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• Draw up a diagnostic and treatment plan on the basis of the probability diagnosis?
• Would it make any difference to your differential diagnosis if the child was 1 day old rather than 3 day old ? OR 10 day old? Give reasons for your answer.
Learning Objectives
n ro uction
Jaundice occurs in approximately 60% of newborns but only a few will require investigation and treatment.
LFTs:
Aspartate aminotransferase (ASAT ) and alanine aminotransferase (ALAT ) levels are elevated in:
Hepatocellular disease.
Alkaline phosphatase and γ-glutamyltransferase(GGT) levels are often elevated in:
cholestatic disease.
Toxoplasmosis, rubella, herpes
simplex
Surface swabs including umbilicus,
throat swabs, urine culture, blood
culture, lumbar puncture, CXR.
Infection screen:
Blood type and Rh determination in mother and
infant.
Reticulocyte count.
Haemoglobin and haematocrit values.
Direct coombs test
Peripheral blood film for erythrocyte morphology.
Red cell enzyme assays: glucose-6-phosphate
dehydrogenase activity (G6PD deficiency), pyruvate
kinase deficiency.
Hemolytic work-up :
Ultrasound, radionuclide scan, liver biopsy
may be required for cholestatic jaundice in
the differentiation between hepatitis and
biliary atresia.
Doctors, nurses, and family members will
watch for signs of jaundice at the hospital
and after the newborn goes home.
When treatment is needed,
the type will depend on:
•The baby's bilirubin level.
•How fast the level has been
rising.
•Whether the baby was born
early .
•How old the baby is.
IFPhysiological
jaundice :The type seen in most newborns -- does not require
aggressive treatment.
with frequent feedings the baby often (up to 12 times a day) to encourage frequent bowel movements. These help remove bilirubin through the stools. And exposure to indirect sunlight at home.
It will typically disappear in a few days (within 1 -2wk.)
Doctors may test the baby's bilirubin levels during that time to make sure it has not gotten worse.
Phototherapy treatment
Exchange transfusion
Intravenous immunoglobulin
IF baby has more severe jaundice, she/he may need
treatment including:
When unconjugated bilirubin is > 12 mg/dl (> 205.2 μmol/L)
And when unconjugated bilirubin is > 15 mg/dl at 25 to 48 h, 18 mg/dl at 49 to 72 h, and 20 mg/dl at > 72 h
Phototherapy is not indicated for conjugated hyperbilirubinemia.
Indication:
Phototherapy treatment
Phototherapy is the use of light to photoisomerize
unconjugated bilirubin into forms that are more water-
soluble and can be excreted rapidly by the liver and
kidney.
It provides definitive treatment of neonatal
hyperbilirubinemia and prevention of kernicterus.
Phototherapy treatment
Treatment with phototherapy is
successful for almost all infants.
Side effects:
• Phototherapy is very safe, but it can have
temporary side effects, including a skin rash and
loose bowel movements.
• Overheating and dehydration can occur if the infant
does not get enough breast milk or formula.
Phototherapy is stopped when bilirubin levels decline
to a safe level.
is done to prevent or minimize
bilirubin-related brain damage.
The transfusion replaces an infant's
blood with donated blood in an attempt
to quickly lower bilirubin levels.
performed in infants who have not
responded to other treatments
Exchange transfusion :
oBilirubin >340 micromol/L
oWho have signs of or are at significant
neurologic risk of bilirubin toxicity
Indications:
Risks of exchange transfusions:(uncommon) include:
bradycardiavasospasmair embolisminfectionthrombosis
If a baby have different blood types, may get immunoglobulin (a blood protein) through a needle
into a vein.
This can help her treat her jaundice so that she’s less likely to need an
exchange transfusion.
Intravenous immunoglobulin
(also called IVIg):
Would it make any difference to your
differential diagnosis if the child was 1 day old rather than 3 day old ?
OR 10 day old? Give reasons for your
answer.
Best classified by age of onset and
duration:
1.Early: within 24 hrs of life.
2. Intermediate: 2 days to 2
weeks.
3.Late: persists for >2 weeks.
Early:
Haemolytic causes: Rh incompatibility- ABO incompatibility-
G6PD deficiency
Congenital infection .
Increased haemolysis due to haematoma.
Maternal autoimmune haemolytic anaemia: eg, systemic lupus
erythematosus.
Crigler-Najjar syndrome.
Gilbert's syndrome.
• Physiological jaundice
• Breast milk jaundice (inadequate
intake)
• Sepsis
• Haemolysis
• Crigler-Najjar syndrome (glucuronyl
transferase absent/reduced)
• Polycythaemia
• Hypothyroidism, hypopituitarism.
• Galactosaemia.
Intermediate:
• Conjugated (dark urine, pale stools):
– Bile duct obstruction
– Biliary atresia
– Neonatal hepatitis
• Unconjugated:
– Physiological (rare).
– Breast milk jaundice
– Infection
– Hypothyroidism
References
• Kliegman Book.
• Merck Manual
• http://www.health.vic.gov.au/neonatalhandbook/conditions/jaundice-in-
neonates.htm
• http://www.nlm.nih.gov/medlineplus/ency/article/001559.htm
• http://www.emedicinehealth.com
• http://www.healthline.com
• http://www.patient.co.uk/doctor/neonatal-jaundice-pro
• http://www.nhs.uk/conditions/jaundice-newborn/pages/treatment.aspx