重度双胎输血综合征宫内激光消融治疗后出生儿童的预后

A.G Sutcliffe , N.J Sebire , A.J Pigott , B Taylor , P.R Edwards , K.H Nicolaides
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引用次数: 0

摘要

目的观察重度双胎输血综合征宫内激光消融治疗后新生儿的发育情况。设计回顾性队列结果研究,评估神经发育和身体健康。设置哈里斯出生权中心,伦敦国王学院医院。参与者:双胞胎和单胎幸存者在四年的时间里接受了双胎输血综合征的激光消融治疗。方法在54个参与研究的家庭中,有24个家庭参加了儿科评估,这些家庭在四年期间接受了双胎输血综合征的治疗;使用格里菲斯智力发展量表对12对双胞胎和12对单胎幸存者进行围产期、神经系统和神经发育结果的评估。在与全科医生接触后,对另外20个家庭进行了形式评估。这些组的比较显示,有反应者(44个家庭,81.5%)和无反应者(10个家庭)在社会人口学因素或疾病严重程度方面没有显著差异。结果一名儿科医生评估的儿童组出生体重低(供体体重1619g,受体体重1814g,单胎体重1877g),早产(双胞胎体重33周,单胎体重31.2周),并伴有复苏、新生儿住院(平均40天)和辅助分娩的增加。平均Griffiths评分在正常能力范围内(供体91.2分,受体97.7分,单例101.6分),唯一显著差异是在运动分量表上,供体82.6分,受体85.3分低于单例:-99.1分(p < 0.05)。在单胎幸存者中没有脑瘫,但在双胞胎组中有5例。除一名四肢瘫痪患儿外,所有患儿的格里菲斯平均分均在正常范围内。在GP形式组中,双胞胎中有一例脑瘫。结论脑瘫总发生率为9%,单胎存活组为0%,双胎存活组为13.3%。这一试点数据强调需要对受双胞胎输血综合征影响的儿童进行仔细的长期随访。
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Outcome for children born after in utero laser ablation therapy for severe twin-to-twin transfusion syndrome

Objective To examine the postnatal development of a group of children born after in utero laser ablation therapy for severe twin-to-twin transfusion syndrome.

Design Retrospective cohort outcome study involving assessment of neurodevelopment and physical well being.

Setting Harris Birthright Centre, King’s College Hospital, London.

Participants Twins and singleton survivors treated via laser ablation therapy for twin-to-twin transfusion syndrome over a four-year period.

Methods Of 54 families contacted to participate in the study, who had been treated for twin-to-twin transfusion syndrome during a four-year period, 24 families attended for paediatric assessment; 12 pairs of twins and 12 singleton survivors were assessed for perinatal, neurological and neurodevelopmental outcome using the Griffiths scales of mental development. A further 20 families were assessed via a proforma after contact with their general practitioner. A comparison of these groups showed no significant differences in sociodemographic factors or severity of disease between responders (44 families, 81.5%) and non-responders (10 families).

Results The group of children assessed by a paediatrician had low birthweight (1619g donor, 1814g recipient, 1877g singleton) and had been born preterm (33 weeks twins, 31.2 weeks singleton) with attendant increased resuscitation, neonatal unit admission (mean 40 days) and instrumental delivery. Mean Griffiths scores were within the normal range of ability (91.2 donor vs 97.7 recipient and 101.6 singletons) with the only significant difference being in the locomotor subscale where donor (82.6) and recipient (85.3) were less than singletons: -99.1 (P<0.05). There was no cerebral palsy in the singleton survivors, but there were five cases in the twin group. All except one affected child (with quadriplegia) had mean Griffiths scores in the normal range. In the GP proforma group there was one case, in a twin, of cerebral palsy.

Conclusion The overall cerebral palsy rate was 9%: 0% in the singleton survivors group and 13.3% in the twin survivors group. This pilot data highlights the need for careful long term follow up of children affected by twin-to-twin transfusion syndrome.

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