Norwood W I, Kirklin J K, Sanders S P
Am J Cardiol. 1980 Jan;45(1):87-91. doi: 10.1016/0002-9149(80)90224-6.
Aortic atresia is a form of hypoplastic left heart syndrome always complicated by associated severe hypoplasia of the ascending aorta and various degrees of mitral valve and left ventricular hypoplasia. At present it is a universally fatal lesion in early infancy. This is a report of a new palliative procedure for hypoplastic left heart syndrome that has resul;ed in early ongoing survival of two infants with aortic atresia. On the basis of experience with a third patient, an operation for future physiologic correction is proposed.
主动脉闭锁是左心发育不全综合征的一种形式，常伴有升主动脉严重发育不全以及不同程度的二尖瓣和左心室发育不全。目前，这是一种在婴儿早期普遍致命的病变。本文报告了一种针对左心发育不全综合征的新姑息性手术，该手术使两名患有主动脉闭锁的婴儿早期得以存活。基于对第三名患者的经验，提出了一种未来进行生理性矫正的手术方案。
