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Gastro-oesophageal reflux in infants under 6 months with cystic fibrosis
  1. Ralf G Heinea,
  2. Brenda M Buttonb,
  3. Anthony Olinskyc,
  4. Peter D Phelanc,
  5. Anthony G Catto-Smitha
  1. aRoyal Children’s Hospital, Melbourne, Australia: Department of Gastroenterology, bDepartment of Physiotherapy, cDepartment of Thoracic Medicine
  1. Dr A G Catto-Smith, Department of Gastroenterology, Royal Children’s Hospital, Flemington Road, Parkville, Victoria 3052, Australia. e-mail:cattosmt{at}


AIM To establish the incidence of pathological gastro-oesophageal reflux (GOR) in newly diagnosed infants with cystic fibrosis and to identify clinical predictors of increased reflux.

METHODS 26 infants with cystic fibrosis less than 6 months of age (14 male, 12 female; mean (SEM) age 2.1 (0.21) months, range 0.8 to 5.6 months) underwent prolonged oesophageal pH monitoring (mean duration 27.1 (0.49) hours; range 21.3 to 30.2 hours). Reflux symptoms, anthropometric variables, pancreatic status, meconium ileus, genotype, and chest x ray findings were correlated with pH monitoring data.

RESULTS Five infants (19.2%) had an abnormal fractional reflux time of greater than 10%, seven (26.9%) of 5–10%, and 14 (53.8%) of below 5%. Infants who presented with frequent vomiting had a significantly higher fractional reflux time than infants who had infrequent or no vomiting. There was no significant association between abnormal chest x rays and pathological GOR. Sex, genotype, nutritional status, meconium ileus, and pancreatic enzyme supplementation were not significantly associated with pathological GOR.

CONCLUSIONS About one in five newly diagnosed infants with cystic fibrosis had pathological GOR. Pathologically increased reflux was present before radiological lung disease was established. Apart from frequent vomiting, no useful clinical predictors of pathological reflux were found.

  • gastro-oesophageal reflux
  • cystic fibrosis
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