Competency information

Details

Provide transfusion support for pregnant women with red cell antibodies.

Considerations

  • Aetiology, and clinical presentation of HDFN, and the specificities of red cell antibodies implicated.
  • The antenatal testing requirements of those antibodies known to cause HDFN:
    • anti-D
    • anti-c
    • Kell-related antibodies.
  • Prediction of risk/severity of HDFN from laboratory testing during pregnancy:
    • titration of antibodies and the selection of cells and reagents to perform the titration
    • quantification of antibodies
    • significant levels for anti-D, anti-c, anti-K and other potentially clinically significant red cell antibodies
    • which specificities do not cause HDFN and why
    • role of immunoglobulin class and subclasses in the severity of HDFN
    • phenotyping of the father to predict the phenotype of the fetus and likelihood of HDFN
    • the criteria and limitations when free fetal DNA testing for the fetal genotype can be employed
    • non-serological monitoring of the fetus throughout pregnancy, e.g. middle cerebral artery Doppler and ultrasound.
  • The significance of a positive DAT in a neonatal sample.
  • Strategies for the reduction of impact on the fetus of HDN:
    • IUT
    • premature delivery
    • exchange transfusion, top-up transfusions and phototherapy
    • new and emerging strategies.
  • Logistics of ongoing support throughout pregnancy and delivery for women requiring rare blood and liaison with reference services.
  • Additional specifications of units suitable for IUT, neonatal top-up and neonatal exchange.
  • Cross-matching considerations for neonates.

Relevant learning outcomes

# Outcome
# 5 Outcome Select and perform tests to predict and monitor haemolytic disease of the fetus and newborn (HDFN), and provide appropriate transfusion therapy for the fetus and neonate.