MANAGEMENT
Previously, blood was transfused into the fetal abdomi-nal cavity, where absorption of the red cells could take place over several days through the lymphatic channels.
Currently, transfusion of antigen-negative red blood cells (depending on the
blood group involved) to the fetus is indicated when PUBS determines that the
fetus has mod-erate or severe anemia with a hematocrit less than 30%. Direct transfusion under ultrasound guidance
into the umbilical vein has become the preferred technique. The procedure
has a1% to 3% risk of complications, including fetal death and preterm
delivery, which must be weighed against the pre-dicted course of the fetus if
left untreated or delivered. The volume of red blood cells to be transfused can
be calculated based on the gestational age, estimated fetal weight, the
hematocrit of the unit of blood, and the differ-ence between the current fetal
hematocrit and the desired hematocrit. Because the transfused cells are
antigen-negative, they are not subject to hemolysis by the mater-nal antibody
and the predicted lifespan of the red cell is the only determinant of how long
they persist in the fetal circulation. The timing and need for further
transfusions can be based either on the predicted course given the severity of
the disease, or on MCA Doppler assessments. After 2 to 3 transfusions, most of
the circulating red cells in a fetus are transfused cells, as the hematopoietic
system in the fetus has been suppressed.
Box 19.1
Maternal antibody identification and titer Careful obstetric history for prior affected fetus
Paternal antigen testing, possible fetal DNA
testing
Assessment of risk for fetal anemia if a critical
titer is found or if there has been a prior affected child
Amniotic fluid bilirubin assessment
Serial antibody titers, if first sensitized pregnancy Middle cerebral artery Doppler Ultrasound
Cordocentesis/percutaneous umbilical blood
sampling if monitoring test is abnormal
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