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High-definition optical magnification with digital chromoendoscopy detects gastric mucosal changes in dyspeptic-patients

BACKGROUND: Accurate detection of gastric infection by Helicobacter pylori (H. pylori) and premalignant lesions are important for effective provision of treatment, preventing the development of gastric neoplasia. Optical enhancement systems with optical magnification improved the identification of m...

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Autores principales: Robles-Medranda, Carlos, Valero, Manuel, Puga-Tejada, Miguel, Oleas, Roberto, Baquerizo-Burgos, Jorge, Soria-Alcívar, Miguel, Alvarado-Escobar, Haydee, Pitanga-Lukashok, Hannah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2020
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6939121/
https://www.ncbi.nlm.nih.gov/pubmed/31942231
http://dx.doi.org/10.4253/wjge.v12.i1.23
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author Robles-Medranda, Carlos
Valero, Manuel
Puga-Tejada, Miguel
Oleas, Roberto
Baquerizo-Burgos, Jorge
Soria-Alcívar, Miguel
Alvarado-Escobar, Haydee
Pitanga-Lukashok, Hannah
author_facet Robles-Medranda, Carlos
Valero, Manuel
Puga-Tejada, Miguel
Oleas, Roberto
Baquerizo-Burgos, Jorge
Soria-Alcívar, Miguel
Alvarado-Escobar, Haydee
Pitanga-Lukashok, Hannah
author_sort Robles-Medranda, Carlos
collection PubMed
description BACKGROUND: Accurate detection of gastric infection by Helicobacter pylori (H. pylori) and premalignant lesions are important for effective provision of treatment, preventing the development of gastric neoplasia. Optical enhancement systems with optical magnification improved the identification of mucosal superficial and vascular patterns in patients with dyspepsia. AIM: To evaluate an optical enhancement system with high-definition magnification, for diagnosis of normal gastric mucosa, H. pylori-associated gastritis, and gastric atrophy. METHODS: A cross-sectional, nonrandomized study from November 2015 to April 2016 performed in a single-tertiary academic center from Ecuador. Seventy-two consecutive patients with functional dyspepsia according to the Rome III criteria, were tested for H. pylori using a stool antigen test and were assigned to an Hp(+) group or an Hp(−) control group. Esophagogastroduodenoscopy with high-definition optical magnification and digital chromoendoscopy was performed, and patients were classified into 4 groups, in accordance to the microvascular-architecture pattern of the mucosa. Interobserver and intraobserver agreement among operators were calculated. RESULTS: Of the 72 participants, 35 were Hp(+) and 37 were Hp(−). Among 10 patients with normal mucosal histology in biopsy samples, 90% had a Type I pattern of microvascular architecture by endoscopy. Among participants with type IIa and type IIb patterns, significantly more were Hp(+) than Hp(−) (32 vs 8), and most (31 out of 40) had histological diagnoses of chronic active gastritis. Two of the three participants with a histological diagnosis of atrophy had a type III microvascular pattern. The type I pattern predicted normal mucosa, type IIa–IIb predicted H. pylori infection, and type III predicted atrophy with sensitivities of 90.0%, 91.4%, and 66.7%, respectively. The intraobserver and interobserver agreements had kappa values of 0.91 and 0.89, respectively. CONCLUSION: High-definition optical magnification with digital chromoendoscopy is useful for diagnosis of normal gastric mucosa and H. pylori-associated gastritis with high accuracy, but further studies are needed to determine whether endoscopic diagnosis of gastric atrophy is feasible.
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spelling pubmed-69391212020-01-16 High-definition optical magnification with digital chromoendoscopy detects gastric mucosal changes in dyspeptic-patients Robles-Medranda, Carlos Valero, Manuel Puga-Tejada, Miguel Oleas, Roberto Baquerizo-Burgos, Jorge Soria-Alcívar, Miguel Alvarado-Escobar, Haydee Pitanga-Lukashok, Hannah World J Gastrointest Endosc Clinical Trials Study BACKGROUND: Accurate detection of gastric infection by Helicobacter pylori (H. pylori) and premalignant lesions are important for effective provision of treatment, preventing the development of gastric neoplasia. Optical enhancement systems with optical magnification improved the identification of mucosal superficial and vascular patterns in patients with dyspepsia. AIM: To evaluate an optical enhancement system with high-definition magnification, for diagnosis of normal gastric mucosa, H. pylori-associated gastritis, and gastric atrophy. METHODS: A cross-sectional, nonrandomized study from November 2015 to April 2016 performed in a single-tertiary academic center from Ecuador. Seventy-two consecutive patients with functional dyspepsia according to the Rome III criteria, were tested for H. pylori using a stool antigen test and were assigned to an Hp(+) group or an Hp(−) control group. Esophagogastroduodenoscopy with high-definition optical magnification and digital chromoendoscopy was performed, and patients were classified into 4 groups, in accordance to the microvascular-architecture pattern of the mucosa. Interobserver and intraobserver agreement among operators were calculated. RESULTS: Of the 72 participants, 35 were Hp(+) and 37 were Hp(−). Among 10 patients with normal mucosal histology in biopsy samples, 90% had a Type I pattern of microvascular architecture by endoscopy. Among participants with type IIa and type IIb patterns, significantly more were Hp(+) than Hp(−) (32 vs 8), and most (31 out of 40) had histological diagnoses of chronic active gastritis. Two of the three participants with a histological diagnosis of atrophy had a type III microvascular pattern. The type I pattern predicted normal mucosa, type IIa–IIb predicted H. pylori infection, and type III predicted atrophy with sensitivities of 90.0%, 91.4%, and 66.7%, respectively. The intraobserver and interobserver agreements had kappa values of 0.91 and 0.89, respectively. CONCLUSION: High-definition optical magnification with digital chromoendoscopy is useful for diagnosis of normal gastric mucosa and H. pylori-associated gastritis with high accuracy, but further studies are needed to determine whether endoscopic diagnosis of gastric atrophy is feasible. Baishideng Publishing Group Inc 2020-01-16 2020-01-16 /pmc/articles/PMC6939121/ /pubmed/31942231 http://dx.doi.org/10.4253/wjge.v12.i1.23 Text en ©The Author(s) 2019. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.
spellingShingle Clinical Trials Study
Robles-Medranda, Carlos
Valero, Manuel
Puga-Tejada, Miguel
Oleas, Roberto
Baquerizo-Burgos, Jorge
Soria-Alcívar, Miguel
Alvarado-Escobar, Haydee
Pitanga-Lukashok, Hannah
High-definition optical magnification with digital chromoendoscopy detects gastric mucosal changes in dyspeptic-patients
title High-definition optical magnification with digital chromoendoscopy detects gastric mucosal changes in dyspeptic-patients
title_full High-definition optical magnification with digital chromoendoscopy detects gastric mucosal changes in dyspeptic-patients
title_fullStr High-definition optical magnification with digital chromoendoscopy detects gastric mucosal changes in dyspeptic-patients
title_full_unstemmed High-definition optical magnification with digital chromoendoscopy detects gastric mucosal changes in dyspeptic-patients
title_short High-definition optical magnification with digital chromoendoscopy detects gastric mucosal changes in dyspeptic-patients
title_sort high-definition optical magnification with digital chromoendoscopy detects gastric mucosal changes in dyspeptic-patients
topic Clinical Trials Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6939121/
https://www.ncbi.nlm.nih.gov/pubmed/31942231
http://dx.doi.org/10.4253/wjge.v12.i1.23
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