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[儿童早期喉气管成形术]

[Laryngotracheoplasty in early childhood].

作者信息

Schultz-Coulon H J, Laubert A

机构信息

Klinik für Hals-Nasen-Ohrenkrankheiten, Kopf- und Halschirurgie, plastische Operationen, Lukaskrankenhaus, Neuss.

出版信息

HNO. 1988 Jan;36(1):1-12.

PMID:3280524
Abstract

Because of increased risk of surgery in infancy and because surgery at this age may affect laryngotracheal growth it is preferable to postpone open surgical correction of congenital or acquired laryngotracheal stenoses until pre-school or even school age. However, early intervention by one of the surgical methods available today appears to be justified if a child with a tracheostomy has unsatisfactory home surroundings, if the tracheostomy impedes a rehabilitation programme or if the laryngeal stenosis does not allow voice production. Of 42 children with congenital (14) or acquired (28) laryngotracheal stenosis, 13 were operated between the ages of 3 months and 6 years. The following surgical methods were used, depending on the type and degree of stenosis: (1) submucosal scar resection (5 cases); (2) "stepped incision" as described by Evans and Todd (2 cases); (3) widening of the anterior wall by an autogenous cartilage graft as described by Cotton (2 cases); (4) laminotomy with interposition of an autogenous cartilage graft as described by Rethi (3 cases); (5) multiple-staged laryngotracheal reconstruction with regional skin flaps and repeated cartilage grafting (1 case). The soft silicon Montgomery T tube was preferred in all cases for stenting the reconstructed laryngotracheal lumen, because it seems to be the most convenient and safest method. The importance of painstaking postoperative intensive care is emphasized. Up to now 11 patients have been extubated, but 4 of them show a mild restenosis. The history of one child who has not yet been decannulated is reported in detail to demonstrate the limits of laryngotracheoplasty in early childhood.

摘要

由于婴儿期手术风险增加,且这个年龄段的手术可能会影响喉气管的生长,因此最好将先天性或后天性喉气管狭窄的开放性手术矫正推迟到学龄前甚至学龄期。然而,如果气管切开术患儿的家庭环境不理想、气管切开术妨碍康复计划,或者喉狭窄导致无法发声,那么采用目前可用的手术方法之一进行早期干预似乎是合理的。在42例先天性(14例)或后天性(28例)喉气管狭窄患儿中,13例在3个月至6岁之间接受了手术。根据狭窄的类型和程度,采用了以下手术方法:(1)黏膜下瘢痕切除术(5例);(2)Evans和Todd描述的“阶梯状切口”(2例);(3)Cotton描述的自体软骨移植扩大前壁(2例);(4)Rethi描述的自体软骨移植置入的板层切开术(3例);(5)用局部皮瓣和重复软骨移植进行多阶段喉气管重建(1例)。所有病例均首选柔软的硅胶蒙哥马利T形管支撑重建的喉气管腔,因为它似乎是最方便、最安全的方法。强调了术后精心重症监护的重要性。到目前为止,已有11例患者拔管,但其中4例有轻度再狭窄。详细报告了1例尚未拔管患儿的病史,以说明幼儿期喉气管成形术的局限性。

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