11 results
Threshold for Initiating Exchange Transfusion by Risk Stratum. Bhutani et al. Pediatrics. 1999.

#Peds #Pediatrics #Diagnosis #Management
Threshold for Initiating ... Pediatrics. 1999 ... #Peds #Pediatrics ... Management #Neonatal #Jaundice ... Neurotoxicity #Thresholds
Infant of a Diabetic Mother - complications - pathophysiology learning schema
Information source: UpToDate

#Infant #Diabetic #Mother #Pediatrics
Diabetic Mother - complications ... - pathophysiology ... Diabetic #Mother #Pediatrics ... #Maternal #Complications ... #Peds #Newborn
Inherited forms of Hyperbilirubinemia
Major pathways involved in bilirubin production, conjugation, and excretion. Notes: Both the UB
Decreased MRP2 - Conjugated ... Decreased OATP1B - Conjugated ... Hyperbilirubinemia #pathophysiology ... congenital #hepatology #pediatrics ... #peds
gestational diabetes algorithm
#Infant #Diabetic #Mother #Pediatrics #Neonatology #IDM #NICU #OBGYN #Diagnosis #Pathophysiology #Maternal #Complications #Peds #Newborn
Diabetic #Mother #Pediatrics ... OBGYN #Diagnosis #Pathophysiology ... #Maternal #Complications ... #Peds #Newborn
Assess risk for developing subsequent neurotoxicity.

This will tell you: a) phototherapy or b) exchange transfusion

#Peds #Pediatrics
transfusion #Peds ... #Pediatrics #Diagnosis ... Management #Neonatal #Jaundice ... Neurotoxicity #Thresholds
Risk Stratification for Developing Severe Hyperbilirubinemia. Bhutani et al. Pediatrics. 1999.

In general, babies at low-risk and
Pediatrics. 1999 ... #Peds #Pediatrics ... Management #Neonatal #Jaundice ... Nomogram #RiskZones #Thresholds
Prader-Willi Syndrome: Pathogenesis and clinical findings
 • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Signs/Symptoms/Complications ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
Acute Otitis Media: Pathogenesis and Clinical Findings (in Children)
Upper Respiratory Tract Infection: 
 - Bacterial: Streptococcus
resolve by 72 hours Complications ... #OtitisMedia #pathophysiology ... symptoms #signs #peds ... #pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds ... #pediatrics
Childhood Immunization Schedule: Why we immunize
 • Diphtheria Toxin -> URT inflammation causes pseudomembrane with hardened
anorexia, nausea, jaundice ... #Immunization #peds ... #pediatrics #pathophysiology