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February 2017Neonatal jaundice
Jaundice, usually mild unconjugated bilirubinemia, affects many newborns. Although most cases are physiological, some are indicative of serious underlying disorders.
(list not exhaustive)
Unconjugated hyperbilirubinemia
Increased bilirubin production
Hemolytic causes (e.g., Coombs positive, Coombs negative)
Decreased bilirubin conjugation
Metabolic or genetic (e.g., Gilbert syndrome, hypothyroidism)
Physiologic (e.g., breast milk jaundice)
Gastrointestinal (e.g., sequestered blood)
Conjugated hyperbilirubinemia
Decreased bilirubin uptake
Infections (e.g., sepsis, neonatal hepatitis)
Cholestasis (e.g., total parenteral nutrition)
Metabolic
Genetic
Obstructive (e.g., biliary atresia)
Given a patient with neonatal jaundice, the candidate will diagnose the cause, severity, and complications, and will initiate an appropriate management plan. Particular attention should be paid to jaundice which presents within the first three days after birth or with a rapid onset.
Given a patient with neonatal jaundice, the candidate will
list and interpret critical clinical findings, including
determining whether the neonate meets the criteria for treatment of physiologic jaundice;
identifying features of serious underlying disorders;
list and interpret critical investigations, including
those investigations which differentiate disorders associated with conjugated or unconjugated hyperbilirubinemia;
construct an effective initial management plan, including
monitoring and managing physiologic jaundice;
referring the patient to appropriate specialists in the case of non-physiologic jaundice;
counselling and reassuring parents, as appropriate.