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外周肺动脉狭窄修复的手术技术

Surgical Techniques for Repair of Peripheral Pulmonary Artery Stenosis.

作者信息

Mainwaring Richard D, Hanley Frank L

机构信息

Division of Pediatric Cardiac Surgery, Lucile Packard Children's Hospital/Stanford University, Stanford, California.

Division of Pediatric Cardiac Surgery, Lucile Packard Children's Hospital/Stanford University, Stanford, California.

出版信息

Semin Thorac Cardiovasc Surg. 2017;29(2):198-205. doi: 10.1053/j.semtcvs.2017.05.001. Epub 2017 May 17.

Abstract

Peripheral pulmonary artery stenosis is a rare form of congenital heart disease frequently associated with Williams and Alagille syndromes. Patients with this disease typically have systemic level right ventricular pressures secondary to obstruction at the lobar, segmental, and subsegmental branches. The current management of patients with peripheral pulmonary artery stenosis remains somewhat controversial. We have pioneered an entirely surgical approach to the reconstruction of peripheral pulmonary artery stenosis. This approach initially entailed surgical patch augmentation of all major lobar branches and effectively reduced right ventricular pressures by more than half. This was the first report demonstrating an effective approach to the disease. Over the past 5 years, we have gradually evolved the technique to extend the reconstruction's reach to include segmental and subsegmental branch stenoses. An important technical aspect of this approach entails division of the main pulmonary and separation of the branch pulmonary arteries to access the lower lobe branches. Pulmonary artery homograft patches are used to augment hypoplastic pulmonary artery branches. In addition, we perform a Heineke-Mikulicz type ostioplasty for isolated ostial stenoses. The technical details of the surgical approach to peripheral pulmonary artery stenosis are outlined in this article, and can also be used for other complex peripheral pulmonary artery reconstructions.

摘要

外周肺动脉狭窄是一种罕见的先天性心脏病,常与威廉姆斯综合征和阿拉吉列综合征相关。患有这种疾病的患者通常由于叶、节段和亚节段分支处的梗阻而出现体循环水平的右心室压力。目前对外周肺动脉狭窄患者的治疗仍存在一定争议。我们开创了一种完全手术的方法来重建外周肺动脉狭窄。这种方法最初需要对所有主要叶分支进行手术补片扩大,并有效地将右心室压力降低了一半以上。这是第一份证明该疾病有效治疗方法的报告。在过去的5年里,我们逐渐改进了该技术,将重建范围扩大到包括节段和亚节段分支狭窄。这种方法的一个重要技术方面是对主肺动脉进行分割,并将分支肺动脉分离以显露下叶分支。肺动脉同种异体移植物补片用于扩大发育不全的肺动脉分支。此外,对于孤立的开口狭窄,我们进行海涅克-米库利奇式造口成形术。本文概述了外周肺动脉狭窄手术方法的技术细节,也可用于其他复杂的外周肺动脉重建。

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