脊髓小脑共济失调 1 型患者的麻醉管理

Sakura Takeda, Sumire Idzuchi, Kentaro Mizuta
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摘要

脊髓小脑共济失调 1 型(SCA1)是常染色体显性脊髓小脑变性(SCD)疾病之一,以进行性小脑共济失调、肌肉萎缩和周围神经病变为特征。我们报告了一名 43 岁男性 SCA1 患者在下颌骨骨折切开复位内固定术中接受全身麻醉的治疗情况。虽然有报道称 SCD 患者在麻醉过程中会出现声带麻痹,但使用视频喉镜进行鼻气管插管时并无大碍。考虑到 SCD 患者术后呼吸抑制的风险增加,罗库溴铵的剂量经过了仔细滴定,手术期间没有使用芬太尼。在为 SCA 患者提供全身麻醉时,为预期的困难气道做好准备并避免明显的呼吸抑制至关重要1。
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 Patient With Spinocerebellar Ataxia Type 1.

Spinocerebellar ataxia type 1 (SCA1) is one of the autosomal dominant spinocerebellar degeneration (SCD) diseases characterized by progressive cerebellar ataxia, muscle atrophy, and peripheral neuropathy. We report the management of a 43-year-old man with SCA1 who underwent general anesthesia for open reduction and internal fixation of a mandibular fracture. Although anesthesia-induced vocal cord paralysis has been reported in patients with SCD, nasotracheal intubation was performed uneventfully with video laryngoscope. After taking into consideration the increased risk of postoperative respiratory depression in patients with SCD, rocuronium dosing was titrated carefully, and fentanyl was not used during surgery. Preparation for an anticipated difficult airway and avoiding significant respiratory depression are crucial when providing general anesthesia for patients with SCA1.

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