Seminars in Fetal & Neonatal Medicine
Volume 15, Issue 3 , Pages 176-182, June 2010

Hyperbilirubinemia in African American neonates: clinical issues and current challenges

Division of Newborn Medicine, Department of Pediatrics, University of Pittsburgh School of Medicine, Children's Hospital of Pittsburgh, Magee-Women's Research Institute, Magee-Women's Hospital, 300 Halket Street, Pittsburgh, PA 15213, USA

published online 26 November 2009.

Summary 

African American neonates evidence a low incidence of hyperbilirubinemia yet account for more than 25% of the reported kernicterus cases in the USA. Glucose-6-phosphate dehydrogenase (G6PD) deficiency accounts for ∼60%, and late preterm gestation and ABO hemolytic disease ∼40% of these cases. Females heterozygous for G6PD A− harbor a population of G6PD-deficient red blood cells and are at risk for hyperbilirubinemia. Pre-discharge bilirubin measurement coupled with gestational age enhances the identification of neonates at hyperbilirubinemia risk. Parental education at the time of birth hospitalization discharge combined with timely follow-up may help to reduce the risk of developing hazardous hyperbilirubinemia.

Keywords: African American, Female heterozygote, G6PD deficiency, Kernicterus, Late preterm gestation, Neonatal jaundice

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PII: S1744-165X(09)00108-5

doi:10.1016/j.siny.2009.11.001

Seminars in Fetal & Neonatal Medicine
Volume 15, Issue 3 , Pages 176-182, June 2010