Ross-Konno Operation for Patients with Shone Complex

被引：1

作者：

Aeba, Ryo ^{[1
]}

Okamoto, Kazuma ^{[1
]}

Yozu, Ryohei ^{[1
]}

机构：

[1] Keio Univ, Div Cardiovasc Surg, Shinjuku Ku, Tokyo 1608582, Japan

来源：

TEXAS HEART INSTITUTE JOURNAL | 2010年 / 37卷 / 02期

关键词：

Aortic valve stenosis/congenital/surgery; cardiac surgical procedures/methods; child; preschool; heart defects; congenital/mortality/pathology/surgery; mitral valve/abnormalities/pathology/surgery; reoperation; risk assessment; treatment outcome; ventricular outflow obstruction/complications/congenital/surgery; AUTOGRAFT;

D O I：

暂无

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

We report the cases of 2 pediatric patients who had Shone complex. Each child had severe left ventricular outflow tract obstruction and marginal mitral obstruction, and both underwent the Ross-Konno operation. The mitral valve was left alone. Both patients survived the operations, and serial follow-up echocardiography up to 4 years later showed a decreased or decreasing trend in the peak mitral diastolic velocity. The Ross-Konno procedure can be an acceptable approach for a subgroup of patients who have Shone complex. (Tex Heart Inst J 2010;37(2):240-1)

引用

页码：240 / 241

页数：2

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