对一名患有菲佛综合征的儿科患者的麻醉管理。

Anesthesia progress Pub Date : 2024-09-09 DOI:10.2344/523400
Emiko Inoue, Chikako Owada, Ayumi Kiyohara, Tomoyuki Miyata, Hina Wajima, Yasuko Iwahori, Gentaro Tsujimoto, Asako Yasuda, Yoshiki Shionoya
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引用次数: 0

摘要

费弗氏综合征(PS)是一种罕见的遗传性疾病,主要影响颅面部和四肢骨骼,也可包括上下气道异常。在三种亚型中,PS 2 型和 PS 3 型最为严重。我们描述了一名患有 PS 2 型的 10 岁男孩在全身麻醉下接受牙科治疗的麻醉处理过程。由于他有 Chiari 畸形病史,我们建议他避免颈部过度伸展,以防神经功能恶化。术前计算机断层扫描显示他的鼻腔明显狭窄,但气管没有异常。考虑到鼻气管插管的难度,我们计划进行口腔插管。我们使用七氟醚、氧化亚氮和氧气以及口咽气道进行全身麻醉。在口咽部局部涂抹利多卡因后,在自主通气的情况下进行光纤气管插管,以尽量减少头颈部的活动。使用地氟醚和瑞芬太尼维持麻醉,未观察到术后并发症。PS 患者的全身麻醉需要仔细规划,其中应包括术前气道评估,以确定鼻气管插管的可行性并识别气道异常。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anesthetic Management of a Pediatric Patient With Pfeiffer Syndrome.

Pfeiffer syndrome (PS) is a rare inherited disorder that affects the craniofacial and extremity bones but can also include anomalies of the upper and lower airways. Among the 3 subtypes, PS types 2 and 3 are the most severe. We describe the anesthetic management of a 10-year-old boy with PS type 2 scheduled for dental treatment under general anesthesia. Because of his history of Chiari malformation, avoiding neck hyperextension was recommended to prevent worsening of his neurologic function. Preoperative computed tomography revealed significant nasal stenosis but no tracheal anomalies. Considering the difficulty of nasotracheal intubation, we planned for an oral intubation. General anesthesia was induced using sevoflurane, nitrous oxide, and oxygen along with an oropharyngeal airway. After lidocaine was topically applied to the oropharynx, fiber-optic orotracheal intubation was performed under spontaneous ventilation to minimize head and neck movement. Anesthesia was maintained using desflurane and remifentanil, and no postoperative complications were observed. General anesthesia for patients with PS requires careful planning, which should include preoperative assessment of the airway to determine the feasibility of nasotracheal intubation and identify airway irregularities.

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