Test ID FMB Fetomaternal Bleed, Flow Cytometry, Blood
Useful For
Determining the volume of fetal-to-maternal hemorrhage for the purposes of recommending an increased dose of the Rh immune globulin
Method Name
Flow Cytometry
Reporting Name
Fetomaternal Bleed,Flow Cytometry,BSpecimen Type
Whole Blood EDTASpecimen must arrive within 120 hours (preferably 24-72 hours) of draw.
Container/Tube: Lavender top (EDTA)
Specimen Volume: Full tube
Collection Instructions:
1. Do not centrifuge or aliquot.
2. Invert several times to mix blood.
3. Send specimen in original tube.
Specimen Minimum Volume
1 mL
Specimen Stability Information
Specimen Type | Temperature | Time |
---|---|---|
Whole Blood EDTA | Refrigerated (preferred) | 5 days |
Ambient | 5 days |
Clinical Information
In hemolytic disease of the newborn, fetal red cells become coated with IgG alloantibody of maternal origin, directed against an antigen on the fetal cells that is of paternal origin and absent on maternal cells. The IgG-coated cells undergo accelerated destruction, both before and after birth. The clinical severity of the disease can vary from intrauterine death to hematological abnormalities detected only if blood from an apparently healthy infant is subject to serologic testing.
Pregnancy causes immunization when fetal red cells possessing a paternal antigen foreign to the mother enter the maternal circulation, an event described as fetomaternal hemorrhage (FMH). FMH occurs in up to 75% of pregnancies, usually during the third trimester and immediately after delivery. Delivery is the most common immunizing event, but fetal red cells can also enter the mother's circulation after amniocentesis, spontaneous or induced abortion, chorionic villus sampling, cordocentesis, or rupture of an ectopic pregnancy, as well as blunt trauma to the abdomen.(1)
Rh immune globulin (RhIG, anti-D antibody) is given to Rh-negative mothers who are pregnant with an Rh-positive fetus. Anti-D antibody binds to fetal D-positive red cells, preventing development of the maternal immune response. RhIG can be given either before or after delivery. The volume of FMH determines the dose of RhIG to be administered.
Reference Values
≤1.5 mL of fetal RBCs in normal adults
Cautions
Clinical conditions exist that may result in an increased level of fetal hemoglobin-containing red cells, including hereditary persistence of fetal hemoglobin and thalassemia. Such red cells (also referred to as F cells) are detected by this assay. Results must be interpreted with caution in these situations.
This test is not used to detect the hereditary persistence of fetal hemoglobin (see HPFH / Hemoglobin F, Red Cell Distribution, Blood).
Day(s) Performed
Monday through Sunday; Varies
Report Available
Same day/1 dayPerforming Laboratory

Test Classification
This test has been cleared or approved by the U.S. Food and Drug Administration and is used per manufacturer's instructions. Performance characteristics were verified by Mayo Clinic in a manner consistent with CLIA requirements.CPT Code Information
88184-Flow cytometry, cell surface, cytoplasmic