hyper-bilirunemia. history earliest work on jaundice from baumes-1785, and hervieux-1847 ...

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Page 1: HYPER-BILIRUNEMIA. History  Earliest work on jaundice from Baumes-1785, and Hervieux-1847  Kernicterus was first described by Johannes Orth, 1875

HYPERHYPER--BILIRUNEMIABILIRUNEMIA

Page 2: HYPER-BILIRUNEMIA. History  Earliest work on jaundice from Baumes-1785, and Hervieux-1847  Kernicterus was first described by Johannes Orth, 1875

History Earliest work on jaundice from Baumes-1785, and

Hervieux-1847

Kernicterus was first described by Johannes Orth, 1875He postulated that jaundice might have hematologic

originsHe noted that the brain in jaundiced adults wasn’t

affected

Christian Schmorl coined the term in 1904Translated, Kernicterus means jaundice of the “kern”

or nuclear region of the brain

Page 3: HYPER-BILIRUNEMIA. History  Earliest work on jaundice from Baumes-1785, and Hervieux-1847  Kernicterus was first described by Johannes Orth, 1875

Jaundice… Exaggerated Hyperbilirubinemia

Polycythemia

HemolysisRh incompatibilityABO incompatibilityAbnormal RBCs—G6PD,

spherocytosis, thalassemia

Birth Trauma—Bruising, Cephalohematoma

Metabolic Abnormalities—Crigler Najjar, Gilbert Syndrome, Galactosemia

Medications—SulfonamidesDisplaces bilirubin from

albumin; same binding site

Page 4: HYPER-BILIRUNEMIA. History  Earliest work on jaundice from Baumes-1785, and Hervieux-1847  Kernicterus was first described by Johannes Orth, 1875

Causes of Hyper-bilirubinemia in the newborns:

Page 5: HYPER-BILIRUNEMIA. History  Earliest work on jaundice from Baumes-1785, and Hervieux-1847  Kernicterus was first described by Johannes Orth, 1875

Jaundice

Page 6: HYPER-BILIRUNEMIA. History  Earliest work on jaundice from Baumes-1785, and Hervieux-1847  Kernicterus was first described by Johannes Orth, 1875

Zona 1: 4 a 7 mg/dl; Zona 2: 5 a 8,5 mg/dl;  Zona 3: 6 a 11,5 mg/dl;  Zona 4: 9 a 17 mg/dl;  Zona 5: > de 15 mg/dl.  Adaptado de Kramer: AJDC 1069;118:454 y Finn: Acta Obstet Gynecol Scand 1975; 54:329

Page 7: HYPER-BILIRUNEMIA. History  Earliest work on jaundice from Baumes-1785, and Hervieux-1847  Kernicterus was first described by Johannes Orth, 1875
Page 8: HYPER-BILIRUNEMIA. History  Earliest work on jaundice from Baumes-1785, and Hervieux-1847  Kernicterus was first described by Johannes Orth, 1875

Pathophysiology

RBCs are broken down

Bilirubin is an end product of heme metabolism

Bilirubin is conjugated in the liverEnzyme: UDP-Glucuronyl Transferase

Conjugated bili is excreted via the GI tractEnzyme: Beta-Glucuronidase can

unconjugate bili in the small intestine and bili is reabsorbed

Page 9: HYPER-BILIRUNEMIA. History  Earliest work on jaundice from Baumes-1785, and Hervieux-1847  Kernicterus was first described by Johannes Orth, 1875

Pathophysiology of Newborn Hyperbilirubinemia

Relatively high hematocrit; more cells to break down

UDP-Glucuronyl Transferase is not fully functional until 3-4 months of life

Relative starvation state and slow transit time, especially in breastfeeders

Breastmilk contains beta-glucuronidase; enterohepatic circulation is increased

Page 10: HYPER-BILIRUNEMIA. History  Earliest work on jaundice from Baumes-1785, and Hervieux-1847  Kernicterus was first described by Johannes Orth, 1875

Pathophysiology

UCB is lipophilic and crosses the Blood-Brain BarrierIn vitro, free UCB will not precipitate out

of solution unless in the presence of a polar lipid membrane

In theory, only free UCB crosses, albumin-bound does not.

BBB of infants is more permeable than adults, and acidosis causes it to be even more permeable.

Page 11: HYPER-BILIRUNEMIA. History  Earliest work on jaundice from Baumes-1785, and Hervieux-1847  Kernicterus was first described by Johannes Orth, 1875

Pathophysiology…cont

UCB has an affinity for the basal ganglia, hippocampus, cranial nerve nucleiMechanism is widely studied, but still

unknown

UCB interrupts metabolism in glial cells and causes apoptosis of neuronsExact mechanisms are unknown, but

definitely separate pathways.Age of the cell is inversely proportional to

susceptibility

Page 12: HYPER-BILIRUNEMIA. History  Earliest work on jaundice from Baumes-1785, and Hervieux-1847  Kernicterus was first described by Johannes Orth, 1875
Page 13: HYPER-BILIRUNEMIA. History  Earliest work on jaundice from Baumes-1785, and Hervieux-1847  Kernicterus was first described by Johannes Orth, 1875
Page 14: HYPER-BILIRUNEMIA. History  Earliest work on jaundice from Baumes-1785, and Hervieux-1847  Kernicterus was first described by Johannes Orth, 1875

Phases of Physiological jaundice

Page 15: HYPER-BILIRUNEMIA. History  Earliest work on jaundice from Baumes-1785, and Hervieux-1847  Kernicterus was first described by Johannes Orth, 1875

In pre-term infant, bilirubin levels may peak as high as 10-12mg/dl at 4-5 days and decrease slowly over 2-4 weeks.

Newborns produce twice as much bilirubin as do adults, because of:

Page 16: HYPER-BILIRUNEMIA. History  Earliest work on jaundice from Baumes-1785, and Hervieux-1847  Kernicterus was first described by Johannes Orth, 1875

Types of UnTypes of Un--conjugated Hyperconjugated Hyper--bilirubinemiabilirubinemia

Page 17: HYPER-BILIRUNEMIA. History  Earliest work on jaundice from Baumes-1785, and Hervieux-1847  Kernicterus was first described by Johannes Orth, 1875

Physiological JaundicePhysiological Jaundice

Immature hepatic function + increased bilirubin load from RBCs hemolysis..

Page 18: HYPER-BILIRUNEMIA. History  Earliest work on jaundice from Baumes-1785, and Hervieux-1847  Kernicterus was first described by Johannes Orth, 1875

Breast feeding associated Breast feeding associated jaundicejaundice--earlyearly milk intake

few calories

Enterohepatic shunting

In the intestine the enzyme (B-glucuronidase is able to convert conjugated bilirubin into unconjigated form reabsorbed by the intestinal mucosa transported to the liver

Page 19: HYPER-BILIRUNEMIA. History  Earliest work on jaundice from Baumes-1785, and Hervieux-1847  Kernicterus was first described by Johannes Orth, 1875

Hemolytic diseaseBreast-milk jaundice (late onset)

Blood antigen incompatibility cause hemolytic or large numbers of RBCs where liver is unable to conjugate and excrete excess bilirubin from hemolysis.

Caused by possible factors in the breast milk that prevent bilirubin conjugation, or less frequent stooling.

Page 20: HYPER-BILIRUNEMIA. History  Earliest work on jaundice from Baumes-1785, and Hervieux-1847  Kernicterus was first described by Johannes Orth, 1875

Dx: serum level of bilirubin.

Normal values: Unconjugated bilirubin= 0.2 to 1.4 mg/dl.

Clinical dx depends on:TSB (Total serum bilirubin level) time on onset for the S&S GA at birth age in days post delivery. Family Hx and mother’s Rh factor evidence of hemolysis feeding methodInfant physiological status

Diagnostic evaluation

Page 21: HYPER-BILIRUNEMIA. History  Earliest work on jaundice from Baumes-1785, and Hervieux-1847  Kernicterus was first described by Johannes Orth, 1875

Laboratory Measures

There is currently no lab value that correlates well with the development of kernicterus; there seem to be many factors that lead to its development

Guidelines for initiating therapy for hyperbilirubinemia currently include the variables of UCB and age of baby. There are no good guidelines for preterm infantsAn unconjugated bilirubin level of 25 or less in TERM,

HEALTHY babies has not been correlated with kernicterus

Pediatrics 1995; Case reports of Term, Healthy, Breastfed babies—UCB levels associated with clinical Kernicterus were 39-50

It has been hypothesized that measuring UNBOUND UCB can be correlated, but not well supported as of yet

Page 22: HYPER-BILIRUNEMIA. History  Earliest work on jaundice from Baumes-1785, and Hervieux-1847  Kernicterus was first described by Johannes Orth, 1875

Pathological JaundiceAppearance of jaundice within 24 hours of birth.Persistent jaundice after 1 week in full-terms babies, and more than 2 weeks for pre-term neonates.TSB > 12mg/dl.Increase in serum bilirubin 5mg/dl/dayDirect bilirubin > 1.5 mg/dl.

Page 23: HYPER-BILIRUNEMIA. History  Earliest work on jaundice from Baumes-1785, and Hervieux-1847  Kernicterus was first described by Johannes Orth, 1875

Jaundice

Page 24: HYPER-BILIRUNEMIA. History  Earliest work on jaundice from Baumes-1785, and Hervieux-1847  Kernicterus was first described by Johannes Orth, 1875

Def: is a syndrome of sever brain damage resulting from the deposition of unconjugated bilirubin In brain cells.

The damage occurs when the serum concentration reaches toxic levels and crosses the BBB.

ComplicationsComplications……Kernicterus Kernicterus ((Bilirubin Bilirubin encephalopathyencephalopathy))

Page 25: HYPER-BILIRUNEMIA. History  Earliest work on jaundice from Baumes-1785, and Hervieux-1847  Kernicterus was first described by Johannes Orth, 1875
Page 26: HYPER-BILIRUNEMIA. History  Earliest work on jaundice from Baumes-1785, and Hervieux-1847  Kernicterus was first described by Johannes Orth, 1875

The yellow staining in the brain of a neonate is known as kernicterus.

There is a coronal section of medulla on the left and cerebral hemisphere on the right demonstrating kernicterus in deep grey matter of hemisphere and brain stem.

Kernicterus is more likely to occur with prematurity, low birth weight, and increased bilirubin levels.

Page 27: HYPER-BILIRUNEMIA. History  Earliest work on jaundice from Baumes-1785, and Hervieux-1847  Kernicterus was first described by Johannes Orth, 1875

-Serum bilirubin level can’t predict the risk for brain injury alone, other factors put the newborn at high risk for encephalo-pathy are:Metabolic acidosis low serum albumin levels Intracranial infection as meningitis increased blood pressure any conditions that may increase metabolic demands for oxygen or glucose, (e.g. fetal distress, hypoxia, hypthermia, hypoglycemia).

S&S:

CNS depression or excitation, Lethargy and decreased activity, Irritability, Hypotonia and seizures…. May progress to defness, cerebral palsy, or mental retardation.

Complications…….cont

Page 28: HYPER-BILIRUNEMIA. History  Earliest work on jaundice from Baumes-1785, and Hervieux-1847  Kernicterus was first described by Johannes Orth, 1875

Therapeutic Management

Page 29: HYPER-BILIRUNEMIA. History  Earliest work on jaundice from Baumes-1785, and Hervieux-1847  Kernicterus was first described by Johannes Orth, 1875

Prevention: Treatment of HyperbilirubinemiaPhototherapy

Initiate based on UCB level and baby’s ageIsomerizes UCB to Lumirubin, soluble in water and

excreted via the kidney

Exchange transfusionInitiate if phototherapy fails, repeat as neededIncidence of kernicterus has dropped since the

advent

Sn-MesoporphyrinInhibits Heme-oxygenase, which is the rate-limiting

enzyme in heme catabolism.Only case reports thus far, where exchange transfusion

was refused

Page 30: HYPER-BILIRUNEMIA. History  Earliest work on jaundice from Baumes-1785, and Hervieux-1847  Kernicterus was first described by Johannes Orth, 1875

Jaundice

Page 31: HYPER-BILIRUNEMIA. History  Earliest work on jaundice from Baumes-1785, and Hervieux-1847  Kernicterus was first described by Johannes Orth, 1875
Page 32: HYPER-BILIRUNEMIA. History  Earliest work on jaundice from Baumes-1785, and Hervieux-1847  Kernicterus was first described by Johannes Orth, 1875

Phototherapy ………( blue fluorescent light)

Bilirubin by photoisomerization soluble lumirubin (best in 1st 24-48hrs)

What are the major nursing

intervention at this stage?

Pharmacological action of phenobarbital are:Increase bilirubin conjugation

&hepatic clearance of the pigment in the bile

2. Increase albumin level thus increasing binding sites

Feeding Feeding ( ( intestinal motility, establish Nintestinal motility, establish N..Flora, Flora, ) ) hepatic shuntinghepatic shunting..

Page 33: HYPER-BILIRUNEMIA. History  Earliest work on jaundice from Baumes-1785, and Hervieux-1847  Kernicterus was first described by Johannes Orth, 1875

Some infants may also benefit from a fiberoptic pad underneath them, especially in the breastfed infant who is encouraged to feed 8-12 times in 24 hours.

Serum bilirubin levels above 25 mg/dL or higher at any time is a medical emergency and the infant should be evaluated immediately for exchange transfusion

Page 34: HYPER-BILIRUNEMIA. History  Earliest work on jaundice from Baumes-1785, and Hervieux-1847  Kernicterus was first described by Johannes Orth, 1875
Page 35: HYPER-BILIRUNEMIA. History  Earliest work on jaundice from Baumes-1785, and Hervieux-1847  Kernicterus was first described by Johannes Orth, 1875

Jaundice

Page 36: HYPER-BILIRUNEMIA. History  Earliest work on jaundice from Baumes-1785, and Hervieux-1847  Kernicterus was first described by Johannes Orth, 1875

Jaundice

Page 37: HYPER-BILIRUNEMIA. History  Earliest work on jaundice from Baumes-1785, and Hervieux-1847  Kernicterus was first described by Johannes Orth, 1875

Phototherapy at home

Page 38: HYPER-BILIRUNEMIA. History  Earliest work on jaundice from Baumes-1785, and Hervieux-1847  Kernicterus was first described by Johannes Orth, 1875

When drwing blood samples, turn the light off, cover the sample

Page 39: HYPER-BILIRUNEMIA. History  Earliest work on jaundice from Baumes-1785, and Hervieux-1847  Kernicterus was first described by Johannes Orth, 1875

Def: an excessive level of accumulated billirubin in the blood.

Jaundice mask

Page 40: HYPER-BILIRUNEMIA. History  Earliest work on jaundice from Baumes-1785, and Hervieux-1847  Kernicterus was first described by Johannes Orth, 1875

MRI of an infant who suffered from severe Erythroblastosis Fetalis

Page 41: HYPER-BILIRUNEMIA. History  Earliest work on jaundice from Baumes-1785, and Hervieux-1847  Kernicterus was first described by Johannes Orth, 1875

Sources

Ahlfors, CE: Unbound Bilirubin Associated with Kernicterus: A Historical Approach. Journal of Pediatrics 2000; 137(4): 540-544.

Brodersen, R and L. Stern: Deposition of Bilirubin Acid in the CNS—A Hypothesis for the Development of Kernicterus: Acta Paediatr Scand 1990; 79: 12-19.

Hansen, TR: Pioneers in the Scientific Study of Neonatal Jaundice and Kernicterus. Pediatrics 2000; 106(2): e15.

Kappas, A, et al: Sn-Mesoporphyrin Interdiction of Severe Hyperbilirubinemia in Jehovah’s Witness Newborns as an Alternative to Exchange Transfusion. Pediatrics 2001; 108(6): 1374-1377.