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Additional corpus biopsy enhances the detection of Helicobacter pylori infection in a background of gastritis with atrophy

BACKGROUND: The best sites for biopsy-based tests to evaluate H. pylori infection in gastritis with atrophy are not well known. This study aimed to evaluate the site and sensitivity of biopsy-based tests in terms of degree of gastritis with atrophy. METHODS: One hundred and sixty-four (164) uninvest...

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Autores principales: Lan, Hung-Chieh, Chen, Tseng-Shing, Li, Anna Fen-Yau, Chang, Full-Young, Lin, Han-Chieh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3573986/
https://www.ncbi.nlm.nih.gov/pubmed/23272897
http://dx.doi.org/10.1186/1471-230X-12-182
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author Lan, Hung-Chieh
Chen, Tseng-Shing
Li, Anna Fen-Yau
Chang, Full-Young
Lin, Han-Chieh
author_facet Lan, Hung-Chieh
Chen, Tseng-Shing
Li, Anna Fen-Yau
Chang, Full-Young
Lin, Han-Chieh
author_sort Lan, Hung-Chieh
collection PubMed
description BACKGROUND: The best sites for biopsy-based tests to evaluate H. pylori infection in gastritis with atrophy are not well known. This study aimed to evaluate the site and sensitivity of biopsy-based tests in terms of degree of gastritis with atrophy. METHODS: One hundred and sixty-four (164) uninvestigated dyspepsia patients were enrolled. Biopsy-based tests (i.e., culture, histology Giemsa stain and rapid urease test) and non-invasive tests (anti-H. pylori IgG) were performed. The gold standard of H. pylori infection was defined according to previous criteria. The sensitivity, specificity, positive predictive rate and negative predictive rate of biopsy-based tests at the gastric antrum and body were calculated in terms of degree of gastritis with atrophy. RESULTS: The prevalence rate of H. pylori infection in the 164 patients was 63.4%. Gastritis with atrophy was significantly higher at the antrum than at the body (76% vs. 31%; p<0.001). The sensitivity of biopsy-based test decreased when the degree of gastritis with atrophy increased regardless of biopsy site (for normal, mild, moderate, and severe gastritis with atrophy, the sensitivity of histology Giemsa stain was 100%, 100%, 88%, and 66%, respectively, and 100%, 97%, 91%, and 66%, respectively, for rapid urease test). In moderate to severe antrum or body gastritis with atrophy, additional corpus biopsy resulted in increased sensitivity to 16.67% compare to single antrum biopsy. CONCLUSIONS: In moderate to severe gastritis with atrophy, biopsy-based test should include the corpus for avoiding false negative results.
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spelling pubmed-35739862013-02-16 Additional corpus biopsy enhances the detection of Helicobacter pylori infection in a background of gastritis with atrophy Lan, Hung-Chieh Chen, Tseng-Shing Li, Anna Fen-Yau Chang, Full-Young Lin, Han-Chieh BMC Gastroenterol Research Article BACKGROUND: The best sites for biopsy-based tests to evaluate H. pylori infection in gastritis with atrophy are not well known. This study aimed to evaluate the site and sensitivity of biopsy-based tests in terms of degree of gastritis with atrophy. METHODS: One hundred and sixty-four (164) uninvestigated dyspepsia patients were enrolled. Biopsy-based tests (i.e., culture, histology Giemsa stain and rapid urease test) and non-invasive tests (anti-H. pylori IgG) were performed. The gold standard of H. pylori infection was defined according to previous criteria. The sensitivity, specificity, positive predictive rate and negative predictive rate of biopsy-based tests at the gastric antrum and body were calculated in terms of degree of gastritis with atrophy. RESULTS: The prevalence rate of H. pylori infection in the 164 patients was 63.4%. Gastritis with atrophy was significantly higher at the antrum than at the body (76% vs. 31%; p<0.001). The sensitivity of biopsy-based test decreased when the degree of gastritis with atrophy increased regardless of biopsy site (for normal, mild, moderate, and severe gastritis with atrophy, the sensitivity of histology Giemsa stain was 100%, 100%, 88%, and 66%, respectively, and 100%, 97%, 91%, and 66%, respectively, for rapid urease test). In moderate to severe antrum or body gastritis with atrophy, additional corpus biopsy resulted in increased sensitivity to 16.67% compare to single antrum biopsy. CONCLUSIONS: In moderate to severe gastritis with atrophy, biopsy-based test should include the corpus for avoiding false negative results. BioMed Central 2012-12-29 /pmc/articles/PMC3573986/ /pubmed/23272897 http://dx.doi.org/10.1186/1471-230X-12-182 Text en Copyright ©2012 Lan et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Lan, Hung-Chieh
Chen, Tseng-Shing
Li, Anna Fen-Yau
Chang, Full-Young
Lin, Han-Chieh
Additional corpus biopsy enhances the detection of Helicobacter pylori infection in a background of gastritis with atrophy
title Additional corpus biopsy enhances the detection of Helicobacter pylori infection in a background of gastritis with atrophy
title_full Additional corpus biopsy enhances the detection of Helicobacter pylori infection in a background of gastritis with atrophy
title_fullStr Additional corpus biopsy enhances the detection of Helicobacter pylori infection in a background of gastritis with atrophy
title_full_unstemmed Additional corpus biopsy enhances the detection of Helicobacter pylori infection in a background of gastritis with atrophy
title_short Additional corpus biopsy enhances the detection of Helicobacter pylori infection in a background of gastritis with atrophy
title_sort additional corpus biopsy enhances the detection of helicobacter pylori infection in a background of gastritis with atrophy
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3573986/
https://www.ncbi.nlm.nih.gov/pubmed/23272897
http://dx.doi.org/10.1186/1471-230X-12-182
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