Anesthetic Management of an Infant With Postnatally Diagnosed Tracheal Agenesis Undergoing Tracheal Reconstruction: A Case Report.

Brittany L Willer, Kayla G Bryan, Daiva E Parakininkas, Michael R Uhing, Susan R Staudt, Kathleen M Dominguez, Michael E McCormick, Michael E Mitchell, John C Densmore, Keith T Oldham, Richard J Berens
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引用次数: 4

Abstract

A term infant born cyanotic failed multiple intubation attempts and tracheostomy placement. After esophageal intubation resulted in the ability to ventilate, he was presumed to have tracheal agenesis and distal bronchoesophageal fistula. He was transferred to our institution where he was diagnosed with Floyd Type II tracheal agenesis. He underwent staged tracheal reconstruction. He was discharged to home at 4 months of age with a tracheostomy collar, cervical spit fistula, and gastrostomy tube. He represents the sole survivor-to-discharge of tracheal agenesis in the United States. We describe the anesthetic considerations for a patient with tracheal agenesis undergoing reconstruction.

产后诊断为气管发育不全的婴儿进行气管重建的麻醉处理:1例报告。
一个足月婴儿出生紫绀失败多次插管尝试和气管切开术安置。经食管插管恢复通气后,推测患者有气管发育不全和远端支气管食管瘘。他被转移到我们的机构,在那里他被诊断为弗洛伊德II型气管发育不全。他接受了分阶段气管重建。他在4个月大时出院回家,气管造口领、颈口吐瘘和胃造口管。他是美国唯一一位因气管发育不全而出院的幸存者。我们描述了麻醉考虑的病人与气管发育不全进行重建。
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