Transcatheter aortic valve replacement (TAVI) is an established treatment for inoperable patients or patients at high surgical risk with severe aortic stenosis. Herein, we illustrate the key design features of the main new generation devices that are entering contemporary clinical practice, the labeled and off-labeled indications, the basic principles of screening process, and the clinical outcomes of the TAVI procedure.Answer questions and earn CME: https://wileyhealthlearning.com/Activity2/ 4193543/Activity.aspx
TAVI New TechnologyDespite growing experience with transcatheter aortic valve replacement (TAVI) the first-generation devices were associated with several limitations such as: valve malpositioning, vascular complications, paravalvular regurgitation (PVR), and conduction disorders [1,2]. Several new generation TAVI devices (Table 1), aimed at addressing these issues.
Medtronic Evolut-R TMThe Evolut-R TM is the new iteration of the Medtronic CoreValve â (MCV), ( Figure 1A). Several key features of the MCV have been preserved, namely the trileaflet porcine pericardial tissue, the supra-annular position of the valve leaflets, the self-expanding nitinol stent frame and the architecture in three levels of function: inflow portion with a high radial force for anchoring within the aortic annulus, mid portion with a constrained structure for preservation of the coronary flow, and outflow portion with a high hoop strength for coaxiality with the aortic root. However, the new generation Evolut-R TM presents several improvements namely:) the inflow portion is wider and more cylindrical providing a flatter landing zone to ensure maximum over-sizing within the full target implant depth range, (iii) the geometry of the distal diamond cell of the inflow portion has been modified with a slightly asymmetric configuration and extended length for better conformability and consistent radial force across a range of annulus sizes, (iv) the distal skirt has been extended with a scalloped design creating a longer landing zone for better sealing, (v) the prosthesis is fully repositionable and retrievable before final detachment of the hooks (up to three times) and, (vi) the 14 Fr profile of the delivery system (true outer diameter 18 Fr), with the option of proceeding to sheath-less procedures reduces the rate of vascular complications. At the moment the device is available in three sizes (23, 26, and 29 mm) covering aortic annuli from 18 to 26 mm. In addition, whereas positioning of the actual MCV can be sometimes challenging, the 1:1 ratio applied to the handle and prosthesis unsheathing-resheathing response aims at ª 2016 Hellenic College of Cardiology