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胎儿先天性膈疝的宫内矫治IX:预后不良(肝脏疝出和低肺头比)的胎儿可通过胎儿镜下临时气管闭塞术获救。

Correction of congenital diaphragmatic hernia in utero IX: fetuses with poor prognosis (liver herniation and low lung-to-head ratio) can be saved by fetoscopic temporary tracheal occlusion.

作者信息

Harrison M R, Mychaliska G B, Albanese C T, Jennings R W, Farrell J A, Hawgood S, Sandberg P, Levine A H, Lobo E, Filly R A

机构信息

The Fetal Treatment Center and the Department of Surgery, University of California, San Francisco 94143-0570, USA.

出版信息

J Pediatr Surg. 1998 Jul;33(7):1017-22; discussion 1022-3. doi: 10.1016/s0022-3468(98)90524-3.

Abstract

BACKGROUND/PURPOSE: Fetuses with congenital diaphragmatic hernia (CDH) who have a "poor prognosis" with postnatal treatment now can be identified on the basis of liver herniation, early diagnosis (before 25 weeks' gestation) and a low lung-to-head ratio (LHR). Because complete in utero repair proved unsuccessful for this group, the strategy of temporary tracheal occlusion was developed to gradually enlarge the hypoplastic fetal lung. The purpose of this study is to compare the outcome of patients in the poor-prognosis group treated by one of three methods: (1) standard postnatal care, (2) fetal tracheal occlusion via open hysterotomy, and (3) the recently developed video-fetoscopic (Fetendo) technique of tracheal occlusion without hysterotomy.

METHODS

In the past 3 years, 34 of 86 fetuses with an isolated left CDH met criteria for the poor-prognosis group. Thirteen families chose postnatal treatment at an extracorporeal membrane oxygenation (ECMO) center, 13 underwent open fetal tracheal occlusion, and eight underwent fetoscopic tracheal occlusion.

RESULTS

The survival rate was 38% in the group treated by standard postnatal therapy, 15% in the open tracheal occlusion group, and 75% in the Fetendo group. There were less postoperative pulmonary complications noted in mothers who underwent the Fetendo procedure versus the open tracheal occlusion. All but one Fetendo clip patient had a striking physiological response demonstrated by sonographic enlargement of the small left lung that was documented postnatally by plain radiographs and its subjective appearance during repair of the CDH. In contrast, only 5 of the 13 open tracheal occlusion patients demonstrated lung growth.

CONCLUSION

Fetuses with a left CDH who have liver herniation and a low LHR are at high risk of neonatal demise and appear to benefit from temporary tracheal occlusion when performed fetoscopically, but not when performed by open fetal surgery.

摘要

背景/目的:目前,可依据肝脏疝出、早期诊断(妊娠25周前)及低肺头比(LHR)来识别出生后治疗“预后不良”的先天性膈疝(CDH)胎儿。由于对这组胎儿进行子宫内完全修复未获成功,因此制定了临时气管阻塞策略,以逐步扩大发育不全的胎儿肺。本研究的目的是比较采用以下三种方法之一治疗的预后不良组患者的结局:(1)标准出生后护理;(2)经腹开放式子宫切开术进行胎儿气管阻塞;(3)最近开发的无需子宫切开术的视频胎儿镜(Fetendo)气管阻塞技术。

方法

在过去3年中,86例孤立性左侧CDH胎儿中有34例符合预后不良组标准。13个家庭选择在体外膜肺氧合(ECMO)中心进行出生后治疗,13例接受开放式胎儿气管阻塞,8例接受胎儿镜气管阻塞。

结果

标准出生后治疗组的存活率为38%,开放式气管阻塞组为15%,Fetendo组为75%。与开放式气管阻塞相比,接受Fetendo手术的母亲术后肺部并发症较少。除1例Fetendo夹子患者外,所有患者均有明显的生理反应,表现为左侧小肺超声检查显示增大,出生后经X线平片证实,且在CDH修复过程中外观上有主观变化。相比之下,13例开放式气管阻塞患者中只有5例显示肺生长。

结论

有肝脏疝出和低LHR的左侧CDH胎儿有很高的新生儿死亡风险,经胎儿镜进行临时气管阻塞似乎有益,但经开放式胎儿手术进行则不然。

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