While surgical aortic valve replacement has been an extraordinarily effective treatment for symptomatic aortic stenosis, it has been estimated that over 40% of patients with this condition go untreated. 1 Many of these face prohibitive operative risk, due to a number of factors such as porcelain aorta, cirrhosis, severe emphysema, and other comorbidities. Recently, transfemoral transcatheter aortic valve implantation (TAVI) has demonstrated clinical benefit in a patient population at prohibitively high risk for complications following traditional surgical valve implantation. 2 The initial application of this technology in human patients utilized an antegrade approach via the femoral vein, a transseptal puncture, and guidance of the prosthesis across the mitral valve and out through the left ventricular outflow tract. 3 Although this approach avoids the complications associated with large-bore access of the iliofemoral arterial system, it proved cumbersome for most operators and was associated with a high risk of other major complications, includingcardiacperforationandmajorstructuraldamageto the mitral valve. In recent years, TAVI procedures with a balloon-expandable system have been performed retrograde either through a transfemoral arterial approach (TF) or through a transapical approach involving a limited left thoracotomy and exposure of the apex of the heart. For the purposes of this article, we focusontheTFtechniqueusingtheEdwardsSapienballoonexpandable platform (Fig. 1; Edwards Lifesciences, Irvine, CA). This device is not currently approved for marketing in the United States and is limited to investigational use; it is currently the only device in clinical trial in the United States, although it has been Conformite European (CE) mark approved for use in Europe since September 2007. Another transcatheter aortic valve device, the Medtronic Corevalve (Medtronic, Inc, Minneapolis, MN), has impending clinical trials in the United States and has also received CE mark approval. A number of other innovative transcatheter valve devices are in various stages of preclinical and clinical testing internationally. Because our experience has been solely with the Edwards Sapien device, we limit our discussion to this system. The preoperative steps of this procedure, other than general patient selection, include proper evaluation of iliofemoral and aortic access for retrograde device deployment and accurate annulus sizing. The critical procedural steps include the following: reassessment of annular size, vascular access, accurate valve positioning, reliable rapid ventricular pacing, valve deployment, valve assessment, and control of vascular access and closure. The procedural steps of retrograde valve positioning and deployment have been well described 4 and we focus much of this discussion on our technique for total percutaneous device placement. These techniques can also prove useful for other largebore arterial access systems, such as endovascular aortic stent-graft placement.