When is RhoGAM (Rho(D) immune globulin) given to pregnant women?

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When to Administer RhoGAM (Rh(D) Immune Globulin) in Pregnancy

RhoGAM should be administered to unsensitized Rh-negative women at 28 weeks gestation, within 72 hours after delivery of an Rh-positive infant, and following any potentially sensitizing event including spontaneous or induced abortion, regardless of gestational age. 1

Standard Prophylaxis Protocol

  • RhoGAM should be administered to all unsensitized Rh-negative pregnant women at 28 weeks gestation when fetal blood type is unknown or known to be Rh-positive 1
  • A second dose should be given within 72 hours after delivery if the infant is Rh-positive 1, 2
  • This two-dose protocol reduces the rate of RhD alloimmunization from approximately 1.8% to between 0.1% and 0.2% 1, 3
  • Postpartum RhoGAM alone decreases the rate of anti-D alloimmunization from 13-17% to 1-2% 1, 2

Administration for Pregnancy Complications

  • Spontaneous or Induced Abortion:

    • For abortions before 12 weeks gestation: A minimum dose of 50 μg RhoGAM within 72 hours is adequate 1
    • For abortions after 12 weeks gestation: A standard 300 μg dose should be given 1, 4
    • The Society for Maternal-Fetal Medicine recommends offering both RhD testing and RhoGAM for spontaneous and induced abortion at <12 weeks gestation despite some conflicting guidelines 5
  • Threatened Abortion/Vaginal Bleeding:

    • RhoGAM should be administered in cases of threatened abortion with heavy bleeding, abdominal pain, or when the event occurs near 12 weeks 1
    • For bleeding events before 12 weeks gestation, a minimum dose of 50 μg RhoGAM within 72 hours is adequate 1
  • Invasive Procedures:

    • After amniocentesis: 300 μg dose 1, 4
    • After chorionic villus sampling: 120 μg during first 12 weeks, 300 μg after 12 weeks 4
    • After cordocentesis: 300 μg 4
  • Other Indications:

    • Ectopic pregnancy: 120 μg before 12 weeks, 300 μg after 12 weeks 4
    • Molar pregnancy: RhoGAM should be given due to possibility of partial mole 4
    • Minor trauma in pregnancy: Consider RhoGAM as 28% of pregnant patients with minor trauma have fetomaternal hemorrhage 1

Special Considerations

  • If RhoGAM is not given within 72 hours of a potentially sensitizing event, it should still be administered up to 28 days after the event 4
  • For large fetomaternal hemorrhage (>15 mL of fetal red blood cells), additional doses of RhoGAM may be required 2, 4
  • Women with "weak D" (Du-positive) should not receive RhoGAM 4
  • If RhoGAM supply is limited, postpartum patients and antenatal patients at later gestational ages should be prioritized 1

Mechanism and Rationale

  • Fetal RBCs display red cell antigens from as early as 6 weeks gestation, making maternal sensitization possible even in early pregnancy 5, 1
  • RhoGAM suppresses the maternal immune response to fetal RhD-positive red blood cells, preventing the production of anti-D antibodies 2
  • Prevention of alloimmunization is critical given its substantial impact on pregnancy outcomes including hemolytic disease of the fetus/newborn, need for fetal transfusion, fetal hydrops, and stillbirth 1

Common Pitfalls to Avoid

  • Failing to administer RhoGAM in early pregnancy based on misconceptions that sensitization cannot occur before 12 weeks 5, 1
  • Not recognizing that a large fetomaternal hemorrhage may require additional doses of RhoGAM 2
  • Overlooking the need for RhoGAM in cases of minor trauma during pregnancy 1
  • Administering RhoGAM to women with "weak D" (Du-positive) who do not require it 4
  • Delaying administration beyond 72 hours, though it may still be beneficial up to 28 days after exposure 4

References

Guideline

Management Guidelines for Rh Negative Pregnancy

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Prevention of Rh alloimmunization.

Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obstetrique et gynecologie du Canada : JOGC, 2003

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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