RHESUS ISOIMMUNIZATION
Rh blood group incompatibility
arises when an Rh-negative woman conceives an Rh-positive fetus. RBCs from the
fetus can enter the woman’s circulation during pregnancy or, more commonly,
during birth. These “foreign” RBCs stimulate the production of maternal
anti-bodies against the Rh factor. Spontaneous or induced abortions of an
Rh-positive fetus can also result in isoimmunization. In subsequent
pregnancies, transplacental transmission of the maternal anti-Rh antibody leads
to hemolytic anemia in the fetus or neonate. The resulting disease, called erythroblastosis
fetalis, may be fatal. Unless a woman was previously sensitized by
transfusion, a first pregnancy rarely leads to erythroblastosis fetalis.
Isoimmunization does not have signs or symptoms during pregnancy, although
hydrops fetalis and fetal demise may occur in severe cases. In less severe
cases, bilirubin levels in the newborncan increase dramatically because of the
hemolytic anemia. This can lead to kernicterus, characterized by decreased
tone, poor feeding, apnea, seizures, and death. Survivors of kernicterus can be
left with mental retardation, choreoathetosis, and hearing loss.
High maternal anti-Rh antibody
titers, checked in Rh-negative women at the first prenatal visit and at week
26, suggest sensitization of the mother. Amniocentesis showing high bilirubin
levels in theamniotic fluid suggests more severe disease and potential for
fetal death.
If bilirubin levels are elevated,
intrauterine transfusions to the fetus can be performed at 2-week intervals.
Delivery should be minimally traumatic, and the placenta should not be manually
removed.
Inthe neonate, hyperbilirubinemia may
necessitate phototherapy or an exchange transfusion.
At the first prenatal checkup, all patients should be screened for Rh type. If the patient is Rhnegative, maternal Rh antibody titers should be checked early in the pregnancy and repeated at the twenty-sixth week of gestation. A previously unsensitized mother will not normally produce anti-Rh antibody until after delivery, when mixing of the maternal and fetal blood occurs. Rh isoimmunization can be prevented by injecting the mother with anti-Rh immunoglobulin (RhoGAM) at 28 weeks and within 3 days of delivery. Immunoglobulin C binds the fetal Rh factor and prevents the mother from developing anti-Rh antibodies but is too large to pass though the placenta to the Rh-positive fetus. RhoGAM should be given at the termination of each pregnancy, whether a delivery, ectopic pregnancy, or abortion, as well as any other time when feto-maternal hemorrhage may occur (e.g., amniocentesis or trauma).
At the first prenatal checkup, all patients should be screened for Rh type. If the patient is Rhnegative, maternal Rh antibody titers should be checked early in the pregnancy and repeated at the twenty-sixth week of gestation. A previously unsensitized mother will not normally produce anti-Rh antibody until after delivery, when mixing of the maternal and fetal blood occurs. Rh isoimmunization can be prevented by injecting the mother with anti-Rh immunoglobulin (RhoGAM) at 28 weeks and within 3 days of delivery. Immunoglobulin C binds the fetal Rh factor and prevents the mother from developing anti-Rh antibodies but is too large to pass though the placenta to the Rh-positive fetus. RhoGAM should be given at the termination of each pregnancy, whether a delivery, ectopic pregnancy, or abortion, as well as any other time when feto-maternal hemorrhage may occur (e.g., amniocentesis or trauma).