This study evaluates the effectiveness and safety of Percutaneous Device Closure for Significant Paravalvular Leakage after transcatheter or surgical valve replacement.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
percutaneous transcatheter approach into cardiac valve
Asan Medical Center
Seoul, South Korea
Degree of para-valvular leakage
classified as none, mild, moderate or severe by doppler echocardiography according to Valve Academic Research Consortium-2(VARC-2)
Time frame: 1 month
Event rate of all cause death
Time frame: up to 5 years
Event rate of cardiac death
Time frame: up to 5 years
Event rate of stroke
Time frame: up to 5 years
Event rate of myocardial infarction
Time frame: up to 5 years
Event rate of rehospitalization
Time frame: up to 5 years
Event rate of infection
Valve related infection or infective endocarditis
Time frame: up to 5 years
Event rate of acute kidney injury
Time frame: 1 month
Event rate of vascular complication
Time frame: 1 month
Event rate of bleeding
Time frame: 1 month
Event rate of device success
Time frame: 1 month
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.