EARLY PREDICTION OF HEMOLYTIC DISEASE OF THE NEWBORN BASED ON CLINICAL INDICATORS
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Abstract
Hemolytic disease of the newborn (HDN) is an immune-mediated condition caused by maternal alloantibodies against fetal red blood cell antigens, most commonly involving the Rh and ABO blood group systems. Early identification of neonates at risk is crucial to prevent severe anemia, hyperbilirubinemia, kernicterus, and perinatal mortality. This article reviews and synthesizes current evidence on early clinical and laboratory indicators predictive of HDN, including maternal blood group status, direct antiglobulin test (DAT) positivity, reticulocyte percentage (RET%), lactate dehydrogenase (LDH), γ-glutamyltransferase (γ-GT), hemoglobin levels, and early-onset jaundice. Evidence suggests that combined laboratory predictors improve diagnostic accuracy compared to single markers. Early screening strategies integrating maternal risk assessment and neonatal biochemical indicators can significantly enhance timely diagnosis and intervention.
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