General anesthesia using propofol infusion for implantation of an implantable cardioverter defibrillator in a pediatric patient with Andersen-Tawil syndrome: a case report.

Seyeon Park, Wonjae Heo, Sang-Wook Shin, Hye-Jin Kim, Yeong Min Yoo, Hee Young Kim
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Abstract

Andersen-Tawil syndrome (ATS) is a rare genetic disease characterized by a triad of episodic flaccid muscle weakness, ventricular arrhythmias, and physical anomalies. ATS patients have various cardiac arrhythmias that can cause sudden death. Implantation of an implantable cardioverter-defibrillator (ICD) is required when life-threatening cardiac arrhythmias do not respond to medical treatment. An 11-year-old girl underwent surgery for an ICD implantation. For general anesthesia in ATS patients, anesthesiologists should focus on the potentially difficult airway, serious cardiac arrhythmias, such as ventricular tachycardia (VT), and delayed recovery from neuromuscular blockade. We followed the difficult airway algorithm, avoided drugs that can precipitate QT prolongation and fatal cardiac arrhythmias, and tried to maintain normoxia, normocarbia, normothermia, normoglycemia, and pain control for prevention of sympathetic stimulation. We report the successful application of general anesthesia for ICD implantation in a pediatric patient with ATS and recurrent VT.

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应用异丙酚输注全身麻醉植入可植入式心律转复除颤器1例安徒生-塔威尔综合征患儿。
安徒生-塔威尔综合征(ATS)是一种罕见的遗传性疾病,其特征是间歇性弛缓性肌无力、室性心律失常和身体异常。ATS患者有各种可能导致猝死的心律失常。当危及生命的心律失常药物治疗无效时,需要植入植入式心律转复除颤器(ICD)。一名11岁的女孩接受了ICD植入手术。对于ATS患者的全身麻醉,麻醉医师应关注潜在的气道困难,严重的心律失常,如室性心动过速(VT),以及神经肌肉阻滞后的延迟恢复。我们遵循困难气道算法,避免使用可能导致QT间期延长和致死性心律失常的药物,并尽量维持常氧、常碳、常体温、常血糖,控制疼痛以防止交感刺激。我们报告成功的应用全麻ICD植入儿童患者ATS和复发性VT。
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