Sese A, Kouda Y, Ueno Y, Kuboyama I, Kisizaki K, Kurisu K, Masaki H, Toujou T, Jou K
Nihon Kyobu Geka Gakkai Zasshi. 1989 Jan;37(1):49-55.
From December, 1984, through April, 1987, ten infants with coarctation of the aorta and six with interrupted aortic arch underwent staged repair of aorta and other cardiac lesions. Simultaneous pulmonary artery banding was performed in six of 8 patients with ventricular septal defect (VSD) and in all of seven patients with complex cardiac lesions. With first operation, there were no operative deaths and two late deaths. Eight of 14 survivors underwent total correction of associated lesions at three to 17 months after initial operation. VSD was closed in five patients with one operative death. One patient required pulmonary artery debanding alone because of decrease of VSD size. The Damus-Kaye-Stansel operation was performed successfully in one patient with Taussig-Bing anomaly and the Jatene operation was done in one with transposition of the great arteries. Based on these results, we prefer staged repair with pulmonary artery banding for coarctation or interruption of the aorta associated with complex cardiac lesions.
从1984年12月至1987年4月,10例主动脉缩窄婴儿和6例主动脉弓中断婴儿接受了主动脉及其他心脏病变的分期修复。8例室间隔缺损(VSD)患者中的6例以及7例复杂心脏病变患者全部同时进行了肺动脉环扎术。首次手术时无手术死亡病例,有2例晚期死亡。14名幸存者中有8例在初次手术后3至17个月接受了相关病变的完全矫正。5例VSD患者进行了VSD修补,有1例手术死亡。1例患者因VSD尺寸减小仅需进行肺动脉解扎术。1例陶西格-宾畸形患者成功进行了达姆斯-凯-斯坦塞尔手术,1例大动脉转位患者进行了贾滕手术。基于这些结果,我们倾向于对合并复杂心脏病变的主动脉缩窄或中断采用分期修复并结合肺动脉环扎术。