婴儿气管成形术后实现正常肺功能。

0 CARDIAC & CARDIOVASCULAR SYSTEMS
Ciara Harrison, Jo Harrison, Tyson A Fricke, Igor E Konstantinov
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引用次数: 0

摘要

婴儿长段先天性气管狭窄(LTS)非常罕见,是一种具有挑战性的临床病例。我们描述了一名患儿的治疗情况,该患儿在呼吸骤停后需要进行体外膜肺氧合,并在婴儿期因重度 LTS 而接受了滑动气管成形术,但因反复出现气管肉芽而需要反复进行支气管镜再介入治疗。孩子 9 岁时肺功能测试正常,运动耐量正常。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Achieving normal pulmonary function following tracheoplasty in infancy.

Infant long-segment congenital tracheal stenosis (LTS) is rare and presents a challenging clinical scenario. We describe the management of a child who required extracorporeal membrane oxygenation following a respiratory arrest and underwent slide tracheoplasty in infancy for severe LTS and required repeated bronchoscopic reinterventions for recurrent tracheal granulations. At 9 years of age, the child has normal pulmonary function testing and a normal exercise tolerance.

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