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母体静脉注射免疫球蛋白治疗不能预防胎儿同种免疫性血小板减少症中的颅内出血。

Maternal intravenous immunoglobulin treatment does not prevent intracranial haemorrhage in fetal alloimmune thrombocytopenia.

作者信息

Kroll H, Kiefel V, Giers G, Bald R, Hoch J, Hanfland P, Hansmann M, Mueller-Eckhardt C

机构信息

Institute for Clinical Immunology and Transfusion Medicine, Justus Liebig University, Giessen, Germany.

出版信息

Transfus Med. 1994 Dec;4(4):293-6. doi: 10.1111/j.1365-3148.1994.tb00266.x.

Abstract

In fetal alloimmune thrombocytopenia (FAIT) the fetus is threatened by intracranial haemorrhage (ICH); therefore early diagnostic and therapeutic intervention is required. We followed the clinical course of a 30-year-old woman during her fifth pregnancy after she had given birth to a child with alloimmune thrombocytopenia due to anti-Zwa. The fetus was monitored by 13 fetal blood samplings (FBS) always followed by transfusion of either maternal or compatible donor platelets. Intravenous immunoglobulin (ivIg) treatment of the mother was begun at 20 weeks of gestation when the fetal platelet count was 36 x 10(9)/l. The fetal platelets were typed Zwa positive by DNA analysis. Despite 11 weeks of maternal ivIg treatment fetal platelet counts progressively declined to 6 x 10(9)/l and ICH occurred. Subsequently, the fetus was successfully managed by intrauterine platelet transfusions at shorter intervals (3-5 days) and elective Cesarean section was carried out at 35 weeks of gestation. We conclude that maternal ivIg treatment does not prevent ICH in FAIT. The treatment of choice for severely affected cases is serial FBS combined with transfusion of compatible platelets.

摘要

在胎儿同种免疫性血小板减少症(FAIT)中,胎儿受到颅内出血(ICH)的威胁;因此需要早期诊断和治疗干预。我们跟踪了一名30岁女性在其第五次怀孕期间的临床过程,她此前曾生下一名因抗Zwa导致同种免疫性血小板减少症的孩子。通过13次胎儿血液采样(FBS)对胎儿进行监测,每次采样后均输注母亲或匹配供体的血小板。当胎儿血小板计数为36×10⁹/L时,在妊娠20周开始对母亲进行静脉注射免疫球蛋白(ivIg)治疗。通过DNA分析,胎儿血小板被确定为Zwa阳性。尽管母亲接受了11周的ivIg治疗,但胎儿血小板计数仍逐渐下降至6×10⁹/L并发生了ICH。随后,通过更短间隔(3 - 5天)的宫内血小板输注成功处理了胎儿,并在妊娠35周时进行了选择性剖宫产。我们得出结论,母亲的ivIg治疗不能预防FAIT中的ICH。对于严重受影响的病例,首选治疗方法是连续FBS联合输注匹配的血小板。

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