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Related Concept Videos

Esophageal Achalasia01:27

Esophageal Achalasia

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 (VIP)...
Gastrointestinal Motility Disorders01:20

Gastrointestinal Motility Disorders

Gastrointestinal or GI motility disorders are characterized by irregular gastrointestinal tract movements, disrupting food transit from the mouth to the anus. They are caused by damage or dysfunction in gut muscles or nerves. These disorders can cause symptoms such as severe constipation, diarrhea, abdominal pain, and swallowing difficulties. Disorders can affect any segment of the GI tract and range widely in severity, from common conditions like GERD to life-threatening conditions like...
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Gastroesophageal Reflux Disease

Gastroesophageal reflux disease (GERD) is the backward flow of stomach contents (acid, pepsin, or bile) into the esophagus, causing mucosal inflammation known as esophagitis. It results from failure of antireflux mechanisms, mainly the lower esophageal sphincter (LES), influenced by mechanical and physiological factors.Etiology and Risk FactorsGERD develops when LES function is weakened or when intra-abdominal pressure increases. Risk factors include aging, obesity, and sliding hiatal hernia,...
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Gastroesophageal Reflux Disease (GERD) involves the recurrent backflow of the stomach or duodenal contents into the esophagus, leading to troublesome symptoms and potential esophageal mucosal damage. Although GERD is often referred to as a disease, it is more accurately described as a syndrome, as it encompasses a range of symptoms and complications rather than a singular pathological entity, impacting a large number of individuals as the most prevalent upper gastrointestinal problem. Roughly...
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Robotic Myotomy and Partial Fundoplication for Achalasia
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Esophageal dysmotility: characterization and pathophysiology.

A Aspirot1, C Faure

  • 1Division of Pediatric Surgery, Sainte-Justine University Health Center, Montreal, Quebec, Canada H3T 1C5. ann.aspirot.hsj@ssss.gouv.qc.ca

Diseases of the Esophagus : Official Journal of the International Society for Diseases of the Esophagus
|May 18, 2013
PubMed
Summary

Esophageal dysmotility is common in patients with esophageal atresia (EA). High-resolution manometry helps characterize specific motility patterns, but correlations with symptoms and long-term evolution remain unclear.

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Area of Science:

  • Gastroenterology
  • Pediatric Surgery
  • Developmental Biology

Background:

  • Esophageal dysmotility is a significant long-term complication in patients with esophageal atresia (EA).
  • Previous studies utilized esophageal manometry to assess motility defects in operated EA patients.
  • Advancements in high-resolution manometry offer improved characterization of esophageal function.

Purpose of the Study:

  • To review normal esophageal motility and detail specific defects in EA patients.
  • To characterize esophageal motility patterns in operated EA patients using high-resolution manometry.
  • To discuss pathophysiological hypotheses for esophageal dysmotility in EA.

Main Methods:

  • Review of normal esophageal motility.
  • Application of high-resolution manometry in patients with operated EA.
  • Description of identified esophageal motility patterns: aperistalsis, pressurization, and distal peristalsis.

Main Results:

  • Three distinct esophageal motility patterns (aperistalsis, pressurization, distal peristalsis) were identified in operated EA patients.
  • No correlation was found between the severity of dysmotility and patient symptomatology.
  • Potential contributing factors include developmental neuronal defects, surgical trauma, and esophagitis from impaired acid clearance.

Conclusions:

  • High-resolution manometry provides enhanced characterization of esophageal motility in EA patients.
  • The etiology of esophageal dysmotility in EA is multifactorial, involving congenital and acquired factors.
  • Further research is needed to understand the long-term evolution of esophageal dysmotility in repaired EA.