[The airway management and treatment of newborns with micrognathia and laryngomalacia].

Q4 Medicine
Jing Wang, Mengrou Xu, Lei Jin, Meizhen Gu, Xiaoyan Li
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引用次数: 0

Abstract

Objective:To explore the perioperative airway management and treatment of newborns with micrognathia and laryngomalacia. Methods:From January to December 2022, a total of 6 newborns with micrognathia and laryngomalacia were included. Preoperative laryngoscopy revealed concomitant laryngomalacia. These micrognathia were diagnosed as Pierre Robin sequences. All patients had grade Ⅱ or higher symptoms of laryngeal obstruction and required oxygen therapy or non-invasive ventilatory support. All patients underwent simultaneous laryngomalacia surgery and mandibular distraction osteogenesis. The shortened aryepiglottic folds were ablated using a low-temperature plasma radiofrequency during the operation. Tracheal intubation was maintained for 3-5 days postoperatively. Polysomnography(PSG) and airway CT examination were performed before and 3 months after the surgery. Results:Among the 6 patients, 4 required oxygen therapy preoperatively and 2 required non-invasiveventilatory support. The mean age of patients was 40 days at surgery. The inferior alveolar nerve bundle was not damaged during the operation, and there were no signs of mandibular branch injury such as facial asymmetry after the surgery. Laryngomalacia presented as mixed type: type Ⅱ+ type Ⅲ. The maximum mandibular distraction distance was 20 mm, the minimum was 12 mm, and the mean was 16 mm. The posterior airway space increased from a preoperative average of 3.5 mm to a postoperative average of 9.5 mm. The AHI decreased from a mean of 5.65 to 0.85, and the lowest oxygen saturation increased from a mean of 78% to 95%. All patients were successfully extubated after the surgery, and symptoms of laryngeal obstruction such as hypoxia and feeding difficulties disappeared. Conclusion:Newborns with micrognathia and laryngomalacia have multi-planar airway obstruction. Simultaneous laryngomalacia surgery and mandibular distraction osteogenesis are safe and feasible, and can effectively alleviate symptoms of laryngeal obstruction such as hypoxia and feeding difficulties, while significantly improving the appearance of micrognathia.

新生儿小颌伴喉软化症的气道管理与治疗。
目的:探讨新生儿小颌畸形伴喉软化的围手术期气道管理及治疗。方法:选取2022年1 - 12月收治的6例小颌畸形伴喉软化新生儿。术前喉镜检查发现伴发性喉软化。这些小颌畸形被诊断为Pierre Robin序列。所有患者都有Ⅱ级或更高级别的喉梗阻症状,需要吸氧或无创通气支持。所有患者同时接受了喉软化手术和下颌牵张成骨术。术中使用低温等离子体射频消融缩短的动脉粥样硬化皱襞。术后气管插管维持3 ~ 5天。术前和术后3个月分别行多导睡眠图(PSG)和气道CT检查。结果:6例患者中术前氧疗4例,无创呼吸支持2例。手术时患者的平均年龄为40天。术中未损伤下牙槽神经束,术后无面部不对称等下颌分支损伤征象。喉软化表现为混合型:Ⅱ型+Ⅲ型。下颌牵张距离最大20 mm,最小12 mm,平均16 mm。后气道间隙从术前平均3.5 mm增加到术后平均9.5 mm。AHI由平均5.65下降到0.85,最低血氧饱和度由平均78%上升到95%。所有患者术后均成功拔管,缺氧、进食困难等喉梗阻症状消失。结论:新生儿小颌畸形伴喉软化伴多平面气道阻塞。喉软化术联合下颌牵张成骨术安全可行,可有效缓解缺氧、进食困难等喉部梗阻症状,同时显著改善小颌畸形外观。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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