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一名患有埃布斯坦畸形的青少年在脊柱后路融合术中的麻醉护理

Anesthetic Care During Posterior Spinal Fusion in an Adolescent With Ebstein's Anomaly.

作者信息

Phi Kenneth, Martin David P, Beebe Allan, Klamar Jan, Tobias Joseph D

机构信息

The Ohio State University School of Medicine, Columbus, OH, USA.

Department of Anesthesiology & Pain Medicine, Nationwide Children's Hospital, Columbus, OH, USA.

出版信息

J Med Cases. 2020 Mar;11(3):68-72. doi: 10.14740/jmc3449. Epub 2020 Mar 26.

Abstract

Ebstein's anomaly is a rare form of cyanotic congenital heart disease (CHD) that involves malformation and dysfunction of the tricuspid valve and right ventricle (RV). The severity of the defect impacts clinical presentation, survival, and treatment options. Presentation during the neonatal period with hypoxemia and cyanosis is noted in patients with severe tricuspid valve malformation, a hypoplastic RV, or RV outflow tract obstruction. However, presentation later in infancy is more common when there is a moderate tricuspid valve malformation and no associated RV outflow tract obstruction. Although Ebstein's anomaly is not generally associated with other congenital defects, patients may occasionally require surgery for other comorbid conditions. We describe the perioperative anesthetic management of an adolescent with Ebstein's anomaly for posterior spinal fusion. Previous reports of anesthetic care in this clinical scenario are reviewed, anesthetic considerations discussed, and options for intraoperative monitoring and anesthetic care presented.

摘要

埃布斯坦畸形是一种罕见的青紫型先天性心脏病(CHD),涉及三尖瓣和右心室(RV)的畸形与功能障碍。缺损的严重程度影响临床表现、生存率及治疗选择。严重三尖瓣畸形、右心室发育不全或右心室流出道梗阻的患者在新生儿期会出现低氧血症和发绀。然而,当存在中度三尖瓣畸形且无相关右心室流出道梗阻时,婴儿期后期发病更为常见。虽然埃布斯坦畸形一般不与其他先天性缺陷相关,但患者偶尔可能因其他合并症需要手术治疗。我们描述了一名患有埃布斯坦畸形的青少年行后路脊柱融合术的围手术期麻醉管理。回顾了此前该临床场景下的麻醉护理报告,讨论了麻醉考虑因素,并介绍了术中监测和麻醉护理的选择。

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本文引用的文献

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