A randomized controlled trial of fetal endoscopic tracheal occlusion versus postnatal management of severe isolated congenital diaphragmatic hernia


Autoria(s): Ruano, Rodrigo; Yoshizaki, Carlos Tadashi; Silva, M. M. da; Ceccon, M. E. J.; Grasi, M. S.; Tannuri, Uenis; Zugaib, Marcelo
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

07/11/2013

07/11/2013

2012

Resumo

Objective Severe pulmonary hypoplasia and pulmonary arterial hypertension are associated with reduced survival in congenital diaphragmatic hernia (CDH). We aimed to determine whether fetal endoscopic tracheal occlusion (FETO) improves survival in cases of severe isolated CDH. Methods Between May 2008 and July 2010, patients whose fetuses had severe isolated CDH (lung-to-head ratio < 1.0, liver herniation into the thoracic cavity and no other detectable anomalies) were assigned randomly to FETO or to no fetal intervention (controls). FETO was performed under maternal epidural anesthesia supplemented with fetal intramuscular anesthesia. Tracheal balloon placement was achieved with ultrasound guidance and fetoscopy between 26 and 30 weeks of gestation. All cases that underwent FETO were delivered by the EXIT procedure. Postnatal therapy was the same for both treated fetuses and controls. The primary outcome was survival to 6 months of age. Other maternal and neonatal outcomes were also evaluated. Results Twenty patients were enrolled randomly to FETO and 21 patients to standard postnatal management. The mean gestational age at randomization was similar in both groups (P = 0.83). Delivery occurred at 35.6 +/- 2.4 weeks in the FETO group and at 37.4 +/- 1.9 weeks in the controls (P < 0.01). In the intention-to-treat analysis, 10/20 (50.0%) infants in the FETO group survived, while 1/21 (4.8%) controls survived (relative risk (RR), 10.5 (95% CI, 1.5-74.7), P < 0.01). In the receivedtreatment analysis, 10/19 (52.6%) infants in the FETO group and 1/19 (5.3%) controls survived (RR, 10.0 (95% CI, 1.4-70.6) P < 0.01). Conclusion FETO improves neonatal survival in cases with isolated severe CDH. Copyright (C) 2011 ISUOG. Published by John Wiley & Sons, Ltd.

CNPq (Conselho Nacional de Desenvolvimento de Pesquisa e Tecnologia do Brasil)

CNPq (Conselho Nacional de Desenvolvimento de Pesquisa e Tecnologia do Brasil) [SISNEP CAAE - 0926.0.015.000-07]

Identificador

ULTRASOUND IN OBSTETRICS & GYNECOLOGY, MALDEN, v. 39, n. 1, pp. 20-27, JAN, 2012

0960-7692

http://www.producao.usp.br/handle/BDPI/42886

10.1002/uog.10142

http://dx.doi.org/10.1002/uog.10142

Idioma(s)

eng

Publicador

WILEY-BLACKWELL

MALDEN

Relação

ULTRASOUND IN OBSTETRICS & GYNECOLOGY

Direitos

restrictedAccess

Copyright WILEY-BLACKWELL

Palavras-Chave #CONGENITAL DIAPHRAGMATIC HERNIA #FETAL ABNORMALITIES #FETAL SURGERY #FETO #FETOSCOPY #PRENATAL DIAGNOSIS #PULMONARY HYPERTENSION #PULMONARY HYPOPLASIA #HEAD CIRCUMFERENCE RATIO #LUNG-VOLUME #SURVIVAL #PREDICTION #FETUSES #DOPPLER #AREA #ACOUSTICS #OBSTETRICS & GYNECOLOGY #RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Tipo

article

original article

publishedVersion