-12-16 /pmc/articles/PMC9053217/ /pubmed/35602200 http://dx.doi.org/10.1038/s43856-021-00062-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Liu, Chin-Fu Hsu, Johnny Xu, Xin Ramachandran, Sandhya Wang, Victor Miller, Michael I. Hillis, Argye E. Faria, Andreia V. Deep learning-based detection and segmentation of diffusion abnormalities in acute ischemic stroke |
title | Deep learning-based detection and segmentation of diffusion abnormalities in acute ischemic stroke |
title_full | Deep learning-based detection and segmentation of diffusion abnormalities in acute ischemic stroke |
title_fullStr | Deep learning-based detection and segmentation of diffusion abnormalities in acute ischemic stroke |
title_full_unstemmed | Deep learning-based detection and segmentation of diffusion abnormalities in acute ischemic stroke |
title_short | Deep learning-based detection and segmentation of diffusion abnormalities in acute ischemic stroke |
title_sort | deep learning-based detection and segmentation of diffusion abnormalities in acute ischemic stroke |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9053217/ https://www.ncbi.nlm.nih.gov/pubmed/35602200 http://dx.doi.org/10.1038/s43856-021-00062-8 |
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