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Characterization and risk factors for aortic dilatation in pediatric patients with bicuspid aortic valve
Anna Sabaté-Rotés1, Laura Sabidó Sanchez1, Ferran Gran Ipiña1
1Cardiología Pediátrica, Hospital Universitari Vall d'Hebron, Universitat Autònoma de Barcelona, Barcelona, España.
Insights
Pediatric patients with bicuspid aortic valve often experience aortic dilatation, particularly of the ascending aorta. Early medical follow-up is crucial for managing this common valve impairment.
Area of Science:
- Cardiovascular Medicine
- Pediatric Cardiology
- Medical Genetics
Background:
- Bicuspid aortic valve (BAV) is a common congenital heart defect associated with aortic dilatation, a significant cause of morbidity and mortality.
- Ascending aortic dilatation in adults with BAV is well-documented, but pediatric involvement requires further characterization.
Purpose of the Study:
- To identify the prevalence and characteristics of aortic involvement in pediatric patients with BAV.
- To determine risk factors associated with aortic dilatation in this population.
Main Methods:
- Retrospective analysis of aortic measurements in pediatric patients with BAV from 1997-2015.
- Exclusion of patients with syndromic aortic dilatation.
Main Results:
- Aortic dilatation (z-score>2) was observed in over one-third of 206 pediatric BAV patients.
- Ascending aorta was primarily affected (70/80 patients), with the aortic root often spared.
- Absence of coarctation and a vertical valve opening pattern were associated with ascending aorta dilatation.
Conclusions:
- Pediatric patients with BAV frequently exhibit aortic dilatation, particularly of the ascending aorta.
- Regular medical follow-up is essential for early detection and management of aortic abnormalities in these children.
- Identifying risk factors like valve opening pattern can aid in risk stratification.
Introduction And Objectives:
Dilatation of the ascending aorta associated with bicuspid aortic valve is a major cause of morbidity and mortality in adults. The main objective was to recognize the aortic involvement in children, its characteristics and risk factors.
Methods:
Aortic measures of all pediatric patients with bicuspid aortic valve followed in a tertiary pediatric hospital between 1997 and 2015 were retrospectively taken. Patients with syndromes associated with aortic dilatation were excluded (n=17).
Results:
Two hundred and six patients were included, 67.9% males. The commonest opening pattern was horizontal: 137 (66.7%). Half of the patients (101) had a history of surgical aortic coarctation, 46 (22.3%) had≥moderate aortic valve stenosis and 13 (6%) had≥moderate aortic insufficiency. Mean follow-up time was 6.1 (4.9) years; diagnosis of aortic dilatation was made during the first year of follow-up. Progression of the dilatation of the ascending aorta was noted in 17.1%, and of the aortic root in 2.5%. More than one-third (80/206) had aortic dilatation (z-score>2). The ascending aorta was exclusively affected in 70/80 patients, with sparing of the aortic root. In the multivariate analysis, patients with dilatation of the ascending aorta were associated with absence of coarctation (P=.001) and vertical opening pattern (P=.007).
Conclusions:
Pediatric patients with bicuspid aortic valve warrant medical follow-up for the frequent association with valve impairment and/or dilatation of the ascending aorta.
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