450 consecutive patients in high operative risk underwent TAVI with the Medtronic Corevalve (Medtronic, Minneapolis, MN, USA) or Edwards Sapien (Edwards Lifesience, Irvine, CA, USA) prostheses at our institution between June 2008 and February 2012. Full data of 341 patients was collected. Of these, 190 patients presented with normal-flow, high gradient (NFHG) AS (aortic surface area (ASA) < 1.0 cm2, mean gradient (ΔPmean) > 30 mmHg, left ventricular ejection fraction (LVEF) > 50%) and 28 patients with PLFLG AS (ASA < 1.0 cm2, ΔPmean < 30 mmHg, LVEF > 50%, stroke volume index (SVI) < 35 ml/m2). Clinical follow-up, echocardiography and measurements of NT-pro-BNP levels were analyzed at 10 days, 4 weeks, 6 month and 1 year after TAVI.