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

被引:62
作者
Kohl, T [1 ]
Hering, R
Bauriedel, G
Van de Vondel, P
Heep, A
Keiner, S
Müller, A
Franz, A
Bartmann, P
Gembruch, U
机构
[1] Univ Bonn, Sch Med, German Ctr Fetal Surg & Minimally Invas Therapy, Dept Obstet & Prenatal Med, D-53105 Bonn, Germany
[2] Univ Bonn, Dept Anesthesiol, D-53105 Bonn, Germany
[3] Univ Bonn, Dept Internal Med Cardiol 2, D-53105 Bonn, Germany
[4] Univ Bonn, Dept Neonatol, D-53105 Bonn, Germany
[5] Univ Bonn, Clin ENT Head & Neck Surg, D-53105 Bonn, Germany
[6] Univ Childrens Hosp Munster, Dept Cardiol, Munster, Germany
关键词
CHAOS; fetal surgery; fetoscopy; fetus; Fraser syndrome; laryngeal atresia;
D O I
10.1002/uog.1974
中图分类号
O42 [声学];
学科分类号
070206 ; 082403 ;
摘要
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. Copyright (c) 2005 ISUOG. Published by John Wiley & Sons, Ltd.
引用
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页码:84 / 88
页数:5
相关论文
共 11 条
[1]   Successful EXIT (ex utero intrapartum treatment) procedure in a fetus diagnosed prenatally with congenital high-airway obstruction syndrome due to laryngeal atresia [J].
Bui, TH ;
Grunewald, C ;
Frenckner, B ;
Kuylenstierna, R ;
Dahlgren, G ;
Edner, A ;
Granström, L ;
Selldén, H .
EUROPEAN JOURNAL OF PEDIATRIC SURGERY, 2000, 10 (05) :328-333
[2]  
CROMBLEHOLME TM, 2001, UNBORN PATIENT, P357
[3]   Successful ex utero intrapartum treatment (EXIT) procedure for congenital high airway obstruction syndrome (CHAOS) owing to laryngeal atresia [J].
DeCou, JM ;
Jones, DC ;
Jacobs, HD ;
Touloukian, RJ .
JOURNAL OF PEDIATRIC SURGERY, 1998, 33 (10) :1563-1565
[4]   EFFECT OF TRACHEOSTOMY ON LUNG DEVELOPMENT IN FETAL LAMBS [J].
FEWELL, JE ;
HISLOP, AA ;
KITTERMAN, JA ;
JOHNSON, P .
JOURNAL OF APPLIED PHYSIOLOGY, 1983, 55 (04) :1103-1108
[5]   A case of laryngeal atresia (congenital high airway obstruction. syndrome) with chromosome 5p deletion syndrome rescued by ex utero intrapartum treatment [J].
Kanamori, Y ;
Kitano, Y ;
Hashizume, K ;
Sugiyama, M ;
Tomonaga, T ;
Takayasu, H ;
Egami, S ;
Goishi, K ;
Shibuya, K ;
Kawana, Y ;
Marumo, G ;
Kikuchi, A ;
Kozuma, S ;
Taketani, Y ;
Sekiyama, Y .
JOURNAL OF PEDIATRIC SURGERY, 2004, 39 (01) :E25-28
[6]   Amniotic air insufflation during minimally invasive fetoscopic fetal cardiac interventions is safe for the fetal brain in sheep [J].
Kohl, T ;
Reckers, J ;
Strümper, D ;
Hartlage, MG ;
Gogarten, W ;
Gembruch, U ;
Vogt, J ;
Van Aken, H ;
Scheld, HH ;
Paulus, W ;
Rickert, CH .
JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 2004, 128 (03) :467-471
[7]   Intra-amniotic multimodal fetal echocardiography in sheep: A novel imaging approach during fetoscopic interventions and for assessment of high-risk pregnancies in which conventional imaging methods fail [J].
Kohl, T ;
Hartlage, MG ;
Westphal, M ;
Kienitz, D ;
Aryee, S ;
Achenbach, S ;
Buller, T ;
Kossobutzki, C ;
Gogarten, W ;
Vogt, J ;
Scheld, HH ;
Van Aken, H ;
Gembruch, U .
ULTRASOUND IN MEDICINE AND BIOLOGY, 2002, 28 (06) :731-736
[8]  
KOHL T, 1999, EUR HEART J, V20, pA644
[9]   Congenital high airway obstruction syndrome: Natural history and management [J].
Lim, FY ;
Crombleholme, TM ;
Hedrick, HL ;
Flake, AW ;
Johnson, MP ;
Howell, LJ ;
Adzick, NS .
JOURNAL OF PEDIATRIC SURGERY, 2003, 38 (06) :940-945
[10]   Congenital high airway obstruction syndrome successfully managed with ex-utero intrapartum treatment [J].
Oepkes, D ;
Teunissen, AKK ;
Van de Velde, M ;
Devlieger, H ;
Delaere, P ;
Deprest, J .
ULTRASOUND IN OBSTETRICS & GYNECOLOGY, 2003, 22 (04) :437-439