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      Identifying hiatal hernia with impedance planimetry during esophageal distension testing

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          Abstract

          Introduction

          Functional luminal imaging probe (FLIP) Panometry evaluates the esophageal response to distension involving biomechanics and motility. We have observed that hiatus hernia (HH) is evident during FLIP studies as a separation between the crural diaphragm (CD) and lower esophageal sphincter (LES) like what is seen with high‐resolution manometry (HRM). The aim of this study was to compare FLIP findings to endoscopy and HRM in the detection of HH.

          Methods

          A total of 100 consecutive patients that completed FLIP during sedated endoscopy and HRM were included. LES‐CD separation was assessed on FLIP and HRM with the presence of HH defined as LES‐CD ≥1 cm. The agreement was evaluated using the kappa ( κ) statistic.

          Results

          Hiatal hernia was detected in 32% of patients on HRM and 44% of patients on FLIP with a substantial agreement between studies (84% agreement; κ = 0.667). On FLIP, a ‘new’ HH (i.e. HH not observed on HRM) occurred in 14 patients and an “enlarged” HH (i.e., LES‐CD ≥2 cm larger than on HRM) occurred in 11 patients. Among patients that also completed, timed barium esophagogram (TBE), delayed esophageal emptying on TBE was more common in patients with new or enlarged HH on FLIP than those without: 7/11 (64%) versus 2/12 (17%); p = 0.017.

          Conclusion

          FLIP can detect HH with a substantial agreement with HRM, though esophageal distension with FLIP testing appeared to elicit and/or enlarge a HH in an additional 25% of patients. Although this unique response to esophageal distension may represent a mechanism of dysphagia or susceptibility to reflux, additional study is needed to clarify its significance.

          Abstract

          Functional lumen imaging probe (FLIP) Panometry can detect hiatal hernia with a substantial agreement with high‐resolution manometry, though esophageal distension with FLIP testing appeared to elicit and/or enlarge a HH in an additional 25% of patients.

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          Most cited references30

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          Esophageal motility disorders on high‐resolution manometry: Chicago classification version 4.0 ©

          Chicago Classification v4.0 (CCv4.0) is the updated classification scheme for esophageal motility disorders using metrics from high-resolution manometry (HRM). Fifty-two diverse international experts separated into seven working subgroups utilized formal validated methodologies over two-years to develop CCv4.0. Key updates in CCv.4.0 consist of a more rigorous and expansive HRM protocol that incorporates supine and upright test positions as well as provocative testing, a refined definition of esophagogastric junction (EGJ) outflow obstruction (EGJOO), more stringent diagnostic criteria for ineffective esophageal motility and description of baseline EGJ metrics. Further, the CCv4.0 sought to define motility disorder diagnoses as conclusive and inconclusive based on associated symptoms, and findings on provocative testing as well as supportive testing with barium esophagram with tablet and/or functional lumen imaging probe. These changes attempt to minimize ambiguity in prior iterations of Chicago Classification and provide more standardized and rigorous criteria for patterns of disorders of peristalsis and obstruction at the EGJ.
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            Validation of the GerdQ questionnaire for the diagnosis of gastro-oesophageal reflux disease.

            The diagnosis of gastro-oesophageal reflux disease (GERD) remains a challenge as both invasive methods and symptom-based strategies have limitations. The symptom-based management of GERD in primary care may be further optimised with the use of a questionnaire. To assess the diagnostic validity of the GerdQ questionnaire in patients with symptoms suggestive of GERD. Patients with symptoms suggestive of GERD without alarm features, underwent upper endoscopy, and if normal, pH-metry. Patients were followed for 4 weeks and GerdQ was completed blinded to the investigator at both visits. Reflux oesophagitis or pathological acid exposure was used as diagnostic references for GERD. The diagnostic accuracy for GERD on symptom response to proton pump inhibitor (PPI) was assessed. Among the 169 patients, a GerdQ cutoff ≥9 gave the best balance with regard to sensitivity, 66% (95% CI: 58-74), and specificity, 64% (95% CI: 41-83), for GERD. The high prevalence of reflux oesophagitis (81%) resulted in a high proportion of true positives, but at the same time a high proportion of false-negatives. Consequently, GerdQ had a high positive predictive value, 92% (95% CI: 86-97), but a low negative predictive value, 22% (95% CI: 13-34), for GERD. Symptom resolution on PPI therapy had high sensitivity, 76% (95% CI: 66-84), but low specificity, 33% (95% CI: 17-53), for GERD. GerdQ is a useful complementary tool for the diagnosis of gastro-oesophageal reflux disease in primary care. The implementation of GerdQ could reduce the need for upper endoscopy and improve resource utilisation. Symptom resolution on proton pump inhibitor did not predict gastro-oesophageal reflux disease. © 2013 Blackwell Publishing Ltd.
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              Evaluation of Esophageal Motility Utilizing the Functional Lumen Imaging Probe.

              Esophagogastric junction (EGJ) distensibility and distension-mediated peristalsis can be assessed with the functional lumen imaging probe (FLIP) during a sedated upper endoscopy. We aimed to describe esophageal motility assessment using FLIP topography in patients presenting with dysphagia.
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                Author and article information

                Contributors
                dustin-carlson@northwestern.edu
                Journal
                Neurogastroenterol Motil
                Neurogastroenterol Motil
                10.1111/(ISSN)1365-2982
                NMO
                Neurogastroenterology and Motility
                John Wiley and Sons Inc. (Hoboken )
                1350-1925
                1365-2982
                27 September 2022
                February 2023
                : 35
                : 2 ( doiID: 10.1111/nmo.v35.2 )
                : e14470
                Affiliations
                [ 1 ] Division of Gastroenterology and Hepatology, Department of Medicine, Feinberg School of Medicine Northwestern University Chicago Illinois USA
                [ 2 ] Department of Biomedical Sciences Humanitas University Pieve Emanuele Italy
                [ 3 ] Department of Surgery, Feinberg School of Medicine Northwestern University Chicago Illinois USA
                Author notes
                [*] [* ] Correspondence

                Dustin A. Carlson, Division of Gastroenterology and Hepatology, Department of Medicine, Feinberg School of Medicine, Northwestern University, 676 St Clair St, Suite 1400, Chicago, IL 60611‐2951, USA.

                Email: dustin-carlson@ 123456northwestern.edu

                Author information
                https://orcid.org/0000-0002-1702-7758
                https://orcid.org/0000-0002-8260-1250
                https://orcid.org/0000-0003-2582-2070
                Article
                NMO14470 NMO-00104-2022.R1
                10.1111/nmo.14470
                10078178
                36168153
                240b4868-f7c4-49e8-8d28-b600d68ab79c
                © 2022 The Authors. Neurogastroenterology & Motility published by John Wiley & Sons Ltd.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

                History
                : 29 July 2022
                : 14 March 2022
                : 12 September 2022
                Page count
                Figures: 4, Tables: 4, Pages: 9, Words: 5220
                Funding
                Funded by: American College of Gastroenterology , doi 10.13039/100007827;
                Funded by: National Institute of Diabetes and Digestive and Kidney Diseases , doi 10.13039/100000062;
                Categories
                Original Article
                Original Articles
                Custom metadata
                2.0
                February 2023
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.2.7 mode:remove_FC converted:06.04.2023

                Gastroenterology & Hepatology
                esophagogastric junction,heartburn,hernia,hiatal,manometry,motility
                Gastroenterology & Hepatology
                esophagogastric junction, heartburn, hernia, hiatal, manometry, motility

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