Rutter Michael J, Cotton Robin T
Division of Pediatric Otolaryngology/Head & Neck Surgery, Aerodigestive and Sleep Center, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio 45229-3039, USA.
Arch Otolaryngol Head Neck Surg. 2004 Jun;130(6):737-9. doi: 10.1001/archotol.130.6.737.
To review our experience using posterior cricoid grafts to manage pediatric patients with isolated posterior glottic stenosis (PGS).
Retrospective review over a 12-year period.
Tertiary care pediatric hospital.
All patients with isolated PGS treated between 1990 and 2002, in whom PGS was the dominant airway lesion and laryngotracheoplasty was required. Patients with concomitant vocal cord paralysis, a history of posterior laryngeal clefting, a Bogdasarian type I stenosis, or subglottic stenosis worse than grade I were excluded.
Cause, operative intervention, decannulation rate, failure rate, and requirement for secondary procedures.
A total of 29 patients ranging in age from 2 to 8 years were treated (21 with a history of prolonged intubation and 8 with a history of laryngeal trauma). Twenty patients had tracheotomies in place at the time of airway reconstruction and the remainder had stridor. Costal cartilage was the preferred graft material and was used in 27 patients. Six patients were referred with a diagnosis of bilateral vocal cord paralysis, but on evaluation were found to have PGS and mobile vocal cords. In 12 patients, repair was accomplished in a single-stage procedure; a suprastomal stent was placed in 17 patients. Overall decannulation rate was 97%, though a second procedure was required in 4 patients. One patient remained tracheotomy dependent; 4 had poor voice, including 2 with a history of laryngeal fracture; and 2 had late arytenoid prolapse.
Isolated PGS in children is effectively managed with costal cartilage grafting of the posterior cricoid. This series has seen an evolution in management, with shorter stenting periods, placement of flanged posterior grafts without sutures, and graft placement without complete laryngofissure.
回顾我们使用环状软骨后移植物治疗小儿单纯性声门后狭窄(PGS)患者的经验。
对12年期间进行回顾性研究。
三级儿科护理医院。
1990年至2002年间所有接受治疗的单纯性PGS患者,其中PGS是主要气道病变且需要进行喉气管成形术。排除伴有声带麻痹、有喉后裂病史、Bogdasarian I型狭窄或声门下狭窄超过I级的患者。
病因、手术干预、拔管率、失败率以及二次手术需求。
共治疗29例年龄在2至8岁之间的患者(21例有长期插管史,8例有喉部创伤史)。20例患者在气道重建时已行气管切开术,其余患者有喘鸣。肋软骨是首选的移植材料,27例患者使用。6例患者初诊为双侧声带麻痹,但经评估发现为PGS且声带活动正常。12例患者通过一期手术完成修复;17例患者放置了造口上支架。总体拔管率为97%,不过4例患者需要二次手术。1例患者仍依赖气管切开术;4例患者声音不佳,其中2例有喉部骨折史;2例患者出现晚期杓状软骨脱垂。
小儿单纯性PGS采用环状软骨后肋软骨移植治疗有效。本系列研究在治疗方法上有所改进,包括缩短支架置入时间、放置无缝线的带凸缘后移植物以及在不进行完全喉裂开的情况下放置移植物。