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Rh incompatibility
arises when a pregnant woman lacks the Rh (D) antigen on her red blood cells
(Rh-negative) while the fetus inherits it from an Rh-positive father. During
pregnancy or delivery, fetal blood may enter the maternal circulation,
triggering the mother's immune response to produce anti-Rh antibodies. These
IgG antibodies can cross the placenta in subsequent pregnancies, destroying
fetal RBCs and causing hemolytic disease of the fetus and newborn (HDFN).
Mechanism and Risk
Sensitization often happens
via minor fetal-maternal hemorrhage from trauma, miscarriage, or procedures
like amniocentesis. First pregnancies are usually unaffected as
antibodies form late, but risks escalate in later Rh-positive pregnancies.
Without intervention, it leads to fetal anemia, jaundice, hydrops fetalis, or
stillbirth.
Prevention
RhoGAM (Rh immunoglobulin)
injections at 28 weeks of gestation and postpartum neutralize
fetal Rh antigens, preventing antibody formation in 99% of cases. Non-invasive
prenatal testing monitors fetal Rh status early.
Diagnosis and Treatment
Maternal antibody titers, ultrasound for fetal anemia, and Doppler middle cerebral artery velocity aid diagnosis. Severe cases require intrauterine transfusions; newborns receive phototherapy, IVIG, or exchange transfusion for hyperbilirubinemia.