Management of Bilirubin 289 μmol/L (17 mg/dL) at 72 Hours
This 72-hour-old newborn with a bilirubin of 289 μmol/L (17 mg/dL) requires immediate phototherapy initiation and close monitoring, as this level is above the 95th percentile for age and approaches treatment thresholds for most term infants. 1, 2
Immediate Actions Required
1. Initiate Phototherapy
- Start intensive phototherapy immediately if the infant is at or above the phototherapy threshold based on gestational age and risk factors 3, 2
- For a term infant at 72 hours with a bilirubin of 17 mg/dL, this level typically warrants phototherapy for most risk categories 2
- Do not subtract direct bilirubin from total bilirubin when making treatment decisions 3
2. Recheck Bilirubin Levels
- Measure total serum bilirubin within 4-24 hours to assess trajectory and phototherapy efficacy 2
- If risk factors for neurotoxicity exist or bilirubin is rising rapidly (>0.2 mg/dL/hour), recheck within 4-12 hours 2
- For stable infants without risk factors, recheck within 12-24 hours 2
3. Evaluate for Underlying Causes
Obtain the following laboratory tests immediately: 1, 2
- Blood type and Coombs' test (if not already done)
- Complete blood count with smear
- Direct or conjugated bilirubin measurement
- Reticulocyte count (optional but helpful)
- G6PD screening (particularly important as G6PD deficiency causes 31.5% of kernicterus cases) 1
Risk Stratification
Major Risk Factors to Assess: 1
- Gestational age: 35-36 weeks carries higher risk than ≥39 weeks
- Hemolytic disease: ABO/Rh incompatibility, G6PD deficiency
- Feeding status: Exclusive breastfeeding with poor intake/excessive weight loss increases risk
- Cephalohematoma or significant bruising
- East Asian race (higher risk) vs. Black race (lower risk)
- Jaundice observed in first 24 hours
Assess for Hemolysis: 2
- A rise >0.2 mg/dL/hour after 24 hours suggests hemolysis
- If bilirubin continues rising despite intensive phototherapy, hemolysis is very likely 3
Treatment Monitoring
Phototherapy Efficacy: 3, 4
- Phototherapy reduces risk of bilirubin >20 mg/dL by 10-17% in healthy jaundiced infants
- Measure total serum bilirubin after starting phototherapy to verify efficacy 2
- If bilirubin does not fall or continues rising despite intensive phototherapy, consider exchange transfusion 3
Exchange Transfusion Considerations: 4
- Reserved for bilirubin levels approaching exchange thresholds (typically >25-30 mg/dL depending on risk factors)
- Mortality risk: 3-4 per 1,000 term infants without serious hemolytic disease
- Permanent sequelae risk: 5-10% in sick infants who survive
Special Considerations
If Direct Bilirubin is Elevated: 3
- Direct bilirubin >1.0 mg/dL is abnormal if total bilirubin ≤5 mg/dL
- Phototherapy efficacy is reduced in cholestasis, and bronze infant syndrome may develop
- Do not withhold phototherapy if needed—direct hyperbilirubinemia is not a contraindication 3
- If direct bilirubin is ≥50% of total bilirubin, consult an expert 3
Breastfeeding Management: 5
- Do not interrupt breastfeeding unnecessarily, as this increases risk of early discontinuation
- Ensure adequate caloric intake and assess feeding adequacy 1
- Monitor weight loss and voiding/stooling patterns 1
Follow-Up Plan
Short-Term: 1, 2
- Continue phototherapy until bilirubin falls below treatment threshold
- Recheck bilirubin 4-24 hours after starting phototherapy
- Monitor for signs of bilirubin encephalopathy (lethargy, poor feeding, high-pitched cry, hypotonia)
Post-Discharge: 1
- Ensure follow-up within 24-48 hours if discharged before bilirubin peaks
- Provide written and verbal information to parents about jaundice monitoring
- Instruct parents on when to seek immediate medical attention
Critical Pitfalls to Avoid
- Do not rely on visual assessment alone—always measure bilirubin levels, especially in darkly pigmented infants 1
- Do not delay phototherapy while waiting for laboratory results if clinical jaundice is significant 2
- Do not subtract direct bilirubin from total bilirubin when determining treatment thresholds 3
- Do not discharge without ensuring appropriate follow-up, particularly if risk factors are present 1