Follow-up of Congenital Diaphragmatic Hernia: Need for Routinary Assessment of Acid Gastroesophageal Reflux with pH-metry

Eur J Pediatr Surg. 2018 Dec;28(6):502-507. doi: 10.1055/s-0037-1607290. Epub 2017 Oct 11.

Abstract

Introduction: We aim to assess gastroesophageal reflux (GER) in patients treated for congenital diaphragmatic hernia (CDH) and to determine whether a pH-metry investigation should be routinely performed in follow-up.

Materials and methods: Twenty-four-hour pH-metry at 1 year was performed in all patients treated for CDH between January 2014 and April 2015 (Group 1). We compared pH-metry results to those of two other groups: children treated for esophageal atresia (EA) (Group 2) and normal babies presenting with typical symptoms (Group 3). All the pH-metric findings were analyzed and compared. Intra-group analysis was performed in Group 1.

Results: Group 1 consisted of 21, Group 2 of 24, and Group 3 of 21 patients. Mean pH-metry values for Groups 1, 2, and 3 were, respectively: reflux index (RI) 4.3, 5.1, and 3.9; total number of refluxes (NR) 79.5, 88.8, and 88.7; refluxes longer than 5' (R > 5) 1.7, 2.3, and 1.47; and longest reflux episode (LR) 11.4, 13.3, and 8.6. No significant differences were found between Group 1 and the others. Only two CDH patients presented with GER-related symptoms. Patch was associated with significantly higher RI (8.5 vs. 2.98, p = 0.03). The worse was the defect, the worse were the pH-metric results (RI: A3.09, B3.15, and C9.1).

Conclusion: We believe that a routine GER assessment should be performed in all CDH patients regardless the presence of symptoms.

Level of evidence: This is a Level II study.

Publication types

  • Clinical Trial

MeSH terms

  • Aftercare / methods*
  • Esophageal pH Monitoring*
  • Female
  • Follow-Up Studies
  • Gastroesophageal Reflux / diagnosis*
  • Gastroesophageal Reflux / etiology
  • Hernias, Diaphragmatic, Congenital / surgery*
  • Herniorrhaphy* / instrumentation
  • Herniorrhaphy* / methods
  • Humans
  • Infant
  • Infant, Newborn
  • Male
  • Postoperative Complications / diagnosis*
  • Prospective Studies
  • Treatment Outcome