Safety and efficacy of the Amplatzer™ Trevisio™ intravascular delivery system: Post-approval study results.

Hascoet, Sebastien; Baruteau, Alban-Elouen; Jalal, Zakaria; Demkow, Marcin; de Winter, Robbert; Gaio, Gianpiero; Clerc, Jean-Michel; Sabiniewicz, Robert; Eberli, Franz; Santoro, Giuseppe; Dauphin, Claire; Schubert, Stephan; Smolka, Grzegorz; Lutz, Matthias; Moreno, Raul; Pan, Manuel; Gutierrez-Larraya, Federico; Godart, Francois; Carminati, Mario; Ovaert, Caroline; Batteux, Clement; Guerin, Patrice; Thambo, Jean-Benoit; Ewert, Peter

doi:10.1016/j.acvd.2023.10.006

journal article

Titel:: Safety and efficacy of the Amplatzer™ Trevisio™ intravascular delivery system: Post-approval study results.
Dokumenttyp:: Article; Observational Study; Journal Article
Autor(en):: Hascoet, Sebastien; Baruteau, Alban-Elouen; Jalal, Zakaria; Demkow, Marcin; de Winter, Robbert; Gaio, Gianpiero; Clerc, Jean-Michel; Sabiniewicz, Robert; Eberli, Franz; Santoro, Giuseppe; Dauphin, Claire; Schubert, Stephan; Smolka, Grzegorz; Lutz, Matthias; Moreno, Raul; Pan, Manuel; Gutierrez-Larraya, Federico; Godart, Francois; Carminati, Mario; Ovaert, Caroline; Batteux, Clement; Guerin, Patrice; Thambo, Jean-Benoit; Ewert, Peter
Abstract:: BACKGROUND: The Amplatzer™ Trevisio™ Intravascular Delivery System (Trevisio DS; Abbott Laboratories, Chicago, IL, USA) facilitates the delivery of Amplatzer™ Occluders and features an ultraflexible tip, which improves assessment of occluder position before release. AIMS: To assess the safety and efficacy of the Trevisio DS for transcatheter closure of patent foramen ovale and atrial septal defect. METHODS: The Amplatzer™ Trevisio™ Intravascular Delivery System Post-Approval Study was a prospective, postmarket, single-arm, multicentre, observational study of the Trevisio DS. Enrolled patients were indicated for transcatheter closure of patent foramen ovale or atrial septal defect. In all procedures, the Trevisio DS was used to deliver Amplatzer™ Occluders. Technical success was defined as successful deployment and release of at least one occluder. Device- or procedure-related serious adverse events were tracked until discharge or day 7, whichever occurred earlier. RESULTS: The study enrolled 144 patients with patent foramen ovale and 107 patients with atrial septal defect at 22 European sites; 53 patients with atrial septal defect (49.6%) were aged<18years. The rate of technical success was 98.4% (97.2% for atrial septal defect, 99.3% for patent foramen ovale). There was one serious adverse event (0.4%), an acute periprocedural device embolization that occurred after occluder release in a patient with atrial septal defect; the device was retrieved percutaneously. This was determined by the implanter to be unrelated to the performance of the Trevisio DS. CONCLUSIONS: The Trevisio DS exhibited a high rate of technical success and an excellent safety profile during transcatheter closure of patent foramen ovale and atrial septal defect.
Zeitschriftentitel:: Arch Cardiovasc Dis
Jahr:: 2023
Band / Volume:: 116
Heft / Issue:: 12
Seitenangaben Beitrag:: 580-589
Volltext / DOI:: doi:10.1016/j.acvd.2023.10.006
PubMed:: http://view.ncbi.nlm.nih.gov/pubmed/37951755
Print-ISSN:: 1875-2136
TUM Einrichtung:: Klinik für Kinderkardiologie und angeborene Herzfehler (DHM) (Prof. Ewert)
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mediaTUM Gesamtbestand Einrichtungen Schools TUM School of Medicine and Health Departments Clinical Medicine Lehr- und Forschungskooperationen mit den Kliniken und Instituten am Deutschen Herzzentrum Klinik für Kinderkardiologie und angeborene Herzfehler (DHM) (Prof. Ewert)2023