How likely is hemolytic disease of the newborn?
The probability of neonatal hemolytic disease may be around 20% to 30%.
In clinical practice, neonatal hemolytic disease refers to a pathological condition caused by blood type incompatibility between the mother and fetus. The most common type is ABO blood group incompatibility, which accounts for approximately 85% of all cases of neonatal hemolytic disease. The second most common type is Rh blood group incompatibility, which accounts for about 15%. According to available data, blood type incompatibility occurs in approximately 20% to 30% of pregnancies. When such incompatibility exists, it may lead to hemolytic disease in newborns; therefore, the incidence rate of neonatal hemolytic disease may be relatively high, around 20% to 30%.
Neonatal hemolytic disease may cause a rapid rise in bilirubin levels after birth, leading to severe jaundice. If not promptly treated, it may result in bilirubin encephalopathy, causing brain damage in the newborn and potentially leaving long-term sequelae such as intellectual impairment and delayed growth and development.