NEONATAL JAUNDICE
Hyperbilirubinemia is a common and, in most cases, benign
problem in neonates. Nonetheless, untreated, severe indirect
hyperbilirubinemia is potentially neurotoxic, whereas conjugated
direct hyperbilirubinemia often signifies a serious hepatic or
systemic illness.
hyperbilirubinemia is potentially neurotoxic, whereas conjugated
direct hyperbilirubinemia often signifies a serious hepatic or
systemic illness.
Jaundice is observed during the 1st wk of life in
approximately 60% of term infants and 80% of preterm infants,
this is because of the followings:-
this is because of the followings:-
The color usually results from:-
Either the accumulation in skin of unconjugated, lipid-soluble
bilirubin pigment (indirect reacting) formed from hemoglobin
by the action of heme oxygenase, biliverdin reductase, and
nonenzymatic reducing agents in the reticuloendothelial cells,
Or the jaundice may also be due to deposition of the pigment
after it has been converted in the liver cells by the enzyme
uridine diphosphoglucuronic acid (UDP)-glucuronyl
transferase to the water-soluble direct reacting bilirubin.
heme
Heme oxygenase
Biliverdin reductase
Hemoglobin
globin
Fat soluble indirect
bilirubin
Glucuronyl
transferase
water soluble
direct bilirubin
bilirubin pigment (indirect reacting) formed from hemoglobin
by the action of heme oxygenase, biliverdin reductase, and
nonenzymatic reducing agents in the reticuloendothelial cells,
Or the jaundice may also be due to deposition of the pigment
after it has been converted in the liver cells by the enzyme
uridine diphosphoglucuronic acid (UDP)-glucuronyl
transferase to the water-soluble direct reacting bilirubin.
heme
Heme oxygenase
Biliverdin reductase
Hemoglobin
globin
Fat soluble indirect
bilirubin
Glucuronyl
transferase
water soluble
direct bilirubin
The unconjugated form is neurotoxic in infants at certain
concentrations and under various conditions. Conjugated
bilirubin is not neurotoxic but indicates a potentially serious
disorder.
bilirubin is not neurotoxic but indicates a potentially serious
disorder.
Unconjugated hyperbilirubinemia may be caused or increased by
any factor that:
1. Increase the load of bilirubin to be metabolized by the liver as
in hemolytic anemias, polycythemia, shortened red cell life as
a result of immaturity or transfused cells or use of oxytocin
during delivery, infection, enterohepatic circulation.
1. Increase the load of bilirubin to be metabolized by the liver as
in hemolytic anemias, polycythemia, shortened red cell life as
a result of immaturity or transfused cells or use of oxytocin
during delivery, infection, enterohepatic circulation.
2. Damages or reduces the activity of the transferase enzyme
(genetic deficiency, hypoxia, infection, hypothermia and
thyroid deficiency).
thyroid deficiency).
3. Competes for or blocks the transferase enzyme as drugs and
other substances requiring glucuronic acid conjugation for
excretion).
excretion).
4. Reduction of bilirubin uptake by liver cells (genetic defect,
prematurity).
Diferential diagnosis of neonatal jaundice:-
Neonatal jaundice may be either:-
-Indirect hyperbilirubinemia.
-Direct hyperbilirubinemia (when the direct bilirubin is more
than 20% of the total serum bilirubin.
Indirect hyperbilirubinemia:-
1. Physiologic jaundice(icterus neonatorum).
2. Pathologic (mainly hemolytic).
3. Breast milk jaundice.
-Indirect hyperbilirubinemia.
-Direct hyperbilirubinemia (when the direct bilirubin is more
than 20% of the total serum bilirubin.
Indirect hyperbilirubinemia:-
1. Physiologic jaundice(icterus neonatorum).
2. Pathologic (mainly hemolytic).
3. Breast milk jaundice.
Physiologic jaundice:-
Causes:
-There is marked physiological release of haemoglobin
from the breakdown of red cells because of the high Hb
concentration at birth.
-The red cell life span of newborn infants (70-90 days) is
markedly shorter than that of adults (120 days).
-Hepatic bilirubin metabolism is slow during the first few days of life.
-There is marked physiological release of haemoglobin
from the breakdown of red cells because of the high Hb
concentration at birth.
-The red cell life span of newborn infants (70-90 days) is
markedly shorter than that of adults (120 days).
-Hepatic bilirubin metabolism is slow during the first few days of life.
Criteria of physiologic jaundice:
- It starts during the 2nd or the 3rd day of life.
- The peak of jaundice in fullterm baby is at the 2nd to 4th day
of life, while in preterm baby it peaks at 5th to 7th day of life.
- Decline to below 2mg/dl by the 7th day of life in term & by
the 10th day in preterm baby.
- Jaundice disappear completely within 2 weeks of life.
- The raise in the bilirubin is less than 5 mg/dl/24 hours.
- The peak level of bilirubin is less than 12mg/dl, although
10% of these babies having higher bilirubin level as in babies
of diabetic mothers, prematurity, polycythemia, vit k
administration, male sex, Down syndrome, cephalhematoma,
cutaneous bruising oxytocin during labor, dehydration and
calory deprivation, delay bowel motion.
- The peak of jaundice in fullterm baby is at the 2nd to 4th day
of life, while in preterm baby it peaks at 5th to 7th day of life.
- Decline to below 2mg/dl by the 7th day of life in term & by
the 10th day in preterm baby.
- Jaundice disappear completely within 2 weeks of life.
- The raise in the bilirubin is less than 5 mg/dl/24 hours.
- The peak level of bilirubin is less than 12mg/dl, although
10% of these babies having higher bilirubin level as in babies
of diabetic mothers, prematurity, polycythemia, vit k
administration, male sex, Down syndrome, cephalhematoma,
cutaneous bruising oxytocin during labor, dehydration and
calory deprivation, delay bowel motion.
Pathologic Jaundice(hemolytic):-
The criteria of this jaundice are:-
- It starts during the 1st 24 hr of life.
- The rise in serum bilirubin is more than 5mg/dl/24 hr.
- The serum bilirubin is higher than 12mg/dl.
- Jaundice persist for more than 2 weeks.
- May be positive family history of hemolytic disease, pallor,
hepatosplenomegaly, signs of kernecterus.
- Lab. findings may show evidence of Rh or ABO incompatability
low hemoglobin, reticulocytosis, and may be a positive
Coombs test.
- It starts during the 1st 24 hr of life.
- The rise in serum bilirubin is more than 5mg/dl/24 hr.
- The serum bilirubin is higher than 12mg/dl.
- Jaundice persist for more than 2 weeks.
- May be positive family history of hemolytic disease, pallor,
hepatosplenomegaly, signs of kernecterus.
- Lab. findings may show evidence of Rh or ABO incompatability
low hemoglobin, reticulocytosis, and may be a positive
Coombs test.
Breast milk jaundice:
An estimated of 2% of breast fed term infants develops an
elevated level of uncongugated bilirubin after the7th day of life reaching maximal concentrations as high as 10-30mg per dl during the 2nd & 3rd week.If breast feeding continued the hyperbilirubinemia gradually decrases & then may persist for 3-10 weeks at lower levels. These infants show no signs of illness and kernicterus is very rarely reported.
elevated level of uncongugated bilirubin after the7th day of life reaching maximal concentrations as high as 10-30mg per dl during the 2nd & 3rd week.If breast feeding continued the hyperbilirubinemia gradually decrases & then may persist for 3-10 weeks at lower levels. These infants show no signs of illness and kernicterus is very rarely reported.
The milk of some of these mothers contains a non esterified
long chain fatty acids which acts as an inhibitory substances
to glucuronyl trasferase conjucating activity.In others the milk
contains a glucuronidase that may be responsible for jaundice.
to glucuronyl trasferase conjucating activity.In others the milk
contains a glucuronidase that may be responsible for jaundice.
Kernicterus:
Is a neurologic syndrome results from a deposition of
uncongugated bilirubin in the brain cells particularly in the basal
ganglia, hippocumpus,and cerebellum. Lipid soluble indirect
bilirubin may cross the blood brain barrier and enter the brain
by diffusion.
uncongugated bilirubin in the brain cells particularly in the basal
ganglia, hippocumpus,and cerebellum. Lipid soluble indirect
bilirubin may cross the blood brain barrier and enter the brain
by diffusion.
The factors which increase the toxic effects of elevated
levels of unconjugated bilirubin in the serum are:-
- Factors that reduce the retention of bilirubin in the circulation
i.e increase of free bilirubin in the circulation as in:-
(hypoproteinemia, displacement of bilirubin from its binding
sites on albumin by competitive binding of drugs such as
sulfisoxazole and acidosis, increased free fatty acid
concentration secondary to hypoglycemia, starvation, or
hypothermia).
- Factors that increase the permeability of the blood-brain
barrier or nerve cell membranes to bilirubin or increase the
susceptibility of brain cells to its toxicity, such as asphyxia,
prematurity, hyperosmolality, and infection.
Clinical features: signs & symptoms of kernicterus usually appear in the 1st week of life although kernicterus can occur at any time during the neonatal period.
The early signs may be subtle & indistinguishable from sepsis,
asphyxia, hypoglycemia or intracranial hrg which are:-
Lethargy poor feeding & absence Moro reflex are common initial signs.
In advanced cases there is irritability, increased muscle tone causing the baby to lie with an arched back (opisthotonos),
twitching, seizures, high pitched cry, bulging fontanel, coma with the infant stiffly extended his arms with inward rotation.
- Factors that reduce the retention of bilirubin in the circulation
i.e increase of free bilirubin in the circulation as in:-
(hypoproteinemia, displacement of bilirubin from its binding
sites on albumin by competitive binding of drugs such as
sulfisoxazole and acidosis, increased free fatty acid
concentration secondary to hypoglycemia, starvation, or
hypothermia).
- Factors that increase the permeability of the blood-brain
barrier or nerve cell membranes to bilirubin or increase the
susceptibility of brain cells to its toxicity, such as asphyxia,
prematurity, hyperosmolality, and infection.
Clinical features: signs & symptoms of kernicterus usually appear in the 1st week of life although kernicterus can occur at any time during the neonatal period.
The early signs may be subtle & indistinguishable from sepsis,
asphyxia, hypoglycemia or intracranial hrg which are:-
Lethargy poor feeding & absence Moro reflex are common initial signs.
In advanced cases there is irritability, increased muscle tone causing the baby to lie with an arched back (opisthotonos),
twitching, seizures, high pitched cry, bulging fontanel, coma with the infant stiffly extended his arms with inward rotation.
opisthotonos
Many infants who progress to these severe neurologic signs die, the survivors are usually seriously damaged but may appear to recover & for 2-3 months manifest few abnormalities.
Later in the 1st year of life opisthotonos, muscular rigidity,
irregular movements, and convulsions tends to recur.
In the 2nd year opisthotonos & convulsions abate,but irregular
involuntary movements, muscular rigidity or in some infants
hypotonia increase gradually.
In the 2nd year opisthotonos & convulsions abate,but irregular
involuntary movements, muscular rigidity or in some infants
hypotonia increase gradually.
By 3 years of age the syndrome is completely developed
consisting of bilateral chorioathetosis with involuntary
muscle spasm,seizures, mental deficiency, dysarthric speech,
high frequency hearing loss,squints, and defective upward movement of the eyes.
In mildly affected infants, the syndrome may be characterized only by mild to moderate neuromuscular incoordination,partial
deafness, or minimal brain dysfunction.
muscle spasm,seizures, mental deficiency, dysarthric speech,
high frequency hearing loss,squints, and defective upward movement of the eyes.
In mildly affected infants, the syndrome may be characterized only by mild to moderate neuromuscular incoordination,partial
deafness, or minimal brain dysfunction.
Treatment of hyperbilirubinemia:
Either there is no need for treatment especially if there is no
hemolysis, full term baby, healthy active & the jaundice is not
deep with criteria of physiologic jaundice.
2. Phototherapy: usually started when the bilirubin level is at 50-
70% of the maximal accepted value.
3. Exchange transfusion.
4. Intravenous immunoglobulin: for ABO and Rh incompata-bility in a dose of 0.5-1 grams/kg/dose repeated every 12 hours.
hemolysis, full term baby, healthy active & the jaundice is not
deep with criteria of physiologic jaundice.
2. Phototherapy: usually started when the bilirubin level is at 50-
70% of the maximal accepted value.
3. Exchange transfusion.
4. Intravenous immunoglobulin: for ABO and Rh incompata-bility in a dose of 0.5-1 grams/kg/dose repeated every 12 hours.
Birth weight(g) uncomplicated complicated
-------------------------------------------------------------------------
<1000 12-13 10-12
1000-1250 12-14 10-12
2000-2500 20-22 18-20
1251-1499 14-16 12-14
1500-1999 16-20 15-17
2000-2500 20-22 18-20
Maximal accepted bilirubin value
according to weight
<1000 12-13 10-12
1000-1250 12-14 10-12
2000-2500 20-22 18-20
1251-1499 14-16 12-14
1500-1999 16-20 15-17
2000-2500 20-22 18-20
Maximal accepted bilirubin value
according to weight
Phototherapy:-
Clinical jaundice & indirect hyperbilirubinemia reduced on
exposure to a high intensity of light in a wave length of
420-470nm. Bilirubin in the skin absorbs light energy which by
photoisomerization converts the toxic unconjugated bilirubin to
a product which can be excreted in bile without the need for
conjugation, also phototherapy converts uncojugated bilirubin to lumirubin which excreted in urine by the kidney.
Prophylactic phototherapy in VLBW infants may prevents
hyperbilirubinemia & may reduce the need for exchange
transfusion.
exposure to a high intensity of light in a wave length of
420-470nm. Bilirubin in the skin absorbs light energy which by
photoisomerization converts the toxic unconjugated bilirubin to
a product which can be excreted in bile without the need for
conjugation, also phototherapy converts uncojugated bilirubin to lumirubin which excreted in urine by the kidney.
Prophylactic phototherapy in VLBW infants may prevents
hyperbilirubinemia & may reduce the need for exchange
transfusion.
The therapeutic effect depends on:-
1. The light energy emitted on in the effective wavelengths.
2. The distance between the lights & the infants.
3. The amount of skin exposed.
4. The rate of hemolysis if present.
5. Rate of metabolism & excretion of bilirubin.
2. The distance between the lights & the infants.
3. The amount of skin exposed.
4. The rate of hemolysis if present.
5. Rate of metabolism & excretion of bilirubin.
Conventional phototherapy is applied continuously & the
infant should be turned frequently for max skin exposure.
Serum bilirubin & PCV should be measured every 4-8 hrs in infants with hemolysis or when bilirubin level near the toxic
range,others particularly older infants may be monitored every 12-24 hrs.
Monitoring should continue for at least 24 hrs after cessation of phototherapy in infants with hemolytic disease that unexpected
rise of bilirubin sometimes occur & require further treatment.
Skin color can not be relied on for evaluation of the effectiveness of phototherapy that the skin of babies exposed
to light may appear without jaundice in the presence of marked hyperbilirubinemia.
The infants eyes should be closed & adequately covered to prevent exposure to light. Body temp also should be monitored.
Serum bilirubin & PCV should be measured every 4-8 hrs in infants with hemolysis or when bilirubin level near the toxic
range,others particularly older infants may be monitored every 12-24 hrs.
Monitoring should continue for at least 24 hrs after cessation of phototherapy in infants with hemolytic disease that unexpected
rise of bilirubin sometimes occur & require further treatment.
Skin color can not be relied on for evaluation of the effectiveness of phototherapy that the skin of babies exposed
to light may appear without jaundice in the presence of marked hyperbilirubinemia.
The infants eyes should be closed & adequately covered to prevent exposure to light. Body temp also should be monitored.
Complications of phototherapy:
1. loose stool.
2. Erythematous macular rashes.
3. Overheating.
4. Dehydration.
5. Bronze baby syndrome when there is direct
hyperbilirubinemia.
6. Eye injury and nasal obstruction.
Phtotherapy is contraindicated in cases of porphyria.
2. Erythematous macular rashes.
3. Overheating.
4. Dehydration.
5. Bronze baby syndrome when there is direct
hyperbilirubinemia.
6. Eye injury and nasal obstruction.
Phtotherapy is contraindicated in cases of porphyria.
Exchange transfusion:-
It is used to remove bilirubin from the circulation when phototherapy fails, is especially used for infants with increased
it bilirubin production from immune mediated hemolysis
because the circulating antibodies and the sensitized RBCs
are also removed.
it bilirubin production from immune mediated hemolysis
because the circulating antibodies and the sensitized RBCs
are also removed.
Exchange transfusion will:-
- Clear excess bilirubin.
- Correct the anemia without causing circulatory overload.
- Removes maternal antibodies.
- Removes sensitized RBCs.
- Correct the anemia without causing circulatory overload.
- Removes maternal antibodies.
- Removes sensitized RBCs.
Technique: a double volume exchange transfusion removes
approximately twice the infant circulating blood volume
170ml/kg body wt blood volume of the (infant is approximately
80-90 ml/kg body wt) replacing it with crossed-matched whole
blood.The procedure involves placement of a central catheter
and removing & placing blood in a volume that is approximately
10% or less of the infant blood volume.
Most of the bilirubin is extravascular, as a result exchange transfusion removes approximately 25% of the total body bilirubin, after the procedure serum bilirubin falls to
approximately 1/2 of the pre exchange value, then increase
to approximately 2/3 of that level as the extravascular & vascular bilirubin reequilibirate. A double volume exchange trnsfusion replace approximately 85% of the infants red blood cells.
170ml/kg body wt blood volume of the (infant is approximately
80-90 ml/kg body wt) replacing it with crossed-matched whole
blood.The procedure involves placement of a central catheter
and removing & placing blood in a volume that is approximately
10% or less of the infant blood volume.
Most of the bilirubin is extravascular, as a result exchange transfusion removes approximately 25% of the total body bilirubin, after the procedure serum bilirubin falls to
approximately 1/2 of the pre exchange value, then increase
to approximately 2/3 of that level as the extravascular & vascular bilirubin reequilibirate. A double volume exchange trnsfusion replace approximately 85% of the infants red blood cells.
Risks:
The risks of exchange transfusion are either to the use of blood products or from the procedure itself,these includes:-
- blood born infection.
thrombocytopenia.
-metabolic acidosis.
-volume overload.
- coagulopathy.
- graft versus host disease.
- necrotizing enterocolitis.
- portal vein thrombosis.
- electrolytes disturbance.
- hypoglycemia, hypocalcemia.
- cardiac arrhythmias.
- sudden death.
- blood born infection.
thrombocytopenia.
-metabolic acidosis.
-volume overload.
- coagulopathy.
- graft versus host disease.
- necrotizing enterocolitis.
- portal vein thrombosis.
- electrolytes disturbance.
- hypoglycemia, hypocalcemia.
- cardiac arrhythmias.
- sudden death.
Direct hyperbilirubinemia:
When the direct bilirubin level is more than 2mg /dl then the problem is termed as direct hyperbilirubinemia.
Common causes:-
- biliary atresia.
- idiopathic neonatal hepatitis.
Less common causes as:-
cystic fibrosis, galactosemia, Wilson disease, tyrosinemia,
fructosemia, alpha 1 antitrypsin deficiency, TORCH infection,
choledochal cyst, total parenteral nutrition.
Common causes:-
- biliary atresia.
- idiopathic neonatal hepatitis.
Less common causes as:-
cystic fibrosis, galactosemia, Wilson disease, tyrosinemia,
fructosemia, alpha 1 antitrypsin deficiency, TORCH infection,
choledochal cyst, total parenteral nutrition.
Comments
Post a Comment