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羊膜腔镜腹部减压术治疗先天性膈疝的肺脏体视学参数变化:一项初步研究

Stereological Lung Parameters After Fetoscopic Abdominal Decompression of Congenital Diaphragmatic Hernia in an Ovine Model: A Pilot Study.

机构信息

Department of General, Visceral, Thoracic, Transplant, and Pediatric Surgery, UKSH University Hospital of Schleswig-Holstein Kiel Campus, Kiel, Germany.

Department of Pediatric Surgery, University Medical Center Hamburg-Eppendorf (UKE), Hamburg, Germany.

出版信息

J Laparoendosc Adv Surg Tech A. 2021 Jun;31(6):712-718. doi: 10.1089/lap.2020.0954. Epub 2021 Apr 28.

Abstract

Fetoscopic endoluminal tracheal occlusion (FETO) improves lung maturation in severe cases of congenital diaphragmatic hernia (CDH) but it does not ameliorate lung compression by herniated abdominal organs. Surgically opening the fetal abdomen (abdominal decompression [AD]) reduces the intrathoracic pressure by diverting the abdominal organs into the amniotic cavity-a probable causal therapy for lung hypoplasia and pulmonary hypertension in CDH. Open surgical abdominal decompression has been reported: we describe a minimally invasive approach in an ovine model of CDH as a probable fetoscopic intervention. Eight fetuses were included, 2 were kept as HEALTHY controls. A CDH (left side, liver down) was created by open fetal surgery at midgestation in 6 fetuses, 2 were taken as CDH controls. Fetoscopic abdominal decompression (fAD) was performed 21 days later in 4 animals. The fetuses were retrieved at the end of gestation and evaluated by lung stereology. fAD led to a near total evacuation of the thoracic cavity in 2 of the 4 animals. Fetuses with CDH had a lower total volume and fraction of alveolar air space, a lower volume fraction of the parenchyma, and an increase of the volume fraction of the alveolar septa and atelectasis, as well as an increased mean thickness of alveolar septa compared with HEALTHY fetuses. Fetuses treated with abdominal decompression showed an improvement of stereological parameters. In spite of relevant limitations (pilot study, small groups, spontaneous closure of the abdominal incision) we were able to demonstrate that abdominal decompression for CDH can be performed by fetoscopy. Our results support the hypothesis of causally improving lung development by abdominal decompression, thus implying increased survival in extreme cases of CDH. A refinement of the fetoscopic techniques and direct comparison to FETO appears warranted.

摘要

胎儿镜腔内气管阻塞术(FETO)可改善严重先天性膈疝(CDH)患者的肺成熟度,但不能改善疝入的腹部器官对肺的压迫。通过打开胎儿腹部(腹部减压[AD])将腹部器官转移到羊膜腔中,可以减少胸腔内压力,这可能是 CDH 中肺发育不全和肺动脉高压的因果治疗方法。已经有报道称开腹手术进行腹部减压:我们描述了一种在 CDH 羊模型中的微创方法,这可能是一种胎儿镜干预。纳入了 8 只胎儿,其中 2 只为健康对照组。在中期妊娠时通过开放胎儿手术在 6 只胎儿中创建 CDH(左侧,肝向下),其中 2 只为 CDH 对照组。21 天后在 4 只动物中进行胎儿镜下腹部减压(fAD)。在妊娠末期取回胎儿,并通过肺体视学进行评估。fAD 导致 4 只动物中的 2 只胸腔几乎完全排空。与健康胎儿相比,CDH 胎儿的总容积和肺泡空气空间分数较低,实质容积分数较低,肺泡间隔和肺不张的容积分数增加,肺泡间隔的平均厚度增加。接受腹部减压治疗的胎儿显示体视学参数的改善。尽管存在相关限制(试点研究、小样本组、腹部切口自发闭合),我们能够证明 CDH 的腹部减压可以通过胎儿镜完成。我们的结果支持通过腹部减压改善肺发育的假设,从而意味着在极端 CDH 病例中生存率提高。需要进一步完善胎儿镜技术并直接与 FETO 进行比较。

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