RhoGAM Administration for Obstetric Vaginal Bleeding
RhoGAM should be administered to all Rh-negative pregnant women with any vaginal bleeding during pregnancy, regardless of the trimester or cause of bleeding.
Rationale and Indications
Vaginal bleeding during pregnancy can indicate potential fetal-maternal hemorrhage, which may lead to maternal sensitization in Rh-negative women. This sensitization can cause hemolytic disease of the fetus and newborn in subsequent pregnancies.
First Trimester Bleeding
- Even minimal bleeding in early pregnancy warrants RhoGAM administration in Rh-negative women
- Common causes include:
- Threatened abortion
- Ectopic pregnancy
- Gestational trophoblastic disease
- Spontaneous abortion 1
Second and Third Trimester Bleeding
- Higher risk of significant fetal-maternal hemorrhage
- Common causes include:
- Placenta previa
- Placental abruption
- Vasa previa
- Uterine rupture
- Preterm labor with bleeding 1
Dosing Guidelines
Standard Dosing
- Microdose (50 μg): For first trimester bleeding (<12 weeks)
- Full dose (300 μg): For bleeding after 12 weeks gestation
Special Considerations
- For significant bleeding or trauma, quantification of fetal-maternal hemorrhage using Kleihauer-Betke test should be performed to determine if additional doses are needed 2
- The standard dose of RhoGAM (300 μg) covers approximately 30 mL of fetal blood
Timing of Administration
- RhoGAM should be administered as soon as possible after bleeding is identified
- Effectiveness is greatest when given within 72 hours of the bleeding episode
- Can still provide some protection if given up to 28 days after exposure
Clinical Algorithm
Identify patient blood type
- If Rh-negative, proceed with RhoGAM administration
- If Rh-positive, no RhoGAM needed
Assess gestational age
- <12 weeks: Microdose (50 μg)
- ≥12 weeks: Full dose (300 μg)
Evaluate severity of bleeding
- For major trauma or significant bleeding: Perform Kleihauer-Betke test to quantify fetal-maternal hemorrhage 2
- Calculate additional doses if needed (1 dose per 30 mL fetal blood)
Document administration
- Record lot number, dose, and time of administration
- Document patient education regarding the purpose of RhoGAM
Important Considerations
- RhoGAM should be given regardless of the viability of the pregnancy
- Administration should not be delayed pending confirmation of the cause of bleeding by ultrasound 2
- For Rh-negative trauma patients in pregnancy, RhoGAM should be given regardless of the apparent severity of injury 2
- Domestic violence should be considered as a potential cause of vaginal bleeding in pregnancy 2
Common Pitfalls to Avoid
- Failing to identify Rh status - Always check blood type in any pregnant woman with vaginal bleeding
- Delaying administration - Do not wait for diagnostic confirmation before giving RhoGAM
- Inadequate dosing - Ensure proper dosing based on gestational age and extent of bleeding
- Missing repeat dosing - For ongoing bleeding, additional doses may be required every 12 weeks
- Overlooking quantification - In cases of significant trauma or bleeding, Kleihauer-Betke testing is essential to determine adequate dosing
By following these guidelines, healthcare providers can prevent Rh sensitization and protect future pregnancies from hemolytic disease of the fetus and newborn.