TY - JOUR
T1 - Three-Year Outcomes With a Contemporary Self-Expanding Transcatheter Valve From the Evolut PRO US Clinical Study
AU - Wyler von Ballmoos, Moritz C.
AU - Reardon, Michael J.
AU - Williams, Mathew R.
AU - Mangi, Abeel A.
AU - Kleiman, Neal S.
AU - Yakubov, Steven J.
AU - Watson, Daniel
AU - Kodali, Susheel
AU - George, Isaac
AU - Tadros, Peter
AU - Zorn, George L.
AU - Brown, John
AU - Kipperman, Robert
AU - Oh, Jae K.
AU - Qiao, Hongyan
AU - Forrest, John K.
N1 - Funding Information:
Dr. von Ballmoos serves as a consultant and on an advisory board to Boston Scientific and LivaNova and as a proctor for LivaNova; Dr. Reardon has received fees to his institution from Medtronic for consulting and providing educational services; Dr. Williams serves as a consultant for Edwards Lifesciences and Medtronic; as a speaker for Abbott Laboratories; and has received research grants from Medtronic. Dr. Forrest has received grant support/research contracts and consultant fees/honoraria/speakers' bureau fees from Edwards Lifesciences and Medtronic; Dr. Mangi has received speaking fees and consulting fees from Thoratec Corporation; and speaking, training, and proctoring fees from Medtronic Corporation and Edwards LifeSciences; Dr. Kleiman has received fees for providing educational services from Medtronic. Dr. Yakubov has received institutional research grants from Medtronic and Boston Scientific; and serves on an advisory board for Medtronic and Boston Scientific; Dr. Watson serves on the speakers' bureau and is a proctor for Boston Scientific, Edwards, Medtronic, and Liva Nova; Dr. Kodali has received grant/research support from Boston Scientific, Claret Medical, Edwards Lifesciences, and Medtronic; serves on the steering committee for Claret Medical, Edwards Lifesciences, and Meril; holds equity in Thubrikar Aortic Valve and Dura Biotech; and received honoraria from Claret Medical and St. Jude Medical; Dr. George is a consultant for CardioMech, Vdyne, WL Gore and Atricure; Dr. Tadros is a consultant and proctor and has received research support from Medtronic and St. Jude Medical; Dr. Zorn receives consulting fees from Medtronic; Dr. Kipperman is a consultant for Medtronic; Dr. Oh is the director of the echocardiographic core laboratory for the Evolut PRO US Study; Dr. Qiao is an employee and shareholder of Medtronic, plc; Dr. Forrest has received grant support/research contracts and consultant fees/honoraria/speakers' bureau fees from Edwards Lifesciences and Medtronic. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose.
Publisher Copyright:
© 2020 Elsevier Inc.
PY - 2021/5
Y1 - 2021/5
N2 - Background: Paravalvular regurgitation (PVR) following transcatheter aortic valve replacement (TAVR) is associated with increased morbidity and mortality. PVR continues to plague TAVR jeopardizing long-term results. New device iterations, such as the self-expandable Evolut PRO valve, aim to decrease PVR while maintaining optimal hemodynamics. This study sought to evaluate clinical and hemodynamic performance of the Evolut PRO system at 3 years. Methods: The Evolut PRO US Clinical Study included 60 patients at high or extreme surgical risk undergoing TAVR with the Evolut PRO valve at 8 centers in the United States. Clinical outcomes were evaluated using Valve Academic Research Consortium (VARC)-2 criteria and included all-cause mortality, cardiovascular mortality, disabling stroke and valve complications. An independent core laboratory centrally assessed all echocardiographic measures. Results: At 3 years, all-cause mortality was 25.8% (cardiovascular mortality 16.5%) and the disabling stroke rate was 10.7%. There were no cases of repeat valve intervention, endocarditis or coronary obstruction. Valve thrombosis was identified in 1 patient 2 years post-procedure and was treated medically. Hemodynamics at 3 years included a mean gradient of 7.2 ± 4.5 mm Hg, an effective orifice area of 2.0 ± 0.5 cm2, and 88.2% of patients had no or trace PVR. The remaining patients had mild PVR. Most of the surviving patients (80.6%) had New York Heart Association class I symptoms at 3 years. Conclusion: Outcomes at 3-years following TAVR with a contemporary self-expanding prosthesis are favorable, with no signal of valve deterioration, excellent hemodynamics including very low prevalence of PVR.
AB - Background: Paravalvular regurgitation (PVR) following transcatheter aortic valve replacement (TAVR) is associated with increased morbidity and mortality. PVR continues to plague TAVR jeopardizing long-term results. New device iterations, such as the self-expandable Evolut PRO valve, aim to decrease PVR while maintaining optimal hemodynamics. This study sought to evaluate clinical and hemodynamic performance of the Evolut PRO system at 3 years. Methods: The Evolut PRO US Clinical Study included 60 patients at high or extreme surgical risk undergoing TAVR with the Evolut PRO valve at 8 centers in the United States. Clinical outcomes were evaluated using Valve Academic Research Consortium (VARC)-2 criteria and included all-cause mortality, cardiovascular mortality, disabling stroke and valve complications. An independent core laboratory centrally assessed all echocardiographic measures. Results: At 3 years, all-cause mortality was 25.8% (cardiovascular mortality 16.5%) and the disabling stroke rate was 10.7%. There were no cases of repeat valve intervention, endocarditis or coronary obstruction. Valve thrombosis was identified in 1 patient 2 years post-procedure and was treated medically. Hemodynamics at 3 years included a mean gradient of 7.2 ± 4.5 mm Hg, an effective orifice area of 2.0 ± 0.5 cm2, and 88.2% of patients had no or trace PVR. The remaining patients had mild PVR. Most of the surviving patients (80.6%) had New York Heart Association class I symptoms at 3 years. Conclusion: Outcomes at 3-years following TAVR with a contemporary self-expanding prosthesis are favorable, with no signal of valve deterioration, excellent hemodynamics including very low prevalence of PVR.
KW - Outer pericardial wrap
KW - Paravalvular regurgitation
KW - Transcatheter aortic valve implantation
KW - Transcatheter aortic valve replacement
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U2 - 10.1016/j.carrev.2020.11.007
DO - 10.1016/j.carrev.2020.11.007
M3 - Article
C2 - 33199247
AN - SCOPUS:85096369747
VL - 26
SP - 12
EP - 16
JO - Cardiovascular Revascularization Medicine
JF - Cardiovascular Revascularization Medicine
SN - 1553-8389
ER -