Gariod S, Brossard Y, Poissonnier M-H, Vuilliez B, Deutsch V, Jouk P-S, Pons J-C
Département d'Obstétrique, Gynécologie et Médecine de la Reproduction, CHU de Grenoble, BP 217, 38043 Grenoble Cedex 09, France.
J Gynecol Obstet Biol Reprod (Paris). 2004 Nov;33(7):637-48. doi: 10.1016/s0368-2315(04)96605-7.
Kell alloimmunization is a rare disease, although its incidence is the highest after after anti-D alloimmunization.
We report two recent cases and a review of the literature to describe practical management of Kell alloimmunization in pregnancy.
When an immunization against the Kell antigen was diagnosed, amniocentesis was performed at 14 weeks gestation to determine the fetal blood group. If the fetus was Kell positive, a first fetal blood sample was drawn at 17 weeks gestation in case of fetal hydrops, and at 20 weeks without fetal hydrops. The diagnosis of anemia led to in utero transfusion. A second fetal blood sample was taken at 8 to 10 days, every two weeks during the second trimester and every three or four weeks during the third trimester. Fetal well-being was assessed with weekly sonography and rates of hemoglobin decline. These measures enable adapting the frequency of fetal blood sampling.
尽管凯尔血型同种免疫的发病率在抗-D血型同种免疫之后是最高的,但它仍是一种罕见疾病。
我们报告了两例近期病例并对文献进行综述,以描述孕期凯尔血型同种免疫的实际管理方法。
当诊断出针对凯尔抗原的免疫反应时,在妊娠14周时进行羊膜穿刺术以确定胎儿血型。如果胎儿为凯尔阳性,若出现胎儿水肿,则在妊娠17周时采集第一份胎儿血样;若无胎儿水肿,则在妊娠20周时采集。贫血的诊断导致进行宫内输血。在8至10天时采集第二份胎儿血样,妊娠中期每两周采集一次,妊娠晚期每三或四周采集一次。通过每周超声检查和血红蛋白下降率评估胎儿健康状况。这些措施有助于调整胎儿血样采集的频率。