Search engine for discovering works of Art, research articles, and books related to Art and Culture
ShareThis
Javascript must be enabled to continue!

Retrospective study on symptoms and treatment modalities used and short‐term follow up of achalasia cardia in Indian setting

View through CrossRef
AbstractBackgroundAchalasia cardia is a rare esophageal motor disorder that is frequently diagnosed late.AimThe aim of this study was to study the symptoms, treatment given, and response to treatment in patients with achalasia cardia in an Indian setting.Materials and methodsThis retrospective study included all patients diagnosed with achalasia cardia on high‐resolution esophageal manometry, using Chicago Classification v 3.0. On follow up, patients were contacted by telephone, and details of the treatment given and response were recorded in a predesigned pro forma. We excluded overseas patients, postoperative cases of achalasia, and those in whom the manometry catheter could not be passed across the gastroesophageal junction.ResultsA total of 452 patients (260 males, median age 44.5 years) were included in the study cohort. The major symptoms included dysphagia for solids and liquids (428, 94.7%), regurgitation (360, 79.6%), naso‐oral regurgitation (182, 40.3%), weight loss (322, 71.3%), and chest pain (158, 35%). Type 2 achalasia (229, 50.6%) was the most common subtype, followed by type 3 (154, 34.1%). Chest pain was more common in type 3, and weight loss and naso‐oral regurgitation were more common in type 2 achalasia. A majority of patients underwent Heller's myotomy and pneumatic dilatation. Of 280 patients for whom treatment details were available, 98% reported good response to endoscopic/surgical management.ConclusionThe predominant symptoms of achalasia cardia vary per the manometric subtype. Heller's myotomy and pneumatic dilatation are the most commonly used treatment options. Response to treatment is good. The choice of treatment modality was likely influenced by financial reasons and availability of local expertise.
Title: Retrospective study on symptoms and treatment modalities used and short‐term follow up of achalasia cardia in Indian setting
Description:
AbstractBackgroundAchalasia cardia is a rare esophageal motor disorder that is frequently diagnosed late.
AimThe aim of this study was to study the symptoms, treatment given, and response to treatment in patients with achalasia cardia in an Indian setting.
Materials and methodsThis retrospective study included all patients diagnosed with achalasia cardia on high‐resolution esophageal manometry, using Chicago Classification v 3.
On follow up, patients were contacted by telephone, and details of the treatment given and response were recorded in a predesigned pro forma.
We excluded overseas patients, postoperative cases of achalasia, and those in whom the manometry catheter could not be passed across the gastroesophageal junction.
ResultsA total of 452 patients (260 males, median age 44.
5 years) were included in the study cohort.
The major symptoms included dysphagia for solids and liquids (428, 94.
7%), regurgitation (360, 79.
6%), naso‐oral regurgitation (182, 40.
3%), weight loss (322, 71.
3%), and chest pain (158, 35%).
Type 2 achalasia (229, 50.
6%) was the most common subtype, followed by type 3 (154, 34.
1%).
Chest pain was more common in type 3, and weight loss and naso‐oral regurgitation were more common in type 2 achalasia.
A majority of patients underwent Heller's myotomy and pneumatic dilatation.
Of 280 patients for whom treatment details were available, 98% reported good response to endoscopic/surgical management.
ConclusionThe predominant symptoms of achalasia cardia vary per the manometric subtype.
Heller's myotomy and pneumatic dilatation are the most commonly used treatment options.
Response to treatment is good.
The choice of treatment modality was likely influenced by financial reasons and availability of local expertise.

Related Results

The Current Surgical Management of Achalasia Cardia: Review Article
The Current Surgical Management of Achalasia Cardia: Review Article
The surgical management of achalasia cardia has been evolving over the past decade since the introduction of Heller’s myotomy. Laparoscopic Heller’s myotomy is the current gold sta...
ALLGROVE SYNDROME(TRIPLE-A SYNDROME):A CASE REPORT
ALLGROVE SYNDROME(TRIPLE-A SYNDROME):A CASE REPORT
Triple-A syndrome, also known as Allgrove syndrome, is an uncommon disorder which is inherited as an autosomal recessive pattern of inheritance, associated with mutations in the AA...
PS01.115: ESOPHAGECTOMY FOR ACHALASIA CARDIA: A SINGLE TEAM EXPERIENCE
PS01.115: ESOPHAGECTOMY FOR ACHALASIA CARDIA: A SINGLE TEAM EXPERIENCE
Abstract Background In the era of per oral endoscopic myotomy, advancement in manometry and laparoscopy the treatment for achala...
THE SURGICAL TREATMENT OF ACHALASIA ON LAPAROSCOPIC HELLER MYOTOMY WITH DOR ANTIREFLUX PROCEDURE AT HUE CENTRAL HOSPITAL
THE SURGICAL TREATMENT OF ACHALASIA ON LAPAROSCOPIC HELLER MYOTOMY WITH DOR ANTIREFLUX PROCEDURE AT HUE CENTRAL HOSPITAL
Background: Achalasia is a primary motor disorder of the esophagus characterized by insufficient lower esophageal sphincter relaxation and loss of esophageal peristalsis. Diagnosis...
Case Report and Therapeutic Approach for Achalasia Cardia
Case Report and Therapeutic Approach for Achalasia Cardia
Achalasia cardia is an uncommon esophageal motility disorder characterized by the impaired relaxation of the lower esophageal sphincter (LES) and the absence of peristaltic contrac...
Differential Diagnosis of Neurogenic Thoracic Outlet Syndrome: A Review
Differential Diagnosis of Neurogenic Thoracic Outlet Syndrome: A Review
Abstract Thoracic outlet syndrome (TOS) is a complex and often overlooked condition caused by the compression of neurovascular structures as they pass through the thoracic outlet. ...

Back to Top