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Anti-D prophylaxis principles in early pregnancy

Essential points for quick revision.

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Treat the bleeding emergency first

Anti-D never replaces resuscitation, urgent imaging or operative control of a ruptured ectopic pregnancy or major miscarriage haemorrhage.

Action: Use an ABCDE approach, obtain senior gynaecology and anaesthetic help, activate the major-haemorrhage pathway when indicated, then revisit RhD prophylaxis once immediate danger is controlled.

Synopsis

Apply the June 2026 NICE anti-D thresholds accurately, explain sensitisation and consent simply, and prevent both unnecessary treatment before 12 weeks and missed prophylaxis at 12 weeks.

  • Anti-D immunoglobulin prevents an RhD-negative, non-sensitised pregnant person forming immune anti-D after exposure to RhD-positive fetal red cells.
  • Do not offer anti-D for ectopic pregnancy, miscarriage or threatened miscarriage up to and including 11+6 weeks, even after surgical management.
  • Use ultrasound gestation rather than the last menstrual period when the two estimates disagree.

Key red flags

Syncope, shoulder-tip pain, severe unilateral pelvic pain or peritonism suggesting a ruptured ectopic pregnancy.

Investigation priorities

01
Ultrasound datingFirst step

Establish the best gestational estimate and pregnancy location or viability where clinically required.

Management branches

Up to 11+6 weeksDo not offer anti-D

Ultrasound gestation is no more than 11+6 weeks and the event is ectopic pregnancy, miscarriage or threatened miscarriage.

  1. Manage pain, bleeding, pregnancy location and viability through the appropriate urgent or early-pregnancy pathway.
  2. Do not prescribe anti-D, including after manual vacuum aspiration, laparoscopy or other surgical management below 12+0 weeks.

Key medicines

Anti-D immunoglobulinAt 12+0 to 12+6 weeks give at least 250 IU (50 micrograms), using the authorised intramuscular or intravenous route for the selected product; a larger stocked dose may be used when the minimum-size vial is unavailable.
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Sources and review status4 sources · checked 27 Aug 2026 · clinical review pending
Sources

Sources and review status

National guidance is shown before implementation-dependent detail. Typical adult dose examples remain subject to patient factors, contraindications and the live BNF or specialist protocol. Source check completed 27 Aug 2026; clinical approval remains outstanding.

Authoring stateRapid draftClinical stateAwaiting reviewJurisdictionUnited Kingdom