Dual ProGlide versus ProGlide and FemoSeal for vascular access haemostasis after transcatheter aortic valve implantation

Large-bore arteriotomy for transcatheter aortic valve implantation (TAVI) requires percutaneous vascular closure devices, but real-world data comparing different closure strategies are limited. We sought to compare a dual ProGlide strategy vs a combination of one ProGlide and one FemoSeal for vascul...

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Veröffentlicht in:EuroIntervention 2022-11, Vol.18 (10), p.812-819
Hauptverfasser: Gmeiner, Jonas M D, Linnemann, Marie, Steffen, Julius, Scherer, Clemens, Orban, Martin, Theiss, Hans, Mehilli, Julinda, Sadoni, Sebastian, Peterß, Sven, Joskowiak, Dominik, Hagl, Christian, Tsilimparis, Nikolaos, Curta, Adrian, Maurus, Stefan, Doldi, Philipp M, Löw, Kornelia, Haum, Magda, Roden, Daniel, Hausleiter, Jörg, Massberg, Steffen, Rizas, Konstantinos, Deseive, Simon, Braun, Daniel
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Sprache:eng
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Zusammenfassung:Large-bore arteriotomy for transcatheter aortic valve implantation (TAVI) requires percutaneous vascular closure devices, but real-world data comparing different closure strategies are limited. We sought to compare a dual ProGlide strategy vs a combination of one ProGlide and one FemoSeal for vascular closure after TAVI. We retrospectively analysed 874 propensity score-matched patients undergoing TAVI at the Munich University Hospital from August 2018 to October 2020. From August 2018 to August 2019, a dual ProGlide strategy was used for vascular closure. From October 2019 to October 2020, a combination of one ProGlide and one FemoSeal was used. The primary endpoint was defined as access-related major vascular complications or bleeding ≥Type 2 according to Valve Academic Research Consortium 3 criteria. Patients in the dual ProGlide group (n=437) had a higher incidence of the primary endpoint than patients treated with one ProGlide and one FemoSeal (n=437; 11.4% vs 3.0%; p
ISSN:1774-024X
1969-6213
DOI:10.4244/EIJ-D-22-00311