In the newborn, jaundice is a bilirubin-and-time question with a treatment threshold; in the older child it is a liver question.
18 hours
Hemolysis: this is never physiological.
Differential
ABO or Rh incompatibility
G6PD deficiency
Sepsis
Hereditary spherocytosis
What changes
A bilirubin now, a blood group and direct antiglobulin test, a blood count and a reticulocyte count. Plot the bilirubin on the hour-specific nomogram; phototherapy thresholds are lower in the first day and in preterm or hemolysing infants.
4 days
Physiological or breastfeeding jaundice, and the bilirubin level that needs phototherapy.
Measure, do not estimate: visual assessment is unreliable, especially in darker skin. Weigh the baby, assess feeding and output, plot the level, and treat by the nomogram. Ask about a sibling who needed phototherapy.
3 weeks
Prolonged jaundice: is any of it conjugated? Biliary atresia has a surgical clock.
Differential
Breast milk jaundice (unconjugated, thriving, a diagnosis after the rest are excluded)
Biliary atresia (conjugated, pale stools, dark urine)
Hypothyroidism
Urinary tract infection
Neonatal hepatitis, metabolic disease
What changes
Jaundice beyond 14 days in a term infant needs a split bilirubin. A conjugated fraction that is raised is a liver problem; pale stools with dark urine is biliary atresia until an ultrasound and a hepatology review say otherwise, and the Kasai procedure works best before 60 days.
12 years
Hepatitis, hemolysis, and the drug or the autoimmune disease behind the liver.
Adult-style liver panel logic: hepatocellular versus cholestatic pattern, split bilirubin, a synthetic function check with the INR. Ask about acetaminophen and about supplements.
A 3-week-old, breastfed, still jaundiced, thriving, with pale stools and dark urine. What is the single most important test?