Fetal Cell Count™ Kit

The Fetal Cell Count™ Kit is used for the Diagnosis of Fetomaternal Hemorrhage (FMH). It is a complete solution for the assay for routine diagnosis of Fetomaternal Hemorrhage using Anti-CA and Anti-HbF.

Features

  • Unique quantification of Fetomaternal Hemorrhage by flow cytometry
  • Complete assay for routine diagnosis of Fetomaternal Hemorrhage
  • Detection as low as 0.02% fetal cells in maternal blood
  • Detection of fetal haemoglobin (HbF) and Carbonic Anhydrase (CA)
  • Simple and easy handling procedure
  • IVD/CE registered
  • Determination of Fetomaternal Hemorrhage
  • Pregnancy with suspected RhD incompatibilities
  • Abdominal trauma
  • Recognize fetal cells in maternal Thalaessemia circulation
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Product code: IQP-363

Introduction

Detection and quantification of fetal red blood cells (fRBCs) in maternal blood samples is essential for obstetrical management. Measurement of fRBCs is critical as the extent of Fetomaternal Hemorrhage (FMH), the transplacental passage of fRBCs into the maternal circulation, has consequences for further treatment of mother and child. Frequency and size of FMH is directly influenced by complications in abdominal trauma, suspected placental injury or after a caesarean section. Severe FMH may lead to intra-uterine death. In case of antigen incompatibility between mother and child FMH may result in respiratory problems or anaemia, like Haemolytic Disease of the Newborn.

Adult RBC’s contains a population of HbF (F-cells), which can be differ between 0 and 14%. The F-cells can give a positive result in the Kleihauer-Betke acid-elution test or single HbF flow cytometry test. These F-cells may be the result of physiological variations during pregnancy or traits such as thalassemia, sickle cell anaemia or hereditary persistence of fetal haemoglobin.

The detection (and thus enumeration) of fRBCs is used to calculate the extent of FMH, either in case of trauma with suspected placental injury or in the situation of a RhD incompatibility between the fetus and the mother. The amount of fRBCs is a measure for the prevention of hemolytic disease of the newborn using (prophylactic) anti-D therapy.

Principle of the Fetal Cell Count™ Kit

The Fetal Cell Count™ Kit assay is a flow cytometry product. The assay is based on a  patented combination of two antibodies. One is directed against HbF while the second is specific for carbonic anhydrase (CA), an enzyme present in adult RBCs and, at very low detectable level, in late pregnancy stage. •    Results within 90 minutes •    Precise and accurate detection of fRBCs •    Intracellular detection of HbF and CA •    Distinguishes between fRBCs and maternal F-cells and RBCs, it eliminates subjective interpretations an empiric signal cutoffsCytogramm_FetalCellCount_Kit - IQ ProductsCytograms illustrating typical data obtained with the Fetal Cell Count Kit A1; fetal RBCs / A2; F-cells / A4; maternal RBCs.

Conclusion
The data demonstrate the usefulness of CA as a red blood cell marker. It allows, in combination with HbF, an accurate discrimination between the different RBC populations in maternal blood. Without the use of this second marker, discrimination between the fetal RBCs and the variable concentrations of HbF containing maternal F-cells becomes less precise.

1. Valérie Porra et al,  Identification and quantification of fetal red blood cells in maternal blood by a dual-color flow cytometric method:evaluation of the Fetal Cell Count kit, Transfusion, 2007;47:1281-1289

2. Liesbeth Bakker-Jonges et al, The Detection of Foetal Red Blood Cells in Maternal Blood Samples by Dual Flow Cytometry, Haematology, 2008, 58-60

3. Marek Lubusky et al, Fetomaternal hemorrhage in normal vaginal delivery and in delivery by cesarean section, Transfusion, 2012

4. Waltraut M Merz et al, Dual-colour flow cytometry for the analysis of Fetomaternal haemorrhage during delivery, J Clin Pathol, 2012;65;No 2:186-187

Question: I use cord blood as a positive control but I detect CA+HBF+ cells in my sample. Should I include these cells in my Hbf+ cell gate?
Answer: No, even though these CA+Hbf+ cells are likely to be present in cord blood. Already very late in pregnancy, fetal red blood cells start to express CA to prepare for birth and life outside the womb. However, analysis has learned that the number of events in Q2 in general is negligible compared to the HbF+ cell population in Q1. In addition, when a patient sample is analyzed Q2 may contain maternal F-cells. Therefore, this quadrant is excluded when considering Hbf+ fetal erythrocytes.
When analyzing the data, it is essential to always place the vertical line F directly left from the maternal F-cells (CA+/HbF+) and the horizontal line just below the fetal Hbf+ cell population, as shown in figure 1. All cells in the upper region in Q4 are maternal erythrocytes (F cells) that express both CA and Hbf (F cells) and should not be included in Q2.

figure-1-representative-result
Figure 1. Representative result obtained with a sample containing 1% umbilical cord and 99% whole blood (male) analyzed with the Fetal Cell Count kit.

Question: What is the clinically relevant percentage of Hbf+ cells to state FMH?
Answer: The threshold to determine whether these is a clinically relevant amount of FMH is 0.1% Hbf+ cells1. The calculated amount of mL can be used to either calculate the dose of anti-D or, in case of a trauma,  to assess the impact of the bleeding with knowledge of the age of the fetus and its (estimated) blood volume.

Question: Why are my results with the Fetal Cell Count kit IQP-363 different from my results with the IQP-379?
Answer: This difference is caused by an improvement in the Carbonic Anhydrase antibody. We developed a monoclonal antibody to replace the polyclonal antibody from the IQP-379 kit. Due to this improvement, the signal of the CA antibody is more uniform and stronger, therefore, it is vital to re-assess your compensation settings! Analyze S1-S4 (all the controls, see package insert of the Fetal Cell Count kit page 2) with the new kit and assess your compensation settings. Use a 5% spike with cord blood for your positive control to have a proper HbF- PE signal.

Question: How long can a blood sample be stored before performing the assay and in what conditions?
Answer: Blood samples should be stored at either 2-8 °C or at room temperature (20–25 °C) up to 3 days until processing.

Question: Can you use blood from newborns instead of cord blood as a positive control for HbF?
Answer: Yes that is possible, but the HbF signal can be lower and the CA signal will be higher than cord blood fetal cells. This will result in a lower percentage cell detected when mixed with an adult blood sample.

Question: What is recommended to use as positive control for HbF if you don’t have cord blood available?
Answer: FETALtrol™  can be used as an external control. This is a quality controlled tri-level stabilized blood control with known HbF positive cells content in adult blood.

 

1 Guidelines for the Estimation of Fetomaternal Hemorrhage. E Austin, S Abtes, M de Silva, D Howarth, A Lubenko, M Rowley, M Scott, E Thomas, J White, M Williams. (January 2011).

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