Problems Common to Newborn Flashcards
What is the most common cause of Respiratory Distress of a newborn?
Hyaline Membrane Disease
Hypoglycemia: General Characteristics
Defined as blood glucose
Hypoglycemia: Pathophysiology
Infant does not have sufficient glycogen stores in muscle or liver nor sufficient fat for release of fatty acids for energy
Hypoglycemia: Signs & Sx’s
Asymptomatic Poor feeding Lethargy Tremulousness Irritability Apnea Seizures
Hypoglycemia: Diagnostic Studies
Heel blood tested w/glucometer
Abnormal results should be confirmed w/ serum blood glucose
Normal glucose level is 50-80 mg/dL @ 3 hrs of age
Abnormal level is glucose
Hypoglycemia: Treatment
- Bolus of dextrose & water (D10W) & IV glucose as needed
- Continue to monitor
- Usually resolves by day 5
- Failure to resolve should prompt investigation for less likely causes
Neonatal Jaundice: Bilirubin Pathophysiology
- Bilirubin is final product of heme degradation
- Insoluble in plasma & requires protein binding w/ albumin
- After conjugation in liver, it’s excreted in bile
- Newborns produce bilirubin 2X the rate as adults
- Due to polycythemia & ↑ RBC turnover
- ↓ to adult level w/in 10-14 days after birth
Neonatal Jaundice: General Characteristics
- Total serum bilirubin > 5 mg/dL
- Typically results from deposition of unconjugated bilirubin pigment in the skin & mucus membranes
Pathologic if:
- Presents w/in 1st 24 hrs after birth
- Total serum bilirubin rises by > 5 mg/dL per day
- > 17 mg/dL
- (+) signs & sx’s suggestive of serious illness
> 65% of infants have bilirubin level > 5 mg/dL in first week of life
Neonatal Jaundice: Most common causes
- Physiologic
- Appears after 24 hr
- Peaks @ 3-5 days - Prematurity
- Appears w/in 24 hr of birth - Breast feeding
- Appears 2nd – 3rd day of life
- ↓ volume & frequency of feedings → dehydration & delayed passage of meconium
Neonatal Jaundice: Etiology
- Overproduction of bilirubin
a. Elevated reticulocyte count
- Hemolysis 2° to blood group sensitizations
- (+) Coombs test
- ABO incompatibility
- Rh incompatibility
b. Hemolysis 2° to congenital hemolytic anemia
- (-) Coombs test
- Hereditary spherocytosis
- G6PD deficiency
c. Hemolysis 2° to sepsis - Decreased rate of conjugation
a. Normal reticulocyte count
- Physiologic jaundice 2° to ABO incompatibility
- Bilirubin increases by
Neonatal Jaundice: Physical Exam
- Jaundice begins @ head
a. Extends to chest & extremities as bilirubin increases - Scleral icterus & jaundiced oral mucosa help distinguish jaundice in dark skinned infants
- Splenomegaly may be present in hereditary spherocytosis
Neonatal Jaundice: Diagnostic Studies
- CBC
a. Anemia
- Monitor H&H if acute hemolysis - Peripheral smear
a. Poikilocytosis, schistocytes, nucleated RBC’s - Bili – total, direct, indirect
- Retic count
- Coombs test
- G6PD test
a. African, Asian or Mediterranean descent - Septic work-up if indicated
Neonatal Jaundice: Complications
- Kernicterus
- Abnormal accumulation of bile pigment in the brain & other nerve tissue
- Leads to encephalopathy
- Bilirubin > 20-25 mg/dL
Early Effects of Bilirubin Toxicity
Lethargy
Poor Feeding
High-pitched cry
Hypotonia
Late Effects of Bilirubin Toxicity
Irritability Opisthotonos Seizures Apnea Hypertonia Fever