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Updated: Jun 26, 2026

Robotic Myotomy and Partial Fundoplication for Achalasia
Published on: August 11, 2023
A National Experience in Paediatric Achalasia: Symptom Recurrence, Reintervention, and Transition Challenges
Insights
Pediatric achalasia interventions offer initial symptom relief but are not curative, necessitating lifelong management and transition to adult care for improved long-term quality of life.
Area of Science:
- Pediatric Gastroenterology
- Surgical Innovation
- Quality of Life Research
Background:
- Esophageal achalasia is a chronic condition requiring long-term management.
- Interventions aim to alleviate symptoms but may not provide a permanent cure.
Purpose of the Study:
- To evaluate the long-term outcomes and quality of life (QOL) in pediatric patients treated for achalasia.
- To assess the effectiveness of interventions over an 18-year period.
Main Methods:
- Retrospective review of 31 pediatric achalasia patients (2006-2024).
- Analysis of demographics, surgical techniques, and pre/post-intervention Eckardt scores.
- Post-intervention QOL assessment using Eckardt and Achalasia Scoring Questionnaire (ASQ).
Main Results:
- 28 patients analyzed; 75% underwent laparoscopic Heller myotomy.
- Mean follow-up of 7.6 years; mean pre-op Eckardt score 6.9, post-op 2.9.
- 57% transitioned to adult care; current mean ASQ score 19.4 (indicating persistent symptoms).
Conclusions:
- Achalasia interventions provide initial relief but require ongoing management.
- Lifelong follow-up and smooth transition to adult care are crucial for QOL.
- ASQ tool can aid outpatient monitoring of achalasia patients.
Aims:
To assess the long-term outcomes and quality of life (QOL) of patients who underwent intervention for esophageal achalasia in a national Paediatric centre over an 18-year period.
Methods:
All patients who underwent surgical or radiological intervention after a diagnosis of achalasia between 2006 and 2024 were identified. A retrospective review of patient demographics, operative technique and Eckardt score before intervention was undertaken. Patients were contacted via telephone to re-assess QOL using Eckardt and Achalasia Scoring Questionnaire (ASQ) scoring systems.
Results:
In total, 31 patients were identified and 28 were included in the analysis (15 female and 13 male). The majority 21(75%) underwent laparoscopic Heller Myotomy. The mean age at intervention was 11.6 years. The mean duration of follow-up was 7.6 years. The mean pre-operative Eckardt score was 6.9. The mean post-operative Eckardt score was 2.9. Twenty-one patients (75%) were initially symptom free for an average of 17.4 months and 7 (25%) remain symptom free to this day. Eleven (39%) required further interventions. In terms of quality of life, the current mean ASQ score is 19.4 (scoring system 10-31, with 10 representing symptom free). Of the patients who are now adults, 12 (57%) had a formal transition of care to adult services.
Conclusion:
Although surgery may initially improve achalasia symptoms, it is not curative. Patients require lifelong follow-up and support to manage this challenging chronic condition. Ensuring patients are transitioned from Paediatric to adult services could help improve future QOL and tools such as ASQ could help monitor this in an outpatient setting.
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