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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,B

Specimen Type

Whole Blood EDTA

Specimen 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 day

Performing Laboratory

Mayo Medical Laboratories in Rochester

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

NY State Approved

Yes