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Published on: June 5, 2014
Causes of prolonged jaundice in infancy: 3-year experience in a tertiary paediatric centre
1Paediatric Outpatient Department, Christchurch Hospital, 2 Riccarton Avenue, Christchurch, 4710, New Zealand. drmargaretandre@gmail.com.
Insights
Prolonged jaundice (PJ) in infants often requires further investigation beyond a normal clinical exam. Hypothyroidism was the most common pathological cause identified in this study of infants with prolonged jaundice.
Area of Science:
- Neonatal Medicine
- Pediatric Gastroenterology
Background:
- Prolonged jaundice (PJ) is common in infants, but diagnostic approaches vary, especially for well-appearing infants.
- Significant underlying pathologies can manifest as PJ in this demographic.
Purpose of the Study:
- To determine the causes of prolonged jaundice in infants referred to a tertiary pediatric center.
- To evaluate the diagnostic yield of investigations for PJ in infancy.
Main Methods:
- Retrospective review of 167 infants with PJ over a 3-year period.
- Analysis of clinical documentation, electronic records, and investigation results.
Main Results:
- 58% of infants were older than 28 days.
- 18% of infants had a specific medical diagnosis contributing to PJ, with hypothyroidism being the most frequent (6 cases).
- Normal clinical examination and exclusion of conjugated hyperbilirubinemia did not rule out pathological causes.
Conclusions:
- Clinical assessment alone is insufficient to exclude serious causes of PJ.
- Late referrals were common, highlighting the need for improved management guidelines.
- Enhanced education and clear guidelines are necessary for optimal management of prolonged jaundice in infants.
Unlabelled:
Although prolonged jaundice (PJ) commonly occurs in infancy, there is not yet agreement as to the appropriate extent of investigations, particularly in otherwise well children. Significant pathologies may present with PJ in this age group and need to be considered.
Aim:
The aim of this retrospective study was to ascertain the causes of PJ in infants referred to a single tertiary paediatric centre.
Methods:
Infants referred with PJ over a 3-year period were identified. Clinical documentation, electronic notes and results of investigations performed prior to and after referral were reviewed.
Results:
One hundred and sixty-seven infants with PJ were seen. Fifty-eight percent were over 28 days of age. Four patients had conjugated hyperbilirubinaemia. Eighteen percent of patients were found to have a specific medical diagnosis causing or contributing to PJ, almost half of whom had normal clinical examination. The single most common pathological cause for PJ was hypothyroidism found in six patients.
Conclusions:
This study demonstrates that normal clinical examination and exclusion of conjugated hyperbilirubinaemia are insufficient to exclude pathological causes of PJ. Overall, these children were referred late. Guidelines, in conjunction with education initiatives, are required to optimise the management of prolonged jaundice in infancy.
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