Deka D, Buckshee K, Kinra G
Department of Obstetrics and Gynaecology, All India Institute of Medical Sciences, New Delhi, India.
J Obstet Gynaecol Res. 1996 Dec;22(6):561-7. doi: 10.1111/j.1447-0756.1996.tb01071.x.
Maternal high dose intravenous immunoglobulin (IVIG) has shown promise in the management of severe Rh-immunization. Intravenous immunoglobulin, blocks Fe mediated antibody transport across the placenta and blocks destruction of fetal red cells and reduces maternal antibody levels. We have tried this new therapy in 6 patients with severe Rh-immunization, with high maternal antibody titres and previous hydrops and intrauterine deaths. Intravenous immunoglobulin was given from 13-18 weeks of gestation 3-4 weekly, till intrauterine transfusion (IUT) or delivery. Intensive fetal monitoring was done. No fetal hydrops or deaths occurred in any of the 6 cases. Only 2 cases needed intrauterine transfusion. IVIG delayed the onset of fetal anemia by 8-17 weeks thus deferring the need for IUT. All pregnancies continued till 32-36 weeks and all 6 babies did well in the neonatal period.
母亲大剂量静脉注射免疫球蛋白(IVIG)在严重Rh血型免疫的治疗中显示出了前景。静脉注射免疫球蛋白可阻断铁介导的抗体通过胎盘转运,阻止胎儿红细胞的破坏,并降低母体抗体水平。我们对6例严重Rh血型免疫、母体抗体效价高且既往有胎儿水肿和宫内死亡情况的患者尝试了这种新疗法。在妊娠13至18周期间,每3至4周给予一次静脉注射免疫球蛋白,直至进行宫内输血(IUT)或分娩。进行了密集的胎儿监测。6例患者中无一例发生胎儿水肿或死亡。只有2例需要进行宫内输血。IVIG将胎儿贫血的发生推迟了8至17周,从而推迟了进行IUT的必要性。所有妊娠均持续至32至36周,所有6名婴儿在新生儿期情况良好。