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. 2013 Feb 1;14(2):10.1542/neo.14-2-e63.
doi: 10.1542/neo.14-2-e63.

Neonatal Cholestasis

Amy G Feldman  1 , Ronald J Sokol
Affiliations

Neonatal Cholestasis

Amy G Feldman et al. Neoreviews. .

Abstract

Cholestatic jaundice is a common presenting feature of neonatal hepatobiliary and metabolic dysfunction. Any infant who remains jaundiced beyond age 2 to 3 weeks should have the serum bilirubin level fractionated into a conjugated (direct) and unconjugated (indirect) portion. Conjugated hyperbilirubinemia is never physiologic or normal. The differential diagnosis of cholestasis is extensive, and a step-wise approach based on the initial history and physical examination is useful to rapidly identify the underlying etiology. Early recognition of neonatal cholestasis is essential to ensure timely treatment and optimal prognosis. Even when specific treatment is not available, infants who have cholestasis benefit from early medical management and optimization of nutrition. Future studies are necessary to determine the most reliable and cost-effective method of universal screening for neonatal cholestasis.

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