Tiller Heidi, Husebekk Anne, Ahlen Maria Therese, Stuge Tor B, Skogen Bjørn
Immunology Research Group, Faculty of Health Sciences, UiT, The Arctic University of Norway.
Division of Diagnostic Services, Department of Laboratory Medicine.
Int J Womens Health. 2017 Apr 19;9:223-234. doi: 10.2147/IJWH.S90753. eCollection 2017.
Differences in platelet type between the fetus and the mother can lead to maternal immunization and destruction of the fetal platelets, a condition named fetal and neonatal alloimmune thrombocytopenia (FNAIT). FNAIT is reported to occur in ~1 per 1,000 live born neonates. The major risk is intracranial hemorrhage in the fetus or newborn, which is associated with severe neurological complications or death. Since no countries have yet implemented a screening program to detect pregnancies at risk, the diagnosis is typically established after the birth of a child with symptoms. Reports on broader clinical impact have increased clinical concern and awareness. Along with new treatment options for FNAIT, the debate around antenatal screening to detect pregnancies at risk of FNAIT has been revitalized.
胎儿与母亲血小板类型的差异可导致母体免疫及胎儿血小板破坏,这种情况称为胎儿和新生儿同种免疫性血小板减少症(FNAIT)。据报道,FNAIT在每1000例活产新生儿中约有1例发生。主要风险是胎儿或新生儿颅内出血,这与严重的神经并发症或死亡有关。由于尚无国家实施筛查计划来检测有风险的妊娠,因此通常在出现症状的患儿出生后才确诊。关于更广泛临床影响的报告增加了临床关注和认识。随着FNAIT新治疗方案的出现,围绕产前筛查以检测有FNAIT风险的妊娠的争论再度兴起。