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ACHALASIA CARDIA
PRESENTER: DR LALTHLAMUANA
DEPARTMENT OF GENERAL SURGERY
CIVIL HOSPITAL AIZAWL.
INTRODUCTION
• The term achalasia originated from the Greek word ‘khalasis’,meaning ‘failure to relax’.
• It is uncommon, with a prevalence of 1.8–12.6 per 100 000 persons per year.
• Primary Esophageal motility disorder.
• Also called as cardiospasm -because of severe spasm of the circular muscles of the lower end
of the esophagus.
• The contracted segment doesn’t relax during swallowing as a result there is a dilation,
tortuosity and hypertrophy of the esophagus above.
PATHOLOGY AND AETIOLOGY
• Remains uncertain but is postulated to be due to loss of the inhibitory ganglion cells in the
myenteric (Auerbach’s) plexus, possibly related to a virus-induced autoimmune effect.
• Histology of muscle specimens generally shows a reduction in the number of ganglion
cells with a variable degree of chronic inflammation.
• During a normal swallow, the food bolus will trigger primary peristalsis in the esophagus
by sequential activation of excitatory lower motor neurons.
• At the same time, relaxation of the LOS allows esophageal emptying.
PATHOLOGY AND AETIOLOGY
• With time, the esophagus dilates and contractions disappear, so that the esophagus empties
mainly by the hydrostatic pressure of its contents.
• This is nearly always incomplete, leaving residual food and fluid.
• The esophagus becomes progressively more tortuous and dilated (megaesophagus);
• Persistent retention esophagitis due to fermentation of food residues may predispose to the
increased incidence of carcinoma of the esophagus.
CLINICAL FEATURES
• The disease is most commonly diagnosed between 30 and 60 years of age.
• It typically presents with dysphagia (to both solid and liquid)
• Regurgitation and heartburn (often mistaken for GORD),
• Chest pain/odynophagia is also common in the early stages.
• Patients often present late and, having had relatively mild symptoms, remain untreated for
many years.
CLINICAL FEATURES
• Patients may or may not have experienced weight loss.
• Frequently, patients will adjust their diet according to symptoms and can maintain their body weight after an initial
drop.
• An ‘Eckardt score’ was developed to assess the severity of symptoms and monitor treatment outcome
• Aspiration-related respiratory symptoms and pneumonia can also occur when there is significant stasis of food
residue in the dilated esophagus.
• The retained food substance can cause fermentation and therefore halitosis.
• Patients may report regurgitating food that they have ingested before.
GRADING/STAGING
• 1 Proximal dilatation < 4cm
• 11 Dilatation between 4-7 cm
• 111 Dilatation > 6cm
• 1V Sigmoid Dilatation
DIAGNOSIS
• A high index of suspicion is needed in the diagnosis of achalasia as symptoms can be mild
and chronic and can be easily misdiagnosed as GORD.
• Endoscopy typically shows frothy saliva pooling in the esophagus and the presence of food
residue.
• The esophagus may be dilated and can be tortuous.
• The OGJ appears tight and spastic but can usually allow an endoscope to pass with gentle
pressure.
• A normal endoscopy however does not exclude achalasia, as 30–40% of endoscopies are
reported as normal before a final diagnosis of achalasia is made.
DIAGNOSIS
• Barium contrast study typically shows a hold-up of contrast in the distal esophagus.
• Abnormal contractions in the esophageal body and a tapering stricture in the distal
esophagus, described as a ‘bird’s beak’ or ‘rat’s tail.’
• All these investigations are suggestive of achalasia but definitive diagnosis relies on
HRM.
• HRM- (GOLD STANDARD)
• It shows unrelaxed LES with high resting pressure
• It shows failure of the LES to relax completely during swallowing and complete absence
of peristalsis.
• It is an important investigation to exclude ‘pseudo-achalasia’, often
referring to cancer of the gastric cardia mimicking achalasia.
• Oesophagoscope is done to confirm the diagnosis and to rule out carcinoma esophagus.
• It shows totally closed LES with atonic, dilated proximal esophagus.
• Biopsy of the mucosa at LES should be done.
TREATMENT
• The treatment goal of achalasia is for symptom palliation since there is no therapy to
reverse the neuronal degeneration.
• Therapies target the LOS, aiming to reduce its contractility by pharmacological means or
by destroying the muscle fibers using endoscopic or surgical methods.
MEDICAL THERAPY
• Calcium channel blockers, nitrates or 5′-phosphodiesterase inhibitors are used to
reduce the LOS pressure.
• Most have limited efficacy in symptom improvement.
• There are also significant side effects, such as headache, oedema and hypotension, after
repeated doses.
• Medical therapy should be reserved for selected patients who are poor candidates for
endoscopic or surgical treatments
BOTULINUM TOXIN
• Botulinum toxin is a potent presynaptic inhibitor of acetylcholine release from nerve endings.
• When injected endoscopically into the LOS, it interferes with the LOS cholinergic excitatory
neural activity and paralyses the sphincter muscle.
• The injection usually has to be repeated after few months. Because the effect is temporary, it is sometimes used
when the diagnosis of achalasia is in doubt.
• Repeated injection may result in scarring, making subsequent treatments more difficult.
• It should not be offered as first-line treatment in patients who are suitable for myotomy or pneumatic dilatation
and its indication is usually restricted to elderly patients with comorbidities.
PNEUMATIC DILATATION
• This involves stretching the LOS with a non-compliant balloon to disrupt the sphincter
muscle and render it less competent.
• Plastic (polyethene) balloons with a precisely controlled external diameter are used.
• Balloons of 30–40 mm in diameter are available and are inserted over a guidewire. There
is no standardized dilatation protocol.
• Generally, it is preferred to have serial dilatations in a graded manner, from 30 mm to 35
mm and 40 mm.
• Serial pneumatic dilatation has similar efficacy to surgical myotomy in selected patients.
PNEUMATIC DILATATION
• Perforation is uncommon; the reported incidence averaged about 1.9% (0–16%).
• With a 30-mm balloon, the chance of perforation should be less than 0.5%.
• The risk of perforation increases with bigger balloons, which should be used cautiously
for progressive dilatation over weeks.
• It is important to have an experienced endoscopist performing the procedure and surgical
back-up in case of perforation
HELLER'S MYOTOMY
• This involves cutting the muscle of the lower esophagus and gastric cardia.
• Typically, anterior myotomy is performed for at least 6 cm proximally at the esophageal side and 2–3 cm distally into
the gastric cardia.
• Transabdominal or transthoracic approaches have been advocated.
• Currently, the standard procedure is a laparoscopic approach.
• The major complication is GORD, which can occur in up to 40% of patients.
• The addition of a partial fundoplication (anterior Dor or posterior Toupet) has been shown to be effective in reducing
the incidence of GORD.
HELLER'S MYOTOMY
• A complete 360° fundoplication (Nissen) is considered contraindicated because the
increase in outflow resistance against a peristaltic esophageal body which will probably
result in postoperative dysphagia.
• Laparoscopic myotomy is superior to single pneumatic dilatation in efficacy
and durability.
PERORAL ENDOSCOPIC MYOTOMY
• Peroral endoscopic myotomy (POEM) involves opening the mucosa at a short distance proximal to
the intended myotomy site.
• Entrance is gained into the submucosal plane, which is extended distally to about 2–3 cm into the
gastric cardia. The circular +/– longitudinal muscles are then cut using ESD instruments.
• Typically, the myotomy extends a minimum of 6 cm in the esophagus proximally and 2 cm into the
gastric cardia distally. The mucosal opening is then closed with endo clips.
• POEM has the advantage in that it can extend the length of the myotomy proximally
• POEM can also be utilized to treat other types of ‘spastic’ esophageal motility disorders
such as distal esophageal spasm and hypercontractile esophagus.
• Randomized controlled trials have demonstrated similar efficacy of POEM to pneumatic
dilatation and Heller’s myotomy in relieving dysphagia.
• Without any antifix procedure, the incidence of GORD is expectedly higher in POEM
compared with Heller’s myotomy with partial fundoplication.
• The incidence of esophagitis at 3 months after POEM can be as high as 57%, which may
subject patients to lifelong acid suppression therapy or subsequent antireflux operation.
OESOPHAGECTOMY
• Oesophagectomy is reserved only for the treatment of patients with ‘end-stage’ achalasia
with a sigmoidal or megaesophagus who are not responding to other methods.
• A grossly dilated oesophagus predisposes to regurgitation and aspiration pneumonia.
• Balancing the risk of an oesophagectomy with the patient’s quality of life and risk of
aspiration complication, surgery can be a reasonable option for surgically fit patients.
FOLLOW UP
• Treatment success is usually define by symptom relief.
• The Eckardt score is quantified and compared with the preoperative score.
• Patients should be counselled on a post-treatment diet as the oesophageal body motility
remains defective.
• Ideally,HRM, barium contrast study, endoscopy and 24-hour pH monitoring should be
performed postoperatively to objectively assess LOS function, bolus retention, response to
treatment, presence of oesophagitis and acid reflux.
• This depends on the availability of resources and patients’ preference.
THANK YOU

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Achalasia cardia.pptx

  • 1. ACHALASIA CARDIA PRESENTER: DR LALTHLAMUANA DEPARTMENT OF GENERAL SURGERY CIVIL HOSPITAL AIZAWL.
  • 2. INTRODUCTION • The term achalasia originated from the Greek word ‘khalasis’,meaning ‘failure to relax’. • It is uncommon, with a prevalence of 1.8–12.6 per 100 000 persons per year. • Primary Esophageal motility disorder. • Also called as cardiospasm -because of severe spasm of the circular muscles of the lower end of the esophagus. • The contracted segment doesn’t relax during swallowing as a result there is a dilation, tortuosity and hypertrophy of the esophagus above.
  • 3. PATHOLOGY AND AETIOLOGY • Remains uncertain but is postulated to be due to loss of the inhibitory ganglion cells in the myenteric (Auerbach’s) plexus, possibly related to a virus-induced autoimmune effect. • Histology of muscle specimens generally shows a reduction in the number of ganglion cells with a variable degree of chronic inflammation. • During a normal swallow, the food bolus will trigger primary peristalsis in the esophagus by sequential activation of excitatory lower motor neurons. • At the same time, relaxation of the LOS allows esophageal emptying.
  • 4. PATHOLOGY AND AETIOLOGY • With time, the esophagus dilates and contractions disappear, so that the esophagus empties mainly by the hydrostatic pressure of its contents. • This is nearly always incomplete, leaving residual food and fluid. • The esophagus becomes progressively more tortuous and dilated (megaesophagus); • Persistent retention esophagitis due to fermentation of food residues may predispose to the increased incidence of carcinoma of the esophagus.
  • 5. CLINICAL FEATURES • The disease is most commonly diagnosed between 30 and 60 years of age. • It typically presents with dysphagia (to both solid and liquid) • Regurgitation and heartburn (often mistaken for GORD), • Chest pain/odynophagia is also common in the early stages. • Patients often present late and, having had relatively mild symptoms, remain untreated for many years.
  • 6. CLINICAL FEATURES • Patients may or may not have experienced weight loss. • Frequently, patients will adjust their diet according to symptoms and can maintain their body weight after an initial drop. • An ‘Eckardt score’ was developed to assess the severity of symptoms and monitor treatment outcome • Aspiration-related respiratory symptoms and pneumonia can also occur when there is significant stasis of food residue in the dilated esophagus. • The retained food substance can cause fermentation and therefore halitosis. • Patients may report regurgitating food that they have ingested before.
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  • 8. GRADING/STAGING • 1 Proximal dilatation < 4cm • 11 Dilatation between 4-7 cm • 111 Dilatation > 6cm • 1V Sigmoid Dilatation
  • 9. DIAGNOSIS • A high index of suspicion is needed in the diagnosis of achalasia as symptoms can be mild and chronic and can be easily misdiagnosed as GORD. • Endoscopy typically shows frothy saliva pooling in the esophagus and the presence of food residue. • The esophagus may be dilated and can be tortuous. • The OGJ appears tight and spastic but can usually allow an endoscope to pass with gentle pressure. • A normal endoscopy however does not exclude achalasia, as 30–40% of endoscopies are reported as normal before a final diagnosis of achalasia is made.
  • 10. DIAGNOSIS • Barium contrast study typically shows a hold-up of contrast in the distal esophagus. • Abnormal contractions in the esophageal body and a tapering stricture in the distal esophagus, described as a ‘bird’s beak’ or ‘rat’s tail.’ • All these investigations are suggestive of achalasia but definitive diagnosis relies on HRM.
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  • 14. • HRM- (GOLD STANDARD) • It shows unrelaxed LES with high resting pressure • It shows failure of the LES to relax completely during swallowing and complete absence of peristalsis.
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  • 17. • It is an important investigation to exclude ‘pseudo-achalasia’, often referring to cancer of the gastric cardia mimicking achalasia. • Oesophagoscope is done to confirm the diagnosis and to rule out carcinoma esophagus. • It shows totally closed LES with atonic, dilated proximal esophagus. • Biopsy of the mucosa at LES should be done.
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  • 19. TREATMENT • The treatment goal of achalasia is for symptom palliation since there is no therapy to reverse the neuronal degeneration. • Therapies target the LOS, aiming to reduce its contractility by pharmacological means or by destroying the muscle fibers using endoscopic or surgical methods.
  • 20. MEDICAL THERAPY • Calcium channel blockers, nitrates or 5′-phosphodiesterase inhibitors are used to reduce the LOS pressure. • Most have limited efficacy in symptom improvement. • There are also significant side effects, such as headache, oedema and hypotension, after repeated doses. • Medical therapy should be reserved for selected patients who are poor candidates for endoscopic or surgical treatments
  • 21. BOTULINUM TOXIN • Botulinum toxin is a potent presynaptic inhibitor of acetylcholine release from nerve endings. • When injected endoscopically into the LOS, it interferes with the LOS cholinergic excitatory neural activity and paralyses the sphincter muscle. • The injection usually has to be repeated after few months. Because the effect is temporary, it is sometimes used when the diagnosis of achalasia is in doubt. • Repeated injection may result in scarring, making subsequent treatments more difficult. • It should not be offered as first-line treatment in patients who are suitable for myotomy or pneumatic dilatation and its indication is usually restricted to elderly patients with comorbidities.
  • 22. PNEUMATIC DILATATION • This involves stretching the LOS with a non-compliant balloon to disrupt the sphincter muscle and render it less competent. • Plastic (polyethene) balloons with a precisely controlled external diameter are used. • Balloons of 30–40 mm in diameter are available and are inserted over a guidewire. There is no standardized dilatation protocol. • Generally, it is preferred to have serial dilatations in a graded manner, from 30 mm to 35 mm and 40 mm. • Serial pneumatic dilatation has similar efficacy to surgical myotomy in selected patients.
  • 23. PNEUMATIC DILATATION • Perforation is uncommon; the reported incidence averaged about 1.9% (0–16%). • With a 30-mm balloon, the chance of perforation should be less than 0.5%. • The risk of perforation increases with bigger balloons, which should be used cautiously for progressive dilatation over weeks. • It is important to have an experienced endoscopist performing the procedure and surgical back-up in case of perforation
  • 24. HELLER'S MYOTOMY • This involves cutting the muscle of the lower esophagus and gastric cardia. • Typically, anterior myotomy is performed for at least 6 cm proximally at the esophageal side and 2–3 cm distally into the gastric cardia. • Transabdominal or transthoracic approaches have been advocated. • Currently, the standard procedure is a laparoscopic approach. • The major complication is GORD, which can occur in up to 40% of patients. • The addition of a partial fundoplication (anterior Dor or posterior Toupet) has been shown to be effective in reducing the incidence of GORD.
  • 25. HELLER'S MYOTOMY • A complete 360° fundoplication (Nissen) is considered contraindicated because the increase in outflow resistance against a peristaltic esophageal body which will probably result in postoperative dysphagia. • Laparoscopic myotomy is superior to single pneumatic dilatation in efficacy and durability.
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  • 27. PERORAL ENDOSCOPIC MYOTOMY • Peroral endoscopic myotomy (POEM) involves opening the mucosa at a short distance proximal to the intended myotomy site. • Entrance is gained into the submucosal plane, which is extended distally to about 2–3 cm into the gastric cardia. The circular +/– longitudinal muscles are then cut using ESD instruments. • Typically, the myotomy extends a minimum of 6 cm in the esophagus proximally and 2 cm into the gastric cardia distally. The mucosal opening is then closed with endo clips.
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  • 29. • POEM has the advantage in that it can extend the length of the myotomy proximally • POEM can also be utilized to treat other types of ‘spastic’ esophageal motility disorders such as distal esophageal spasm and hypercontractile esophagus. • Randomized controlled trials have demonstrated similar efficacy of POEM to pneumatic dilatation and Heller’s myotomy in relieving dysphagia. • Without any antifix procedure, the incidence of GORD is expectedly higher in POEM compared with Heller’s myotomy with partial fundoplication. • The incidence of esophagitis at 3 months after POEM can be as high as 57%, which may subject patients to lifelong acid suppression therapy or subsequent antireflux operation.
  • 30. OESOPHAGECTOMY • Oesophagectomy is reserved only for the treatment of patients with ‘end-stage’ achalasia with a sigmoidal or megaesophagus who are not responding to other methods. • A grossly dilated oesophagus predisposes to regurgitation and aspiration pneumonia. • Balancing the risk of an oesophagectomy with the patient’s quality of life and risk of aspiration complication, surgery can be a reasonable option for surgically fit patients.
  • 31. FOLLOW UP • Treatment success is usually define by symptom relief. • The Eckardt score is quantified and compared with the preoperative score. • Patients should be counselled on a post-treatment diet as the oesophageal body motility remains defective. • Ideally,HRM, barium contrast study, endoscopy and 24-hour pH monitoring should be performed postoperatively to objectively assess LOS function, bolus retention, response to treatment, presence of oesophagitis and acid reflux. • This depends on the availability of resources and patients’ preference.
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