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Fetal Cell Screen
Test CodeRHOG
Preferred Specimen
Lavender Top Tube, Plasma (EDTA), 3 ml
Patient Preparation
Maternal specimen collected after delivery of all products of conception. It is best to wait approximately 1 hour after delivery to allow fetal cells to mix with maternal circulation if present.
Testing is not required if patient is less than 20 weeks gestation. Testing can only be performed if the mother is Rh-negative and the infant is Rh-positive. If Rh is unknown, does not qualify, or either is weak D positive, Kleihauer-Betke testing must be performed instead.
Minimum Volume
2 ml
Instructions
Testing performed ASAP to permit administration of RhIG within 72 hours of delivery.
Transport Container
Lavender Top Tube
Transport Temperature
Room Temperature
Specimen Stability
Room Temp: Perform ASAP
Refrigerated: 2 days
Frozen: Unacceptable
Refrigerated: 2 days
Frozen: Unacceptable
Reject Criteria (Eg, hemolysis? Lipemia? Thaw/Other?)
Do not use grossly hemolyzed samples for testing. Bacterial contamination may cause false positive results.
Methodology
A red blood cell suspension from a D-negative mother is incubated with reagent containing anti-D and then washed to remove unbound antibody. A weak suspension of D-positive red blood cells is added. The red blood cell mixture is centrifuged and examined microscopically for mixed-field agglutination.
Setup Schedule
Daily
Report Available
Daily
Reference Range
Not Applicable
Clinical Significance
Rho (D) Immune Globulin (RhIG) is used to prevent isoimmunization in the Rh negative individual exposed to Rh positive blood as a result of a fetomaternal hemorrhage. A full dose (300 μg) is sufficient to counteract the immunizing effects of 15mL of D-positive red cells; this corresponds to approximately 30 mL of fetal whole blood. The fetal bleed test is a screen to detect a feto-maternal hemorrhage of an amount greater than that covered by a standard dose of RhIG.
Performing Laboratory
Shady Grove Medical Center Only