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Gastroesophageal reflux in patients with cystic fibrosis

The Journal of Pediatrics
|February 1, 1985
PubMed

Insights

Children with cystic fibrosis (CF) experience more gastroesophageal reflux symptoms than siblings. Nighttime nasogastric feeding safely aids nutrition in CF patients with reflux.

Area of Science:

  • Pediatrics
  • Gastroenterology
  • Pulmonology

Background:

  • Gastroesophageal reflux (GER) is a common concern in pediatric patients.
  • Cystic Fibrosis (CF) is a genetic disorder affecting multiple organs, including the digestive system.
  • Understanding GER incidence and management in CF is crucial for patient care.

Purpose of the Study:

  • To determine the incidence of symptomatic gastroesophageal reflux in children with CF.
  • To compare GER symptoms and objective reflux measures between CF patients and healthy siblings.
  • To evaluate the safety and efficacy of continuous nighttime nasogastric feeding in CF patients with GER.

Main Methods:

  • Survey of CF patients and asymptomatic siblings for GER symptoms (heartburn, regurgitation).
  • Esophageal manometry, 24-hour esophageal pH monitoring, and pulmonary function tests in a subgroup of CF patients.
  • Assessment before and after initiation of supplemental continuous nighttime nasogastric feeds.

Main Results:

  • 20.6% of CF patients reported regurgitation, 26.5% reported heartburn; significantly higher than asymptomatic siblings.
  • CF patients showed significantly increased reflux episodes and duration compared to controls.
  • Nighttime nasogastric feeding increased reflux episodes but did not worsen pH or pulmonary function.

Conclusions:

  • Symptomatic GER and objective reflux are more prevalent in children with CF.
  • Continuous nighttime nasogastric feeding is a safe and effective method for nutritional rehabilitation in CF patients with GER.
  • GER management should be considered in the overall care of pediatric CF patients.

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