Kainz A, Harabacz I, Cowlrick I S, Gadgil S D, Hagiwara D
Safety Information Centre, Fujisawa GmbH, Munich, Germany.
Transplantation. 2000 Dec 27;70(12):1718-21. doi: 10.1097/00007890-200012270-00010.
The increasing use of tacrolimus as a primary immunosuppressant is paralleled by a growing number of pregnancies occurring in mothers receiving tacrolimus systemically.
In this retrospective analysis during 1992-1998; data sources were case reports from clinical studies, spontaneous reports from health care professionals, routine surveys by transplant registries, and the published literature.
One hundred pregnancies in 84 mothers were recorded. Mean maternal age was 28 years. All except one mother (autoimmune disease) were solid organ transplant recipients (66% liver and 27% kid- ci ney). Mean time from transplantation to conception was 26 months. The mean daily dose of tacrolimus (range 11.7-12.8 mg/day) and the mean tacrolimus whole blood level (range 8.5-11.5 ng/ml) remained fairly constant from preconception through the third trimester. The most frequent maternal complications were graft rejection followed by preeclampsia, renal impairment, and infection. All cases of rejection were successfully treated with corticosteroids and did not result in graft loss. Of 100 pregnancies, 71 progressed to delivery (68 live births, 2 neonatal deaths, and 1 stillbirth), 24 were terminated (12 spontaneous and 12 induced), 2 pregnancies were ongoing, and 3 were lost to follow-up. Mean gestation period was 35 weeks with 59% deliveries being premature (<37 weeks). The birth weight (mean 2573 g) was appropriate for gestational age in 90% of cases. Most common complications in the neonate were hypoxia, hyperkalemia, and renal dysfunction. These were transient in nature. Four neonates presented with malformations, without any consistent pattern of affected organs.
Pregnancy in tacrolimus-treated transplant recipients resulted in a favourable outcome. Complications of the mother and neonate were similar to those previously described with other immunosuppressants.
随着他克莫司作为主要免疫抑制剂的使用日益增加,接受全身性他克莫司治疗的母亲怀孕的数量也在不断增多。
在这项1992年至1998年的回顾性分析中,数据来源包括临床研究的病例报告、医护人员的自发报告、移植登记处的常规调查以及已发表的文献。
记录了84名母亲的100次怀孕情况。母亲的平均年龄为28岁。除一名母亲(患有自身免疫性疾病)外,所有母亲均为实体器官移植受者(66%为肝脏移植,27%为肾脏移植)。从移植到受孕的平均时间为26个月。从受孕前到孕晚期,他克莫司的平均每日剂量(范围为11.7 - 12.8毫克/天)和他克莫司全血水平(范围为8.5 - 11.5纳克/毫升)保持相当稳定。最常见的母亲并发症是移植排斥反应,其次是先兆子痫、肾功能损害和感染。所有排斥反应病例均成功用皮质类固醇治疗,未导致移植器官丧失。在100次怀孕中,71次进展至分娩(68例活产、2例新生儿死亡和1例死产),24次终止妊娠(12例自然流产和12例人工流产),2次妊娠仍在继续,3次失访。平均妊娠期为35周,59%的分娩为早产(<37周)。90%的病例中出生体重(平均2573克)与孕周相符。新生儿最常见的并发症是缺氧、高钾血症和肾功能障碍。这些并发症本质上是短暂的。4名新生儿出现畸形,受累器官无任何一致的模式。
接受他克莫司治疗的移植受者怀孕产生了良好的结局。母亲和新生儿的并发症与先前使用其他免疫抑制剂时所描述的相似。