2020
DOI: 10.1155/2020/7189519
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Clinical Performance of the Automated LIAISON® Meridian H. pylori SA Stool Antigen Test

Abstract: 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 SA chemiluminescent immunoassay against more invasive biopsy tests that are considered to be the “gold standard” (Composite Reference Method). Methods. This prospective multisite study enrolled patients undergoing an esophagogastroduodenoscopy with… Show more

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Cited by 17 publications
(13 citation statements)
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References 37 publications
(32 reference statements)
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“…The test was used on 277 patients for whom an endoscopy was performed. Compared to a composite reference test including histology, culture and a RUT, the LIAISON ® Meridian H pylori SAT gave a sensitivity of 95.5% and a specificity of 97.6% confirming its usefulness in detecting H pylori 37 …”
Section: Non‐invasive Testsmentioning
confidence: 83%
“…The test was used on 277 patients for whom an endoscopy was performed. Compared to a composite reference test including histology, culture and a RUT, the LIAISON ® Meridian H pylori SAT gave a sensitivity of 95.5% and a specificity of 97.6% confirming its usefulness in detecting H pylori 37 …”
Section: Non‐invasive Testsmentioning
confidence: 83%
“…This test uses a monoclonal antibody sandwich method and chemiluminescent immunoassay technology. A sensitivity of 95.5% and a specificity of 97.6% were obtained for LIAISON, in comparison to a sensitivity and specificity exceeding 80% in previously used monoclonal antibody-based tests [ 100 ]. In a recent comparison of LIAISON ® with an ELISA test procedure (RIDASCREEN ® , R-Biopharm, Darmstadt, Germany) and an immunochromatography test from the same company (RIDAQUICK ® ), very comparable results were demonstrated for the diagnostic accuracy of the mentioned tests [ 101 ].…”
Section: Noninvasive Methodsmentioning
confidence: 95%
“…Eradication of H. pylori was defined by a negative stool antigen test, according to standard clinical practice in our center, performed 4–8 weeks after the end of retreatment. The test used was “LIAISON ® Meridian H. pylori SA”, a chemiluminescent immunoassay (CLIA) stool antigen test, which applies monoclonal antibodies (DiaSorin Iberia S.A., Madrid, Spain) [ 35 ].…”
Section: Methodsmentioning
confidence: 99%