A multicenter registry study on percutaneous electrical nerve field stimulation for pediatric disorders of gut-brain

Ashish Chogle1, Khalil El-Chammas2, Neha Santucci2

  • 1Department of Pediatrics, Division of Pediatric Gastroenterology, Hepatology and Nutrition, Children's Hospital of Orange County, Orange, California, USA.

Insights

Percutaneous electrical nerve field stimulation (PENFS) effectively improved gastrointestinal symptoms and functionality in children with disorders of gut-brain interaction (DGBI). This multicenter study confirms PENFS as a promising therapy for pediatric DGBI.

Area of Science:

  • Pediatric Gastroenterology
  • Neuromodulation
  • Disorders of Gut-Brain Interaction (DGBI)

Background:

  • Pediatric abdominal pain-related disorders of gut-brain interaction (DGBI) are common and challenging to treat.
  • Single-center trials suggested percutaneous electrical nerve field stimulation (PENFS) as a potential therapy for pediatric DGBI.
  • A need exists to evaluate PENFS efficacy in a broader, multicenter setting.

Purpose of the Study:

  • To explore the efficacy of PENFS as a standard therapy for pediatric DGBI.
  • To assess the impact of PENFS on gastrointestinal symptoms and functional disability in a multicenter registry.
  • To evaluate the long-term effectiveness of PENFS in pediatric patients.

Main Methods:

  • A multicenter, prospective, open-label registry involving 292 children (8-18 years) with DGBI across seven tertiary care centers.
  • Patients were classified by Rome IV criteria, and subtypes included functional dyspepsia.
  • Abdominal Pain Index (API), Nausea Severity Scale (NSS), and Functional Disability Inventory (FDI) were administered pre-therapy and at follow-up visits up to 1 year.

Main Results:

  • Significant reductions in child-reported API scores were observed within 3 weeks (p < 0.001) and persisted at 3 months (p < 0.001).
  • Nausea Severity Scale (NSS) scores improved significantly and were sustained at 3 and 6 months (p < 0.001).
  • Functional Disability Inventory (FDI) scores showed reductions at 3 months (p = 0.01), with parent-reported scores aligning with child reports.

Conclusions:

  • This large, multicenter registry demonstrates the efficacy of PENFS in improving gastrointestinal symptoms and functionality for pediatric DGBI.
  • PENFS represents a valuable therapeutic option for children suffering from DGBI.
  • The findings support the broader implementation of PENFS in pediatric gastroenterology practice.
Abstract

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