Shuhaiber Jeffrey H, Ho Sieuw Yen, Rigby Michael, Sethia Babulal
Department of Cardiothoracic Surgery, Royal Brompton Hospital, Sydney Street, London, United Kingdom.
Eur J Cardiothorac Surg. 2009 May;35(5):891-900. doi: 10.1016/j.ejcts.2009.01.009. Epub 2009 Feb 24.
A wealth of experience has been gained in the management of atrioventricular septal defect (AVSD) since the first complete correction of this malformation in 1955. The success of surgical therapy followed an enhanced understanding of morphology and physiology as well as major improvements in imaging of this congenital heart defect. Therapeutic success in the management of patients with AVSD has been extended to include those with associated lesions such as tetralogy of Fallot, double outlet right ventricle and relative degrees of ventricular hypoplasia. Although operative mortality is low and long-term survival is relatively good, important detrimental residual or AVSD-related complications such as left atrioventricular valve regurgitation, left ventricular outflow tract obstruction still carry significant late morbidity in a proportion of patients. This article reviews our current understanding of the morphology of this defect, aspects of diagnosis and surgical treatment options.
自1955年首次成功完全矫正房室间隔缺损(AVSD)以来,在其治疗方面积累了丰富的经验。随着对该先天性心脏缺陷形态学和生理学的深入理解以及成像技术的重大改进,外科治疗取得了成功。AVSD患者治疗的成功已扩展到包括患有相关病变的患者,如法洛四联症、右心室双出口和不同程度的心室发育不全。尽管手术死亡率低且长期生存率相对较好,但重要的有害残余或与AVSD相关的并发症,如左房室瓣反流、左心室流出道梗阻,在一部分患者中仍会导致显著的晚期发病。本文综述了我们目前对该缺陷形态学、诊断方面及手术治疗选择的理解。