3. Clinical features
History
Family history
Maternal history
Infants history
Poor breast feedinding or poor calorie
intake
Vomiting
Delayed passage of meconium or
infrequent stools
4. Physical finding
Jaundice
Areas of bleeding
Hepatosplenomegaly
Physical signs of prematurity, IUGR,
postmaturity
Pallor
Large infant
Abnormal neurologic sign
5. Kernicturus
Definition: a neurologic syndrome resulting
from the deposition of unconjugated bilirubin
in the basal ganglia and brainstem nuclei
Pathogenesis: multifactorial
Incidence
Level and duration of exposure
6. Clinical manifestations
Acute form
Phase 1(1st-2nd d): poor sucking, stuper,
hypotonia, seizure
Phase 2(middle of 1st wk): hypertonia
of extensor muscles, opisthotonus,
retrocollis, fever
Phase 3(after 1 wk): hypertonia
7. Chronic form
1st year: hypotonia, active deep
tendon reflexes, obligatory tonic neck
reflex, delayed motor skill
After 1st year:movement
disorder(choreoathetosis,ballismus,
tremor), upward gaize, sensorineural
hearing loss
8. Prevention
1. For any neonate with jaundice within 24hrs,
serum bilirubin level should be checked
2. Follow up within 2-3d of discharge for all
neonate discharged earlier than 48hr
3. Recognize the presence of possible risk
factor
4. Never underestimate the severity of jaundice
by visual assessment
5. Early initiation of phototherapy in those with
elevated bilirubin
6. Recognize parental concern regarding
jaundice, poor feeding, lethargy
9. Investigation
Serum biluribin levels
CBC with differentials, reticulocyte
count and peripheral morphology
Blood group
Direct Coomb’s test
10. Sepsis screen
Liver and thyroid function test
TORCH antibody titer
G6PD enzyme assay
Urine for reducing agents
15. Exchange transfusion
Indications
If intensive phototherapy fails
If the risk of kernicterus exceeds the
risk of procedure
If signs of kernicterus are evident
If the TSB is in the range for
exchange