Fetus-Placenta-Newborn
Fetoscopic temporary tracheal occlusion by means of detachable balloon for congenital diaphragmatic hernia

https://doi.org/10.1067/mob.2001.117344Get rights and content

Abstract

Occlusion of the fetal trachea blocks the egress of fetal lung fluid and stimulates the growth of hypoplastic lungs in fetuses with diaphragmatic hernia. Accomplishing temporary and reversible occlusion of the fetal trachea has proven difficult without invasive fetal surgery. Using simultaneous real-time ultrasonography and fetal bronchoscopy through a single uterine port, we placed a detachable balloon in the trachea of 2 fetuses with severe diaphragmatic hernia. In both fetuses the fetal lung subsequently enlarged, allowing survival after birth. (Am J Obstet Gynecol 2001;185:730-3.)

Section snippets

Case 1

A 31-year-old gravida 3, para 0 woman carrying a fetus with a right-sided CDH, a normal karyotype, and no other detectable abnormalities came to the University of California, San Francisco Fetal Treatment Center at 26 weeks’ gestation for fetal ultrasonography, echocardiography, and magnetic resonance imaging (MRI), which demonstrated a severe right-sided CDH, a large amount of liver herniated into the right hemithorax, a low LHR of 0.52, signs of fetal hydrops (ascites and pleural fluid), and

Fetendo balloon technique

The Fetendo balloon technique is shown in Figure 1.

. Access to the fetus is through a single 5-mm uterine port. The fetus is positioned with the neck extended, and tracheoscopy is performed with a 4.5-mm (OD) Bettochi constant perfusion hysteroscope. A detachable balloon loaded on a catheter is passed through the working port of the fetoscope and into the fetal trachea. It is positioned with both endoscopic and ultrasonographic visualization during inflation. Gentle traction on the catheter

Prenatal course

In both cases the balloon was successfully placed in the fetal trachea with a single 5-mm uterine port. The intraoperative course was uneventful, and the procedure time was less than half of that required for the Fetendo clip procedure.11 The postoperative course for mother and fetus was also uneventful, with a mean hospital stay of 7 days. In both cases the mothers were weaned from postoperative tocolytics, indomethacin, and magnesium sulfate and discharged on the oral calcium channel blocker

Comment

The clinical management for a prenatally diagnosed diaphragmatic hernia has evolved rapidly over the last decade and is based on a careful prognostic evaluation of the severity of the lesion. Fetuses with mild lesions have no herniation of the liver into the chest and reasonable lung volumes, as determined by LHR. Families can be reassured that these fetuses have an excellent prognosis with standard postnatal care after term delivery. On the other hand, fetuses with severe lesions have liver

References (21)

There are more references available in the full text version of this article.

Cited by (102)

  • In Utero Therapy for Congenital Diaphragmatic Hernia

    2022, Clinics in Perinatology
    Citation Excerpt :

    Fetal endoscopic tracheal occlusion (FETO) was developed as a minimally invasive method to obstruct the fetal airway, wherein a detachable silicone balloon was placed with the use of fetal bronchoscopy through a single 4- to 5-mm uterine port. Given encouraging initial results,39 the UCSF group conducted a randomized controlled trial comparing endoscopic tracheal occlusion to standard postnatal care in fetuses with severe CDH (LHR of <1.5 between 22 and 27 weeks, liver up).40 The trial was closed early after 24 patients had been enrolled, owing to the finding that tracheal occlusion did not improve survival or morbidity rates and was associated with higher rates of premature rupture of the membranes and preterm delivery.

  • Minimally Invasive Fetal Surgery

    2017, Clinics in Perinatology
    Citation Excerpt :

    Fetal endoscopic (Fetendo) tracheal clipping, first performed in a human fetus in 1997, involved a maternal laparotomy, followed by 4 trocars through the maternal uterus to access and clip the fetal trachea.80 Owing to complications of tracheal damage and vocal cord paralysis related to clipping, this technique evolved to the use of fetoscopic balloon tracheal occlusion, which avoids fetal neck dissection and requires only 1 uterine port (Fig. 6).81 Fetal endoscopic tracheal occlusion (FETO) is generally performed between 26 and 30 weeks of gestation.

View all citing articles on Scopus

Reprint requests: Michael R. Harrison, MD, The Fetal Treatment Center, University of California, San Francisco, 513 Parnassus Avenue, HSW-1601, San Francisco, CA 94143-0570.

View full text