Achalasia is an esophageal motility disorder characterized by impaired lower esophageal sphincter (LES) relaxation and failed peristalsis. Common clinical manifestations include dysphagia to solid and liquid foods, chest pain, regurgitation,… Click to show full abstract
Achalasia is an esophageal motility disorder characterized by impaired lower esophageal sphincter (LES) relaxation and failed peristalsis. Common clinical manifestations include dysphagia to solid and liquid foods, chest pain, regurgitation, and weight loss, resulting in significant morbidity and healthcare burden. Historically surgical Heller myotomy and pneumatic dilation represented first-line therapeutic options for achalasia. This convention was shaken in 2009 when Inoue and colleagues introduced an endoscopic approach to dissect the muscle fibers of the LES, known as per-oral endoscopic myotomy (POEM). Since incorporation of POEM into standard practice, the overall myotomy technique has remained unchanged, however, adaptations in the thickness and length of myotomy have evolved. Full thickness myotomy is recognized to have similar clinical success and faster procedure times compared to selective circular muscle myotomy. While myotomy length for Type 1 and Type 2 achalasia has classically been >6 cm, recent studies demonstrate similar outcomes with reduction of myotomy length to <3cm. Length of myotomy for type 3 achalasia has been tailored to treat the entire length of spastic muscle segment, and the modality to gauge the optimal thickness and length of myotomy in this group has yet to be established. In addition to changes in POEM technique, the post-operative management of POEM has also changed, favoring reduced post-procedure imaging, antibiotic use, and hospitalizations.
               
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