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. 2016 Aug 16;3(2):e000420. doi: 10.1136/openhrt-2016-000420

Table 2.

Procedural details according to device

Variables Total 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 (%)
 AS 142 (80%) 115 (91.3%) 27 (52.9%)  
 AS+AR 25 (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 mm 1 (0.6%) 1 (0.8%) 0  
 23 mm 56 (31.6%) 51 (40.5%) 5 (9.8%)
 26 mm 74 (41.8%) 61 (48.4%) 13 (25.5%)
 29 mm 38 (21.5%) 13 (10.3%) 25 (49%)
 31 mm 8 (4.5%) 0 8 (15.7%)
Balloon post dilation, n (%) 13 (7.3%) 4 (3.2%) 9 (17.6%) 0.002
Conversion to heart surgery, n (%) 0 0 0
Death during procedure, n (%) 0 0 0
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.