Types of Jaundice in Pediatrics | Causes, Symptoms & Management

 

Types of Jaundice in Pediatrics

Jaundice in children refers to the yellowish discoloration of the skin, sclera, and mucous membranes due to increased bilirubin levels. It is very common in newborns but can also occur in older children. Below are the main types:

1. Physiological Jaundice

  • Cause: Immature liver enzymes leading to slow bilirubin conjugation.
  • Onset: Appears after 24 hours, peaks at day 3–5, and resolves within 1–2 weeks.
  • Features: Mild, self-limiting, no disease.
  • Management: Monitoring only, usually no treatment.

2. Pathological Jaundice

This occurs when bilirubin rises excessively or too early. It is always abnormal.

  • Causes:
    • Hemolytic: ABO or Rh incompatibility, G6PD deficiency, spherocytosis.
    • Infections: Neonatal sepsis, TORCH infections.
    • Metabolic/Liver disease: Crigler–Najjar syndrome, biliary atresia, galactosemia.
  • Features: Appears within 24 hours, bilirubin rises >5 mg/dL/day, lasts >2 weeks.
  • Risk: Can lead to kernicterus if untreated.

3. Breastfeeding-related Jaundice

  • Breastfeeding Jaundice: Due to insufficient milk intake causing dehydration and increased bilirubin reabsorption (appears in the first week).
  • Breast Milk Jaundice: Due to substances in breast milk that slow bilirubin conjugation (appears after the 1st week, may last up to 12 weeks).
  • Management: Encourage breastfeeding; temporary interruption only if bilirubin is very high.

4. Conjugated (Cholestatic) Jaundice

  • Cause: Impaired excretion of conjugated bilirubin.
  • Onset: Always pathological.
  • Causes: Biliary atresia, neonatal hepatitis, metabolic disorders.
  • Features: Dark urine, pale stools, hepatomegaly, persistent jaundice >2 weeks.
  • Management: Requires urgent referral (e.g., surgery for biliary atresia).

5. Hemolytic Jaundice (Older Children)

  • Cause: Excessive destruction of red blood cells.
  • Causes: Sickle cell disease, G6PD deficiency, malaria.
  • Features: Rapid rise in unconjugated bilirubin, anemia, splenomegaly.

Summary Table

Type Onset Cause Key Features Management
Physiological After 24 hrs (day 2–5) Immature liver enzymes Mild, self-limiting Monitor only
Pathological Within 24 hrs or prolonged Hemolysis, infection, metabolic disease High/early bilirubin, kernicterus risk Investigate & treat cause
Breastfeeding-related 1st week or after 1 week Low milk intake or breast milk factors Prolonged jaundice Encourage breastfeeding
Conjugated (Cholestatic) Anytime (pathological) Biliary atresia, hepatitis, metabolic issues Dark urine, pale stools, hepatomegaly Urgent referral
Hemolytic (Children) Older infants/children Sickle cell, G6PD, malaria Anemia, splenomegaly Treat underlying cause

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