Achalasia cardia, an oesophageal dynamic disorder, is a
relatively rare primary motor oesophageal disease characterised by the
functional loss of plexus ganglion cells in the distal oesophagus and lower
oesophageal sphincter. The management of Achalasia Cardia can be divided into
medical and surgical management. This chapter synthesises the literature
findings to examine the various surgical procedures available for achalasia
cardia, focusing on their respective advantages and potential complications.
The surgical management of achalasia cardia has undergone significant
advancements over the past decade, particularly following the introduction of
Heller's myotomy. Currently, laparoscopic Heller's myotomy, often accompanied
by partial fundoplication, is regarded as the gold standard for the surgical
treatment of achalasia cardia. Additionally, robotic Heller's myotomy is gradually
gaining prominence with the advent of robotic surgical techniques. In contrast,
thoracoscopic myotomy is now infrequently performed, and esophagectomy is
reserved for patients with end-stage achalasia cardia. The choice of surgical
approach is typically individualised, taking into account the patient’s
condition and risk profile.
Author(s) Details
Kumar H.R.
Taylor’s University School of Medicine Clinical Campus,4700 Sg Buloh,
Selangor, Malaysia.
Please see the book here :- https://doi.org/10.9734/bpi/msup/v2/6625
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