Table 2

Procedural details according to device

VariablesTotal population (177)Edwards
SAPIEN
(126)
Medtronic CoreValve (51)p Value
Preventive PCI pre-TAVI, n (%)24 (13.6%)17 (13.5%)7 (13.7%)0.99
Iliac PTA before TAVI, n (%)15 (8.5%)8 (6.3%)7 (13.7%)0.14
PCI during TAVI, n (%)6 (3.4%)3 (2.4%)3 (5.9%)0.54
Valvular pathology, n (%)
 AS142 (80%)115 (91.3%)27 (52.9%) 
 AS+AR25 (14.1%)8 (6.3%)17 (33.3%)
 Degenerated aortic prosthesis (VIV)10 (5.6%)3 (2.4%)7 (13.7%)
Prosthesis size, n (%)
 20 mm1 (0.6%)1 (0.8%)0 
 23 mm56 (31.6%)51 (40.5%)5 (9.8%)
 26 mm74 (41.8%)61 (48.4%)13 (25.5%)
 29 mm38 (21.5%)13 (10.3%)25 (49%)
 31 mm8 (4.5%)08 (15.7%)
Balloon post dilation, n (%)13 (7.3%)4 (3.2%)9 (17.6%)0.002
Conversion to heart surgery, n (%)000
Death during procedure, n (%)000
VARC-2 device non-success, n (%)6 (3.4%)4 (3.2%)2 (3.9%)0.99
  • AR, aortic regurgitation; AS, aortic stenosis; PCI, percutaneous coronary intervention; PTA, percutaneous transluminal angioplasty; VARC-2, Valve Academic Research Consortium; VIV, valve in valve.