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新生儿溶血病的产前诊断与治疗

[Prenatal diagnosis and therapy of hemolytic disease of the newborn].

作者信息

Fischer K, Poschmann A, Hellwege H H, Kitschke H J, Carstensen M, Sprotte C, Schreer I

出版信息

Monatsschr Kinderheilkd. 1985 Mar;133(3):167-70.

PMID:4010672
Abstract

From 1966 to 1983 a total of 586 intra-uterine fetal transfusions on 268 fetuses suffering from severe Rh-erythroblastosis were performed at the Hamburg university hospital. 149 (56%) fetuses survived. 29% of 268 fetuses exhibited ascitic fluid at the beginning of therapy. The survival rate improved to 63% in the last five years. The diagnostic and therapeutic procedures are explained in detail. The amniotic fluid analysis has been improved. In addition to Rh-antibodies, it is important to detect other blood group antibodies such as anti-Jk(a) and anti-Fy(a), that can diminish the survival rate of the donor erythrocytes in the fetus.

摘要

1966年至1983年期间,汉堡大学医院对268例患有严重Rh溶血病的胎儿进行了总计586次宫内胎儿输血。149例(56%)胎儿存活。268例胎儿中有29%在治疗开始时出现腹水。最近五年存活率提高到了63%。详细解释了诊断和治疗程序。羊水分析方法得到了改进。除Rh抗体外,检测其他血型抗体如抗Jk(a)和抗Fy(a)也很重要,这些抗体可降低胎儿体内供体红细胞的存活率。

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