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黏多糖贮积症Ⅰ型(Hurler综合征)中预期困难气道的处理

Management of an anticipated difficult airway in Hurler's syndrome.

作者信息

Gurumurthy T, Shailaja S, Kishan Shetty, Stephen Madona

机构信息

Department of Anaesthesiology, Father Muller Medical College, Mangalore, Karnataka, India.

出版信息

J Anaesthesiol Clin Pharmacol. 2014 Oct;30(4):558-61. doi: 10.4103/0970-9185.142862.

Abstract

Management of an anticipated difficult airway in Hurler syndrome. Hurler syndrome is a subtype of Mucopolysaccharidosis (MPS) type 1. Mucopolysaccharidosis (lysosomal storage diseases) are a group of inherited disorders caused by deficiency of specific lysosomal enzyme required for a normal degradation of glycosaminoglycons (GAGs). Administration of general anaesthesia in patients who have congenital syndromes such as Hurler's is often a challenge because of progressive airway, craniofacial and skeletal abnormalities that may make both the ventilation and intubation difficult. We encountered difficult mask ventilation and endotracheal intubation was not possible and finally ventilated with laryngeal mask airway in a known case of Hurler syndrome posted for umbilical hernia repair.

摘要

黏多糖贮积症I型Hurler综合征患者预期困难气道的管理。Hurler综合征是黏多糖贮积症(MPS)I型的一种亚型。黏多糖贮积症(溶酶体贮积病)是一组遗传性疾病,由正常降解糖胺聚糖(GAGs)所需的特定溶酶体酶缺乏引起。由于进行性气道、颅面和骨骼异常,可能使通气和插管都变得困难,因此对患有Hurler综合征等先天性综合征的患者实施全身麻醉往往是一项挑战。在一例因脐疝修补术而确诊为Hurler综合征的患者中,我们遇到了面罩通气困难且无法进行气管插管的情况,最终使用喉罩进行了通气。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b409/4234796/f43d27bd1583/JOACP-30-558-g001.jpg

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