Jain A, Venkataramanan R, Fung J J, Gartner J C, Lever J, Balan V, Warty V, Starzl T E
The Thomas E. Starzl Transplantation Institute, University of Pittsburgh Medical Center, Pennsylvania 15213, USA.
Transplantation. 1997 Aug 27;64(4):559-65. doi: 10.1097/00007890-199708270-00002.
The maternal and fetal risk of pregnancy after organ transplantation under tacrolimus has not been reported. This was prospectively studied in 27 pregnancies by 21 female liver recipients who were treated with tacrolimus before and throughout gestation.
Twenty-seven babies were born between October 1990 and April 1996. In 15 cases, samples were obtained at or after delivery and stored (-40 degrees C) for comparison of tacrolimus concentration in the maternal blood with different combinations of cord and infant venous blood, breast milk, or a section of the placenta.
The 21 mothers had surprisingly few serious complications of pregnancy and no mortality. Two infants with 23 and 24 weeks gestation died shortly after birth. The mean birth weight of the other 25 was 2638+/-781 g after a gestational period of 36.6+/-3.3 weeks. Mean birth weight percentile for gestational age was 50.2+/-26.2 (median 40). On the day of delivery, the mean tacrolimus concentrations (ng/ml) were 4.3 in placenta versus 1.5, 0.7, and 0.5 in maternal, cord, and child plasma, and 0.6 in the first breast milk specimens. The infants had a 36% incidence of transient perinatal hyperkalemia (K+>7.0 meq/L) and a mild reversible renal impairment, which were thought to reflect in part maternal homeostasis. One newborn had unilateral polycystic renal disease (the only anomaly). All 25 babies have had satisfactory postnatal growth and development with a current mean weight percentile of 62+/-37 (median 80).
Pregnancy by postliver transplant mothers under tacrolimus was possible with a surprisingly low incidence of the hypertension, preeclampsia, and other maternal complications historically associated with such gestations. As in previous experience with other immunosuppressive regimens, preterm deliveries were common. However, prenatal growth for gestational age and postnatal infant growth for postpartum age were normal.
关于接受他克莫司治疗的器官移植受者妊娠的母婴风险尚无报道。本研究对21名在妊娠前及整个妊娠期均接受他克莫司治疗的女性肝移植受者的27次妊娠进行了前瞻性研究。
1990年10月至1996年4月期间共出生27名婴儿。其中15例在分娩时或分娩后采集样本并储存于-40℃,用于比较母体血液与脐带血、婴儿静脉血、母乳或胎盘组织中他克莫司的浓度。
21名母亲妊娠期间严重并发症出奇地少,且无死亡病例。2名分别在孕23周和24周出生的婴儿出生后不久死亡。其余25名婴儿在妊娠36.6±3.3周后出生,平均出生体重为2638±781g。按胎龄计算的平均出生体重百分位数为50.2±26.2(中位数40)。分娩当天,胎盘组织中他克莫司的平均浓度(ng/ml)为4.3,而母体、脐带和婴儿血浆中的浓度分别为1.5、0.7和0.5,初乳样本中的浓度为0.6。婴儿发生短暂围生期高钾血症(血钾>7.0 meq/L)的发生率为36%,并伴有轻度可逆性肾功能损害,这部分被认为反映了母体的内环境稳定。1名新生儿患有单侧多囊肾病(唯一的异常情况)。所有25名婴儿出生后生长发育良好,目前平均体重百分位数为62±37(中位数80)。
接受他克莫司治疗的肝移植术后母亲能够妊娠,与这类妊娠相关的高血压、先兆子痫和其他母体并发症的发生率出奇地低。与以往其他免疫抑制方案的经验一样,早产很常见。然而,胎儿的产前生长和婴儿出生后的产后生长均正常。