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. 2018 Jul 12;5:92. doi: 10.3389/fcvm.2018.00092

Table 1.

Results of major prospective randomized trials on TAVI vs. SAVR in high and intermediate to low risk patients.

PARTNER 1A (6) CoreValve HR (7) PARTNER 2A (10) NOTION (9) SURTAVI (8)
Time of recruitment May 2007–August 2009 February 2011–December 2012 December 2011 –November 2013 December 2009–April 2013 June 2012 –June 2016
THV SAPIEN CoreValve SAPIEN XT CoreValve CoreValve
Primary endpoint All-cause death at 1 year All-cause death at 1 year All-cause death or diasbling stroke at 2 years All-cause death, disabling stroke or myocardial infarction at 1 year All-cause death or disabling stroke at 2 years
TAVI SAVR p TAVI SAVR p TAVI SAVR p TAVI SAVR p TAVI SAVR 95% CI
Number of randomized pts. 348 351 n/a 394 401 n/a 1,011 1,021 n/a 145 135 n/a 864 796 n/a
Age 83.6 ± 6.8 84.5 ± 6.4 0.07 83.2 ± 7.1 83.5 ± 6.3 n/a 81.5 ± 6.7 81.7 ± 6.7 n/a 79.2 ± 4.9 79.0 ± 4.7 n/a 79.9 ± 6.2 79.7 ± 6.1 n/a
Male gender 57.8% 56.7% 0.82 53.6% 52.9% n/a 54.2% 54.8% n/a 53.8% 52.6% n/a 57.6% 55.0% n/a
STS-PROM (%) 11.8 ± 3.3 11.7 ± 3.5 0.61 7.3 ± 3.0 7.5 ± 3.2 n/a 5.8 ± 2.1 5.8 ± 1.9 n/a 2.9 ± 1.6 3.1 ± 1.7 n/a 4.4 ± 1.5 4.5 ± 1.6 n/a
Log. EuroSCORE (%) 29.3 ± 16.5 29.2 ± 15.6 0.93 17.6 ± 13.0 18.4 ± 12.8 n/a n/a n/a n/a 8.4 ± 4 8.9 ± 5.5 n/a 11.9 ± 7.6 11.6.8.0 n/a
Transfemoral access 70.1% n/a 76.3% 96.5% 93.6%
Primary endpoint 24.2% 26.8% 0.44 14.2% 19.1% 0.04 19.3% 21.1% 0.25 13.1% 16.3% 0.43 12.6% 14.0% −5.2 to 2.3
All-cause mortality (30 days) 3.4% 6.5% 0.07 3.3% 4.5% n/a 3.9% 4.1% 0.78 2.1% 3.7% 0.43 2.2% 1.7% −0.9 to 1.8
All-cause mortality (1 year) 24.2% 26.8% 0.44 14.2% 19.1% 0.004 12.3% 12.9% 0.69 4.9% 7.5% 0.38 6.7% 6.8% −2.7 to 2.4
All-cause mortality (2 years) 33.9% 35.0% 0.78 22.2% 28.6% 0.04 16.7% 18.0% 0.45 8.0% 9.8% 0.54 11.4% 11.6% −3.8 to 3.3
Stroke (30 days) 3.8% 2.1% 0.2 4.9% 6.2% 0.46 5.5% 6.1% 0.57 1.4% 3.0% 0.37 3.4% 5.6% −4.2 to−0.2
Myocardial infarction (30 days) 0 0.6% 0.16 0.8% 0.8% 0.92 1.2% 1.9% 0.22 2.8% 6.0% 0.2 0.9% 1.0% −1.0 to 0.9
Major vascular complications (30 days) 11.0% 3.2% <0.001 5.9% 1.7% 0.003 7.9% 5.0% 0.008 5.6% 1.5% 0.1 6.0% 1.0% 3.2 to 6.7
Major or life-threatening bleeding (30 days) 9.3% 3.2% <0.001 13.6% 35.0% <0.001 10.4% 43.4% <0.001 11.3% 20.9% 0.03 12.2% 9.3% −0.1 to 5.9
New permanent pacemaker (30 days) 3.8% 3.6% 0.89 19.8% 7.1% <0.001 8.5% 6.9% 0.17 34.1% 1.6% <0.001 25.9% 6.6% 15.9–22.7
New-onset atrial fibrillation (30 days) 8.6% 16.0% 0.006 11.7% 30.5% <0.001 9.1% 26.4% <0.001 16.9% 57.8% 0.001 12.9% 43.3% −34.7 to −26.4
Acute kidney injury (30 days) 1.2% 1.2% 0.95 6.0% 15.1% <0.001 1.3% 3.1% 0.006 0.7% 6.7% 0.01 1.7% 4.4% −4.4 to −1.0
Moderate or severe PVL (1 year) 6.8% 1.9% <0.001 6.1% 0.5% <0.001 3.4% 0.4% <0.001 15.7% 0.9% 0.001 5.3% 0.6% n/a
Rehospitalization (2 years) 24.7% 21.7% 0.41 n/a n/a 19.6% 17.3% 0.22 n/a n/a 13.2% 9.7% 0.1–7.0
Endocarditis (2 years) 1.5% 1.0% 0.61 0.9% 1.7% 0.35 1.2% 0.7% 0.22 n/a n/a n/a n/a
AV reintervention (2 years) n/a n/a 2.5% 0.4% 0.02 1.4% 0.6% 0.09 n/a n/a 2.7% 0.7% 0.6–3.4

AV, aortic valve; CI, confidence interval; LogES, logistic EuroSCORE; PVL, paravalvular leakage; SAVR, surgical aortic valve replacement; STS-PROM, Society of Thoracic Surgeons predicted risk of operative mortality; TAVI, transcatheter aortic valve intervention; THV, transcatheter heart valve. Values are given as mean ± standard deviation or frequencies and percentages.