Jaundice in early infancy

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  • See also

    Recognition of the seriously unwell neonate and young infant

    Key points

    1. If significant jaundice is clinically suspected, a transcutaneous bilirubinometer (TcB) and/or serum bilirubin level should be performed. Visual assessment alone is unreliable for estimating bilirubin level
    2. Most jaundice in otherwise well infants is physiological and self-limiting, however severe unconjugated hyperbilirubinaemia may cause acute bilirubin encephalopathy and kernicterus
    3. Features suggestive of pathological jaundice include onset <24 hours of age, rapidly rising bilirubin, unwell appearance, prolonged jaundice, conjugated hyperbilirubinaemia, or evidence of haemolysis
    4. Pale or acholic stools at any age require urgent evaluation for cholestatic liver disease, including biliary atresia

    Background

    • Jaundice (hyperbilirubinaemia) occurs in approximately 60% of term and 80% of preterm infants within the first week of life
    • Hyperbilirubinaemia results from an imbalance between bilirubin production, conjugation and elimination
    • Most jaundice is physiological and benign, however severe unconjugated hyperbilirubinaemia may lead to acute bilirubin encephalopathy and kernicterus, which can cause permanent neurological injury
    • Risk factors for severe hyperbilirubinaemia include prematurity, poor feeding, dehydration, excessive weight loss, haemolysis, bruising/cephalhaematoma
    • Clinical assessment aims to
      • identify infants requiring phototherapy or further treatment
      • identify pathological jaundice requiring further investigation and management
    • Early community follow-up and feeding support, including by GPs and maternal child health nurses, are important to reduce the risk of severe hyperbilirubinaemia

    Assessment

    History

    Feature Further information
    Age of onset <24 hours
    Duration >2 weeks is prolonged
    Antenatal course Maternal blood group and antibodies
    Maternal infectious serology
    Birth Gestational age
    Birth trauma
    Instrumental delivery
    Feeding/weight gain Breast vs formula feeds
    Intake assessment: number and volume/duration of feeds per 24-hour period, breast milk supply, formula preparation
    Poor weight gain/significant weight loss >10% in first week of life
    Output (urine/stools) Hydration status
    Dark urine and pale stools (biliary obstruction)
    Family history ABO/Rhesus incompatibility
    Haemolytic conditions eg G6PD deficiency, Hereditary spherocytosis
    Prolonged jaundice
    Thyroid dysfunction
    Sibling/parent who required treatment for neonatal jaundice

    Examination

    • General tone
    • Neurological exam
    • Hydration status: capillary refill time, heart rate, mucous membranes
    • Plethora
    • Bruising/cephalohaematoma
    • Hepatosplenomegaly
    • Stool/urine colour
    • Pattern and degree of jaundice (may be less obvious in infants with darker skin)

    Management

    Investigations

    1. Investigation of jaundice

    Transcutaneous bilirubinometer (TcB) and/or serum bilirubin (SBR) measurements should be performed in any infant with clinically suspected jaundice.

    TcB

    • may be used as a screening tool in well infants
    • ≥35 weeks gestation
    • ≥24 hours old
    • should be confirmed with SBR if:
      • within 50 micromol/L of treatment threshold
      • ≥250 micromol/L
      • Rapidly rising
      • Phototherapy is being considered or has commenced
    • reliability decreases following phototherapy

    SBR

    • Gold standard for diagnosis and treatment decisions
    • Levels should be interpreted according to gestation, postnatal age and clinical risk factors using an appropriate gestation-specific nomogram
    • Fractionated bilirubin (unconjugated/conjugated) should be performed in prolonged jaundice, unwell infants, suspected pathological jaundice, pale stools or dark urine

    2. Investigation for a cause

    The majority of well infants with unconjugated hyperbilirubinemia do not require further investigation or management

    Causes of neonatal jaundice and relevant investigations

    Type Causes Additional investigations
    Early onset: (<24 hours) Pathological
    All should have:
    SBR (fractionated)
    FBE
    Direct antiglobulin test (DAT)
    Sepsis See Recognition of the seriously unwell neonate and young infant

    Haemolysis

    • Isoimmunisation: ABO or Rhesus D alloantibodies
      RBC enzyme defects: G6PD, hereditary spherocytosis, alpha thalassemia
      Haemorrhage: cerebral, intra-abdominal
      Blood extravasation: bruising/birth trauma
    Blood film and reticulocytes
    Neonatal blood group
    G6PD screen
    Peak onset (24 hours-14 days)

    Physiological jaundice

    • Majority of well infants
      Onset after 24 hours
      Peaks day 3-5, lasts 1-2 weeks
    No further investigations required unless red flags
    Dehydration/insufficient feeding/poor weight gain/weight loss Serum sodium, BGL
    No further investigations required
    Sepsis See Recognition of the seriously unwell neonate and young infant

    Haemolysis

    • Features include anaemia, reticulocytosis, hepatosplenomegaly, rapid bilirubin rise, family history  
    FBE, film and reticulocytes
    Neonatal blood group
    DAT (Coombs)
    G6PD screen

    Breast milk jaundice

    • In healthy, thriving breast-fed infants
      Typical onset 5-7 days after birth
      Peaks at 2-3 weeks, can last up to 12 weeks
    Diagnosis of exclusion after considering above causes
    Bruising, birth trauma No further investigations required

    Prolonged (>2 weeks)

    All should have:

    • SBR (fractionated)
      FBE, film and reticulocytes
      TFTs
      Blood Group
      DAT
      LFTs if conjugated bilirubin >10%
    Sepsis See Recognition of the seriously unwell neonate and young infant
    Haemolysis
    Features include anaemia, reticulocytosis, hepatosplenomegaly, rapid bilirubin rise, family history
    G6PD screen
    Dehydration/insufficient feeding Serum sodium, BGL
    Breast milk jaundice Diagnosis of exclusion after considering above causes
    Hypothyroidism TFTs (for central and primary hypothyroidism)
    Conjugated hyperbilirubinaemia (at any age)
    Conjugated bilirubin >20 µmol/L or >20% of total bilirubin
    Refer to gastroenterology
    Neonatal hepatitis LFTs, maternal infectious serology, metabolic screening
    Extrahepatic obstruction: Biliary atresia, choledochal cyst, bile plug LFTs, coags, abdominal US
    Note: a normal ultrasound does not exclude biliary atresia
    Metabolic See Metabolic disorders
    Drugs/parenteral nutrition Investigations as guided by history and exam

    Treatment

    1. Treatment of unconjugated hyperbilirubinaemia

    • Severity of jaundice should be assessed according to gestation, postnatal age, bilirubin level, clinical condition, hydration status and risk factors
    • TcB/SBR should be plotted on an appropriate gestation-specific nomogram. Refer to local bilirubin treatment thresholds (see additional notes – section below)
    • Ensure adequate hydration and feeding support, particularly in breast-fed infants and those with excessive weight loss or poor intake. Consider lactation consultant and maternal and child health nurse involvement

    Phototherapy

    • Refer to local protocol regarding phototherapy intensity, biliblanket use and monitoring
    • Ongoing close monitoring of weight, hydration, and bilirubin levels should be performed during treatment as per local protocol, with serial checks of SBR to ensure resolution of hyperbilirubinaemia

    Exchange transfusion

    • Should only be performed in, or in conjunction with, a Neonatal Intensive Care Unit
    • Contact local paediatric retrieval service for support

    2. Treatment of cause

    Cause Management
    Physiological jaundice See above
    Should resolve by 2–3 weeks
    Breast milk jaundice Diagnosis of exclusion
    Do NOT stop breastfeeding
    May last up to 12 weeks, no further bilirubin levels necessary unless jaundice is deemed to be worsening
    Sepsis Immediate treatment as per SEPSIS – assessment and management with IV antibiotics
    Haemolysis Discuss with local paediatric services
    Hypothyroidism Discuss with local paediatric services
    Extrahepatic obstruction or neonatal hepatitis
    Uncommon but early diagnosis improves outcome
    If suspected discuss with local paediatric gastroenterology services
    Metabolic If suspected discuss with local metabolic services

    Consider consultation with local paediatric team when

    • Child is unwell
    • Cause of jaundice is unclear
    • Conjugated bilirubin is >20% of total level

    Consider transfer when

    • Jaundice level rising despite adequate treatment offered at local centre
    • Child needs exchange transfusion

    For emergency advice and paediatric or neonatal ICU transfers, see Retrieval Services

    Consider discharge when

    • SBR/TcB below the treatment threshold and plan in place for follow-up
    • Causes requiring further treatment or investigation have been excluded
    • Clinically well and feeding well

    Discharge advice

    • Sunlight exposure is not recommended as a treatment for jaundice
    • Arrange early follow-up with maternal and child health nurse and/or GP to ensure adequate oral intake, especially if
      • <7 days old
      • exclusively breastfeeding or still establishing adequate oral feeds
      • bilirubin level is borderline for requiring treatment
    • Re-check bilirubin in 24-48 hours if borderline level or still rising
    • Parents should be advised to seek medical review if
      • jaundice is present for 2-3 weeks and cause has not previously been established
      • parents believe jaundice is worsening or there is any other cause for clinical concern

    Parent information

    Additional notes

    Established treatment nomograms

    NICE treatment threshold graphs

    Bilitool - an online tool to assess the risk of developing hyperbilirubinaemia (American Academy of Paediatrics)

    Local guidelines with nomograms

    New South Wales
    Jaundice Identification and Management in Neonates >32 Weeks Gestation

    Jaundice In Neonatal Care Practice Guideline

    Queensland

    Neonatal Jaundice
    Nomograms for jaundice management for all weight/gestations
    Assessment for jaundice flowchart

    South Australia

    Neonatal Jaundice

    Western Australia

    Jaundice Guideline

    Updated June 2026

  • Reference List

    1. Nice Guidelines 2016, Jaundice in newborn babies under 28 days, National Institute for Health and Care Excellence, viewed August 2020 <http://www.nice.org.uk/nicemedia/live/12986/48678/48678.pdf>
    2. Safer Care Victoria 2020, Jaundice in neonates, Victorian Agency for Health Information, viewed August 2020 <https://www.bettersafercare.vic.gov.au/resources/clinical-guidance/maternity-and-newborn/jaundice-in-neonates>
    3. Queensland Clinical Guidelines 2019, Neonatal Jaundice, Queensland Health, viewed August 2020 <https://www.health.qld.gov.au/__data/assets/pdf_file/0018/142038/g-jaundice.pdf>