Division of Plastic and Reconstructive Surgery, Department of Surgery, Rush University Medical Center, Chicago, IL.
Department of Otorhinolaryngology, Rush University Medical Center, Chicago, IL.
J Craniofac Surg. 2023;34(8):2413-2416. doi: 10.1097/SCS.0000000000009627. Epub 2023 Aug 28.
Tracheostomy is the definitive treatment for airway management in severe cases of craniofacial-associated upper airway obstruction, like the Pierre-Robin sequence, but is associated with significant morbidity. The purpose of this study was to examine tracheostomy-associated morbidities and mortalities in craniofacial patients to identify opportunities to improve clinical care and patient prognosis.
The study was a retrospective review of pediatric craniofacial patients who were tracheostomized between 2016 and 2022. Data regarding their demographics, craniofacial diagnoses, endoscopic airway anomalies, intubation grade of view classification, tracheostomy-related complications, and causes of mortality were analyzed.
Sixteen of the 17 tracheostomized pediatric patients had the Pierre-Robin sequence, with 5 of those patients having an additional syndromic craniofacial diagnosis. Additional airway anomalies were found in 82.4% of the patients. The mean length of hospital stay after tracheostomy was 4.08 months. Infection was the most common complication, observed in 94.1% of patients, followed by stomal granulation in 76.5% of patients. Two mortalities were observed: one following the compassionate removal of ventilator support and the other following the accidental dislodgment of the tracheostomy tube.
Tracheostomy-related complications were observed in all craniofacial patients in this group. Compared with the general pediatric population, tracheostomized craniofacial patients may endure longer hospital stays and greater stomal granulation rates. Mandibular distraction osteogenesis may allow for tracheostomy avoidance in these patients, and future research should focus on comparing the long-term complication rates and outcomes between tracheostomy mandibular distraction osteogenesis in this challenging patient population.
气管切开术是严重颅面相关上气道阻塞(如 Pierre-Robin 序列)气道管理的确定性治疗方法,但与显著的发病率相关。本研究的目的是检查颅面患者气管切开术相关的发病率和死亡率,以确定改善临床护理和患者预后的机会。
本研究是对 2016 年至 2022 年间接受气管切开术的小儿颅面患者进行的回顾性研究。分析了他们的人口统计学、颅面诊断、内镜气道异常、插管视野分级分类、气管切开术相关并发症以及死亡原因的数据。
17 例气管切开术的小儿患者中有 16 例患有 Pierre-Robin 序列,其中 5 例患者有额外的综合征性颅面诊断。82.4%的患者存在其他气道异常。气管切开术后平均住院时间为 4.08 个月。感染是最常见的并发症,94.1%的患者出现感染,其次是 76.5%的患者出现窦道肉芽组织增生。观察到 2 例死亡:1 例是在同情性停止呼吸机支持后,另 1 例是在气管切开管意外移位后。
本研究组所有颅面患者均观察到气管切开术相关并发症。与一般儿科人群相比,气管切开术的颅面患者可能需要更长的住院时间和更高的窦道肉芽组织增生率。下颌骨牵引成骨术可能允许这些患者避免气管切开术,未来的研究应集中比较在这一具有挑战性的患者群体中,气管切开术与下颌骨牵引成骨术的长期并发症发生率和结局。