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先天性瓣上主动脉狭窄与麻醉相关的猝死:谜团何在?

Congenital supravalvular aortic stenosis and sudden death associated with anesthesia: what's the mystery?

作者信息

Burch Thomas M, McGowan Francis X, Kussman Barry D, Powell Andrew J, DiNardo James A

机构信息

Division of Cardiac Anaesthesia, Department of Anesthesiology, Perioperative and Pain Medicine, Children's Hospital Boston and Harvard Medical School, Boston, Massachusetts 02115, USA.

出版信息

Anesth Analg. 2008 Dec;107(6):1848-54. doi: 10.1213/ane.0b013e3181875a4d.

Abstract

Patients with congenital supravalvular aortic stenosis and associated peripheral pulmonary artery stenoses, the majority of whom have Williams-Beuren syndrome, are inherently at risk for development of myocardial ischemia. This is particularly true in the setting of procedural sedation and anesthesia. The biventricular hypertrophy that accompanies these lesions increases myocardial oxygen consumption and compromises oxygen delivery. In addition, these patients often have direct, multifactorial compromise of coronary blood flow. In this article, we review both the pathophysiology of congenital supravalvular aortic stenosis and the literature regarding sudden death in association with sedation and anesthesia. Recommendations as to preoperative assessment and management of these patients are made based on the best available evidence.

摘要

患有先天性主动脉瓣上狭窄及相关周围肺动脉狭窄的患者,其中大多数患有威廉姆斯-贝伦综合征,本身就有发生心肌缺血的风险。在程序性镇静和麻醉的情况下尤其如此。伴随这些病变的双心室肥厚会增加心肌耗氧量并影响氧输送。此外,这些患者往往存在冠状动脉血流的直接、多因素损害。在本文中,我们回顾了先天性主动脉瓣上狭窄的病理生理学以及与镇静和麻醉相关的猝死文献。基于现有最佳证据,对这些患者的术前评估和管理提出了建议。

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