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Clinical Performance of the Automated LIAISON® Meridian H. pylori SA Stool Antigen Test

BACKGROUND: Antigens derived from Helicobacter pylori can be used as stool biomarkers to assist in the diagnosis of H. pylori infection. Since current assays have variable performance, we assessed the clinical performance of the automated LIAISON® Meridian H. pylori infection. Since current assays h...

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Autores principales: Opekun, Antone R., Zierold, Claudia, Rode, Ashli, Blocki, Frank A., Fiorini, Giulia, Saracino, Ilaria Maria, Vaira, Dino, Sutton, Fred M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114771/
https://www.ncbi.nlm.nih.gov/pubmed/32280698
http://dx.doi.org/10.1155/2020/7189519
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author Opekun, Antone R.
Zierold, Claudia
Rode, Ashli
Blocki, Frank A.
Fiorini, Giulia
Saracino, Ilaria Maria
Vaira, Dino
Sutton, Fred M.
author_facet Opekun, Antone R.
Zierold, Claudia
Rode, Ashli
Blocki, Frank A.
Fiorini, Giulia
Saracino, Ilaria Maria
Vaira, Dino
Sutton, Fred M.
author_sort Opekun, Antone R.
collection PubMed
description BACKGROUND: Antigens derived from Helicobacter pylori can be used as stool biomarkers to assist in the diagnosis of H. pylori infection. Since current assays have variable performance, we assessed the clinical performance of the automated LIAISON® Meridian H. pylori infection. Since current assays have variable performance, we assessed the clinical performance of the automated LIAISON® Meridian METHODS: This prospective multisite study enrolled patients undergoing an esophagogastroduodenoscopy with collection of biopsy and stool specimens. Adult patients (≥22 years) participated in the study from February 2017 to August 2018. Specimens of the stomach were tested by three methods, known as the Composite Reference Method: (1) histological evaluation, (2) culture of the organism, and (3) rapid urease detection test. H. pylori infection. Since current assays have variable performance, we assessed the clinical performance of the automated LIAISON® Meridian H. pylori infection. Since current assays have variable performance, we assessed the clinical performance of the automated LIAISON® Meridian RESULTS: 277 patients (63% female) were included in the study. The prevalence of infected subjects was 24.2% in this study cohort. Clinical performance assessed against the Composite Reference Method showed very good agreement (Cohen′s kappa = 0.922), with good sensitivity (95.5%) and specificity (97.6%). Reproducibility study results showed total imprecision ranging from 3.1% to 13.9% CV. CONCLUSION: The automated LIAISON® Meridian H. pylori SA assay brings reliable noninvasive testing for H. pylori to the laboratory that is in very good agreement with the current, more invasive biopsy-based methods such as histology, culture, or rapid urease test. The clinical trial identifiers are NCT03060746 (pretherapy) and NCT03060733 (posttherapy).H. pylori infection. Since current assays have variable performance, we assessed the clinical performance of the automated LIAISON® Meridian H. pylori infection. Since current assays have variable performance, we assessed the clinical performance of the automated LIAISON® Meridian
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spelling pubmed-71147712020-04-11 Clinical Performance of the Automated LIAISON® Meridian H. pylori SA Stool Antigen Test Opekun, Antone R. Zierold, Claudia Rode, Ashli Blocki, Frank A. Fiorini, Giulia Saracino, Ilaria Maria Vaira, Dino Sutton, Fred M. Biomed Res Int Clinical Study BACKGROUND: Antigens derived from Helicobacter pylori can be used as stool biomarkers to assist in the diagnosis of H. pylori infection. Since current assays have variable performance, we assessed the clinical performance of the automated LIAISON® Meridian H. pylori infection. Since current assays have variable performance, we assessed the clinical performance of the automated LIAISON® Meridian METHODS: This prospective multisite study enrolled patients undergoing an esophagogastroduodenoscopy with collection of biopsy and stool specimens. Adult patients (≥22 years) participated in the study from February 2017 to August 2018. Specimens of the stomach were tested by three methods, known as the Composite Reference Method: (1) histological evaluation, (2) culture of the organism, and (3) rapid urease detection test. H. pylori infection. Since current assays have variable performance, we assessed the clinical performance of the automated LIAISON® Meridian H. pylori infection. Since current assays have variable performance, we assessed the clinical performance of the automated LIAISON® Meridian RESULTS: 277 patients (63% female) were included in the study. The prevalence of infected subjects was 24.2% in this study cohort. Clinical performance assessed against the Composite Reference Method showed very good agreement (Cohen′s kappa = 0.922), with good sensitivity (95.5%) and specificity (97.6%). Reproducibility study results showed total imprecision ranging from 3.1% to 13.9% CV. CONCLUSION: The automated LIAISON® Meridian H. pylori SA assay brings reliable noninvasive testing for H. pylori to the laboratory that is in very good agreement with the current, more invasive biopsy-based methods such as histology, culture, or rapid urease test. The clinical trial identifiers are NCT03060746 (pretherapy) and NCT03060733 (posttherapy).H. pylori infection. Since current assays have variable performance, we assessed the clinical performance of the automated LIAISON® Meridian H. pylori infection. Since current assays have variable performance, we assessed the clinical performance of the automated LIAISON® Meridian Hindawi 2020-03-19 /pmc/articles/PMC7114771/ /pubmed/32280698 http://dx.doi.org/10.1155/2020/7189519 Text en Copyright © 2020 Antone R. Opekun et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Study
Opekun, Antone R.
Zierold, Claudia
Rode, Ashli
Blocki, Frank A.
Fiorini, Giulia
Saracino, Ilaria Maria
Vaira, Dino
Sutton, Fred M.
Clinical Performance of the Automated LIAISON® Meridian H. pylori SA Stool Antigen Test
title Clinical Performance of the Automated LIAISON® Meridian H. pylori SA Stool Antigen Test
title_full Clinical Performance of the Automated LIAISON® Meridian H. pylori SA Stool Antigen Test
title_fullStr Clinical Performance of the Automated LIAISON® Meridian H. pylori SA Stool Antigen Test
title_full_unstemmed Clinical Performance of the Automated LIAISON® Meridian H. pylori SA Stool Antigen Test
title_short Clinical Performance of the Automated LIAISON® Meridian H. pylori SA Stool Antigen Test
title_sort clinical performance of the automated liaison® meridian h. pylori sa stool antigen test
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114771/
https://www.ncbi.nlm.nih.gov/pubmed/32280698
http://dx.doi.org/10.1155/2020/7189519
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