NEONATAL CONDITIONS
A practical guide for SCN clinical staff · Jaundice still there at two weeks - the split bilirubin that must not be missed
Factors in breast milk increase enterohepatic recycling and inhibit conjugation; unconjugated bilirubin stays mildly raised for weeks in a well, thriving baby.
Hypothyroidism slows bilirubin conjugation and clearance - usually caught on the newborn screen, but worth confirming.
Continuing haemolysis (G6PD, spherocytosis, isoimmune disease) keeps the unconjugated bilirubin up.
A urinary tract infection, and other sepsis, can present as prolonged jaundice.
Biliary atresia, neonatal hepatitis, a choledochal cyst, metabolic disease and TPN cholestasis block bile flow - the conjugated fraction rises and stools lose colour.
Confirm it is truly prolonged, send a split bilirubin, and split your thinking: conjugated means an urgent liver work-up; unconjugated means the prolonged jaundice screen.
Why does every prolonged jaundice need a split bilirubin?
What are the stool and urine clues to a conjugated (obstructive) cause?
Why is biliary atresia so time-critical?
How do you safely make a diagnosis of breast-milk jaundice?
Take-home message: Prolonged jaundice is jaundice beyond 14 days (term) or 21 days (preterm). The single essential test is a split bilirubin: a conjugated fraction is always pathological and must trigger an urgent work-up to exclude biliary atresia, where the Kasai works best before 6-8 weeks. Prolonged unconjugated jaundice needs the prolonged jaundice screen (TFTs, G6PD, haemolysis, UTI); breast-milk jaundice is a diagnosis of exclusion in a thriving baby. Always check the stools and urine.
For educational purposes only. Always align management to current ANZCOR/NRP guidelines and your local SCN/NICU or NETS protocols.