TY - JOUR
T1 - Percutaneous transcatheter aortic valve implantation
T2 - Past accomplishments, present achievements and applications, future perspectives
AU - Bande, Marta
AU - Michev, Iassen
AU - Sharp, Andrew S P
AU - Chieffo, Alaide
AU - Colombo, Antonio
PY - 2010/5
Y1 - 2010/5
N2 - Surgical aortic valve replacement remains the gold standard for the treatment of severe, symptomatic aortic stenosis. However, percutaneous treatments are challenging this paradigm in high-risk surgical patients. Technological developments have been rapid in the field of percutaneous aortic valve intervention. Two devices have been approved for general use in Europe: the Edwards SAPIEN™ valve (Edwards Lifesciences, Irvine, CA) and the CoreValve ReValving® System (CoreValve ReValving® Technology Medtronic Inc., Minneapolis, MN), with 15 potential new designs for percutaneous aortic valves in development around the world. Both systems can be delivered via the transfemoral, transapical and the axillary/subclavian routes, depending upon patient characteristics, anatomy, and the device available to the operator. Careful selection of appropriate patients is essential to ensure a safe procedure. This necessitates a multidisciplinary approach, with multiple imaging modalities used to fully delineate the peripheral vasculature, aortic anatomy and the valve itself. It is important to remember, however, that just because we can treat aortic valve disease percutaneously, it does not mean that we necessarily should. The gold standard treatment for aortic stenosis remains thoracotomy and surgical replacement of the valve; to this end it is essential that surgeons play a central role in the decision-making processes for transcatheter aortic valve implantation and that they embrace this new and exciting technology, which promises to dramatically change the way their high-risk aortic valve patients are managed over the course of the next 10 years.
AB - Surgical aortic valve replacement remains the gold standard for the treatment of severe, symptomatic aortic stenosis. However, percutaneous treatments are challenging this paradigm in high-risk surgical patients. Technological developments have been rapid in the field of percutaneous aortic valve intervention. Two devices have been approved for general use in Europe: the Edwards SAPIEN™ valve (Edwards Lifesciences, Irvine, CA) and the CoreValve ReValving® System (CoreValve ReValving® Technology Medtronic Inc., Minneapolis, MN), with 15 potential new designs for percutaneous aortic valves in development around the world. Both systems can be delivered via the transfemoral, transapical and the axillary/subclavian routes, depending upon patient characteristics, anatomy, and the device available to the operator. Careful selection of appropriate patients is essential to ensure a safe procedure. This necessitates a multidisciplinary approach, with multiple imaging modalities used to fully delineate the peripheral vasculature, aortic anatomy and the valve itself. It is important to remember, however, that just because we can treat aortic valve disease percutaneously, it does not mean that we necessarily should. The gold standard treatment for aortic stenosis remains thoracotomy and surgical replacement of the valve; to this end it is essential that surgeons play a central role in the decision-making processes for transcatheter aortic valve implantation and that they embrace this new and exciting technology, which promises to dramatically change the way their high-risk aortic valve patients are managed over the course of the next 10 years.
KW - Aortic stenosis
KW - Percutaneous transcatheter aortic valve replacement
KW - Valvuloplasty
UR - http://www.scopus.com/inward/record.url?scp=77951470135&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=77951470135&partnerID=8YFLogxK
U2 - 10.1097/CRD.0b013e3181c42627
DO - 10.1097/CRD.0b013e3181c42627
M3 - Article
C2 - 20395696
AN - SCOPUS:77951470135
VL - 18
SP - 111
EP - 124
JO - Cardiology in Review
JF - Cardiology in Review
SN - 1061-5377
IS - 3
ER -