| Literature DB >> 31839408 |
Mouen A Khashab1, Marcelo F Vela2, Nirav Thosani3, Deepak Agrawal4, James L Buxbaum5, Syed M Abbas Fehmi6, Douglas S Fishman7, Suryakanth R Gurudu2, Laith H Jamil8, Terry L Jue9, Bijun Sai Kannadath3, Joanna K Law10, Jeffrey K Lee11, Mariam Naveed12, Bashar J Qumseya13, Mandeep S Sawhney14, Julie Yang15, Sachin Wani16.
Abstract
Achalasia is a primary esophageal motor disorder of unknown etiology characterized by degeneration of the myenteric plexus, which results in impaired relaxation of the esophagogastric junction (EGJ), along with the loss of organized peristalsis in the esophageal body. The criterion standard for diagnosing achalasia is high-resolution esophageal manometry showing incomplete relaxation of the EGJ coupled with the absence of organized peristalsis. Three achalasia subtypes have been defined based on high-resolution manometry findings in the esophageal body. Treatment of patients with achalasia has evolved in recent years with the introduction of peroral endoscopic myotomy. Other treatment options include botulinum toxin injection, pneumatic dilation, and Heller myotomy. This American Society for Gastrointestinal Endoscopy Standards of Practice Guideline provides evidence-based recommendations for the treatment of achalasia, based on an updated assessment of the individual and comparative effectiveness, adverse effects, and cost of the 4 aforementioned achalasia therapies.Entities:
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Year: 2019 PMID: 31839408 DOI: 10.1016/j.gie.2019.04.231
Source DB: PubMed Journal: Gastrointest Endosc ISSN: 0016-5107 Impact factor: 9.427