Efficacy and tolerability of Creon for Children in infants and toddlers with pancreatic exocrine insufficiency caused by cystic fibrosis: an open-label, single-arm, multicenter study

Pancreas. 2009 Aug;38(6):693-9. doi: 10.1097/MPA.0b013e3181a85eaf.

Abstract

Objectives: To evaluate the efficacy and safety of a pancreatic enzyme preparation specifically developed for infants and small children with cystic fibrosis (CF).

Methods: Twelve patients with CF younger than 24 months with pancreatic exocrine insufficiency and a coefficient of fat absorption (CFA) less than 70% were treated with Creon for Children (Solvay Pharmaceuticals GmbH, Hannover, Germany) minimicrospheres for 8 weeks. The primary end point was the mean change from baseline in the CFA after 2 weeks of treatment, based on 72-hour fat balance assessments.

Results: Two weeks' treatment with Creon for Children resulted in a significant increase in the mean CFA from 58.0% at baseline to 84.7% (P=0.0013) in the full analysis sample. There was a significant reduction of mean stool fat (from 13.3 to 5.3 g/d; P=0.001) and mean fecal energy loss (from 238.5 to 137.9 kJ/d; P=0.018) at 2 weeks. Dietary fat intake did not change, whereas an improvement was observed in stool frequency and characteristics. Patient weight and height increased over 8 weeks of treatment. No serious adverse event was reported.

Conclusions: Creon for Children was well tolerated and significantly decreased fat malabsorption in infants with pancreatic exocrine insufficiency due to CF.

Publication types

  • Clinical Trial
  • Multicenter Study

MeSH terms

  • Cystic Fibrosis / complications*
  • Dietary Fats / pharmacokinetics
  • Exocrine Pancreatic Insufficiency / drug therapy*
  • Exocrine Pancreatic Insufficiency / etiology*
  • Exocrine Pancreatic Insufficiency / physiopathology
  • Feces / chemistry
  • Female
  • Gastrointestinal Agents / adverse effects
  • Gastrointestinal Agents / therapeutic use*
  • Humans
  • Infant
  • Intestinal Absorption / drug effects
  • Intestinal Absorption / physiology
  • Malabsorption Syndromes / drug therapy
  • Malabsorption Syndromes / etiology
  • Malabsorption Syndromes / physiopathology
  • Male
  • Pancrelipase / adverse effects
  • Pancrelipase / therapeutic use*

Substances

  • Dietary Fats
  • Gastrointestinal Agents
  • Pancrelipase