Lopriore Enrico, Nagel Helene T C, Vandenbussche Frank P H A, Walther Frans J
Department of Neonatology, Leiden University Medical Center, Leiden, The Netherlands.
Am J Obstet Gynecol. 2003 Nov;189(5):1314-9. doi: 10.1067/s0002-9378(03)00760-9.
The purpose of this study was to determine the long-term neurodevelopmental outcome in children after twin-to-twin transfusion syndrome.
Maternal and neonatal medical records of all twin-to-twin transfusion syndrome patients who were admitted to our center between 1990 and 1998 were reviewed. Neurologic and mental development at school age was assessed during a home visit in all twin-to-twin transfusion syndrome survivors.
A total of 33 pregnancies with twin-to-twin transfusion syndrome were identified. Four couples opted for termination of pregnancy. All other pregnancies were treated conservatively, 18 pregnancies (62%) with serial amnioreductions and 11 pregnancies (38%) without intrauterine interventions. Mean gestational age at delivery was 28.6 weeks (range, 20-37 weeks). The perinatal mortality rate was 50% (29/58 infants). The birth weight of the donor twins was less than the recipient twins (P<.001). Systolic blood pressure at birth was lower in donors than in recipients (P=.023), and donors required inotropic support postnatally more frequently than did recipients (P=.008). The incidence of hypertension at birth was higher in recipients than in donors (P=.038). Abnormal cranial ultrasonographic findings were reported in 41% of the neonates (12/29 neonates). All long-term survivors (n=29 neonates) were assessed during a home visit. Mean gestational age at birth of the surviving twin was 31.6 weeks (range, 25-37 weeks). The mean age at follow-up was 6.2 years (range, 4-11 years). The incidence of cerebral palsy was 21% (6/29 infants). Five of 6 children with cerebral palsy had an abnormal mental development. The incidence of cerebral palsy in the group of survivors who were treated with serial amnioreduction was 26% (5/19 infants). Four children were born after the intrauterine fetal demise of their co-twin, 2 of which had cerebral palsy.
The incidence of adverse neurodevelopmental outcome in twin-to-twin transfusion syndrome survivors is high, especially after the intrauterine fetal demise of a co-twin.
本研究旨在确定双胎输血综合征患儿的长期神经发育结局。
回顾了1990年至1998年间入住本中心的所有双胎输血综合征患者的母婴医疗记录。对所有双胎输血综合征幸存者进行家访,评估其学龄期的神经和智力发育情况。
共确定33例双胎输血综合征妊娠。4对夫妇选择终止妊娠。所有其他妊娠均采用保守治疗,18例妊娠(62%)进行了系列羊水减量术,11例妊娠(38%)未进行宫内干预。分娩时的平均孕周为28.6周(范围20 - 37周)。围产儿死亡率为50%(29/58例婴儿)。供血双胎的出生体重低于受血双胎(P <.001)。供血双胎出生时的收缩压低于受血双胎(P =.023),且供血双胎出生后比受血双胎更频繁地需要使用强心药物支持(P =.008)。受血双胎出生时高血压的发生率高于供血双胎(P =.038)。41%的新生儿(12/29例新生儿)报告有异常头颅超声检查结果。对所有长期存活者(n = 29例新生儿)进行了家访评估。存活双胎出生时的平均孕周为31.6周(范围25 - 37周)。随访时的平均年龄为6.2岁(范围4 - 11岁)。脑瘫发生率为21%(6/29例婴儿)。6例脑瘫患儿中有5例智力发育异常。接受系列羊水减量术治疗的存活者组中脑瘫发生率为26%(5/19例婴儿)。4例患儿在其同胞双胎宫内死亡后出生,其中2例患有脑瘫。
双胎输血综合征幸存者不良神经发育结局的发生率较高,尤其是在同胞双胎宫内死亡后。