Buchino J J, Meagher D P, Cox J A
J Pediatr Surg. 1982 Apr;17(2):132-7. doi: 10.1016/s0022-3468(82)80196-6.
Tracheal agenesis, though seemingly rare and fatal to date, has been reported from multiple institutions with increasing frequency. Establishment of the diagnosis necessitates a high index of suspicion in an infant in respiratory distress at birth, without a cry and in whom intubation is difficult. Following definitive diagnosis by endoscopy, infants have been given a chance at survival on four occasions by prompt surgical intervention. The procedure proposed by Altman is adequate for initial stabilization. Postoperative management is aided by the use of continuous positive airway pressure (CPAP) and rigorous pulmonary toilet. Definitive correction should be considered at an early stage in order to prevent fatal complications.
气管闭锁虽然迄今为止似乎罕见且致命,但已有多个机构报告其发病率呈上升趋势。对于出生时出现呼吸窘迫、无哭声且插管困难的婴儿,诊断的确立需要高度的怀疑指数。在内镜检查确诊后,通过及时的手术干预,婴儿已有四次存活的机会。奥特曼提出的手术方法足以实现初步稳定。术后管理可借助持续气道正压通气(CPAP)和严格的肺部清洁措施。为防止致命并发症,应在早期考虑进行最终矫正。