Most Appropriate Next Investigation for an 18-Month-Old Child with Acute Jaundice
The most appropriate next investigation is measurement of total and direct (or conjugated) bilirubin levels, followed by a complete blood count, liver function tests, and urinalysis with urine culture. 1, 2
Critical Context: This is NOT Neonatal Jaundice
- An 18-month-old child developing jaundice within one day represents pathologic jaundice requiring urgent evaluation, as this is far beyond the neonatal period where physiological jaundice occurs 1
- The acute onset (within one day) in a toddler suggests serious underlying pathology including hemolysis, hepatitis, sepsis, biliary obstruction, or metabolic disease 1
Initial Laboratory Workup
Immediate blood tests should include:
- Total and direct (conjugated) bilirubin to differentiate obstructive from non-obstructive causes 1, 2
- Complete blood count with peripheral smear to evaluate for hemolysis, infection, or hematologic disorders 1, 2
- Liver function tests including AST, ALT, alkaline phosphatase, GGT, and albumin to assess hepatocellular injury versus cholestasis 1, 3
- Prothrombin time/INR to evaluate synthetic liver function 3
Additional critical tests:
- Blood type and Coombs test if hemolysis is suspected 1, 2
- Reticulocyte count and G6PD level if anemia or hemolysis is present 1, 2, 4
- Urinalysis and urine culture to evaluate for urinary tract infection, which can cause jaundice in young children 1, 5
Fractionated Bilirubin Guides Further Workup
If conjugated (direct) hyperbilirubinemia is present (>20% of total bilirubin):
- This indicates cholestasis or biliary obstruction and requires urgent evaluation for biliary atresia (though less likely at 18 months), choledochal cyst, hepatitis, or metabolic disease 1, 6
- Abdominal ultrasound should be performed to evaluate the biliary tree and liver parenchyma 1
- Evaluate for sepsis with blood cultures if clinically indicated 1, 2
If unconjugated (indirect) hyperbilirubinemia predominates:
- Consider hemolytic causes (G6PD deficiency, autoimmune hemolytic anemia, blood group incompatibility) 1, 4
- Evaluate for sepsis, as this is a common cause of jaundice in children 1
- Consider Gilbert syndrome or other inherited disorders of bilirubin metabolism 1
Imaging Considerations
- Abdominal ultrasound is the initial imaging modality of choice if biliary obstruction or hepatobiliary disease is suspected based on conjugated hyperbilirubinemia or clinical findings 1
- Ultrasound can detect biliary dilation, gallstones, liver masses, and assess liver parenchyma 1
Critical Pitfalls to Avoid
- Never rely on visual estimation of jaundice severity—always obtain objective bilirubin measurements, particularly in children with darker skin pigmentation 1, 2
- Do not delay evaluation—acute jaundice in an 18-month-old is pathologic until proven otherwise and requires same-day assessment 4
- Always measure direct/conjugated bilirubin—failure to do so may miss serious cholestatic liver disease requiring urgent intervention 1, 6, 5
- Consider sepsis as a leading cause—in one U.S. study, sepsis was the most common etiology of new-onset jaundice (22% of cases) 1
- Evaluate stool and urine color—pale stools or dark urine suggest conjugated hyperbilirubinemia and cholestasis 4, 5