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Comparison of the diagnostic accuracy of the updated Sydney system and single biopsy

BACKGROUND: Updated Sydney system (USS) recommends taking biopsies from certain areas of the stomach for the diagnosis of precancerous lesions associated with Helicobacter pylori. Our aim was to evaluate the contribution of each of the biopsy sites to the diagnosis. METHODS: This prospective study i...

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Autores principales: Torun, Cundullah, Yavuz, Arda, Akan, Kubra, Seneldir, Hatice, Toksoz, Ayse Nur, Ulasoglu, Hak Celal, Tuncer, Ilyas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9843512/
https://www.ncbi.nlm.nih.gov/pubmed/35899924
http://dx.doi.org/10.4103/sjg.sjg_146_22
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author Torun, Cundullah
Yavuz, Arda
Akan, Kubra
Seneldir, Hatice
Toksoz, Ayse Nur
Ulasoglu, Hak Celal
Tuncer, Ilyas
author_facet Torun, Cundullah
Yavuz, Arda
Akan, Kubra
Seneldir, Hatice
Toksoz, Ayse Nur
Ulasoglu, Hak Celal
Tuncer, Ilyas
author_sort Torun, Cundullah
collection PubMed
description BACKGROUND: Updated Sydney system (USS) recommends taking biopsies from certain areas of the stomach for the diagnosis of precancerous lesions associated with Helicobacter pylori. Our aim was to evaluate the contribution of each of the biopsy sites to the diagnosis. METHODS: This prospective study included 97 patients aged 40 and over with dyspeptic complaints. Biopsies were taken from five regions: the lesser curvature of the antrum (LCA), the lesser curvature of the corpus (LCC), incisura angularis (IA), the greater curvature of the antrum (GCA), and the greater curvature of the corpus (GCC). Biopsy specimens were stained with hematoxylin–eosin stain, periodic acid Schiff–alcian blue, and Giemsa histochemical stain and evaluated according to the Sydney classification. RESULTS: Thirty-seven (38%) patients were positive for H. pylori in at least one biopsy site. Atrophic gastritis without intestinal metaplasia (IM) was found in 17 (17.5%) of the patients (6.2% in IA, 5.2% in each of LCA, GCA, and LCC, and 2% in GCC). The prevalence of atrophic gastritis with IM was 42.3% (21.6% in LCA, 20.6% in GCA, 20.6% in IA, 14.4% in LCC, and 5.2% in GCC). Endoscopic follow-up was planned in 21 (22%) patients due to the presence of extensive atrophy or incomplete IM. If a single biopsy of the LCA or a biopsy of both LCA and GCA was taken, endoscopic follow-up would have been missed in 12 (57%) or 6 (29%) patients, respectively. CONCLUSION: Taking biopsies in accordance with the USS had higher sensitivity in detecting atrophic gastritis with or without IM compared to single biopsy. One or two biopsies is not sufficient to identify patients for whom endoscopic follow-up is recommended.
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spelling pubmed-98435122023-01-18 Comparison of the diagnostic accuracy of the updated Sydney system and single biopsy Torun, Cundullah Yavuz, Arda Akan, Kubra Seneldir, Hatice Toksoz, Ayse Nur Ulasoglu, Hak Celal Tuncer, Ilyas Saudi J Gastroenterol Original Article BACKGROUND: Updated Sydney system (USS) recommends taking biopsies from certain areas of the stomach for the diagnosis of precancerous lesions associated with Helicobacter pylori. Our aim was to evaluate the contribution of each of the biopsy sites to the diagnosis. METHODS: This prospective study included 97 patients aged 40 and over with dyspeptic complaints. Biopsies were taken from five regions: the lesser curvature of the antrum (LCA), the lesser curvature of the corpus (LCC), incisura angularis (IA), the greater curvature of the antrum (GCA), and the greater curvature of the corpus (GCC). Biopsy specimens were stained with hematoxylin–eosin stain, periodic acid Schiff–alcian blue, and Giemsa histochemical stain and evaluated according to the Sydney classification. RESULTS: Thirty-seven (38%) patients were positive for H. pylori in at least one biopsy site. Atrophic gastritis without intestinal metaplasia (IM) was found in 17 (17.5%) of the patients (6.2% in IA, 5.2% in each of LCA, GCA, and LCC, and 2% in GCC). The prevalence of atrophic gastritis with IM was 42.3% (21.6% in LCA, 20.6% in GCA, 20.6% in IA, 14.4% in LCC, and 5.2% in GCC). Endoscopic follow-up was planned in 21 (22%) patients due to the presence of extensive atrophy or incomplete IM. If a single biopsy of the LCA or a biopsy of both LCA and GCA was taken, endoscopic follow-up would have been missed in 12 (57%) or 6 (29%) patients, respectively. CONCLUSION: Taking biopsies in accordance with the USS had higher sensitivity in detecting atrophic gastritis with or without IM compared to single biopsy. One or two biopsies is not sufficient to identify patients for whom endoscopic follow-up is recommended. Wolters Kluwer - Medknow 2022-07-26 /pmc/articles/PMC9843512/ /pubmed/35899924 http://dx.doi.org/10.4103/sjg.sjg_146_22 Text en Copyright: © 2022 Saudi Journal of Gastroenterology https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Torun, Cundullah
Yavuz, Arda
Akan, Kubra
Seneldir, Hatice
Toksoz, Ayse Nur
Ulasoglu, Hak Celal
Tuncer, Ilyas
Comparison of the diagnostic accuracy of the updated Sydney system and single biopsy
title Comparison of the diagnostic accuracy of the updated Sydney system and single biopsy
title_full Comparison of the diagnostic accuracy of the updated Sydney system and single biopsy
title_fullStr Comparison of the diagnostic accuracy of the updated Sydney system and single biopsy
title_full_unstemmed Comparison of the diagnostic accuracy of the updated Sydney system and single biopsy
title_short Comparison of the diagnostic accuracy of the updated Sydney system and single biopsy
title_sort comparison of the diagnostic accuracy of the updated sydney system and single biopsy
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9843512/
https://www.ncbi.nlm.nih.gov/pubmed/35899924
http://dx.doi.org/10.4103/sjg.sjg_146_22
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