A Real World 10-Year Experience With Vascular Closure Devices and Large-Bore Access in Patients Undergoing Transfemoral Transcatheter Aortic Valve Implantation.
TAVR
VARC III
bleeding
hematoma
pseudoaneurysm
sheath size
vascular closure device
vascular complication
Journal
Frontiers in cardiovascular medicine
ISSN: 2297-055X
Titre abrégé: Front Cardiovasc Med
Pays: Switzerland
ID NLM: 101653388
Informations de publication
Date de publication:
2021
2021
Historique:
received:
08
10
2021
accepted:
17
12
2021
entrez:
7
2
2022
pubmed:
8
2
2022
medline:
8
2
2022
Statut:
epublish
Résumé
Transcatheter aortic valve replacement (TAVR) has established itself as a safe and efficient treatment option in patients with severe aortic valve stenosis, regardless of the underlying surgical risk. Widespread adoption of transfemoral procedures led to more patients than ever being eligible for TAVR. This increase in procedural volumes has also stimulated the use of vascular closure devices (VCDs) for improved access site management. In a single-center examination, we investigated 871 patients that underwent transfemoral TAVR from 2010 to 2020 and assessed vascular complications according to the Valve Academic Research Consortium (VARC) III recommendations. Patients were grouped by the VCD and both, vascular closure success and need for intervention were analyzed. In case of a vascular complication, the type of intervention was investigated for all VCDs. The Proglide VCD was the most frequently used device (
Identifiants
pubmed: 35127860
doi: 10.3389/fcvm.2021.791693
pmc: PMC8814307
doi:
Types de publication
Journal Article
Langues
eng
Pagination
791693Informations de copyright
Copyright © 2022 Heitzinger, Brunner, Koschatko, Dannenberg, Mascherbauer, Halavina, Doná, Koschutnik, Spinka, Nitsche, Mach, Andreas, Wolf, Loewe, Neumayer, Gschwandtner, Willfort-Ehringer, Winter, Lang, Bartko, Hengstenberg and Goliasch.
Déclaration de conflit d'intérêts
MA has received institutional research funding (Edwards, Abbott, Medtronic, LSI) and has served as a proctor/speaker/consultant (Edwards, Abbott, Medtronic). The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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