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Published on: May 28, 2013
Single dose v two-dose antenatal anti-D prophylaxis: a randomised controlled trial
Scott W White1,2, Janice C Cheng3, Blagica Penova-Veselinovic1
1University of Western Australia, Perth, WA.
A two-dose antenatal anti-D prophylaxis regimen resulted in higher detectable Rh(D)-immunoglobulin levels at delivery compared to a single dose. Compliance rates were similar between the Rh(D) prophylaxis regimens.
Area of Science:
- Obstetrics and Gynecology
- Immunology
- Maternal-Fetal Medicine
Background:
- Rh(D) alloimmunization is a significant risk in Rh(D)-negative women carrying Rh(D)-positive fetuses.
- Antenatal anti-D prophylaxis (RAADP) is crucial for preventing Rh(D) sensitization.
- Optimizing RAADP regimens is essential for maximizing protection.
Purpose of the Study:
- To compare the detectability of circulating Rh(D)-immunoglobulin (anti-D) at delivery between single and two-dose antenatal anti-D prophylaxis (RAADP) regimens.
- To assess and compare compliance rates with the single and two-dose RAADP regimens.
Main Methods:
- An open-label, randomized controlled trial was conducted involving 277 Rh(D)-negative pregnant women.
- Participants received either a single 1500 IU dose of anti-D at 28 weeks or two 625 IU doses at 28 and 34 weeks.
- Primary outcome: detectable anti-D levels at delivery; Secondary outcome: compliance with the RAADP regimen.
Main Results:
- Detectable circulating anti-D levels at delivery were significantly higher in the two-dose group (86%) compared to the single-dose group (56%; P < 0.001).
- Compliance rates did not significantly differ between the single-dose (61%) and two-dose (50%) groups (P = 0.06).
Conclusions:
- The two-dose RAADP schedule provides superior protection against Rh(D) sensitization compared to a single-dose regimen.
- Current Australian recommendations for a two-dose RAADP schedule are supported by these findings.
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