Prospective Follow-up of a Cohort of Patients With Aortic Valve Bicuspidia: Multicentre Study
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Aortic Valve, Bicuspid
- Sponsor
- Centre Hospitalier Universitaire, Amiens
- Enrollment
- 232
- Locations
- 1
- Primary Endpoint
- Analysis of 10 year mortality in cardiac surgery in a patient with bicuspid
- Status
- Recruiting
- Last Updated
- 3 years ago
Overview
Brief Summary
The aortic valve bicuspidia (BVA) is a congenital condition corresponding to the presence of 2 sigmoids instead of 3. This is the most common cardiac congenital anomaly affecting 0.5 to 2% of the population The general rule. BVA may be associated with structural damage to the ascending aorta, which exposes BVA patients to a risk of developing ascending aortic aneurysm and acute aortic accidents. Recent data from the literature have revealed that the natural history of BVA is marked by a possible development towards significant valvulopathy and / or an ascending aortic aneurysm often requiring surgical treatment. However, the natural history of bicuspid disease remains poorly understood and the prognostic factors for progression to severe valvulopathy and / or aneurysmal dilatation of the ascending aorta remain to be determined.
Investigators
Eligibility Criteria
Inclusion Criteria
- •All patients examined in the echocardiography laboratory whose objective examination was a bicuspid valve of the aortic valve
- •Bicuspidia may be formerly known
Exclusion Criteria
- •Refusal to participate
- •Patients who had already undergone bicuspid surgery or ascending aorta before being examined at the echocardiography laboratory
Outcomes
Primary Outcomes
Analysis of 10 year mortality in cardiac surgery in a patient with bicuspid
Time Frame: 10 years
Analyzing the natural history of Bicuspidia