Health condition · Clinically reviewed
Infant jaundice, when it’s normal, when it’s not, and what to do next.
Most newborn jaundice is mild and settles on its own. A clear, NICE-based pathway is what keeps the rare, serious causes from being missed.
Why trust this guide
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Clinically reviewed
Written by our editorial team and reviewed by a registered UK clinician before publication.
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Sourced from guidance
Checked against NICE CG98, RCPCH and peer-reviewed neonatal sources you can see at the end.
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Current for 2026
Reflects modern UK guidance on transcutaneous bilirubinometry, LED phototherapy and prolonged-jaundice pathways.
Key facts
Infant jaundice at a glance.
The essentials, in plain English - what it is, how common it is, and how it’s assessed in the UK today.
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What it is
Yellow discoloration of a newborn baby’s skin and eyes caused by a build-up of bilirubin - a normal breakdown product of red blood cells.
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How common
Very common - affects more than 60 per cent of term babies and more than 80 per cent of preterm babies in the first week of life.
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Physiological pattern
Appears after 24 hours, peaks at 3 to 5 days, and resolves over 1 to 2 weeks - usually mild and self-limiting.
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Prolonged jaundice
Beyond 14 days in a term baby or 21 days in a preterm baby - always needs review to exclude liver or metabolic causes.
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Assessment
Transcutaneous bilirubin (TcB) screens babies of 35 weeks and over; serum bilirubin (SBR) plotted on a NICE treatment-threshold graph guides care.
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Why it matters
Very high unconjugated bilirubin can cross into the brain and cause kernicterus - rare, permanent and almost entirely preventable.
Why this guide matters
Common and mostly benign - but never brushed off.
A structured NICE-based approach separates the common physiological pattern from the rare cases that need urgent specialist care.
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Most cases are physiological
Jaundice appearing after 24 hours, peaking at 3 to 5 days and clearing over 1 to 2 weeks is the usual pattern in a well, feeding baby.
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Timing tells you a lot
Jaundice under 24 hours old, or that lasts beyond 14 days in a term baby, is never assumed to be normal.
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Split bilirubin catches biliary atresia
A conjugated component in a prolonged-jaundice screen is the single most important test for finding biliary atresia early - when Kasai surgery works best.
How the diagnosis is made
From first yellow tinge to a clear plan.
The steps a UK midwife, GP or neonatal team will normally follow per NICE CG98 - so you know what to expect and why.
Phase 1 · Assessing
Clinical review and bilirubin measurement
Phase 2 · Confirming
Plot on threshold graph and cause-finding tests
Phase 3 · Preparing
Imaging and specialist referral
- 01
Assessing
Clinical assessment
Onset, feeding, wet nappies, stool colour and family history - jaundice appearing in the first 24 hours is always pathological.
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Assessing
Transcutaneous bilirubin (TcB)
Non-invasive skin measurement used to screen babies of 35 weeks and over per NICE CG98.
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Assessing
Serum bilirubin (SBR)
A capillary or venous blood test when TcB is elevated, in babies under 35 weeks, or when treatment is being considered.
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Confirming
Plot on threshold graph
Bilirubin is plotted against gestation and hours of life on the NICE treatment-threshold chart to decide phototherapy or exchange transfusion.
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Confirming
Cause-finding bloods
FBC and film, blood group, direct Coombs test, G6PD, LFTs and TFTs - arranged by specialist neonatal or paediatric teams.
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Confirming
Split (conjugated) bilirubin
Any conjugated component in a prolonged jaundice screen is always abnormal and prompts urgent specialist paediatric hepatology review.
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Preparing
Imaging and infection screen
Liver ultrasound and infection screen (blood, urine and where indicated CSF) when a pathological cause is suspected - specialist commissioned.
Typical timeline: from screening to a settled plan in hours to days, not weeks.
Symptoms
What infant jaundice actually looks like.
The classic yellow tinge, the feeding pattern that goes with it, and the features that turn a routine review into an emergency.
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Yellow skin and sclerae
Yellow tinge starting at the face and spreading down the trunk and limbs as bilirubin rises.
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Sleepy or reluctant to feed
Higher bilirubin levels can make babies drowsy, which in turn worsens dehydration and jaundice.
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Poor weight gain and dehydration
Fewer wet nappies, dry mouth and weight loss over 10 per cent point to breastfeeding-failure jaundice.
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Pale stools and dark urine
A red flag for conjugated jaundice and possible biliary atresia - needs urgent specialist review.
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Prolonged jaundice
Jaundice persisting beyond 14 days in a term baby or 21 days in a preterm baby is never ignored.
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Bruising or cephalohaematoma
Extensive bruising or a scalp haematoma provides an extra load of red-cell breakdown and higher bilirubin.
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Family or ethnic risk factors
G6PD deficiency, hereditary spherocytosis, ABO or Rh incompatibility and East Asian, African or Mediterranean heritage raise risk.
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Red flag - unwell newborn
Fever, hypothermia, apnoea, high-pitched cry, arching or seizures with jaundice is a neonatal emergency.
Treatment
How infant jaundice is treated in the UK.
Feeding support first, phototherapy for elevated levels, and specialist commissioned care for haemolytic, infective and surgical causes.
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Feeding support and hydration
Frequent breastfeeding, lactation support, expressed breast milk or, where needed, supplemental feeds - the first step in most mild cases.
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Low-dose LED phototherapy
Blue-green light converts unconjugated bilirubin into water-soluble forms the baby can excrete - delivered on a specialist neonatal unit.
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Intensive (multiple) phototherapy
Double or triple lights used when levels are close to exchange thresholds or rising rapidly despite standard phototherapy.
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Intravenous immunoglobulin (IVIG)
For isoimmune haemolysis (Rh or ABO) when bilirubin keeps rising on intensive phototherapy - specialist neonatal decision.
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Exchange transfusion
Replaces the baby’s blood in aliquots to remove bilirubin and antibodies - reserved for very severe unconjugated jaundice at specialist centres.
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Kasai portoenterostomy
Urgent specialist commissioned surgery for biliary atresia, ideally within 60 days of life - see our guide to the Kasai procedure.
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Treat the underlying cause
Infection, hypothyroidism, galactosaemia, G6PD deficiency and hereditary spherocytosis each need their own specialist pathway.
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MDT follow-up
Specialist neonatal team, paediatric hepatology, metabolic and haematology input where required - always specialist commissioned.
What this guide is based on
The sources behind every claim on this page.
UK national guidance and specialist society standards, current at the time of last review.
Key references
Guidelines and standards we relied on.
A quiet reminder
This guide is for information, not medical advice.
Your midwife, health visitor, GP or neonatal team knows your baby and can tell you which parts of this apply. If in doubt, get seen the same day.
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NICE. Jaundice in newborn babies under 28 days (CG98).
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RCPCH. Prolonged neonatal jaundice pathway and standards.
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British Association for Paediatric Hepatology, Gastroenterology and Nutrition (BSPGHAN). Biliary atresia guidance.
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UK National Screening Committee. Newborn and infant physical examination (NIPE) standards.
Red flags
When infant jaundice needs urgent attention.
Most newborn jaundice is safely managed in the community. These are the situations that aren’t - and where specialist neonatal or paediatric hepatology input is needed straight away.
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Jaundice in the first 24 hours
Always pathological until proven otherwise - needs urgent bilirubin measurement and specialist neonatal review.
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Rapidly rising bilirubin
A rise of more than 8.5 micromol/L per hour, or levels close to the exchange line on the NICE chart, is a neonatal emergency.
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Prolonged jaundice
Beyond 14 days in a term baby or 21 days in a preterm baby - triggers a full prolonged-jaundice screen including split bilirubin.
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Pale stools and dark urine
A red flag for biliary atresia. Any conjugated component means urgent paediatric hepatology review - Kasai works best before 60 days.
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Unwell baby with jaundice
Fever, hypothermia, poor feeding, lethargy, apnoea or a bulging fontanelle points to sepsis and needs emergency admission.
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Signs of kernicterus
High-pitched cry, arching (opisthotonos), abnormal tone, seizures or coma - a paediatric emergency and always specialist commissioned.
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Significant weight loss
More than 10 per cent loss of birth weight, fewer than 6 wet nappies a day or dry mucous membranes - review the same day.
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Known haemolytic risk
Rh or ABO incompatibility, G6PD deficiency or hereditary spherocytosis warrants earlier and closer bilirubin monitoring.
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Family history of liver disease
Alagille syndrome, cystic fibrosis or metabolic disease in the family lowers the threshold for a full liver screen.
Living with it
A common condition, with a clear pathway.
Four things that make the biggest difference in the first weeks - feeding, looking, keeping the reviews and knowing when to escalate.
A quiet reminder
You are not being over-anxious for asking.
Midwives, health visitors and GPs would rather see a well baby who turns out fine than miss the one who isn’t. Ask.
- 01 Feeding
Feed early and often
Eight to twelve breastfeeds a day supports hydration and helps clear bilirubin. Ask your midwife or health visitor for feeding support if it’s not going well.
- 02 Watching
Learn what to look for
Check the whites of the eyes and gums in natural daylight, count wet nappies, and note stool colour - pale stools always warrant review.
- 03 Follow-up
Keep the reviews
Midwife, health visitor and GP checks in the first two weeks are how jaundice is caught early - especially the day-5 and day-10 to 14 visits.
- 04 Escalate
Don’t wait if you’re worried
Contact your midwife, GP or 111 the same day if your baby is more yellow, sleepy, feeding poorly or has pale stools.
Frequently asked
Everything we get asked about infant jaundice.
Quick answers on assessment, phototherapy, biliary atresia and breastfeeding.
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What is infant jaundice?
Infant jaundice - also called neonatal jaundice - is yellow discoloration of a newborn’s skin and eyes caused by a build-up of bilirubin from the normal breakdown of red blood cells. It affects more than 60 per cent of term and more than 80 per cent of preterm babies in the first week.
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When is jaundice a worry rather than normal?
Jaundice appearing in the first 24 hours, jaundice that lasts beyond 14 days in a term baby or 21 days in a preterm baby, jaundice with pale stools and dark urine, or an unwell baby with jaundice are all reasons to seek urgent review. Everything else is usually physiological and settles by 1 to 2 weeks.
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How is the bilirubin level measured?
Per NICE CG98, babies of 35 weeks and over are screened with a transcutaneous bilirubinometer - a non-invasive skin measurement. A serum bilirubin blood test is used when the screening result is high, in preterm babies, or when treatment is being considered.
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What is phototherapy and is it safe?
Phototherapy uses blue-green LED light to convert unconjugated bilirubin into forms the baby can excrete. It is safe, well-established and delivered on a specialist neonatal unit. Babies wear eye protection, feeding continues and most only need it for a day or two.
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What is biliary atresia and why is it urgent?
Biliary atresia is a rare progressive disease that blocks the bile ducts of the newborn liver. It causes conjugated jaundice with pale stools. The Kasai portoenterostomy - a specialist commissioned neonatal operation - works best when done before 60 days of life, so any conjugated component in a prolonged-jaundice screen prompts urgent paediatric hepatology review.
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Should I stop breastfeeding if my baby has jaundice?
Almost never. Breast-milk jaundice is common, late-onset and can last 1 to 3 months without any harm. Breastfeeding-failure jaundice - from underfeeding and dehydration - is treated by supporting feeding, not stopping it. Any decision to interrupt breastfeeding is a specialist one and rarely needed.
Related content
Keep reading.
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Jaundice
The adult picture and how it differs from newborn jaundice.
Learn more -
G6PD deficiency
An inherited cause of neonatal haemolytic jaundice.
Learn more -
Hereditary spherocytosis
A red-cell membrane disorder that can drive jaundice.
Learn more -
Breastfeeding
Feeding support that protects against jaundice.
Learn more -
Cystic fibrosis
An occasional cause of neonatal cholestasis.
Learn more -
Kasai portoenterostomy
Specialist surgery for biliary atresia.
Learn more -
Private childhood vaccinations
Wider newborn and infant preventive care.
Learn more -
Private ultrasound scan
Liver imaging used in prolonged jaundice.
Learn more