Snoddy J W, Parr E L, Robertson L W, Mauck H P, McCue C M, Lower R R
Ann Thorac Surg. 1978 Feb;25(2):158-63. doi: 10.1016/s0003-4975(10)63512-6.
Surgical repair of the Taussig-Bing deformity has been successful in 2 children weighting 7.7 and 11.1 kg, respectively. In the first case the right ventricular patch divered left ventricular blood to the pulmonary arter, thus creating a physiologically complete transposition which was then corrected by an interatrial Mustard baffle. In the second case a right ventricular tunnel diverted left ventricular blood to the aorta, and right ventricular blood was directed to the distal pulmonary artery by means of an external conduit bypassing a subpulmonic stenosis. These patients represent the seventh and eighth successful corrections of the Taussig-Bing anomaly. One case (Patient 2) is the youngest to undergo repair and the first to receive an external conduit for bypass of an associated subpulmonic stenosis.
对两名分别重7.7千克和11.1千克的儿童进行的陶西格 - 宾畸形手术修复取得了成功。在第一例中，右心室补片将左心室血液分流至肺动脉，从而形成了生理上完全性大动脉转位，随后通过心房内马斯塔德挡板进行了矫正。在第二例中，右心室隧道将左心室血液分流至主动脉，右心室血液通过绕过肺动脉瓣下狭窄的外部管道被导向远端肺动脉。这些患者是陶西格 - 宾畸形成功矫正的第七例和第八例。其中一例（患者2）是接受修复手术的最年轻患者，也是首例接受外部管道以绕过相关肺动脉瓣下狭窄的患者。
