先天性完全性房室传导阻滞较罕见,本文通过35例报告,以估计苏格兰西南地区本病的发病率和预后,并探讨安装起搏器的指征。方法:18年中收集当地先天性房室传导阻滞病人35例,诊断依据于Yater制定的标准:出生时或年幼时就存在心率缓慢;无引起传导阻滞的白喉或其他心肌炎病史;无缺血性心脏病或心肌病的证据;无心脏手术史。男15例,女20例,最小仅12天,最大85 Congenital complete atrioventricular block is rare, this article through 35 reports to estimate the incidence and prognosis of the disease in southwestern Scotland, and to explore the instructions for the installation of pacemaker. METHODS: Twenty-five local patients with congenital AV block were collected in 18 years. The diagnosis was based on the criteria set by Yater: a slow heart rate at birth or at young age; no history of diphtheria or other myocarditis causing block; Evidence of ischemic heart disease or cardiomyopathy; no history of cardiac surgery. 15 males and 20 females, the smallest only 12 days, the maximum 85