Fisher R D, Bone D K, Rowe R D, Gott V L
J Thorac Cardiovasc Surg. 1975 Aug;70(2):265-71.
Data on 8 children with the combined anomalies of complete atrioventricular canal and tetralogy of Fallot are presented. Six of the children had only a palliative procedure, and only 1 of these patients is doing relatively well at the present time from a clinical standpoint. Two of the remaining 5 children undergoing palliative procedures have not been helped significantly, and 3 of the children in this group subsequently died. Two children have had an attempted total correction of this complicated intracardiac problem. One of these children, in whom the diagnosis of atrioventricular canal was not made preoperatively, died in the early postoperative period. In the other child, the correct diagnosis was made preoperatively, and a satisfactory, totally corrective procedure was achieved. The patient is asymptomatic at this time.
本文报告了8例患有完全性房室通道合并法洛四联症联合畸形患儿的数据。其中6例患儿仅接受了姑息性手术,从临床角度来看,这些患者中目前只有1例情况相对较好。其余接受姑息性手术的5例患儿中,有2例并未得到明显改善,该组中有3例患儿随后死亡。有2例患儿尝试对这一复杂的心内问题进行完全矫正。其中1例患儿术前未诊断出房室通道,术后早期死亡。另一例患儿术前做出了正确诊断,并成功实施了令人满意的完全矫正手术。该患者目前无症状。