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胸腔镜下胸导管结扎术治疗先天性和后天性疾病

Thoracoscopic Thoracic Duct Ligation for Congenital and Acquired Disease.

作者信息

Slater Bethany J, Rothenberg Steven S

机构信息

Rocky Mountain Hospital for Children , Denver, Colorado.

出版信息

J Laparoendosc Adv Surg Tech A. 2015 Jul;25(7):605-7. doi: 10.1089/lap.2014.0360. Epub 2015 Jan 28.

Abstract

PURPOSE

Congenital and acquired chylothorax presents a unique management challenge in neonates and infants. A failure of conservative therapy requires surgical ligation to prevent continued fluid and protein losses. This article examines a 15-year experience with thoracoscopic ligation of the thoracic duct.

PATIENTS AND METHODS

From June 1999 to December 2013, 21 patients presented with chylothorax refractory to conservative management. Sixteen patients presented following cardiac procedures, 1 after tracheoesophageal fistula repair, 1 after extracorporeal membrane oxygenation cannulation, and 1 after trauma, and 2 had congenital chylothorax. Ages ranged from 3 weeks to 5 years, and weights ranged from 2.6 to 12.7 kg. All procedures were performed in the right chest with three ports. All cases consisted of sealing of the duct at the level of the diaphragm, a mechanical pleurodesis, and fibrin glue.

RESULTS

All cases were completed successfully thoracoscopically. Operative time ranged from 20 to 55 minutes. There were no intraoperative complications. One patient with congenital bilateral chylothorax required a left partial pleurectomy. The chest tube duration postoperatively ranged from 4 to 14 days. Ligation failed in 2 patients, requiring a subsequent thoracoscopic pleurectomy and chemical pleurodesis, respectively.

CONCLUSIONS

Thoracoscopic thoracic duct ligation is a safe and effective procedure even in post-cardiac surgery patients. The site of the leak can be identified in the majority of cases, and tissue-sealing technology appears to be effective. The minimally invasive nature of the procedure has led to more expedient operative repair to avoid the morbidity associated with chyle leak.

摘要

目的

先天性和后天性乳糜胸给新生儿和婴儿的治疗带来了独特的挑战。保守治疗失败时需要进行手术结扎,以防止持续的液体和蛋白质流失。本文探讨了15年胸腔镜结扎胸导管的经验。

患者与方法

1999年6月至2013年12月,21例患者出现对保守治疗无效的乳糜胸。16例患者在心脏手术后出现,1例在气管食管瘘修复后出现,1例在体外膜肺氧合插管后出现,1例在创伤后出现,2例患有先天性乳糜胸。年龄范围为3周至5岁,体重范围为2.6至12.7千克。所有手术均通过右侧胸腔的三个切口进行。所有病例均包括在膈肌水平封闭胸导管、机械性胸膜固定术和纤维蛋白胶。

结果

所有病例均成功通过胸腔镜完成。手术时间为20至55分钟。术中无并发症。1例先天性双侧乳糜胸患者需要进行左侧部分胸膜切除术。术后胸管留置时间为4至14天。2例患者结扎失败,分别需要随后进行胸腔镜胸膜切除术和化学性胸膜固定术。

结论

即使在心脏手术后的患者中,胸腔镜胸导管结扎术也是一种安全有效的手术。在大多数病例中可以确定渗漏部位,组织封闭技术似乎有效。该手术的微创性质使得手术修复更加便捷,以避免与乳糜漏相关的发病率。

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