Aortic Valve Repair for Adult Congenital Heart Disease

Background—Aortic valve–preserving procedures have resulted in excellent outcomes in selected patients, particularly those with normal aortic valve leaflets and dilated aortic roots. However, several congenital heart lesions are associated with abnormal aortic valve leaflets. The long-term results of aortic valve repair for these lesions are not well defined. Methods and Results—We reviewed the clinical records of 54 adult (age .18 years) patients who underwent repair of congenital abnormalities of the aortic valve between 1976 and September 1999. Follow-up data were available on 52 (96%) patients (mean 50667 months, range 1 to 266). Patients underwent repair at a mean age of 34614 years with associated diagnoses of subaortic stenosis (n510), ventricular septal defect with prolapsing aortic valve (n517), bicuspid aortic valve (n523), sinus of Valsalva aneurysm (n510), and bacterial endocarditis (n52). There was 1 operative death (1.9%) and 3 late deaths. Survival at 5 and 10 years was 9862% and 74612%, respectively. Freedom from reoperation was 7469% and 51615% at 5 and 10 years, respectively. The presence of a ventricular septal defect predicted failure of valve repair (59% versus 22%, P50.01). A bicuspid aortic valve, subaortic stenosis, or the requirement for mitral valve surgery did not affect outcomes. Conclusions—Aortic valve repair in adult patients with congenital heart disease can be performed with minimal morbidity and mortality rates. The medium-term results of repair are acceptable, regardless of valvular or associated pathology. However, only 31 patients (57%) demonstrated long-term competence of the aortic valve, suggesting that most adult patients with congenital aortic valve disease will eventually require aortic valve replacement. (Circulation. 2000;102[suppl III]:III-40-III-43.)