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先天性膈疝修补术后抗反流手术:呼吁采取个体化方法。

Antireflux surgery after congenital diaphragmatic hernia repair: a plea for a tailored approach.

机构信息

Department of Thoracic Surgery, University Hospitals Leuven, Leuven, Belgium.

出版信息

Eur J Cardiothorac Surg. 2013 Aug;44(2):263-7; discussion 268. doi: 10.1093/ejcts/ezt001. Epub 2013 Jan 25.

Abstract

OBJECTIVES

Preventive antireflux surgery (ARS) at the moment of congenital diaphragmatic hernia (CDH) repair has been suggested by some authors, particularly in subgroups with a liver herniated in the chest or patch requirement. We evaluated the incidence and associated factors of gastro-oesophageal reflux disease (GERD) and the need for subsequent ARS in our CDH patients.

METHODS

We retrospectively reviewed our CDH database. Demographics, prenatal assessment of severity, prenatal treatment, type of repair, intraoperative findings and incidences of gastro-oesophageal reflux and ARS were recorded.

RESULTS

CDH repair was performed in 77 infants between July 1993 and November 2009. Eight died after repair. Seven were lost to follow-up. The median follow-up was 4.0 (0.16-14.88) years. Fourteen of these 62 patients were prenatally treated with fetoscopic endoluminal tracheal occlusion (FETO) because of severe pulmonary hypoplasia. After CDH repair, GERD was diagnosed in 31 patients. In all of them, medical antireflux treatment was started. Thirteen (42%) patients needed ARS at a median age of 64 (37-264) days. One year after starting medical treatment, 14 (45%) patients were completely off antireflux medication. In CDH subgroups with patch repair, liver herniated in the chest or previous FETO, the incidences of gastro-oesophageal reflux and ARS were 61 and 32%, 73 and 38% and 71 and 43%, respectively. Univariable analysis of associated potentially predisposing factors shows that patch repair, liver herniated in the chest, pulmonary hypertension, high-frequency oscillatory ventilation and FETO are associated with subsequent ARS. On multivariable analysis, liver herniated in the chest was the only independent predictor for both gastro-oesophageal reflux and ARS.

CONCLUSIONS

Of all CDH patients, 50% developed gastro-oesophageal reflux and 21% required ARS. For both, liver in the chest was the only independent predictor. Routine ARS in certain subgroups at the time of CDH repair seems not to be justified. Foetal endoluminal tracheal occlusion creates a new cohort of survivors with an increased risk for undergoing ARS. The surgical group, in particular, reflects a more complex gastro-oesophageal reflux physiopathology.

摘要

目的

一些作者建议在先天性膈疝(CDH)修复时预防性抗反流手术(ARS),尤其是在肝脏疝入胸腔或需要修补的亚组中。我们评估了我们的 CDH 患者中胃食管反流病(GERD)的发生率和相关因素,以及随后进行 ARS 的需求。

方法

我们回顾性地查阅了我们的 CDH 数据库。记录了人口统计学资料、产前严重程度评估、产前治疗、修复类型、术中发现以及胃食管反流和 ARS 的发生率。

结果

1993 年 7 月至 2009 年 11 月期间,我们对 77 名婴儿进行了 CDH 修复。修复后有 8 人死亡。有 7 人失访。中位随访时间为 4.0(0.16-14.88)年。这 62 名患者中有 14 名因严重肺发育不良而接受了胎儿内镜腔内气管阻塞(FETO)的产前治疗。CDH 修复后,31 名患者被诊断为 GERD。在所有患者中,均开始了抗反流药物治疗。13 名(42%)患者需要在中位数为 64(37-264)天的时间进行 ARS。开始药物治疗 1 年后,14 名(45%)患者完全停止了抗反流药物治疗。在有补丁修复、肝脏疝入胸腔或有 FETO 史的 CDH 亚组中,胃食管反流和 ARS 的发生率分别为 61%和 32%、73%和 38%以及 71%和 43%。对潜在相关危险因素的单变量分析显示,补丁修复、肝脏疝入胸腔、肺动脉高压、高频振荡通气和 FETO 与随后的 ARS 相关。多变量分析显示,肝脏疝入胸腔是 GERD 和 ARS 的唯一独立预测因素。

结论

在所有 CDH 患者中,有 50%发生胃食管反流,21%需要 ARS。对于这两种情况,肝脏在胸腔都是唯一的独立预测因素。在 CDH 修复时对某些亚组进行常规 ARS 似乎没有道理。胎儿内镜腔内气管阻塞创造了一个新的幸存者队列,他们发生 ARS 的风险增加。手术组特别反映了更复杂的胃食管反流病理生理学。

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