TY - JOUR
T1 - Mid-term outcomes in patients following transcatheter aortic valve implantation in the CoreValve Australia and New Zealand Study
AU - Meredith, Ian T
AU - Walton, Antony
AU - Walters, Darren L
AU - Pasupati, Sanjeevan
AU - Muller, David
AU - Worthley, Stephen Grant
AU - Yong, Gerald
AU - Whitbourn, Robert
AU - Duffy, Stephen James
AU - Ormiston, John A
PY - 2015
Y1 - 2015
N2 - BACKGROUND: Although numerous studies have reported the safety and effectiveness of transcatheter aortic valve implantation (TAVI), integration of this therapy into standard of care varies widely by region. We evaluated mid-term follow-up in 540 patients with severe symptomatic AS at high risk of surgical AV replacement, enrolled in the ongoing Medtronic CoreValve Australia-New Zealand Study. METHODS: Between August 2008 and July 2013, 10 centres in Australia/New Zealand enrolled 540 patients, which includes initial use of the CoreValve System for all investigators. Patients were deemed suitable for TAVI based on consensus of a multidisciplinary Heart Team. Primary endpoints were cardiovascular death and major adverse cardiovascular and cerebrovascular events (MACCE) at 30 days. Data were fully monitored, and an independent Clinical Events Committee employed. RESULTS: Baseline characteristics include; 45 female, mean age 84 years, EuroSCORE 17.3+/-10.7 , and 74.9 had New York Heart Association III/IV symptoms. At 30 days, all deaths were cardiovascular (4.1 ); MACCE was 11.5 . At one and two years, all-cause mortality was 11.9 and 21.2 ; cardiovascular mortality, 9.9 and 15.2 ; and stroke, 8.2 and 10.1 , respectively. CONCLUSIONS: Early experience with the CoreValve System in a large cohort of fully-monitored patients was associated with good early- and mid-term safety outcomes.
AB - BACKGROUND: Although numerous studies have reported the safety and effectiveness of transcatheter aortic valve implantation (TAVI), integration of this therapy into standard of care varies widely by region. We evaluated mid-term follow-up in 540 patients with severe symptomatic AS at high risk of surgical AV replacement, enrolled in the ongoing Medtronic CoreValve Australia-New Zealand Study. METHODS: Between August 2008 and July 2013, 10 centres in Australia/New Zealand enrolled 540 patients, which includes initial use of the CoreValve System for all investigators. Patients were deemed suitable for TAVI based on consensus of a multidisciplinary Heart Team. Primary endpoints were cardiovascular death and major adverse cardiovascular and cerebrovascular events (MACCE) at 30 days. Data were fully monitored, and an independent Clinical Events Committee employed. RESULTS: Baseline characteristics include; 45 female, mean age 84 years, EuroSCORE 17.3+/-10.7 , and 74.9 had New York Heart Association III/IV symptoms. At 30 days, all deaths were cardiovascular (4.1 ); MACCE was 11.5 . At one and two years, all-cause mortality was 11.9 and 21.2 ; cardiovascular mortality, 9.9 and 15.2 ; and stroke, 8.2 and 10.1 , respectively. CONCLUSIONS: Early experience with the CoreValve System in a large cohort of fully-monitored patients was associated with good early- and mid-term safety outcomes.
UR - http://www.sciencedirect.com/science/article/pii/S1443950614007318
U2 - 10.1016/j.hlc.2014.09.023
DO - 10.1016/j.hlc.2014.09.023
M3 - Article
SN - 1443-9506
VL - 24
SP - 281
EP - 290
JO - Heart Lung and Circulation
JF - Heart Lung and Circulation
IS - 3
ER -