Respiratory Center For Children, Goryeb Children's Hospital, Atlantic Health, Morristown, NJ 07962, USA.
J Pediatr Surg. 2009 Nov;44(11):2107-11. doi: 10.1016/j.jpedsurg.2009.04.036.
Tracheoesophageal fistula (TEF) is the most common congenital tracheal abnormality, frequently associated with esophageal atresia. Respiratory symptoms are associated with all types of TEF, even after surgical repair of the fistula. Gastroesophageal reflux (GER) with aspiration of gastric contents, structural instability of the airways (tracheomalacia), abnormal respiratory epithelium, abnormal esophageal motility, recurrent TEF, and esophageal stenosis contribute to postsurgical complications.
We review 7 patients between 4 and 14 years of age with a history of TEF repair and persistent or worsening respiratory symptoms despite conventional airway clearance techniques and treatment of GER.
Bronchoscopic evaluation in all 7 patients revealed tracheomalacia and a diverticulum on the posterior wall of the trachea at the fistula repair site.
We hypothesize that the diverticula impaired airway clearance and contributed to persistent respiratory symptoms. Possible mechanisms for the diverticulum contributing to poor airway clearance include facilitating the pooling of secretions and acting as a "barrier" to the lower airway clearance mechanism. The diagnosis of a diverticulum should be considered early in patients with persistent respiratory symptoms after management of GER and tracheomalacia. Early obliteration of tracheal diverticula might improve respiratory status in some patients.
气管食管瘘(TEF)是最常见的先天性气管异常,常与食管闭锁有关。所有类型的 TEF 都与呼吸症状有关,即使在瘘管修复后也是如此。胃食管反流(GER)伴胃内容物吸入、气道结构不稳定(气管软化)、异常呼吸上皮、异常食管动力、复发性 TEF 和食管狭窄都会导致术后并发症。
我们回顾了 7 名 4 至 14 岁的患者,这些患者均有 TEF 修复史,尽管采用了常规气道清除技术和 GER 治疗,但仍存在持续性或加重的呼吸症状。
所有 7 名患者的支气管镜评估均显示气管软化和瘘管修复部位气管后壁憩室。
我们假设憩室妨碍了气道清除,导致持续性呼吸症状。憩室导致气道清除不良的可能机制包括促进分泌物积聚和充当下气道清除机制的“障碍”。对于 GER 和气管软化管理后持续性呼吸症状的患者,应早期考虑憩室的诊断。早期闭塞气管憩室可能会改善一些患者的呼吸状况。