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 Jaundice is the visible manifestation of
  increased level of bilirubin in the body. It
  is not a disease rather a symptom of
  diseases.
 In adults sclera appears jaundiced when
  serum bilirubin exceeds 2 mg/dl.
 However it is difficult to see sclera in
  newborn due to difficulty in opening
  eye. But in new born it is very easy to see
  jaundice in skin.
 Important problem in the 1st week of life
 Almost all neonates (60% Term and 80%
  Preterm) will have bilirubin > 5 mg/dl in
  the 1st week of life and become visibly
  jaundiced, vast majority being benign
 Some of the term babies (8 to 9%) have
  levels exceeding 15 mg/dl in 1st 7 days of
  life.
 High bilirubin level is toxic to the
  developing CNS
A women who delivered at home
presented on her 5th postpartum day at
pediatric OPD complaining that her baby
looked yellow.
Hyperbilirubinemia in the first week of life is
usually of the indirect variety.
1. Appearing at birth or within 24 hours of
   age
   › Hemolytic disease of newborn
   › Infections: intrauterine viral, bacterial;
     malaria
   › G-6PD deficiency
2. Appearing between 24-72 hours of life

  › Physiological
  › Sepsis neonatorum
  › Polycythemia
  › Concealed hemorrhages:
    cephalhematoma, subarachnoid
    bleed, IVH.
  › Increased enterohepatic circulation
3. Appearing after 72 hrs and within 1st
   week

  a) Sepsis neonatorum (4th - 7th days)
  b) Syphilis
  c) Toxoplasmosis
4. Jaundice appearing after1 week

a) Prolonged direct Jaundice
   › Neonatal hepatitis (common)
   › Extrahepatic biliary atresia
   › Breast milk jaundice
   › Metabolic disorders
   › Intrahepatic biliary atresia
   › Amino acid toxicity
   › Inspissated bile syndrome (uncommon)
Jaundice appearing after1 week contd…

b) Prolonged Indirect Jaundice

› Criggler Najjar Syndrome
› Breast milk jaundice
› Hypothyroidism
› Pyloric stenosis
› Ongoing hemolysis, malaria
On history, the baby started turning yellow
on his 2nd day. The baby was a full term
male child delivered at home. Baby is
currently 120 hours old. There was no history
of any maternal illness during pregnancy.
Delivery was uneventful. Baby immediately
cried after birth and was immediately
breastfed.
Baby passed meconium on his first day.
Urine is normal with no staining of nappies.
Stool also is normal in colour.
On past history, there was no H/O history of
malaria during pregnancy.
On family history, there was no H/O of
jaundice, liver disease. Previous sibling had
no history of neonatal jaundice.
Baby was well looking, feeding well, vitals
were normal, temperature was normal.
There were no rashes and petechiae in the
body. Baby weighed 3 kg. Icterus was
present. Pallor was Absent. On abdominal
examination no organomegaly was
present. Chest was clear and CVS
examination was normal.
1.   Dermal staining (By karmer) progresses
     from head to toe
     › Examined in good day light skin of
       forehead, chest, abdomen, thigh, legs,
        palms, and soles
     › Blanched with digital pressure and the
       underlying color of the skin and
       subcutaneous tissue should be noted.
2.   Transcutaneus bilirubinometer
In new born babies bilirubin metabolism is
immature which results in the occurrence
of hyperbilirubinemia in the first few days of
life. Also there is increased bilirubin load on
the hepatic cell due to physiological
polycythemia.
Immaturity could be at various steps of
bilirubin metabolism like:
  Defective uptake from plasma into liver
   cell
  Defective conjugation
  Decreased excretion
  Increased entero-hepatic circulation
 First appears between        hours of age
 Maximum intensity seen on 4-5th day in
  term and 7th day in preterm neonates
 Does not exceed 15 mg/dl
 Clinically undetectable after 14 days.
 No treatment is required but baby should
  be observed closely for signs of
  worsening jaundice.
Presence of any of the following signs
denotes that the jaundice is pathological.
 Clinical jaundice detected before 24
  hours of age
 Rise in serum total bilirubin by more than
  5 mg/dl/ day (>5mg/dl on first day , 10
  mg/dl on second day and 12- 13 mg/dl
  thereafter in term babies)
  Serum bilirubin more than 15 mg/dl
 Clinical jaundice persisting beyond 14
   days of life
 Clay/white colored stool and/or dark
   urine staining the nappy yellow
 Direct bilirubin >2 mg/dl at any time
Treatment is required in the form of
phototherapy or exchange blood
transfusion. One should investigate to find
the cause of pathological jaundice.
Clinical
                     Jaundice

               Measure
               Billirubin

       > 12 mg/dl and           < 12 mg/dl and
      infant < 24 hr old       infant > 24 hr old


                                        Follow bilirubin
           Coomb’s test
                                             level


Positive              Negative


 Identify antibody           Direct
    Rh, ABO etc             bilirubin
Direct bilirubin


     > 2 mg/dl                         < 2 mg/dl
     Consider
     Hepatitis
Intrauterine,viral,or                  Hematocrit
 Toxoplasmatic inf.
   Biliary obstr.
       Sepsis
  Galactosemia                            Normal or low
    Cholestasis
Hemochromatosis


                                              High
                                         (Polycythemia)
Normal or Low

                      RBC morphology
                     Reticulocyte Count




          NORMAL
   Enclosed hemorrhage                      ABNORMAL
 Increased enterohep. circ.                Spherocytosis
Breast milk, Hypothyroidism,             Elliptocytosis etc.
  Crigler-Najjar syndrome               ABO Incompatibility
  Infant of diabetic mother             Red cell enzyme def
        RDS, Asphyxia                    Alpha thallasemia
     Infections, Drugs(eg                Drugs(eg penicillin
 novobiocin), galactosemia
Investigations were done. Serum total
bilirubin was found to be 10 mg/dl. The
baby was diagnosed as a case of
physiological Jaundice. Parents were
counseled. The baby was discharge and
kept on follow up for serial analysis of
Bilirubin level.
1.   Bhutani V.K., Johnson Lois H., Keren Ron Diagnosis and management
     of hyperbilirubinemia in term neonates for a safer first week,
     Pediatric clinic of North America, Common issues and concerns in
     Newborn Nursery, Part II Aug 2004, vol 5, No. 4
2.   Gowen CW Jr. Anemia and hyperbilirubinemia. In: Kliegman R.
     Nelson Essentials of Pediatrics. 5th ed. Philadelphia, Pa.: Elsevier
     Saunders; 2006:318.
3.   Paul Vinod K, Deorari Ashok K, Agrawal Ramesh et all, Newborn
     infants, Ghai Essential Pediatrics, 2009, 147-51
4.   Internet
Approach to neonatal jaundice
Approach to neonatal jaundice

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Approach to neonatal jaundice

  • 1.
  • 2.  Jaundice is the visible manifestation of increased level of bilirubin in the body. It is not a disease rather a symptom of diseases.  In adults sclera appears jaundiced when serum bilirubin exceeds 2 mg/dl.  However it is difficult to see sclera in newborn due to difficulty in opening eye. But in new born it is very easy to see jaundice in skin.
  • 3.  Important problem in the 1st week of life  Almost all neonates (60% Term and 80% Preterm) will have bilirubin > 5 mg/dl in the 1st week of life and become visibly jaundiced, vast majority being benign  Some of the term babies (8 to 9%) have levels exceeding 15 mg/dl in 1st 7 days of life.  High bilirubin level is toxic to the developing CNS
  • 4. A women who delivered at home presented on her 5th postpartum day at pediatric OPD complaining that her baby looked yellow.
  • 5.
  • 6. Hyperbilirubinemia in the first week of life is usually of the indirect variety. 1. Appearing at birth or within 24 hours of age › Hemolytic disease of newborn › Infections: intrauterine viral, bacterial; malaria › G-6PD deficiency
  • 7. 2. Appearing between 24-72 hours of life › Physiological › Sepsis neonatorum › Polycythemia › Concealed hemorrhages: cephalhematoma, subarachnoid bleed, IVH. › Increased enterohepatic circulation
  • 8. 3. Appearing after 72 hrs and within 1st week a) Sepsis neonatorum (4th - 7th days) b) Syphilis c) Toxoplasmosis
  • 9. 4. Jaundice appearing after1 week a) Prolonged direct Jaundice › Neonatal hepatitis (common) › Extrahepatic biliary atresia › Breast milk jaundice › Metabolic disorders › Intrahepatic biliary atresia › Amino acid toxicity › Inspissated bile syndrome (uncommon)
  • 10. Jaundice appearing after1 week contd… b) Prolonged Indirect Jaundice › Criggler Najjar Syndrome › Breast milk jaundice › Hypothyroidism › Pyloric stenosis › Ongoing hemolysis, malaria
  • 11. On history, the baby started turning yellow on his 2nd day. The baby was a full term male child delivered at home. Baby is currently 120 hours old. There was no history of any maternal illness during pregnancy. Delivery was uneventful. Baby immediately cried after birth and was immediately breastfed.
  • 12. Baby passed meconium on his first day. Urine is normal with no staining of nappies. Stool also is normal in colour. On past history, there was no H/O history of malaria during pregnancy. On family history, there was no H/O of jaundice, liver disease. Previous sibling had no history of neonatal jaundice.
  • 13. Baby was well looking, feeding well, vitals were normal, temperature was normal. There were no rashes and petechiae in the body. Baby weighed 3 kg. Icterus was present. Pallor was Absent. On abdominal examination no organomegaly was present. Chest was clear and CVS examination was normal.
  • 14. 1. Dermal staining (By karmer) progresses from head to toe › Examined in good day light skin of forehead, chest, abdomen, thigh, legs, palms, and soles › Blanched with digital pressure and the underlying color of the skin and subcutaneous tissue should be noted. 2. Transcutaneus bilirubinometer
  • 15.
  • 16. In new born babies bilirubin metabolism is immature which results in the occurrence of hyperbilirubinemia in the first few days of life. Also there is increased bilirubin load on the hepatic cell due to physiological polycythemia.
  • 17. Immaturity could be at various steps of bilirubin metabolism like:  Defective uptake from plasma into liver cell  Defective conjugation  Decreased excretion  Increased entero-hepatic circulation
  • 18.  First appears between hours of age  Maximum intensity seen on 4-5th day in term and 7th day in preterm neonates  Does not exceed 15 mg/dl  Clinically undetectable after 14 days.  No treatment is required but baby should be observed closely for signs of worsening jaundice.
  • 19. Presence of any of the following signs denotes that the jaundice is pathological.  Clinical jaundice detected before 24 hours of age  Rise in serum total bilirubin by more than 5 mg/dl/ day (>5mg/dl on first day , 10 mg/dl on second day and 12- 13 mg/dl thereafter in term babies)
  • 20.  Serum bilirubin more than 15 mg/dl  Clinical jaundice persisting beyond 14 days of life  Clay/white colored stool and/or dark urine staining the nappy yellow  Direct bilirubin >2 mg/dl at any time Treatment is required in the form of phototherapy or exchange blood transfusion. One should investigate to find the cause of pathological jaundice.
  • 21. Clinical Jaundice Measure Billirubin > 12 mg/dl and < 12 mg/dl and infant < 24 hr old infant > 24 hr old Follow bilirubin Coomb’s test level Positive Negative Identify antibody Direct Rh, ABO etc bilirubin
  • 22. Direct bilirubin > 2 mg/dl < 2 mg/dl Consider Hepatitis Intrauterine,viral,or Hematocrit Toxoplasmatic inf. Biliary obstr. Sepsis Galactosemia Normal or low Cholestasis Hemochromatosis High (Polycythemia)
  • 23. Normal or Low RBC morphology Reticulocyte Count NORMAL Enclosed hemorrhage ABNORMAL Increased enterohep. circ. Spherocytosis Breast milk, Hypothyroidism, Elliptocytosis etc. Crigler-Najjar syndrome ABO Incompatibility Infant of diabetic mother Red cell enzyme def RDS, Asphyxia Alpha thallasemia Infections, Drugs(eg Drugs(eg penicillin novobiocin), galactosemia
  • 24. Investigations were done. Serum total bilirubin was found to be 10 mg/dl. The baby was diagnosed as a case of physiological Jaundice. Parents were counseled. The baby was discharge and kept on follow up for serial analysis of Bilirubin level.
  • 25. 1. Bhutani V.K., Johnson Lois H., Keren Ron Diagnosis and management of hyperbilirubinemia in term neonates for a safer first week, Pediatric clinic of North America, Common issues and concerns in Newborn Nursery, Part II Aug 2004, vol 5, No. 4 2. Gowen CW Jr. Anemia and hyperbilirubinemia. In: Kliegman R. Nelson Essentials of Pediatrics. 5th ed. Philadelphia, Pa.: Elsevier Saunders; 2006:318. 3. Paul Vinod K, Deorari Ashok K, Agrawal Ramesh et all, Newborn infants, Ghai Essential Pediatrics, 2009, 147-51 4. Internet

Editor's Notes

  1. Rh, ABO and minor group incompatibility
  2. Neonatal hepatitis (common): it could be idiopathic, congenital infection (TORCH) or acquired (e.g. H1N1, HIV...).Extrahepaticbiliaryatresia: very obvious clay-color stool. The baby looks well, plays &amp; laughs while he&apos;s yellow! Breast milk jaundiceMetabolic disorders : galactosemia, It is diagnosed by: enzyme assay, hypoglycemia &amp; reduced substance in stool (?)Intrahepaticbiliaryatresia: Alagille syndrome is associated with dysmorphic features, congenital heart disease (pulmonary stenosis) &amp; can be mistaken with Rubella infection.Amino acid toxicity: commonly occurs in children with total parenteral nutrition TPN. (+) history of NICU admission.Inspissated bile syndrome (uncommon): the bile duct is obstructed. Treated with rehydration &amp; ERCP.
  3. Maternal and Perinatal HistoryDelivery at period of gestation, Postnatal age in hoursMaternal illness during pregnancy which also includes diabetesPrevious history of malariaTraumatic delivery, delayed cord clamping, oxytocin useBirth asphyxia, delayed feeding, delay in meconium passageFamily history of jaundice, liver diseasePrevious sibling with jaundice for blood group incompatibilityKernicterus: Lethargy, poor feeding, and hypotonia. Some advanced signs are seizures, retrocollis, paralysis of upward gaze and shrill cryBreast feeding
  4. Baby lethargic, poor feeding, temperature instability, with apnea: Sepsis Small for gestation: polycythemia,Cataract, rash: TORCH infectionsExtravascular bleed: cephalhematomaPallor: hemolysis, blood lossPetechiae: sepsis, TORCH infectionsHepatosplenomegaly: Rh-isoimmunization, sepsis, TORCH infectionsDysmorphic features, congenital heart disease (pulmonary stenosis): Intrahepaticbiliaryatresia (Alagille syndrome)
  5. Blood group for abo and rh and other minor antigen
  6. Torch serumtitres, Endoscopy for biliary obstruction,H/O and signs of Sepsis and screeningGalactosemia: Blood glucose and substance in stool and enzyme assaysColour of stool and urine in cholestasis
  7. H/O for enclosed haemorrageBrest feedingHypothyroidism: thyroid levelLiver function test: in HepatitisDiabetic mother: history of diabetes in the motherRDS and asphxia: Birth historyInfection: signs of infectionDrugs: H/O drugs to motherHaemoglobin analysis and ABO grouping