Department of Otolaryngology, Head and Neck Surgery, University Hospital (CHUV), Lausanne, Switzerland.
J Thorac Cardiovasc Surg. 2010 Feb;139(2):411-7. doi: 10.1016/j.jtcvs.2009.05.010. Epub 2009 Jul 1.
We sought to describe our experience in the management of complex glotto-subglottic stenosis in the pediatric age group.
Between 1978 and 2008, 33 children with glotto-subglottic stenosis underwent partial cricotracheal resection, and they form the focus of this study. They were compared with 67 children with isolated subglottic stenosis (no glottic involvement). The outcomes measured were need for revision open surgical intervention, delayed decannulation (>6 months), and operation-specific and overall decannulation rates. Fisher's exact test was used for comparison of outcomes.
Results of preoperative evaluation showed Myer-Cotton grade III or IV stenosis in 32 (97%) patients and grade II stenosis in 1 patient. All patients with glotto-subglottic stenosis were treated with partial cricotracheal resection and simultaneous repair of the glottic pathology. Bilateral fixed vocal cords were seen in 19 (58%) of 33 patients, bilateral restricted abduction was seen in 7 (21%) of 33 patients, and unilateral fixed vocal cord was seen in 7 (21%) of 33 patients. Ten patients underwent single-stage partial cricotracheal resection with excision of interarytenoid scar tissue. The endotracheal tube was kept for a mean period of 7 days as a stent. Twenty-three patients underwent extended partial cricotracheal resection with LT-Mold (Bredam S.A., St. Sulpice, Switzerland) or T-tube stenting. The overall decannulation rate included 26 (79%) patients, and the operation-specific decannulation rate included 20 (61%) patients.
Glotto-subglottic stenosis is a complex laryngeal injury associated with delayed decannulation and decreased overall and operation-specific decannulation rates when compared with those after subglottic stenosis without glottic involvement after partial cricotracheal resection.
我们旨在描述在小儿年龄组中管理复杂会厌-声门下狭窄的经验。
1978 年至 2008 年间,33 名会厌-声门下狭窄的儿童接受了部分环状软骨-气管切除术,这些儿童是本研究的重点。他们与 67 名孤立性声门下狭窄(无声门受累)的儿童进行了比较。测量的结果是需要再次行开放性手术干预、延迟拔管(>6 个月)以及手术特异性和总体拔管率。Fisher 确切概率法用于比较结果。
术前评估结果显示 32 例(97%)患者存在 Myer-Cotton Ⅲ级或Ⅳ级狭窄,1 例患者存在Ⅱ级狭窄。所有会厌-声门下狭窄的患者均接受了部分环状软骨-气管切除术和同时修复声门病变。33 例患者中有 19 例(58%)双侧固定声带,33 例中有 7 例(21%)双侧限制外展,33 例中有 7 例(21%)单侧固定声带。10 例患者行一期部分环状软骨-气管切除术,切除杓状软骨间的瘢痕组织。作为支架,气管内导管保留了 7 天的平均时间。23 例患者行扩展部分环状软骨-气管切除术,使用 LT-Mold(Bredam S.A.,St. Sulpice,瑞士)或 T 型管支架。总体拔管率包括 26 例(79%)患者,手术特异性拔管率包括 20 例(61%)患者。
与单纯行部分环状软骨-气管切除术治疗无声门受累的声门下狭窄相比,会厌-声门下狭窄是一种复杂的喉损伤,会导致延迟拔管以及总体和手术特异性拔管率降低。