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Balloon tracheoplasty as initial treatment for neonates with symptomatic congenital tracheal stenosis

机译:球囊气管成形术作为有症状先天性气管狭窄的新生儿的初始治疗

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Neonates with congenital tracheal stenosis (CTS) sometimes develop respiratory distress and may be difficult to intubate. We used balloon tracheoplasty with a rigid bronchoscope for emergency airway management in neonates with symptomatic CTS. Herein, we describe the balloon tracheoplasty procedure and the early outcomes following its use as the initial treatment of neonatal symptomatic CTS. We performed a retrospective analysis of five neonates with CTS who were initially treated with balloon tracheoplasty at our institution from January 2010 to December 2013. Five patients with a mean birthweight of 2,117 g were treated during the study period. Of these, four developed respiratory distress after birth, and all patients had difficult intubations. In all five patients, definitive diagnosis of CTS was made by rigid bronchoscopy and 3-dimensional reconstruction scan. A total of nine balloon dilatations were performed in five patients. Following balloon tracheoplasty, two patients were extubated, one was extubated after resection and end-to-end anastomosis following initial balloon dilatation, and one remained hospitalized with tracheostomy for tracheomalacia. The remaining patient died from tracheal bleeding associated with congenital heart disease. Although our sample size was small, balloon tracheoplasty is a potentially effective initial treatment for selected cases with neonatal symptomatic CTS.
机译:先天性气管狭窄(CTS)的新生儿有时会出现呼吸窘迫,可能难以插管。我们将硬性支气管镜球囊气管成形术用于有症状CTS的新生儿的紧急气道管理。在本文中,我们描述了球囊气管成形术的程序以及将其用作新生儿症状性CTS的初始治疗后的早期结果。我们对2010年1月至2013年12月在我们机构接受球囊气管成形术治疗的5例CTS新生儿进行了回顾性分析。研究期间对5例平均出生体重为2117 g的患者进行了治疗。其中,四名出生后出现呼吸窘迫,所有患者均插管困难。在所有五名患者中,通过硬支气管镜和3维重建扫描对CTS进行了明确诊断。五名患者共进行了九次球囊扩张术。球囊气管成形术后,有2例患者拔管,其中1例在切除和初始球囊扩张后端对端吻合后拔管,还有1例因气管软化而需行气管切开术。其余患者死于与先天性心脏病相关的气管出血。尽管我们的样本量很小,但是对于某些有症状的CTS病例,气囊气管成形术是一种可能有效的初始治疗方法。

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