Is the Buddha position beneficial in managing Rh negative pregnancies?

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Last updated: October 17, 2025View editorial policy

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Management of Rh Negative Pregnancy: No Evidence for Buddha Position

There is no evidence supporting the use of the Buddha position in managing Rh negative pregnancies. Instead, proper management of Rh negative pregnancies should focus on RhD immune globulin (RhIg) prophylaxis to prevent maternal sensitization and subsequent fetal complications 1.

Standard RhIg Prophylaxis Protocol

  • RhD negative pregnant women should receive RhIg prophylaxis at 28 weeks gestation and within 72 hours after delivery of an Rh positive infant to prevent RhD alloimmunization 1
  • This two-dose protocol reduces the rate of RhD alloimmunization from approximately 1.8% to between 0.1% and 0.2% 1
  • Postpartum RhIg decreases the rate of anti-D alloimmunization from 13-17% to 1-2% 1

RhIg Administration for Pregnancy Complications

  • For spontaneous or induced abortion at <12 weeks gestation, both RhD testing and RhIg administration should be offered to unsensitized Rh negative individuals 2, 1
  • A dose of 50 μg RhIg within 72 hours is adequate for first trimester losses; if unavailable, the standard 300 μg dose should be used 1
  • In cases of threatened abortion with heavy bleeding, abdominal pain, or when the event occurs near 12 weeks, it is prudent to administer RhIg 2, 1
  • RhIg should be administered in cases of minor trauma in Rh negative patients, as 28% of pregnant patients with minor trauma have been shown to have fetomaternal hemorrhage 1

Rationale for RhIg Administration

  • Fetal red blood cells display RhD antigens from as early as 6 weeks of gestation, making maternal sensitization possible even in early pregnancy 2, 1
  • RhD alloimmunization can lead to devastating fetal and neonatal outcomes including hemolytic disease of the fetus/newborn, fetal hydrops, stillbirth, and preterm delivery 1
  • The introduction of a postpartum rhesus prevention program in the United Kingdom in 1969 reduced fetal mortality from Rh hemolytic disease from 120 per 100,000 live births to 1.5 per 100,000 by 1989 2

Special Considerations

  • If RhIg supply is limited, postpartum patients and antenatal patients at later gestational ages should be prioritized 1
  • A woman with "weak D" (also known as Du-positive) should not receive anti-D 3
  • When paternity is certain, Rh testing of the baby's father may be offered to all Rh-negative pregnant women to eliminate unnecessary blood product administration 3

Common Pitfalls to Avoid

  • Not recognizing that fetal RBCs display red cell antigens from as early as 6 weeks gestation, making maternal sensitization possible in early pregnancy 2, 1
  • Failing to administer RhIg within the recommended 72-hour window after a potentially sensitizing event 3
  • Neglecting to quantify fetomaternal hemorrhage in cases of significant placental trauma, which may require additional doses of RhIg 1, 3
  • Overlooking the need for RhIg in early pregnancy loss or termination, as cases of alloimmunization have been reported following first trimester vaginal bleeding 2

Despite the lack of high-quality evidence specifically addressing the efficacy of RhIg after spontaneous miscarriage 4, the potential consequences of maternal sensitization are severe enough to warrant prophylaxis. Even with universal RhIg prophylaxis, a residual Rh immunization prevalence of 0.24% to 0.31% may still occur 5, highlighting the importance of adherence to established protocols.

References

Guideline

Management Guidelines for Rh Negative Pregnancy

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Prevention of Rh alloimmunization.

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

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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