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Authors
Chiarini, Giovanni
Mariani, Silvia
Schaefer, Anne-Kristin
van Bussel, Bas C. T.
Di Mauro, Michele
Wiedemann, Dominik
Saeed, Diyar
Pozzi, Matteo
Botta, Luca
Boeken, Udo
Samalavicius, Robertas
Bounader, Karl
Hou, Xiaotong
Bunge, Jeroen J. H.
Buscher, Hergen
Salazar, Leonardo
Meyns, Bart
Herr, Daniel
Matteucci, Sacha
Sponga, Sandro
Ramanathan, Kollengode
Russo, Claudio
Formica, Francesco
Sakiyalak, Pranya
Fiore, Antonio
Camboni, Daniele
Raffa, Giuseppe Maria
Diaz, Rodrigo
Wang, I-wen
Jung, Jae-Seung
Belohlavek, Jan
Pellegrino, Vin
Bianchi, Giacomo
Pettinari, Matteo
Barbone, Alessandro
Garcia, José P.
Shekar, Kiran
Whitman, Glenn J. R.
Lorusso, Roberto
,
Heuts, Samuel
Conci, Luca
Khalil, Jawad
Lehmann, Sven
Obadia, Jean-Francois
Loforte, Antonio
Pacini, Davide
Kalampokas, Nikolaos
Jankuviene, Agne
Bounader, Karl
Flecher, Erwan
Dos Reis Miranda, Dinis
Sriranjan, Kogulan
Mazzeffi, Michael A.
Di Eusanio, Marco
Vendramin, Igor
MacLaren, Graeme
Sorokin, Vitaly
Costetti, Alessandro
Schmid, Chistof
Castillo, Roberto
Grus, Tomas
Solinas, Marco
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Article History
Received: 5 June 2024
Accepted: 27 July 2024
First Online: 7 August 2024
Declarations
:
: Institutional Review Board (IRB) approval was required for all centers, based on the IRB-approval of the coordinating center (MUMC + , number: METC-2018-0788, date: December 19th, 2018). The study was registered at ClinicalTrials.gov (trial registration ID: NCT03857217). Need for informed consent was waived based on the retrospective nature of the study, the emergency of the performed procedure, and the pseudonymization of shared data. The current study was conducted in accordance with the Declaration of Helsinki.
: Not applicable.
: DW: consultant/proctor for Abbott; scientific advisor for Xenios. RL: consultant for Medtronic, Getinge and LivaNova; Advisory Board Member of Eurosets (honoraria paid as research funding). KR: received honoraria from Baxter and Fresenius Ltd for educational lectures.
