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Gastroesophageal reflux in children with cystic fibrosis

M Bosheva1, D Ivancheva, N Genkova

  • 1Department of Paediatrics, Higher Medical Institute, Plovdiv, Bulgaria.

Folia Medica
|April 17, 1999
PubMed

Insights

Gastroesophageal reflux (GER) is common in children with cystic fibrosis (CF), particularly during sleep. Cisapride treatment for GER in these patients was found to be safe and effective.

Area of Science:

  • Pediatric Gastroenterology
  • Pulmonology
  • Gastrointestinal Motility Disorders

Background:

  • Cystic Fibrosis (CF) affects multiple organs, including the gastrointestinal tract.
  • Gastroesophageal reflux (GER) is a potential complication in children with CF.
  • Understanding GER frequency and management is crucial for CF patient care.

Purpose of the Study:

  • To determine the frequency of GER in pediatric CF patients.
  • To evaluate the effectiveness and safety of GER management strategies in this population.

Main Methods:

  • Twelve children diagnosed with Cystic Fibrosis (CF) were enrolled.
  • 24-hour esophageal pH monitoring was performed during clinical remission of pulmonary symptoms.
  • Patients diagnosed with GER received Cisapride treatment (10 mg post-dinner).

Main Results:

  • GER was confirmed in 7 out of 12 children (58.3%), all over 6 years old.
  • Reflux events occurred exclusively during sleep.
  • No correlation was found between GER and the timing of inhalational therapies.
  • Cisapride treatment demonstrated safety and efficacy in managing GER.

Conclusions:

  • GER is a frequent condition in children with CF, especially in older children and during sleep.
  • Cisapride is a safe and effective therapeutic option for managing GER in pediatric CF patients.
  • Further research may explore the impact of GER on pulmonary status in CF.

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