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Automatic ganglion cell detection for improving the efficiency and accuracy of hirschprung disease diagnosis
Histopathologic diagnosis of Hirschsprung's disease (HSCR) is time consuming and requires expertise. The use of artificial intelligence (AI) in digital pathology is actively researched and may improve the diagnosis of HSCR. The purpose of this research was to develop an algorithm capable of ide...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7870950/ https://www.ncbi.nlm.nih.gov/pubmed/33558593 http://dx.doi.org/10.1038/s41598-021-82869-y |
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author | Greenberg, Ariel Aizic, Asaf Zubkov, Asia Borsekofsky, Sarah Hagege, Rami R. Hershkovitz, Dov |
author_facet | Greenberg, Ariel Aizic, Asaf Zubkov, Asia Borsekofsky, Sarah Hagege, Rami R. Hershkovitz, Dov |
author_sort | Greenberg, Ariel |
collection | PubMed |
description | Histopathologic diagnosis of Hirschsprung's disease (HSCR) is time consuming and requires expertise. The use of artificial intelligence (AI) in digital pathology is actively researched and may improve the diagnosis of HSCR. The purpose of this research was to develop an algorithm capable of identifying ganglion cells in digital pathology slides and implement it as an assisting tool for the pathologist in the diagnosis of HSCR. Ninety five digital pathology slides were used for the construction and training of the algorithm. Fifty cases suspected for HSCR (727 slides) were used as a validation cohort. Image sets suspected to contain ganglion cells were chosen by the algorithm and then reviewed and scored by five pathologists, one HSCR expert and 4 non-experts. The algorithm was able to identify ganglion cells with 96% sensitivity and 99% specificity (in normal colon) as well as to correctly identify a case previously misdiagnosed as non-HSCR. The expert was able to achieve perfectly accurate diagnoses based solely on the images suggested by the algorithm, with over 95% time saved. Non-experts would require expert consultation in 20–58% of the cases to achieve similar results. The use of AI in the diagnosis of HSCR can greatly reduce the time and effort required for diagnosis and improve accuracy. |
format | Online Article Text |
id | pubmed-7870950 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78709502021-02-10 Automatic ganglion cell detection for improving the efficiency and accuracy of hirschprung disease diagnosis Greenberg, Ariel Aizic, Asaf Zubkov, Asia Borsekofsky, Sarah Hagege, Rami R. Hershkovitz, Dov Sci Rep Article Histopathologic diagnosis of Hirschsprung's disease (HSCR) is time consuming and requires expertise. The use of artificial intelligence (AI) in digital pathology is actively researched and may improve the diagnosis of HSCR. The purpose of this research was to develop an algorithm capable of identifying ganglion cells in digital pathology slides and implement it as an assisting tool for the pathologist in the diagnosis of HSCR. Ninety five digital pathology slides were used for the construction and training of the algorithm. Fifty cases suspected for HSCR (727 slides) were used as a validation cohort. Image sets suspected to contain ganglion cells were chosen by the algorithm and then reviewed and scored by five pathologists, one HSCR expert and 4 non-experts. The algorithm was able to identify ganglion cells with 96% sensitivity and 99% specificity (in normal colon) as well as to correctly identify a case previously misdiagnosed as non-HSCR. The expert was able to achieve perfectly accurate diagnoses based solely on the images suggested by the algorithm, with over 95% time saved. Non-experts would require expert consultation in 20–58% of the cases to achieve similar results. The use of AI in the diagnosis of HSCR can greatly reduce the time and effort required for diagnosis and improve accuracy. Nature Publishing Group UK 2021-02-08 /pmc/articles/PMC7870950/ /pubmed/33558593 http://dx.doi.org/10.1038/s41598-021-82869-y Text en © The Author(s) 2021 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 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/. |
spellingShingle | Article Greenberg, Ariel Aizic, Asaf Zubkov, Asia Borsekofsky, Sarah Hagege, Rami R. Hershkovitz, Dov Automatic ganglion cell detection for improving the efficiency and accuracy of hirschprung disease diagnosis |
title | Automatic ganglion cell detection for improving the efficiency and accuracy of hirschprung disease diagnosis |
title_full | Automatic ganglion cell detection for improving the efficiency and accuracy of hirschprung disease diagnosis |
title_fullStr | Automatic ganglion cell detection for improving the efficiency and accuracy of hirschprung disease diagnosis |
title_full_unstemmed | Automatic ganglion cell detection for improving the efficiency and accuracy of hirschprung disease diagnosis |
title_short | Automatic ganglion cell detection for improving the efficiency and accuracy of hirschprung disease diagnosis |
title_sort | automatic ganglion cell detection for improving the efficiency and accuracy of hirschprung disease diagnosis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7870950/ https://www.ncbi.nlm.nih.gov/pubmed/33558593 http://dx.doi.org/10.1038/s41598-021-82869-y |
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