Reijnen, Michel M. P. J. http://orcid.org/0000-0002-5021-1768
van Wijck, Iris
Brodmann, Marianne
Micari, Antonio
Torsello, Giovanni
Rha, Seung-Woon
Menk, Jeremiah
Zeller, Thomas
,
Funding for this research was provided by:
Medtronic
Article History
Received: 19 January 2023
Accepted: 24 May 2023
First Online: 1 August 2023
Declarations
:
: Michel M. P. J. Reijnen, MD, PhD, is a consultant for Bentley Innomed, Medtronic, Terumo Aortic, and W.L. Gore and Associates. Iris Van Wijck, MD, has nothing to disclose. Marianne Brodmann, MD, received speaking honoraria from Bard Peripheral Vascular, Biotronik, Medtronic, Spectranetics, and VIVA Physicians and is a consultant for Bard Peripheral Vascular, Biotronik, Medtronic, and Spectranetics. Antonio Micari, MD, PhD, is a compensated consultant for Medtronic and Boston Scientific Corp. Giovanni Torsello, MD, received grants and speaking honoraria from Biotronik, Boston Scientific Corp., Cordis, W.L. Gore & Associates and Medtronic. Seung-Woon Rha, MD, PhD, has nothing to disclose. Jeremiah Menk, MS, is a full-time employee of Medtronic. Thomas Zeller, MD, PhD, received speaking honoraria from Abbott Vascular, Bard Peripheral Vascular, Biotronik, Boston Scientific Corp, Cook Medical, Cordis, GLG, W.L. Gore & Associates, Medtronic, Philips, Spectranetics, Straub Medical, TriReme, Veryan, and VIVA Physicians; he is a consultant for Abbott Vascular, Bard Peripheral Vascular, Boston Scientific Corp, Cook Medical, W.L. Gore & Associates, Medtronic, and Spectranetics; and his clinic has received study funds or funds for research or clinical trials from 480 Biomedical, Abbott Vascular, B. Braun, Bard Peripheral Vascular, Bayer Pharma, Biotronik, Caveo Med, Contego Medical, Cook Medical, CSI, W.L. Gore & Associates, Innora, Intact Vascular, Medtronic, Mercator, Philips, Pluristem, Shockwave, Spectranetics, Terumo, TriReme, and Veryan.
: For this type of study consent for publication is not required.
: All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. The Institutional Review Board or Ethics Committee at each study site approved the study protocol.
: Informed consent was obtained from all individual participants included in the study.