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Assessment of stool colour in community management of prolonged jaundice in infancy
D J Crofts1, V J Michel, A S Rigby
1Division of Child Health, Children's Hospital, Sheffield, UK.
Insights
Prolonged infant jaundice is often benign breast milk jaundice. Pale stools or dark urine in bottle-fed infants warrant immediate referral for potential cholestatic liver disease.
Area of Science:
- Neonatal Medicine
- Pediatric Gastroenterology
Background:
- Jaundice beyond two weeks necessitates investigation for cholestatic liver disease.
- Breast milk jaundice is a common, benign cause of prolonged infant jaundice.
- Pale stools and dark urine are indicators of potential cholestatic liver disease.
Purpose of the Study:
- To determine the incidence of prolonged jaundice in newborns.
- To evaluate the utility of stool and urine color in identifying cholestatic liver disease in infants.
- To assist primary care staff in referral decisions for prolonged jaundice.
Main Methods:
- A community program was established to track prolonged jaundice.
- Data on normal stool and urine color were collected to create a reference chart.
- Infants with prolonged jaundice were identified and referred for investigation.
Main Results:
- 3661 infants were studied; 127 had jaundice at 28 days, predominantly breastfed (125).
- Incidence of jaundice in breastfed infants at 28 days was 9.2%.
- No infant exhibited abnormal stool or urine color; none were diagnosed with liver disease, despite common abnormal liver function tests (LFTs) in breastfed infants.
Conclusions:
- Well, jaundiced breastfed infants are unlikely to have serious liver disease.
- Elevated LFTs can be consistent with breast milk jaundice.
- Prolonged jaundice in bottle-fed infants or abnormal stool/urine color requires immediate referral.
Abstract:
Jaundice persisting beyond the first 2 wk of life is often regarded as an indication for investigation to exclude cholestatic liver disease. Most babies with prolonged jaundice have breast milk-related jaundice, which is a benign condition. Cholestatic liver disease is usually accompanied by pale stools and yellow or orange urine. A community programme was established to ascertain the incidence of prolonged jaundice and determine whether abnormal stool and urine colour could be used to assist primary care staff in referral decisions. Data were collected on normal stool and urine colour and used to devise a colour chart and information sheet for parents. Babies with prolonged jaundice were identified and referred for investigation. In all, 3661 babies were recruited into the study, of which 127 were jaundiced at 28 d of age. Of these, 125 were breastfed. The incidence of jaundice in breastfed babies at 28 d was 9.2% (95% CI 7.8%-11.0%) Abnormal liver function tests (LFTs) were common, but no baby had abnormal stool or urine colour and none was found to have liver disease. Jaundiced breastfed babies who are well are unlikely to have serious disease. Elevated LFTs are compatible with a diagnosis of breast milk-related jaundice. Prolonged jaundice in bottle-fed babies, and persistent pallor of stools or yellow/orange urine, are rare and merit immediate referral. Parents and professionals can be advised to report pale stools without generating a large number of unnecessary referrals. Further work is needed to determine whether a colour chart reduces the mean age of referral and treatment of infants with cholestatic liver disease.
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