Steinbacher Derek M, Kaban Leonard B, Troulis Maria J
Department of Oral and Maxillofacial Surgery, Massachusetts General Hospital, Boston, MA 02112, USA.
J Oral Maxillofac Surg. 2005 Aug;63(8):1072-9. doi: 10.1016/j.joms.2005.04.013.
The purpose of this study was to evaluate mandibular lengthening by distraction osteogenesis (DO) to achieve decannulation of micrognathic children with "permanent" tracheostomies.
Using a retrospective chart review, patients were included who had 1 ) airway compromise/tracheostomy, 2 ) micrognathia, 3 ) polysomnography-documented obstructive apnea, and 4 ) mandibular advancement using DO. Excluded were 1 ) adults, 2 ) neonates without tracheostomy, and 3 ) patients with central apnea. Patient age, past medical history, age at tracheostomy, and distraction protocol were documented. Oxygen saturation, posterior airway space (in millimeters), and sella-nasion-B point (SNB) angle were recorded. The distraction protocol consisted of a latency of 48 hours and a rate of 1 mm/day.
There were 5 children, aged 2 to 14 years, who received a tracheostomy between ages 2 and 36 months for airway obstruction. All patients underwent bilateral mandibular distraction using semiburied, unidirectional devices. The average latency was 58 hours, the rate was 1 mm/day, the duration of fixation was 40 to 60 days, and the magnitude of advancement was 23 mm. Healing was evaluated by clinical, radiologic, and ultrasound examinations. No complications were experienced. Mean follow-up was 3.2 years. Postdistraction sleep studies demonstrated no obstructive apneic events and a mean oxygen saturation of 98% (preoperative, 76%, P < .005). Cephalometric values improved: posterior airway space 4 to 14 mm; SNB 66 degrees to 72 degrees ( P < .005 for both variables). Four of the 5 patients have been successfully decannulated to date.
The results of this preliminary study indicate that mandibular advancement by DO is a potentially viable treatment option for tracheostomy-dependent children with upper airway obstruction secondary to micrognathia.
本研究旨在评估牵张成骨术(DO)延长下颌骨,以使患有“永久性”气管切开术的小颌畸形儿童拔除气管套管。
采用回顾性病历审查,纳入符合以下条件的患者:1)气道受损/气管切开术;2)小颌畸形;3)多导睡眠图记录的阻塞性呼吸暂停;4)采用DO进行下颌骨前移。排除标准为:1)成年人;2)无气管切开术的新生儿;3)中枢性呼吸暂停患者。记录患者年龄、既往病史、气管切开术时的年龄以及牵张方案。记录氧饱和度、后气道间隙(以毫米为单位)以及蝶鞍-鼻根- B点(SNB)角。牵张方案包括48小时的延迟期和每天1毫米的速率。
有5名年龄在2至14岁之间的儿童,因气道阻塞在2至36个月龄时接受了气管切开术。所有患者均使用半埋入式单向装置进行双侧下颌骨牵张。平均延迟期为58小时,速率为每天1毫米,固定时间为40至60天,前移幅度为23毫米。通过临床、放射学和超声检查评估愈合情况。未发生并发症。平均随访时间为3.2年。牵张后睡眠研究显示无阻塞性呼吸暂停事件,平均氧饱和度为98%(术前为76%,P <.005)。头影测量值有所改善:后气道间隙增加4至14毫米;SNB从66度增加到72度(两个变量的P均<.005)。截至目前,5名患者中有4名已成功拔除气管套管。
这项初步研究的结果表明,对于因小颌畸形导致上气道阻塞且依赖气管切开术的儿童患者,采用DO进行下颌骨前移是一种潜在可行的治疗选择。