What are the recommendations and guidelines for anti-D (RhD immunoglobulin) prophylaxis?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: August 23, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Anti-D Immunoglobulin Prophylaxis Guidelines and Recommendations

Anti-D immunoglobulin should be administered to all RhD-negative non-sensitized women after potentially sensitizing events to prevent RhD alloimmunization and reduce the risk of hemolytic disease of the fetus and newborn in subsequent pregnancies. 1

Indications for Anti-D Prophylaxis

Postpartum Administration

  • Standard dose: 300 μg IM or IV within 72 hours of delivery to RhD-negative women delivering an RhD-positive infant 2
  • If administration is delayed beyond 72 hours, anti-D should still be given up to 28 days after delivery, though efficacy may be reduced 2
  • Additional anti-D may be required for fetomaternal hemorrhage (FMH) greater than 15 mL of fetal red blood cells 2

Antepartum Routine Prophylaxis

  • 300 μg at 28 weeks' gestation when fetal blood type is unknown or known to be RhD-positive 1, 2
  • Alternative regimen: two doses of 100-120 μg, one at 28 weeks and one at 34 weeks 2

Early Pregnancy Events (Before 12 Weeks)

  • Minimum dose: 50-120 μg for:
    • Miscarriage or threatened abortion
    • Induced abortion
    • Ectopic pregnancy
    • Chorionic villus sampling
    • Partial molar pregnancy 2, 3

Later Pregnancy Events (After 12 Weeks)

  • Standard dose: 300 μg for:
    • Amniocentesis
    • Cordocentesis
    • Other invasive prenatal procedures
    • Spontaneous or induced abortion
    • Intrauterine fetal death
    • External cephalic version
    • Abdominal trauma
    • Obstetric hemorrhage 2, 3

Special Considerations

Fetomaternal Hemorrhage (FMH) Assessment

  • Quantitative testing for FMH should be considered following events potentially associated with placental trauma 2
  • If FMH exceeds the amount covered by standard dosing, additional anti-D should be given at 10 μg per 0.5 mL of fetal red blood cells 2, 3

Threatened Abortion

  • Anti-D administration may be unnecessary with threatened abortion and viable fetus before 12 weeks' gestation 4
  • However, anti-D should be considered when there is "heavy" bleeding, associated abdominal pain, or when the event occurs near 12 weeks' gestation 4

Minor Abdominal Trauma

  • Consider anti-D administration in cases of minor trauma in RhD-negative pregnant patients 4
  • 28% of pregnant patients with minor trauma had fetomaternal hemorrhage in one study 4

Ectopic Pregnancy

  • Anti-D should be given to RhD-negative women following ectopic pregnancy 2
  • Failure to administer anti-D after ectopic pregnancy has been associated with high anti-Rh titers in subsequent pregnancies and delivery of nonviable hydropic fetuses 4

Platelet Transfusions

  • Prevention of RhD alloimmunization should be considered for RhD-negative patients receiving platelet transfusions from RhD-positive donors 4, 1
  • Priority should be given to RhD-negative children (particularly girls) and women of childbearing age 4, 1

Administration Guidelines

Route and Timing

  • Anti-D should be administered intravenously (IV) when possible, especially in thrombocytopenic patients 1
  • Should be given before or immediately after exposure to RhD-positive blood, though remains effective if given within 72 hours 1

Dosage Calculation

  • Standard dose calculation: 25 mg (125 IU) of anti-D protects against 1 mL of RhD-positive RBCs 4, 1

Potential Adverse Reactions

  • Although generally considered safe, anti-D administration carries a small risk of hypersensitivity reactions including anaphylaxis 5, 6
  • Management of suspected hypersensitivity reactions requires detailed history, cautious interpretation of skin tests, and in some cases, anti-D challenges 6

Areas of Guideline Discrepancy

  • Management of women expressing weak D blood type (should not receive anti-D according to some guidelines) 2, 7
  • Optimal dose and regimen for routine antenatal prophylaxis (recommendations vary between administration at 28 weeks versus between 28-34 weeks) 7
  • Dosing recommendations for specific sensitizing events vary between guidelines 7

Conclusion

Anti-D immunoglobulin prophylaxis has significantly reduced the incidence of RhD alloimmunization and subsequent hemolytic disease of the fetus and newborn. Following established guidelines for appropriate administration after potentially sensitizing events is crucial for preventing maternal sensitization and protecting future pregnancies.

References

Guideline

Prevention of RhD Alloimmunization

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.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.