Hemolytic disease of the fetus Hemolytic disease of the fetus and newborn (HDFN) is a rare condition that affects 3 out of 100,000 to 80 out of 100,000 patients per year. It occurs when maternal
antibodies cross the
placenta during pregnancy and destroy fetal
red blood cells (RBCs). This process can lead to fetal
anemia, and in severe cases can progress to
hydrops (edema), ascites, heart failure, and death. For HDFN to occur, the fetus must be
antigen positive (paternally inherited) and the mother must have antibodies to the given antigen. Such antibodies typically form when the mother undergoes
alloimmunization to the antigen during a previous pregnancy or transfusion. Historically,
RhD alloimmunization accounted for the majority of cases. However, the rates of these cases have been significantly reduced by RhIg (
RhoGam) administration. Measures are not available for preventing alloimmunization to non-RhD antigens (
Kell,
Duffy,
Rhc,
RhE, etc.), which can also cause HDFN. Fetal anemia is monitored throughout pregnancy using
Doppler measurement of the middle cerebral artery (MCA) peak systolic velocity (PSV). This non-invasive technique is used as a surrogate measurement for assessing fetal anemia. Doppler multiples of median (MoM) measurements exceeding 1.5 are correlated with moderate to severe anemia. At this point, invasive testing via
percutaneous umbilical cord blood sampling (PUBS, also called cordocentesis), potentially followed by fetal transfusion is indicated. == Procedure ==