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Esophageal electromyography in scleroderma patients with functional dysphagia
M Bortolotti1, R Pinotti, P Sarti
1First Medical Clinic, University of Bologna, Italy.
The American Journal of Gastroenterology
|December 1, 1989
Summary
Scleroderma patients with dysphagia exhibit two distinct esophageal motor disorders: one with hyperactivity resembling diffuse esophageal spasm, and another with reduced activity typical of scleroderma.
Area of Science:
- Gastroenterology
- Esophageal Motility Disorders
- Connective Tissue Diseases
Background:
- Scleroderma often causes esophageal dysfunction, leading to functional dysphagia.
- The specific esophageal motor abnormalities in scleroderma-associated dysphagia require further elucidation.
Purpose of the Study:
- To investigate the myoelectric and manometric characteristics of the esophagus in patients with scleroderma and functional dysphagia.
- To differentiate between early and advanced stages of esophageal involvement in scleroderma.
Main Methods:
- Simultaneous esophageal electromyography (EMG) and manometry were performed.
- Patients were divided into two groups based on symptom duration and radiographic findings: Group A (recent dysphagia, normal esophagus) and Group B (long-standing dysphagia, dilated esophagus).
- A control group of healthy subjects was included for comparison.
Main Results:
- Normal subjects displayed coordinated esophageal myoelectric and manometric activity.
- Group A patients showed disorganized myoelectric hyperactivity with pressure waves, mimicking diffuse esophageal spasm (DES).
- Group B patients exhibited reduced myoelectric activity and pressure wave amplitudes, consistent with advanced scleroderma esophageal involvement.
Conclusions:
- Functional dysphagia in scleroderma arises from two distinct esophageal motor disorders: myoelectric hyperactivity and reduced myoelectric activity.
- These patterns correlate with different stages of esophageal involvement in scleroderma.
- Myoelectric findings can identify specific motor abnormalities contributing to dysphagia in scleroderma.