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Heller myotomy for oesophageal achalasia: risk factors for reintervention - a narrative review.

Created on 22 Jul 2026

Authors

Arianna Vittori, Renato Salvador, Luca Provenzano, Giovanni Zaninotto

Published in

Expert review of gastroenterology & hepatology. Jul 22, 2026. Epub Jul 22, 2026.

Abstract

Heller myotomy (HM) is an effective and durable treatment for esophageal achalasia. However, some patients experience persistent or recurrent symptoms that require reintervention. Heterogeneous definitions of failure after HM limit comparability across studies and complicate clinical decision-making.
This narrative review examines definitions and incidence of failure after HM, as well as risk factors for reintervention. Failure is influenced by disease severity, esophageal morphology, manometric subtype, prior endoscopic therapy, surgical technique, and center experience. Reported failure rates vary because of inconsistent definitions, follow-up durations, and patient selection. Symptom-based tools, such as the Eckardt Score, remain central but have limitations, underscoring the need for validated measures. Sigmoid esophagus and type I-III achalasia increase the risk of failure, whereas prior endoscopic therapy does not predict adverse outcomes in high-volume centers. Compared with endoscopic myotomy, HM-fundoplication may reduce postoperative reflux.
Achalasia is irreversible, and treatment is palliative. Laparoscopic HM remains the gold standard, though failures occur, often due to incomplete myotomy or advanced disease. Early intervention, accurate diagnosis, and meticulous surgical technique are essential. Future research should prioritize standardized definitions of failure, subtype-specific outcome reporting, and long-term follow-up to enhance comparability and guide management.

PMID:
42484866
Bibliographic data and abstract were imported from PubMed on 22 Jul 2026.

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