Neonatal jaundice
(Redirected from Kernicterus)
Background
- Neonatal jaundice can affect up to 84% of term newborns and is often a benign process that is quickly corrected once identified. It is also the most common cause for hospital readmission for neonates post birth.[1]
- The most important piece of the evaluation is distinguishing between unconjugated and conjugated hyperbilirubinemia since a conjugated (direct) hyperbilirubinemia is always pathologic and often more severe
Risk Factors
- Isoimmune hemolytic disease
- G6PD deficiency
- Asphyxia
- Significant lethargy
- Temperature instability
- Sepsis
- Acidosis
- Prematurity
- Poor PO intake
Clinical Features
General neonatal jaundice features
- Jaundice within the first 4-7 days of life
- Scleral icterus
- Lethargy, if progression to severe elevation
- Unlikely when caused by a benign process (e.g. breast milk jaundice, breast feeding jaundice)
Differential Diagnosis
Indirect (Unconjugated) Hyperbilirubinemia
More common causes are listed first, followed by less common causes
- Breast milk jaundice
- Due to substances in milk that inhibits glucuronyl transferase. It may start as early as 3rd day and reaches peak by 3rd week of life. It is unlikely to cause kernicterus
- Breast feeding jaundice
- Patient does not receive adequate oral intake which then causes reduced bowel movement/bilirubin excretion. Best diagnosed by looking for signs of dehydration and comparing weight to birth weight.
- Blood group incompatibility: ABO, Rh factor, minor antigens
- Diabetic mother/gestational diabetes
- Internal hemorrhage
- Physiologic jaundice
- Polycythemia
- Sepsis
- Hemoglobinopathies: thalassemia
- Red blood cell enzyme defects: G6PD Deficiency, pyruvate kinase
- Red blood cell membrane disorders: spherocytosis, ovalocytosis
- Hypothyroidism
- Immune thrombocytopenic purpura
- Mutations of glucuronyl transferase (i.e., Crigler-Najjar syndrome, Gilbert syndrome)
Direct (Conjugated) Hyperbilirubinemia
Conjugated bilirubinemia implies a hepatic or post hepatic cause. More common causes are listed first.
- Hyperalimentation cholestasis
- Neonatal hepatitis
- Cytomegalovirus infection
- Sepsis
- TORCH infection (toxoplasma, other/syphilis, rubella, CMV, HSV)
- Biliary atresia
- Cystic fibrosis
- Hepatic infarction
- Inborn errors of metabolism (e.g., galactosemia, tyrosinosis)
Evaluation
Neonatal jaundice workup
The most important component of the workup is differention of direct vs indirect bilirubinemia
- Total and direct bilirubin levels ("neonatal bilirubin")
- CBC (for evaluation of hemolytic anemia or polycythemia vera)
- Consider coombs or T&S (mom & baby)
Neonatal jaundice diagnosis
- Determine if there are red flags or obvious diagnosis based on history and exam
- Mother's blood type (important if mother is RH negative or O blood type)
- Assess for any signs of decreasing oral intake or signs of dehydration?
- Baby's general appearance (well appearing? evidence of sepsis?)
- Determine bilirubinemia type: direct vs indirect
- Direct
- Admit
- Indirect
- Determine risk category
- See table below
- Determine if patient is above of below bilirubin cutoff by age and risk category
- See table below or use BiliTool or phototherapy guide
- Determine risk category
- Direct
Management
- Breast Milk Jaundice
- Do not need to routinely stop breast-feeding
- If bilirubin elevated beyond 10 mg/dL:
- Stop feeding for 1-2 days, substitute with bottle, and then resume breast milk
- Recurrence of prior hyperbilirubinemia is uncommon upon resuming
- Treat with phototherapy when levels exceed 20 mg/dL
- Breast-Feeding Jaundice (Starvation Jaundice)
- Supplement with expressed breast milk or formula
- Exchange transfusion
- Consider if signs of bilirubin encephalopathy, typically only occurs when the indirect bili level exceeds 25
- Hypertonia, arching, retrocollis, opisthotonos
- Consider if signs of bilirubin encephalopathy, typically only occurs when the indirect bili level exceeds 25
Phototherapy guidelines for neonatal jaundice
Age | Low Risk | Medium Risk | High Risk |
Birth | 7.0 | 5.0 | 4.0 |
24h | 11.5 | 9.0 | 8.0 |
48h | 15 | 14 | 10 |
72h | 17.5 | 15 | 14 |
96h | 20 | 17.5 |
14.5 |
5+days | 21 | 17.5 | 15 |
- Low Risk: ≥38 weeks + no risk factors
- Medium Risk: (≥38 weeks + risk factors) or (35-37 weeks and no risk factors)
- High Risk: 35-37 weeks + risk factors
- Phototherapy is only used for an indirect hyperbilirubinemia
Disposition
- Direct hyperbilirubinemia
- If new diagnosis, always admit to the hospital for further evaluation
- Indirect hyperbilirubinemia
- Admit if septic or concerning disease process
- Typically determined by need for phototherapy (see chart above)
See Also
External Links
References
- ↑ Sgro M, Campbell D, Shah V. Incidence and causes of severe neonatal hyperbilirubinemia in Canada. CMAJ. 2006;175(6):587–590.