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埃布斯坦畸形

Ebstein's Malformation.

作者信息

Younoszai AK, Brook MM, Silverman NH

机构信息

Pediatric Cardiology Box 0544, 505 Parnassus Ave., Room HSE 1403, University of California at San Francisco, San Francisco, CA 94143, USA.

出版信息

Curr Treat Options Cardiovasc Med. 1999 Dec;1(4):363-372. doi: 10.1007/s11936-999-0032-6.

Abstract

Ebstein's malformation of the tricuspid valve is a complex and heterogeneous disorder that has diverse hemodynamic and arrhythmic manifestations. Hemodynamic dysfunction is due to valvar regurgitation and decreased pulmonary blood flow, varying in severity from mild tricuspid insufficiency to severe dysplasia of the right ventricle without forward flow. Atrioventricular reentrant tachycardia and atrial tachyarrhythmias are commonly associated with Ebstein's malformation. Treatment ranges from conservative medical management to the ablation of pathways by catheterization to complex surgical repair or palliation. All patients with Ebstein's malformation should be followed on a regular basis by a cardiologist familiar with congenital heart disease. The frequency of evaluations should depend on the severity of the disease and the presence of arrhythmias. A specialist in electrophysiology should also follow those patients with complex arrhythmias.

摘要

三尖瓣埃布斯坦畸形是一种复杂且异质性的疾病,具有多种血流动力学和心律失常表现。血流动力学功能障碍是由于瓣膜反流和肺血流量减少,严重程度从轻度三尖瓣关闭不全到右心室严重发育异常且无前向血流不等。房室折返性心动过速和房性快速心律失常通常与埃布斯坦畸形相关。治疗方法从保守的药物治疗到通过导管消融传导通路,再到复杂的手术修复或姑息治疗。所有埃布斯坦畸形患者都应由熟悉先天性心脏病的心脏病专家定期随访。评估频率应取决于疾病的严重程度和心律失常的存在情况。对于患有复杂心律失常的患者,还应由电生理专家进行随访。

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