When is Rho(D) immune globulin (Rhogam) administered during pregnancy?

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: November 25, 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.

When to Administer Rhogam (Rho(D) Immune Globulin) in Pregnancy

Rh-negative pregnant women should receive RhIg at 28 weeks gestation and within 72 hours after delivery of an Rh-positive infant, with additional doses required for any potentially sensitizing event throughout pregnancy. 1

Standard Prophylaxis Protocol

Routine Antenatal Administration

  • Administer 300 mcg (1500 IU) RhIg at 28 weeks gestation to all unsensitized Rh-negative women when fetal blood type is unknown or known to be Rh-positive 1, 2
  • Alternative dosing: 100-120 mcg at both 28 weeks and 34 weeks gestation 3
  • This two-dose protocol reduces alloimmunization rates from 1.8% to 0.1-0.2% 1

Postpartum Administration

  • Give 300 mcg RhIg within 72 hours of delivery if the infant is Rh-positive 1, 2
  • If not given within 72 hours, administer as soon as recognized up to 28 days after delivery 3
  • Postpartum RhIg alone reduces alloimmunization from 13-17% to 1-2% 1
  • If delivery occurs within 3 weeks of the last antenatal dose, postpartum dose may be withheld unless fetomaternal hemorrhage exceeds 15 mL of fetal red blood cells 2

Pregnancy Complications Requiring RhIg

Early Pregnancy Loss (<12 weeks)

  • Administer 50 mcg (minimum dose) within 72 hours for spontaneous or induced abortion, miscarriage, or ectopic pregnancy 1, 4
  • If 50 mcg dose unavailable, use standard 300 mcg dose 1
  • Fetal RBCs display Rh antigens from as early as 6 weeks gestation, making sensitization possible even in early pregnancy 1, 4

Late First Trimester and Beyond (≥12 weeks)

  • Give 300 mcg RhIg for miscarriage, abortion, or ectopic pregnancy at or beyond 13 weeks 2, 3
  • For molar pregnancy, administer RhIg unless complete mole is certain 3

Bleeding Episodes

  • Administer RhIg for any placental or vaginal bleeding at any gestational age in unsensitized Rh-negative women 1
  • For threatened abortion with heavy bleeding, abdominal pain, or events near 12 weeks, give RhIg 1
  • Dose: 50 mcg before 12 weeks, 300 mcg at or after 12 weeks 1

Invasive Procedures

  • Amniocentesis (15-18 weeks or third trimester): 300 mcg RhIg 2, 3
  • Chorionic villus sampling: 120 mcg before 12 weeks, 300 mcg after 12 weeks 3
  • Cordocentesis: 300 mcg RhIg 3
  • External cephalic version: 300 mcg RhIg 3

Trauma and High-Risk Events

  • Give 300 mcg RhIg for abdominal trauma in second or third trimester, as 28% of pregnant patients with minor trauma have fetomaternal hemorrhage 1
  • Consider for placental abruption, placenta previa with bleeding, or any event with potential placental trauma 3
  • Perform quantitative fetomaternal hemorrhage testing for these high-risk events to determine if additional doses needed 1, 3

Dosing Adjustments for Large Fetomaternal Hemorrhage

  • Standard 300 mcg dose covers up to 15 mL of fetal red blood cells (30 mL whole blood) 2
  • If fetomaternal hemorrhage exceeds 15 mL of fetal RBCs: divide the volume by 15 mL to calculate number of 300 mcg doses needed 2
  • Give additional 10 mcg for every 0.5 mL of fetal red blood cells beyond the amount covered 3
  • If calculation results in a fraction, round up to next whole number of doses 2

Critical Timing Considerations

  • Optimal window: within 72 hours of any potentially sensitizing event 1, 2
  • If multiple events occur requiring RhIg at 13-18 weeks, give another full dose at 26-28 weeks 2
  • Repeat antenatal dose generally not required at 40 weeks if given at 28 weeks 3
  • IgG half-life is 23-26 days; maintain adequate anti-D levels throughout pregnancy 2

Important Caveats

  • Never administer RhIg intravenously (for IM preparations) or to the neonate 2
  • Women with "weak D" (Du-positive) should NOT receive anti-D 3
  • Women with molecularly defined weak D types 1,2,3,4.0,4.1, or Asian-type DEL do not require RhIg 5
  • Obtain verbal or written informed consent before administration 3
  • During supply shortages, prioritize postpartum patients and those at later gestational ages 1

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

Seguimiento Médico para Aborto a las 12 Semanas

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 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.