1.5 MTB Step 3 - The Newborn (Jaundice) Flashcards
JAUNDICE IN THE NEWBORN
DIAGNOSIS
Describe the Flowchart for diagnosing Jaundice in the Newborn.
Physiologic (Indirect/Unconjugated):
-
Coombs (+)
- Rh/ABO Incompatibility
- Thalassemia minor
-
Coombs (-)
-
High Hemoglobin
- Polycythemia
- Twin-Twin transfusion
- Maternal-Fetal transfusion
- Delayed Cord
- IUGR
- IODM
-
Normal/Low Hemoglobin
- Spherocytosis
- Elliptocytosis
- G6PD Deficiency
- Pyruvate Kinase
-
High Hemoglobin
Pathologic (Direct/Conjugated):
- Sepsis
- TORCH Infections
- TPN
- Hypothyroid
- Galactosemia
- Tyrosinemia
- Cystic Fibrosis
- Choledochal Cyst
JAUNDICE IN THE NEWBORN
DIAGNOSIS
Under which (5) Clinical Presentations or Lab Values is Hyperbilirubinemia considered Pathological?
- Appears ON the 1st Day of Life
- Appears AFTER the 2nd Week of Life
- Bilirubin > 5mg/dL/day
- Bilirubin > 12mg/dL in Term Infant
- Direct Bilirubin > 2mg/dL at ANY time
JAUNDICE IN THE NEWBORN
DIAGNOSIS
If Jaundice** presents in the First 24 hours, what are (5**) Tests to include in the Workup?
- Bilirubin: Total & Direct
- Blood Type (Infant & Mother):Look for ABO or Rh incompatibility
- Direct Coombs Test
- CBC, Reticulocyte Count, & Blood Smear:Assess for Hemolysis
- Urinalysis & Urine Culture (if elevated Direct Bilirubin): Assess for Sepsis
JAUNDICE IN THE NEWBORN
DIAGNOSIS
What is the Mechanism for Bilirubin in the Newborn?
- Hemoglobin breaks down to Unconjugated (Indirect) Bilirubin.
- Higher levels of Unconjugated Bilirubin are needed during development when it can cross the placenta and be removed from the Fetus by the Mother.
- Newborns have Low levels of Glucuronosyltransferase (the enzyme that connects or “Conjugates” Unconjugated Bilirubin to Glucose so that it can be Excreted through Feces).
- The RBCs of Newborns also have a Shorter Life Span. Breakdown of RBCs releases Unconjugated Bilirubin.
JAUNDICE IN THE NEWBORN
DIAGNOSIS
What (4) Disorders should you consider if there is Prolonged Jaundice ( > 2 weeks ) and NO Elevation of Conjugated Bilirubin?
- UTI or other Infection
-
Bilirubin Conjugation Abnormalities
- Gilbert Syndrome
- Crigler-Najjar Syndrome
- Hemolysis
-
Intrinsic Red Cell membrane or Enzyme defects
- Spherocytosis
- Elliptocytosis
- G6PD Deficiency
- Pyruvate Kinase Deficiency
JAUNDICE IN THE NEWBORN
DIAGNOSIS
What does the Most Feared Complication of Jaundice (Kernicterus) result from?
Elevated Indirect (Unconjugated) Bilirubin can Cross the Blood-Brain Barrier, deposit in the Basal Ganglia and Brainstem Nuclei, and cause Kernicterus.
JAUNDICE IN THE NEWBORN
DIAGNOSIS
- What Disorder should you consider if there is Prolonged Jaundice ( > 2 weeks ) and Elevated Conjugated Bilirubin?
- What is the Best INITIAL Diagnostic Test for this Disorder?
- What are the (2) Most SPECIFIC Tests for this Disorder?
- Cholestasis
- Liver Function Tests
- Ultrasound & Liver Biopsy
JAUNDICE IN THE NEWBORN
TREATMENT
- What is the Best INITIAL Treatment for Jaundice in the Newborn?
- What is the Treatment for ANY Infant with suspected Bilirubin Encephalopathy or Failure of the best initial therapy to reduce Total Bilirubin and Risk of Kernicterus?
- Phototherapy when Bilirubin > 10 - 20 mg/dL (normally decreases by 2 mg/dL every 4 - 6 hours)
- Exchange Transusion