Miyaji K, Furuse A, Ohtsuka T, Kawauchi M
Department of Cardiothoracic Surgery, Faculty of Medicine, University of Tokyo, Japan.
Jpn Heart J. 1996 Jul;37(4):509-13. doi: 10.1536/ihj.37.509.
A 10-year-old girl was referred to us with a diagnosis of pulmonary atresia and intact ventricular septum with a severely hypoplastic right ventricle and atrial septal defect. Her tricuspid valve diameter (TVD) was 48.5% of normal, with a TVD Z-score of -6.7, while right ventricular end-diastolic volume was 53.4% of normal. As a definitive procedure, one and one half ventricular repair using a bidirectional cavopulmonary shunt (BCPS) was performed instead of a Fontan procedure. The postoperative course was uneventful without episodes of low cardiac output or elevated right atrial pressure. She has been doing well during a follow-up period of 3 years.
一名10岁女孩因诊断为肺动脉闭锁、室间隔完整、右心室严重发育不全和房间隔缺损而被转诊至我院。她的三尖瓣直径(TVD)为正常的48.5%,TVD Z值为-6.7,而右心室舒张末期容积为正常的53.4%。作为确定性手术,采用双向腔肺分流术(BCPS)进行了一又二分之一心室修复,而不是Fontan手术。术后过程顺利,未出现低心输出量或右心房压力升高的情况。在3年的随访期内,她情况良好。