胎儿RHD基因分型研究中抗- d预防研究进展

J. Minon, C. Gérard, F. Chantraine, M. Nisolle
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引用次数: 6

摘要

几年前,目前预防抗d免疫的基础是在高危胎-产妇出血情况下进行系统的产后预防,并进行针对性的产前注射。预防失败的主要原因是不遵守既定的rhg预防指南,以及在妊娠晚期没有任何明显原因而未被发现的胎母自发性出血。为了降低妊娠后抗d免疫残余率,一些国家决定在妊娠第28或29周期间将经典预防与常规产前抗d预防(RAADP)联系起来。大约10年来,母体血浆中胎儿RHD基因分型使我们能够将产前预防仅限于那些携带D+胎儿的D-妇女。本文涉及:在非侵入性胎儿RHD基因分型的情况下产前预防的优势,使预防方案有效的规则,无论应用哪种算法,以及对接受RHD的妇女推荐的免疫血液学随访。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anti-D Prophylaxis Reviewed in the Erea of Foetal RHD Genotyping
A few years ago, the prevention of anti-D immunization was currently based on systematic postnatal prophylaxis associated with targeted antenatal injection in high-risk situations of foeto-maternal haemorrhage. The failures of prevention are mainly due to the non-respect of established guidelines for RhIG prophylaxis, and to spontaneous undetected foetal-maternal haemorrhages without any obvious cause during the third trimester of pregnancy. In order to reduce the rate of residual post-pregnancy anti-D immunization, several countries decided to associate the classical prophylaxis to a routine antenatal anti-D prophylaxis (RAADP) during the 28th or 29th week of gestation. Since about ten years, the foetal RHD genotyping in maternal plasma enables us to limit the antenatal prophylaxis only to those D- women carrying a D+ foetus. This paper deals with: the advantages of an antenatal prevention in the light of non invasive foetal RHD genotyping, the rules rendering prevention protocols efficient whatever the algorithm applied, and the recommended immuno-haematology follow-up of women who have received RhIG.
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