Role of Fetoscopic Airway Evaluation Immediately Preceding EXIT Procedure in Fetuses With Suspected Airway Obstruction.

IF 3.1 2区 医学 Q2 GENETICS & HEREDITY
Prenatal Diagnosis Pub Date : 2026-10-01 Epub Date: 2026-09-11 DOI:10.1002/pd.70243
Daniel Sanin-Ramirez, Joan Sabria, Josep M Martinez, Mar Bennasar, Montserrat Izquierdo, Elisenda Eixarch, Eduard Gratacos
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引用次数: 0

Abstract

Objective: This study describes the role of pre-EXIT (Ex Utero Intrapartum Treatment) fetoscopic airway evaluation in fetuses with suspected airway obstruction.

Methods: Single center, retrospective, observational study including fetuses with suspected airway obstruction undergoing fetoscopic airway evaluation prior to EXIT between 2013 and 2025.

Results: Nine fetuses underwent EXIT with previous fetoscopy at a median gestational age of 35 + 6 weeks (IQR 34 + 4, 37 + 1). The most frequent indications were cervical teratoma (n = 3) and lymphangioma (n = 3). Fetoscopy confirmed airway patency in one case (11.1%), allowing de-escalation to conventional cesarean section. Airway was secured by endotracheal intubation in seven cases (77.8%) and tracheostomy was required in one (11.1%). Survival at the delivery room was 100%, and one neonate died prior to discharge.

Conclusion: Fetoscopic airway evaluation prior to EXIT is a valuable adjunct in fetuses with suspected airway obstruction. It can confirm the need for EXIT, optimize the trajectory for airway access, and potentially avoid tracheostomy, improving the safety and efficiency of airway management.

胎儿镜下气道评估在疑似气道阻塞胎儿出生前的作用。
目的:本研究描述了在怀疑有气道阻塞的胎儿中,胎儿镜下气道评估的作用。方法:单中心、回顾性、观察性研究,纳入2013年至2025年期间在EXIT前接受胎镜气道评估的疑似气道阻塞胎儿。结果:9例胎儿在中位胎龄为35 + 6周(IQR 34 + 4,37 + 1)时接受了EXIT。最常见的适应症是宫颈畸胎瘤(n = 3)和淋巴管瘤(n = 3)。胎儿镜检查证实1例(11.1%)气道通畅,允许降级为常规剖宫产。7例(77.8%)行气管插管,1例(11.1%)行气管切开术。产房的存活率为100%,一名新生儿在出院前死亡。结论:胎儿内镜下气道检查对疑似气道阻塞的胎儿是有价值的辅助手段。它可以确认是否需要退出,优化气道通路轨迹,并可能避免气管切开术,提高气道管理的安全性和效率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Prenatal Diagnosis
Prenatal Diagnosis 医学-妇产科学
CiteScore
5.80
自引率
13.30%
发文量
204
审稿时长
2 months
期刊介绍: Prenatal Diagnosis welcomes submissions in all aspects of prenatal diagnosis with a particular focus on areas in which molecular biology and genetics interface with prenatal care and therapy, encompassing: all aspects of fetal imaging, including sonography and magnetic resonance imaging; prenatal cytogenetics, including molecular studies and array CGH; prenatal screening studies; fetal cells and cell-free nucleic acids in maternal blood and other fluids; preimplantation genetic diagnosis (PGD); prenatal diagnosis of single gene disorders, including metabolic disorders; fetal therapy; fetal and placental development and pathology; development and evaluation of laboratory services for prenatal diagnosis; psychosocial, legal, ethical and economic aspects of prenatal diagnosis; prenatal genetic counseling
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