Morabito A, MacKinnon E, Alizai N, Asero L, Bianchi A
Sheffield Children's Hospital and The Neonatal Surgical Unit, St Mary's Hospital, Manchester, England.
J Pediatr Surg. 2000 Oct;35(10):1456-8. doi: 10.1053/jpsu.2000.16413.
Tracheomalacia occurs as a primary developmental defect or may be secondary to vascular compression. It is common in association with esophageal atresia and tracheoesophageal fistula. Collapse of the weak trachea is a cause of recurrent respiratory symptoms but may be severe and life threatening.
Between 1978 and 1999 at Sheffield Children's Hospital and The Royal Manchester Children's Hospital, of 16 children with clinically significant symptoms of tracheomalacia 8 underwent combined aortopexy and tracheopexy, 1 had aortopexy alone, 4 only had a tracheopexy, and 3 had tracheal reinforcement with free costal cartilage ring grafts. The surgical approach was limited to a low cervical skin crease incision with a midline manubrial split providing extrapleural access to the anterior mediastinum and allowing for all surgery under direct unimpaired vision.
Ten children did not require postoperative ventilatory support. Four underwent ventilation for a few hours or days. One child required CPAP for 4 months for residual tracheomalacia and a further child, who had 3 operations to insert 11 costal cartilage ring grafts, underwent ventilation intermittently for 6 months. Adequate tracheal patency could be verified by intraoperative tracheoscopy and was sustained postoperatively so that only 1 child with associated bilateral vocal cord paralysis came to tracheostomy. Four children required prolonged hospitalization because of residual tracheomalacia, 2 for bronchomalacia and 2 because of esophageal narrowing leading to further surgery. All other children were fit for discharge within 10 to 30 days of surgery. Long-term follow-up has confirmed sustained tracheal improvement and resolution of the life-threatening features of tracheomalacia.
The authors recommend the low skin crease transmanubrial approach, as described by Vaishnav and MacKinnon, for tracheopexy, aortopexy and for tracheal reconstruction for tracheomalacia. The approach gives excellent access for surgery under direct vision through a relatively avascular plane. It is associated with less morbidity than a conventional thoracotomy and leaves a more acceptable aesthetic scar.
气管软化可作为原发性发育缺陷出现,也可能继发于血管压迫。它常与食管闭锁和气管食管瘘相关。薄弱气管的塌陷是反复出现呼吸道症状的一个原因,但可能很严重甚至危及生命。
1978年至1999年间,在谢菲尔德儿童医院和皇家曼彻斯特儿童医院,16例有明显气管软化临床症状的儿童中,8例行主动脉固定术和气管固定术联合手术,1例仅行主动脉固定术,4例仅行气管固定术,3例行游离肋软骨环移植气管强化术。手术入路局限于低位颈部皮肤皱襞切口,沿胸骨柄中线劈开,经胸膜外进入前纵隔,使所有手术能在直视下顺利进行。
10例儿童术后无需通气支持。4例通气数小时或数天。1例儿童因残余气管软化需持续气道正压通气(CPAP)4个月,另1例儿童接受了3次手术植入11个肋软骨环移植,间歇通气6个月。术中气管镜检查可证实气管通畅,术后得以维持,因此只有1例合并双侧声带麻痹的儿童需要行气管切开术。4例儿童因残余气管软化需要延长住院时间,2例因支气管软化,2例因食管狭窄需要进一步手术。所有其他儿童在术后10至30天内适合出院。长期随访证实气管状况持续改善,气管软化的危及生命特征得以消除。
作者推荐采用Vaishnav和MacKinnon描述的低位皮肤皱襞经胸骨柄入路进行气管固定术、主动脉固定术以及气管软化的气管重建术。该入路通过相对无血管的平面提供了极佳的手术直视视野。与传统开胸手术相比,其发病率更低,且留下的美观瘢痕更易接受。