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在一名患有弗雷泽综合征及因喉闭锁导致先天性高位气道梗阻综合征(CHAOS)的人类胎儿中,通过胎儿镜和超声引导对胎儿气管进行减压。

Fetoscopic and ultrasound-guided decompression of the fetal trachea in a human fetus with Fraser syndrome and congenital high airway obstruction syndrome (CHAOS) from laryngeal atresia.

作者信息

Kohl T, Hering R, Bauriedel G, Van de Vondel P, Heep A, Keiner S, Müller A, Franz A, Bartmann P, Gembruch U

机构信息

German Center for Fetal Surgery & Minimally-Invasive Therapy, Department of Obstetrics & Prenatal Medicine, University of Bonn, Bonn, Germany.

Department of Cardiology, University Children's Hospital Münster, Münster, Germany.

出版信息

Ultrasound Obstet Gynecol. 2006 Jan;27(1):84-88. doi: 10.1002/uog.1974.

Abstract

Congenital high airway obstruction syndrome (CHAOS) from laryngeal atresia bears a poor prognosis for hydropic fetuses owing to cardiac failure. We attempted percutaneous fetoscopic and ultrasound-guided tracheal decompression in a hydropic human fetus with CHAOS associated with Fraser syndrome. Percutaneous fetoscopic and ultrasound-guided tracheal decompression was performed using three trocars under general materno-fetal anesthesia at 19 + 5 weeks of gestation. Abnormal fetoplacental blood flow normalized within hours as a result of the intervention. Furthermore, a normalization of lung : heart size and lung echogenicity was observed within days. Resolution of hydrops was complete within 3 weeks. Premature rupture of membranes and premature contractions prompted emergency delivery of the fetus by ex-utero intrapartum treatment (EXIT) at 28 + 2 weeks of gestation. Following delivery, the lungs could be ventilated at low pressures and ambient oxygen concentration. Weaning from ventilation was achieved at 18 days of postnatal life. Our experience indicated that percutaneous fetoscopic and ultrasound-guided decompression of the fetal trachea is feasible and may permit normalization of hemodynamics in hydropic human fetuses with CHAOS from laryngeal atresia. The procedure may also result in normalization of heart : lung size and provide the time needed to regain the function of the overstretched diaphragm in this grave fetal condition.

摘要

由于心力衰竭,先天性喉闭锁引起的先天性高气道梗阻综合征(CHAOS)对水肿胎儿的预后较差。我们尝试对一名患有与弗雷泽综合征相关的CHAOS的水肿人类胎儿进行经皮胎儿镜和超声引导下的气管减压。在孕19 + 5周时,在全身母胎麻醉下使用三个套管针进行经皮胎儿镜和超声引导下的气管减压。干预后数小时内,异常的胎儿 - 胎盘血流恢复正常。此外,数天内观察到肺与心脏大小及肺回声的正常化。水肿在3周内完全消退。胎膜早破和早产宫缩促使在孕28 + 2周时通过产时宫外治疗(EXIT)紧急分娩胎儿。分娩后,肺可在低压力和环境氧浓度下通气。出生后18天实现脱机。我们的经验表明,经皮胎儿镜和超声引导下的胎儿气管减压是可行的,并且可能使患有先天性喉闭锁所致CHAOS的水肿人类胎儿的血流动力学恢复正常。该手术还可能导致心脏与肺大小的正常化,并为在这种严重胎儿状况下恢复过度伸展的膈肌功能提供所需的时间。

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