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通过植入式静脉输液港给予重组活化凝血因子VII成功控制两名严重凝血因子VII缺乏新生儿的中枢神经系统出血。

Successful control of central nervous system bleeding in two newborns with severe factor VII deficiency using rFVIIa administered via Port-a-Cath.

作者信息

Karimi Mehran

机构信息

Department of Pediatrics, Hematology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.

出版信息

Semin Hematol. 2008 Apr;45(2 Suppl 1):S74. doi: 10.1053/j.seminhematol.2008.03.010.

Abstract

We report two cases of newborn infants (15 and 20 days old, respectively; both were full-term infants with normal vaginal deliveries) with severe factor VII (FVII) deficiencies (FVII <1%) who presented with convulsions and poor feeding. Brain sonography and computed tomography scan showed intracranial hemorrhage. Prothrombin time (PT) was severely prolonged, but partial thromboplastin time, platelet count, and bleeding time were normal. FVII assay showed that both infants had FVII levels of less than 1%. Treatment with recombinant activated factor VII (rFVIIa; NovoSeven(((R))), Novo Nordisk, Bagsvaerd, Denmark) was deemed necessary. We started rFVIIa therapy with 20 microg/kg administered intravenously (IV) every 6 hours for 2 to 3 days. This treatment schedule resulted in normalization of PT, control of convulsions, and reduction in central nervous system (CNS) bleeding. Although prophylaxis is currently an off-label use of rFVIIa, the patients then received one IV bolus dose of 20 microg/kg every other day as a prophylaxis regimen, but the symptoms recurred in one patient a few days later. Therefore, we increased the dose to 30 microg/kg IV every 4 hours, and this led to control of convulsions and CNS bleeding. This patient received rFVIIa at a dose of 30 microg/kg every other day via Port-a-Cath (Bistric ATH, France) due to poor venous access. His parents were educated in the use of the Port-a-Cath, and the patient received home treatment with rFVIIa (30 microg/kg IV every other day and then twice per week) for 6 months. He had a normal neurological status at this time. Unfortunately, at the age of 6 months, this infant died from severe post-traumatic CNS bleeding when he was 60 km away from our center. The second patient, who also received prophylactic rFVIIa at a dose of 20 microg/kg every other day with gradual prolongation of the dose interval to once per week, is currently in good condition with a mild neurological deficit caused by repeated CNS bleedings that occurred when she was newborn, before her first presentation to our clinic. She is now 36 months old and on a 3-year rFVIIa prophylactic regimen, which has provided good results to date.

摘要

我们报告了两例新生儿(分别为15天和20天;均为足月顺产的正常婴儿),他们患有严重的凝血因子VII(FVII)缺乏症(FVII<1%),表现为惊厥和喂养困难。脑部超声和计算机断层扫描显示颅内出血。凝血酶原时间(PT)严重延长,但部分凝血活酶时间、血小板计数和出血时间正常。FVII检测显示两名婴儿的FVII水平均低于1%。认为有必要用重组活化凝血因子VII(rFVIIa;诺其(R),丹麦诺和诺德公司, Bagsvaerd)进行治疗。我们开始以20微克/千克的剂量静脉注射rFVIIa,每6小时一次,持续2至3天。这种治疗方案使PT恢复正常,惊厥得到控制,中枢神经系统(CNS)出血减少。尽管目前预防性使用rFVIIa属于超说明书用药,但之后这两名患者接受了每两天一次20微克/千克的静脉推注剂量作为预防方案,但其中一名患者几天后症状复发。因此,我们将剂量增加到每4小时30微克/千克静脉注射,这使得惊厥和CNS出血得到了控制。由于静脉通路不佳,该患者通过法国的巴斯特里克ATH植入式静脉输液港每两天接受一次30微克/千克剂量的rFVIIa治疗。我们对其父母进行了植入式静脉输液港使用方面的培训,该患者在家中接受了6个月的rFVIIa治疗(每两天一次30微克/千克静脉注射,之后每周两次)。此时他的神经状态正常。不幸的是,6个月大时,这名婴儿在距离我们中心60公里处因严重的创伤后CNS出血死亡。第二名患者也接受了每两天一次20微克/千克剂量的预防性rFVIIa治疗,剂量间隔逐渐延长至每周一次,目前状况良好,但因新生儿期首次就诊前反复发生CNS出血而存在轻度神经功能缺损。她现在36个月大,正在接受为期3年的rFVIIa预防方案治疗,迄今为止效果良好。

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