Bussel J B
J Reprod Immunol. 1997 Dec 15;37(1):35-61. doi: 10.1016/s0165-0378(97)00072-7.
Auto- and alloimmune thrombocytopenias in pregnancy may seriously impact on both mother and fetus. Autoimmune thrombocytopenia (ITP) affects both mothers and fetuses but is considered to be quite benign for both groups. The 'facts' are that: 1) ITP occurs commonly in pregnancy; 2) there has been no reported maternal mortality in more than 20 years; 3) management, except at delivery, is similar to management in the non-pregnant state; 4) splenectomy is virtually never required during pregnancy; 5) significant neonatal thrombocytopenia occurs in approximately 10% of cases and intra-cranial hemorrhage (ICH) 1%; 6) the course of the first sibling predicts that of the next sibling; and 7) the fetal platelet count can be successfully determined (if desired) by either fetal blood sampling (FBS) or by fetal scalp sampling. Many other important considerations remain undetermined: 1) non-invasive prediction of severe fetal thrombocytopenia; 2) the appropriate mode of delivery for a thrombocytopenic fetus; 3) the role of anti-platelet antibody testing; and 4) the effects on the fetal platelet count of maternal therapy. Alloimmune thrombocytopenia (AIT) is easier to outline because it is a far more serious fetal disorder: 1) neonatal platelet counts < 20,000/microliter are common in AIT; 2) there is a 10-30% ICH rate in first affected newborns, some of which occur antenatally; 3) there is no universal prenatal screening although this would be scientifically feasible; 4) testing is complex and requires an experienced laboratory that can test at least five platelet antigens and has sufficient typed controls to confirm the specificity of any anti-platelet antibodies detected; 5) the second affected sibling in a family is usually more severely affected than the first; 6) treatment of the thrombocytopenic neonate can be accomplished with intravenous (i.v.) gammaglobulin and/or platelet transfusions; and 7) treatment of the fetal platelet count can be accomplished in most instances by infusing the mother with i.v. gammaglobulin with or without steroids; platelet transfusions to the fetus is another option.
妊娠期间的自身免疫性和同种免疫性血小板减少症可能会对母亲和胎儿都产生严重影响。自身免疫性血小板减少症(ITP)会影响母亲和胎儿,但对这两组人群来说都被认为相当良性。实际情况是:1)ITP在妊娠期间常见;2)20多年来没有孕产妇死亡报告;3)除分娩时外,管理与非妊娠状态下的管理相似;4)妊娠期间几乎从不要求进行脾切除术;5)约10%的病例会出现显著的新生儿血小板减少症,颅内出血(ICH)发生率为1%;6)第一个同胞的情况可预测下一个同胞的情况;7)(如果需要)可通过胎儿血样采集(FBS)或胎儿头皮采样成功测定胎儿血小板计数。许多其他重要问题仍未确定:1)严重胎儿血小板减少症的非侵入性预测;2)血小板减少胎儿的合适分娩方式;3)抗血小板抗体检测的作用;4)母亲治疗对胎儿血小板计数的影响。同种免疫性血小板减少症(AIT)更容易概述,因为它是一种严重得多的胎儿疾病:1)AIT中新生儿血小板计数<20,000/微升很常见;2)首次受影响的新生儿颅内出血发生率为10 - 30%,其中一些发生在产前;3)尽管从科学角度可行,但没有普遍的产前筛查;4)检测复杂,需要一个经验丰富的实验室,该实验室至少能检测五种血小板抗原并有足够的分型对照来确认检测到的任何抗血小板抗体的特异性;5)一个家庭中第二个受影响的同胞通常比第一个受影响更严重;6)血小板减少新生儿的治疗可通过静脉注射(i.v.)丙种球蛋白和/或血小板输注来完成;7)在大多数情况下,可通过给母亲输注静脉丙种球蛋白(无论是否使用类固醇)来提高胎儿血小板计数;给胎儿输注血小板是另一种选择。