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Taking the Next Steps in Endoscopic Visual Assessment of Barrett’s Esophagus: A Pilot Study
PURPOSE: Patients with Barrett’s esophagus (BE) undergo surveillance endoscopies to assess for pre-cancerous changes. We developed a simple endoscopic classification method for predicting non-dysplastic BE (NDBE), low-grade dysplasia (LGD)/indefinite for dysplasia (ID) and high-grade dysplasia (HGD)...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8075180/ https://www.ncbi.nlm.nih.gov/pubmed/33911891 http://dx.doi.org/10.2147/CEG.S293477 |
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author | Chis, Roxana Hew, Simon Hopman, Wilma Hookey, Lawrence Bechara, Robert |
author_facet | Chis, Roxana Hew, Simon Hopman, Wilma Hookey, Lawrence Bechara, Robert |
author_sort | Chis, Roxana |
collection | PubMed |
description | PURPOSE: Patients with Barrett’s esophagus (BE) undergo surveillance endoscopies to assess for pre-cancerous changes. We developed a simple endoscopic classification method for predicting non-dysplastic BE (NDBE), low-grade dysplasia (LGD)/indefinite for dysplasia (ID) and high-grade dysplasia (HGD)/early esophageal adenocarcinoma (EAC). PATIENTS AND METHODS: Twenty-two patients with BE underwent endoscopy using the PENTAX Medical MagniView gastroscope and OPTIVISTA processor. Sixty-six video-still images were analyzed to characterize the microsurface, microvasculature and the presence of a demarcation line. Class A was characterized by regular microvascular and microsurface patterns and absence of a demarcation line, class B by changes in the microvascular and/or microsurface patterns compared to the background mucosa with presence of a demarcation line, and class C by irregular microvascular and/or irregular microsurface patterns with presence of a demarcation line. RESULTS: Of the class A images, 97.9% were NDBE. For class B, 69.2% were LGD/ID and 30.8% NDBE. One hundred percent of the class C samples were HGD/EAC. The sensitivity of our classification system was 93.8%, specificity 92%, positive predictive value 78.9%, negative predictive value 97.9% and an accuracy 92.4%. CONCLUSION: In this study, we developed a simple classification system for the prediction of NDBE, LGD/ID and HGD/EAC. Its real-time clinical applicability will be validated prospectively. |
format | Online Article Text |
id | pubmed-8075180 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-80751802021-04-27 Taking the Next Steps in Endoscopic Visual Assessment of Barrett’s Esophagus: A Pilot Study Chis, Roxana Hew, Simon Hopman, Wilma Hookey, Lawrence Bechara, Robert Clin Exp Gastroenterol Original Research PURPOSE: Patients with Barrett’s esophagus (BE) undergo surveillance endoscopies to assess for pre-cancerous changes. We developed a simple endoscopic classification method for predicting non-dysplastic BE (NDBE), low-grade dysplasia (LGD)/indefinite for dysplasia (ID) and high-grade dysplasia (HGD)/early esophageal adenocarcinoma (EAC). PATIENTS AND METHODS: Twenty-two patients with BE underwent endoscopy using the PENTAX Medical MagniView gastroscope and OPTIVISTA processor. Sixty-six video-still images were analyzed to characterize the microsurface, microvasculature and the presence of a demarcation line. Class A was characterized by regular microvascular and microsurface patterns and absence of a demarcation line, class B by changes in the microvascular and/or microsurface patterns compared to the background mucosa with presence of a demarcation line, and class C by irregular microvascular and/or irregular microsurface patterns with presence of a demarcation line. RESULTS: Of the class A images, 97.9% were NDBE. For class B, 69.2% were LGD/ID and 30.8% NDBE. One hundred percent of the class C samples were HGD/EAC. The sensitivity of our classification system was 93.8%, specificity 92%, positive predictive value 78.9%, negative predictive value 97.9% and an accuracy 92.4%. CONCLUSION: In this study, we developed a simple classification system for the prediction of NDBE, LGD/ID and HGD/EAC. Its real-time clinical applicability will be validated prospectively. Dove 2021-04-22 /pmc/articles/PMC8075180/ /pubmed/33911891 http://dx.doi.org/10.2147/CEG.S293477 Text en © 2021 Chis et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Chis, Roxana Hew, Simon Hopman, Wilma Hookey, Lawrence Bechara, Robert Taking the Next Steps in Endoscopic Visual Assessment of Barrett’s Esophagus: A Pilot Study |
title | Taking the Next Steps in Endoscopic Visual Assessment of Barrett’s Esophagus: A Pilot Study |
title_full | Taking the Next Steps in Endoscopic Visual Assessment of Barrett’s Esophagus: A Pilot Study |
title_fullStr | Taking the Next Steps in Endoscopic Visual Assessment of Barrett’s Esophagus: A Pilot Study |
title_full_unstemmed | Taking the Next Steps in Endoscopic Visual Assessment of Barrett’s Esophagus: A Pilot Study |
title_short | Taking the Next Steps in Endoscopic Visual Assessment of Barrett’s Esophagus: A Pilot Study |
title_sort | taking the next steps in endoscopic visual assessment of barrett’s esophagus: a pilot study |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8075180/ https://www.ncbi.nlm.nih.gov/pubmed/33911891 http://dx.doi.org/10.2147/CEG.S293477 |
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