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Updated: Sep 10, 2026

Full-root Aortic Valve Replacement by Stentless Aortic Xenografts in Patients with Small Aortic Roots
Published on: May 21, 2017
Congenital aortic stenosis. Experience with 43 patients
Insights
Surgical repair of congenital aortic stenosis in children offers effective symptom relief with low risk for older children. However, infants face high operative mortality, yet surgery remains indicated due to poor prognosis.
Area of Science:
- Cardiology
- Pediatric Surgery
- Congenital Heart Disease
Background:
- Congenital aortic stenosis presents diverse forms, including valvular, subvalvular, and supravalvular obstructions.
- Surgical intracardiac repair is a treatment option for congenital aortic stenosis.
Observation:
- A study of 43 patients with congenital aortic stenosis aged 2 days to 24 years undergoing surgical repair.
- Preoperative symptoms and electrocardiogram abnormalities were common; 28% had associated cardiac defects.
Findings:
- Overall hospital mortality was 9%, with no deaths in patients over 3 months old.
- Late results showed excellent or satisfactory outcomes in 59% (valvular, older), 45% (subvalvular), and 66% (diffuse subvalvular).
- Recurrent obstruction required reoperation in six patients; late hemodynamic studies showed gradient increases in symptomatic patients.
Implications:
- Surgical intervention provides effective symptom relief and minimal morbidity in children and adolescents with congenital aortic stenosis.
- Despite high operative mortality, surgery is crucial for symptomatic infants due to their poor prognosis.
- Long-term monitoring and potential reoperations are necessary for optimal management of congenital aortic stenosis.
Abstract:
Between September, 1967, and January, 1975, 43 patients underwent intracardiac repair for congenital aortic stenosis at the Buffalo Children's Hospital. The patients ranged in age from 2 days to 24 years, 6 of them being below one year of age. Valvular aortic stenosis was found in 21 cases (4 infants [Group I-A] and 17 older patients [Group I-B]), discrete subaortic membranous diaphragm in 11 (Group II); diffuse subvalvular muscular obstruction in 3 (Group III), supravalvular stenosis in 4 (Group IV), and multiple-level obstruction in 4 (2 infants [Group V-A] and 2 older patients [Group V-B]). Preoperatively, 58 per cent of the patients were symptomatic and 67 per cent had abnormal electrocardiograms. Associated congenital cardiac defects were found in 28 per cent of the cases. The over-all hospital mortality rate was 9 per cent (3 patients in Group I-A and one in Group V-A), with no deaths occurring in patients older than 3 months of age at the time of operation. Two late deaths occurred (Groups I-B and V-B). A complete heart block developed in one patient (Group III). The average intraoperative peak systolic left ventricular-aortic gradient decreased in all groups after repair but progressively increased in the late hemodynamic studies obtained in symptomatic patients. Six patients were reoperated upon for recurrent obstruction. Late results were evaluated on the basis of symptoms, electrocardiographic findings, valve function, and hemodynamic data. They showed excellent or satisfactory results in 59 per cent of the patients in Group I-B, in 45 per cent in Group II, in 66 per cent in Group III, and in 25 per cent in Group I-V. Results were fair or poor in Groups, I-A, V-A, and V-B. In children and adolescents, effective relief of the obstruction and of the symptoms can be obtained with minimal operative risk and minimal morbidity. In symptomatic infants, despite the high operative mortality rate, surgical intervention is indicated because of the poor prognosis.
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