Treatment of Idiopathic Achalasia in the Pediatric Population: A Systematic Review

Nicole E Sharp1, Shawn D St Peter2

  • 1Department of Pediatric Surgery, The Children's Mercy Hospital, Kansas City, Missouri, United States.

Insights

Current literature lacks definitive evidence for the best initial treatment of pediatric achalasia. More randomized controlled trials are needed to establish optimal treatment algorithms for this rare esophageal disorder.

Area of Science:

  • Gastroenterology
  • Pediatric Surgery
  • Esophageal Disorders

Background:

  • Achalasia is a rare neuromuscular esophageal disorder affecting lower esophageal sphincter relaxation and peristalsis.
  • It presents a diagnostic and therapeutic challenge in pediatric patients.

Purpose of the Study:

  • To determine the optimal first-line treatment for pediatric achalasia.
  • Comparison of outcomes between pneumatic dilatation (PD) and Heller esophagomyotomy (HM).

Main Methods:

  • Systematic review of English-language articles using OVID database.
  • Searched for studies comparing PD and HM in pediatric achalasia treatment.
  • Data extraction performed by a single reviewer.

Main Results:

  • Seven articles were included in the review.
  • Treatment efficacy varied, with HM favored in two studies, PD in one, and equal efficacy in another.
  • Three studies suggested age-dependent treatment selection.

Conclusions:

  • Insufficient comparative data exists to establish the ideal first-line treatment for pediatric achalasia.
  • Need for well-designed randomized controlled trials with long-term follow-up.
  • Development of evidence-based treatment algorithms is crucial.
Abstract

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