Related Experiment Video
Updated: May 4, 2026

14:13
Coordinate Mapping of Hyolaryngeal Mechanics in Swallowing
Published on: May 6, 2014
17.9K
Developing consensus in post-myotomy dysphagia: a Delphi study integrating anatomic and physiologic assessment from
Shree Patel1, Joshua Robertson2, William Breaux2
1Emory University Division of Digestive Diseases, Atlanta, GA, 30309, USA. Sshri72@gmail.com.
Surgical Endoscopy
|March 4, 2026
Summary
Recurrent dysphagia after myotomy is hard to classify. Experts developed a consensus framework prioritizing anatomy over physiology to standardize diagnosis of post-myotomy dysphagia.
Area of Science:
- Gastroenterology
- Esophageal Disorders
- Surgical Outcomes
Background:
- Recurrent dysphagia post-myotomy presents diagnostic challenges due to multifactorial causes.
- Current diagnostic tools like HRM, FLIP, and contrast studies lack a standardized framework for integrating findings.
- The ACTION consortium aimed to address this gap in post-myotomy dysphagia assessment.
Purpose of the Study:
- To evaluate inter-rater agreement among experts on the mechanisms of recurrent dysphagia after esophageal myotomy.
- To develop an early consensus on a standardized diagnostic framework for post-myotomy dysphagia using a modified Delphi process.
Main Methods:
- Part 1: Six experts assessed 42 anonymized cases, assigning failure mechanisms and measuring inter-rater agreement (Fleiss' kappa).
- Physiologic data (IRP, DI) were analyzed across agreement levels.
- Part 2: A modified Delphi process with 13 experts refined consensus statements over two rounds.
Main Results:
- Fair inter-rater agreement (κ=0.25) was observed in initial case reviews.
- Physiologic measures alone did not consistently predict expert interpretation.
- A consensus was reached on 13 of 15 statements, advocating an anatomy-first approach with context-dependent physiologic data interpretation.
Conclusions:
- Significant variability exists in expert assessment of post-myotomy dysphagia.
- The study established early consensus on key myotomy failure mechanisms.
- Reproducible anatomic subtypes were identified to support standardized diagnostic pathways for post-myotomy dysphagia.
Related Concept Videos
Imaging Studies III: Gastrointestinal Motility Studies and Virtual Colonoscopy
663
This lesson explores three gastrointestinal imaging techniques: radionuclide testing, colonic transit studies, and virtual colonoscopy.
Radionuclide Testing
Radionuclide testing is a sophisticated medical technique for assessing gastrointestinal motility. It focuses on gastric emptying and colonic transit time. Radioactive markers track the movement of food through the digestive system, providing insights into gastrointestinal disorders.
In gastric emptying studies, a meal's liquid and...
Radionuclide Testing
Radionuclide testing is a sophisticated medical technique for assessing gastrointestinal motility. It focuses on gastric emptying and colonic transit time. Radioactive markers track the movement of food through the digestive system, providing insights into gastrointestinal disorders.
In gastric emptying studies, a meal's liquid and...
663
Endoscopic Procedures I: Esophagogastroduodenoscopy
2.4K
An Esophagogastroduodenoscopy (EGD) is a diagnostic procedure in which an endoscopist uses a flexible, lighted endoscope to visualize the upper gastrointestinal (GI) tract. The procedure includes visualizing the oropharynx, esophagus, stomach, and the first part of the small intestine, the duodenum.
During an EGD, the endoscope can be used to:
During an EGD, the endoscope can be used to:
2.4K
Esophageal Achalasia
45
Esophageal achalasia is a chronic neurogenic disorder characterized by impaired relaxation of the lower esophageal sphincter (LES) and absent or ineffective peristalsis in the distal esophagus. This leads to a functional obstruction without a physical blockage, despite significant disruption of esophageal motility.EtiologyAchalasia is caused by degeneration of the myenteric (Auerbach's) plexus, specifically the loss of inhibitory ganglion cells that produce vasoactive intestinal peptide...
45

