Procedural outcomes in patients with dual versus single antiplatelet therapy prior to transcatheter aortic valve replacement

Abstract The impact of uninterrupted dual antiplatelet therapy (DAPT) on bleeding events among patients undergoing transcatheter aortic valve replacement (TAVR) has not been well studied. We conducted an analysis of 529 patients who underwent transfemoral TAVR in our centre and were receiving either...

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Autores principales: Hatim Seoudy, Maren Thomann, Johanne Frank, Matthias Lutz, Thomas Puehler, Georg Lutter, Oliver J. Müller, Norbert Frey, Mohammed Saad, Derk Frank
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Publicado: Nature Portfolio 2021
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spelling oai:doaj.org-article:32ac1d08759e417ca4f3fccb15c70f612021-12-02T16:23:42ZProcedural outcomes in patients with dual versus single antiplatelet therapy prior to transcatheter aortic valve replacement10.1038/s41598-021-94599-22045-2322https://doaj.org/article/32ac1d08759e417ca4f3fccb15c70f612021-07-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-94599-2https://doaj.org/toc/2045-2322Abstract The impact of uninterrupted dual antiplatelet therapy (DAPT) on bleeding events among patients undergoing transcatheter aortic valve replacement (TAVR) has not been well studied. We conducted an analysis of 529 patients who underwent transfemoral TAVR in our centre and were receiving either DAPT or single antiplatelet therapy (SAPT) prior to the procedure. Accordingly, patients were grouped into a DAPT or SAPT group. Following current guidelines, patients in the SAPT group were switched to DAPT for 90 days after the procedure. The primary endpoint of our analysis was the incidence of bleeding events at 30 days according to the VARC-2 classification system. Any VARC-2 bleeding complications were found in 153 patients (28.9%), while major/life-threatening or disabling bleeding events occurred in 60 patients (11.3%). Our study revealed no significant difference between the DAPT vs. SAPT group regarding periprocedural bleeding complications. Based on multivariable analyses, major bleeding (HR 4.59, 95% CI 1.64–12.83, p = 0.004) and life-threatening/disabling bleeding (HR 8.66, 95% CI 3.31–22.65, p < 0.001) events were significantly associated with mortality at 90 days after TAVR. Both pre-existing DAPT and SAPT showed a comparable safety profile regarding periprocedural bleeding complications and mortality at 90 days. Thus, DAPT can be safely continued in patients undergoing transfemoral TAVR.Hatim SeoudyMaren ThomannJohanne FrankMatthias LutzThomas PuehlerGeorg LutterOliver J. MüllerNorbert FreyMohammed SaadDerk FrankNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-8 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Hatim Seoudy
Maren Thomann
Johanne Frank
Matthias Lutz
Thomas Puehler
Georg Lutter
Oliver J. Müller
Norbert Frey
Mohammed Saad
Derk Frank
Procedural outcomes in patients with dual versus single antiplatelet therapy prior to transcatheter aortic valve replacement
description Abstract The impact of uninterrupted dual antiplatelet therapy (DAPT) on bleeding events among patients undergoing transcatheter aortic valve replacement (TAVR) has not been well studied. We conducted an analysis of 529 patients who underwent transfemoral TAVR in our centre and were receiving either DAPT or single antiplatelet therapy (SAPT) prior to the procedure. Accordingly, patients were grouped into a DAPT or SAPT group. Following current guidelines, patients in the SAPT group were switched to DAPT for 90 days after the procedure. The primary endpoint of our analysis was the incidence of bleeding events at 30 days according to the VARC-2 classification system. Any VARC-2 bleeding complications were found in 153 patients (28.9%), while major/life-threatening or disabling bleeding events occurred in 60 patients (11.3%). Our study revealed no significant difference between the DAPT vs. SAPT group regarding periprocedural bleeding complications. Based on multivariable analyses, major bleeding (HR 4.59, 95% CI 1.64–12.83, p = 0.004) and life-threatening/disabling bleeding (HR 8.66, 95% CI 3.31–22.65, p < 0.001) events were significantly associated with mortality at 90 days after TAVR. Both pre-existing DAPT and SAPT showed a comparable safety profile regarding periprocedural bleeding complications and mortality at 90 days. Thus, DAPT can be safely continued in patients undergoing transfemoral TAVR.
format article
author Hatim Seoudy
Maren Thomann
Johanne Frank
Matthias Lutz
Thomas Puehler
Georg Lutter
Oliver J. Müller
Norbert Frey
Mohammed Saad
Derk Frank
author_facet Hatim Seoudy
Maren Thomann
Johanne Frank
Matthias Lutz
Thomas Puehler
Georg Lutter
Oliver J. Müller
Norbert Frey
Mohammed Saad
Derk Frank
author_sort Hatim Seoudy
title Procedural outcomes in patients with dual versus single antiplatelet therapy prior to transcatheter aortic valve replacement
title_short Procedural outcomes in patients with dual versus single antiplatelet therapy prior to transcatheter aortic valve replacement
title_full Procedural outcomes in patients with dual versus single antiplatelet therapy prior to transcatheter aortic valve replacement
title_fullStr Procedural outcomes in patients with dual versus single antiplatelet therapy prior to transcatheter aortic valve replacement
title_full_unstemmed Procedural outcomes in patients with dual versus single antiplatelet therapy prior to transcatheter aortic valve replacement
title_sort procedural outcomes in patients with dual versus single antiplatelet therapy prior to transcatheter aortic valve replacement
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/32ac1d08759e417ca4f3fccb15c70f61
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