CLIPP case 8. Newborn (jaundice, feeding, stools, supplements) Flashcards
Newborn bilirubin physiology
Breakdown of RBCs -> unconjugated bilirubin binds to albumin -> (low levels of) uridine diphosphate gucuronosyl transferase -> conjugated bilirubin -> excreted into bile -> (in adults metabolized by flora to urobilinogen then stercobilinogen and excreted in stool) -> Neonatal lack of GI flora, so beta-glucuronidase of meconium hydrolyzes it back to unconjugated form -> reabsorption into blood stream and binding to albumin (this is enterohepatic circulation)
Kernicterus
- Basal ganglia and cranial nerve nuclei stained by bilirubin -> loss of suck reflex, lethargy, irritability, seizures, death
- Survivors: opisthotonus, rigidity, oculomotor paralysis, tremors, hearing loss, ataxia
- In past was most common in Rh incompatibility (erythroblastosis fetalis) with Tbili > 25
- Decreased now due to: screening for Rh and tx with RhoGAM; tx of unconjugated hyperbili with phototx
Opisthotonus
In survivors of kernicterus: abnormal posturing with rigidity and sever arching of back with head thrown backward
Etiologies of jaundice
1) Physiologic
2) Breast milk jaundice
3) Hemolysis: ABO or Rh incompatibility (positive direct Coombs or direct antibody test DAT), or antibody negative hemolysis (spherocytosis, G6PD def, pyruvate kinase def)
3) Non-hemolytic RBC breakdown: birth trauma, cephalohematoma, ICH, polycythemia, swallowed blood if large amount
4) Sepsis infection
5) Liver: biliary atresia, hepatitis
6) Metabolic: hypothyroidism, hypoglycemia, galactosemia, urea cycle defect, Crigler-Najjar (UDPGT def), Gilbert’s (UDPGT low)
*SCD and thalassemia do not cause jaundice
Physiologic jaundice
- Due to increased enterohepatic circulation: increased RBC breakdown, low UDP glucuronosyl transferase, low GI flora, high Beta-glucuronidase in meconium, and small oral intake to push meconium through (especially breastfed infants)
- Total bilirubin ≤15 mg/dL in otherwise healthy full term infants, no tx required
- Almost all newborns have hyperbilirubinemia, peak level at day 3-4, resolves by day 5
Jaundice associated with breastfeeding
- Breastfeeding: Low intake in first week causing retention of meconium and increased enterohepatic circulation
- Breastmilk: Beta-glucuronidase in milk (as in meconium) deconjugates bilirubin and increases enterohepatic circulation. Can last 12 weeks, but rarely reaches concerning levels
Successful breastfeeding
8-12 x per day. Initially last long 60 min, but then 10-15 min at each breast. Longer feeds may indicate a problem
Breastmilk
Perfect balance of carbs, lipids (50%), proteins (whey and casein), as well as antibodies, growth factors, etc.
*Most of the fat appears at the end of feeding, so is important to empty each breast
Breastfeeding advantages
Bonding, lower infection, lower SIDS, lower allergies
Healthy appearing infant with jaundice, dark urine, and pale (acholic) stools at 3-6 weeks
Biliary atresia -> Kasai procedure
*Usually presents later, after 2 weeks
Major risk factors for harmful hyperbilirubinemia
*Pre-discharge total bili or total conjugatic bili in “high-risk” zone, jaundice in first 24hr life, blood group incompatibility with +DAT, gestational age 35-36 wk, previous sibling with phototx, cephalohematoma/significant bruising, exclusive breastfeeding if not going well and excess wt loss, East Asian race
Tyenol and codeine in breastfeeding
No. Codeine can metabolize to morphine
Supplements for infants
- Vitamin D (440 IU daily) for all breastfed infants to prevent rickets.
- Iron fortified cereals and meats at 6 months
- Fluoride at 6 months if water supply lacks
Non-hemolysis breakdown of RBCs causing jaundice
1) Head trauma:
- Bruising from birth trauma
-Cephalohematoma (subperiosteal hemorrhage that does NOT cross suture lines) or ICH
(Caput succedaneum (edematous swelling over scalp, overlying periosteum, that crosses suture lines) would not cause hyperbilirubinemia)
2) Polycythemia
3) Swallowed blood during delivery
Risk factors for developmental dysplasia of the hip
- Lef hip 3:1. Can appear later than at birth
- Girls
- Breech
- Caucasian, Native American
- Family hx
DDH screening
*Girls born via breech, in Left hip 3:1, white or Native, family history
- Barlow: dislocatable hips
- Ortolani: dislocated hips
*U/S at 4-6 weeks or a hip/pelvis radiograph at 4 months