Gastroesophageal reflux in the infant with cystic fibrosis

Insights

Gastroesophageal reflux is common in infants with cystic fibrosis, causing vomiting and failure to thrive. Aggressive management, including surgery if needed, significantly improves symptoms and outcomes.

Area of Science:

  • Pediatric Gastroenterology
  • Pulmonology
  • Genetics

Background:

  • Gastroesophageal reflux (GER) sequelae are often overlooked in infants with cystic fibrosis (CF).
  • Significant GER was observed in 20% of newly diagnosed CF infants.

Purpose of the Study:

  • To investigate the prevalence and impact of GER in infants with CF.
  • To evaluate the effectiveness of medical and surgical interventions for GER in this population.

Main Methods:

  • Retrospective review of 40 newly diagnosed infants with CF over 24 months.
  • Diagnostic tools included barium swallow, scintiscan, manometry, and esophagoscopy.
  • Interventions comprised standard medical therapy and Nissen fundoplication.

Main Results:

  • Eight infants (20%) presented with significant GER, manifesting as vomiting, recurrent pneumonia, and failure to thrive.
  • Medical therapy resolved symptoms in 3 infants; 5 required Nissen fundoplication with complete symptom relief.
  • Surgical candidates presented earlier (mean 7 weeks) than medically treated or asymptomatic infants.

Conclusions:

  • GER and its complications can significantly impact the clinical course of infants with CF.
  • Aggressive management of GER, including surgical intervention when necessary, is recommended.
  • Intensive management leads to successful and safe symptom reduction in CF infants with GER.

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