Comes Jean-François, Devignes Jean, Thiebaugeorges Olivier, Briquel Marie-Elisabeth, Lecompte Thomas
CHU de Nancy, service d'hématologie biologique, Vandoeuvre-lès-Nancy, France.
Ann Biol Clin (Paris). 2011 Nov-Dec;69(6):713-9. doi: 10.1684/abc.2011.0623.
Taking in charge the delivery of pregnant women with inherited major deficiency of factor VII (FVII) is poorly reported in literature. We report here the haemorrhagic prophylaxis of delivery by recombinant activated FVII (rFVIIa) in a 27-year-old women, gravida 1, para 0, with major deficiency FVII by missense mutation (p.Arg337Cys). Her parents, first germen, presented a FVII deficiency. She has four brothers and three sisters, of which only one brother has major FVII deficiency with hemorrhagic diathesis in childhood (hematochezia). At her birth, because of dystocia, a right sterno-cleido-mastoid muscle hematoma and left clavicle fracture occurred. The FVII concentration was 0.08 U/mL. At the age of fifteen, a surgery of appendicitis was performed with substitution by FVII from plasma donors without any haemorrhagic complication. Because of anatomic specificity (bifid uterus and vagina), caesarean was planned. After reviewing of the literature, caesarean was performed at 38th week of gestation with haemorrhagic prophylaxis consisting in administration of rFVIIa (eptacog alfa) at a dose of 20 μg/kg, 30 min before surgery, then every 3 h during 48 h. No haemorrhagic complication occurred. Thrombosis prophylaxis was ensured by enoxaparin (4000 UI a day subcutaneously started 6 h after surgery for 5 days). Clinical examination of the newborn was normal. In future, modalities of taking in charge have to be evaluated by prospective studies involving a sufficiently numerous group of woman with FVII major deficiency, or by retrospective studies with the means of national or European registers.
关于患有遗传性重度因子 VII(FVII)缺乏症孕妇分娩的处理,文献报道较少。我们在此报告一例 27 岁、孕 1 产 0、因错义突变(p.Arg337Cys)导致重度 FVII 缺乏的女性患者,通过重组活化 FVII(rFVIIa)进行分娩期出血预防的情况。她的父母是第一代亲属,均有 FVII 缺乏症。她有四个兄弟和三个姐妹,其中只有一个兄弟患有重度 FVII 缺乏症,童年时有出血素质(便血)。她出生时,因难产出现右侧胸锁乳突肌血肿和左侧锁骨骨折。FVII 浓度为 0.08 U/mL。15 岁时,因阑尾炎接受手术,输注血浆供体的 FVII 进行替代,未出现任何出血并发症。由于解剖学特异性(双子宫和阴道),计划行剖宫产。查阅文献后,在妊娠第 38 周行剖宫产,出血预防措施为术前 30 分钟给予剂量为 20 μg/kg 的 rFVIIa(重组凝血因子 VIIa),然后在 48 小时内每 3 小时给药一次。未发生出血并发症。通过依诺肝素(术后 6 小时开始皮下注射 4000 UI/天,共 5 天)进行血栓预防。新生儿临床检查正常。未来,必须通过涉及足够多重度 FVII 缺乏症女性群体的前瞻性研究,或借助国家或欧洲登记系统进行回顾性研究,来评估处理方式。