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Optimal protamine‐to‐heparin dosing ratio for the prevention of bleeding complications in patients undergoing TAVR—A multicenter experience
BACKGROUND: Despite major advances, transcatheter aortic valve replacement (TAVR) is still associated with procedure‐specific complications. Although previous studies reported lower bleeding rates in patients receiving protamine for heparin reversal, the optimal protamine‐to‐heparin dosing ratio is...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9849438/ https://www.ncbi.nlm.nih.gov/pubmed/36259730 http://dx.doi.org/10.1002/clc.23936 |
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author | Al‐Kassou, Baravan Veulemans, Verena Shamekhi, Jasmin Maier, Oliver Piayda, Kerstin Zeus, Tobias Aksoy, Adem Zietzer, Andreas Meertens, Max Mauri, Victor Weber, Marcel Sinning, Jan‐Malte Grube, Eberhard Adam, Matti Bakhtiary, Farhad Zimmer, Sebastian Baldus, Stephan Kelm, Malte Nickenig, Georg Sedaghat, Alexander |
author_facet | Al‐Kassou, Baravan Veulemans, Verena Shamekhi, Jasmin Maier, Oliver Piayda, Kerstin Zeus, Tobias Aksoy, Adem Zietzer, Andreas Meertens, Max Mauri, Victor Weber, Marcel Sinning, Jan‐Malte Grube, Eberhard Adam, Matti Bakhtiary, Farhad Zimmer, Sebastian Baldus, Stephan Kelm, Malte Nickenig, Georg Sedaghat, Alexander |
author_sort | Al‐Kassou, Baravan |
collection | PubMed |
description | BACKGROUND: Despite major advances, transcatheter aortic valve replacement (TAVR) is still associated with procedure‐specific complications. Although previous studies reported lower bleeding rates in patients receiving protamine for heparin reversal, the optimal protamine‐to‐heparin dosing ratio is unknown. HYPOTHESIS: The aim of this study was a comparison of two different heparin antagonization regimens for the prevention of bleeding complications after TAVR. METHODS: The study included 1446 patients undergoing TAVR, of whom 623 received partial and 823 full heparin antagonization. The primary endpoint was a composite of 30‐day mortality, life‐threatening, and major bleeding. Safety endpoints included stroke and myocardial infarction at 30 days. RESULTS: Full antagonization of heparin resulted in lower rates of the primary endpoint as compared to partial heparin reversal (5.6% vs. 10.4%, p < .01), which was mainly driven by lower rates of life‐threatening (0.5% vs. 1.6%, p = .05) and major bleeding (3.2% vs. 7.5%, p < .01). Moreover, the incidence of major vascular complications was significantly lower in patients with full heparin reversal (3.5% vs. 7.5%, p < .01). The need for red‐blood‐cell transfusion was lower in patients receiving full as compared to partial heparin antagonization (10.4% vs. 15.9%, p < .01). No differences were observed in the incidence of stroke and myocardial infarction between patients with full and partial heparin reversal (2.2% vs. 2.6%, p = .73 and 0.2% vs. 0.4%, p = .64, respectively). CONCLUSIONS: Full heparin antagonization resulted in significantly lower rates of life‐threatening and major bleeding after TAVR as compared to partial heparin reversal. The occurrence of stroke and myocardial infarction was low and comparable between both groups. |
format | Online Article Text |
id | pubmed-9849438 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98494382023-01-24 Optimal protamine‐to‐heparin dosing ratio for the prevention of bleeding complications in patients undergoing TAVR—A multicenter experience Al‐Kassou, Baravan Veulemans, Verena Shamekhi, Jasmin Maier, Oliver Piayda, Kerstin Zeus, Tobias Aksoy, Adem Zietzer, Andreas Meertens, Max Mauri, Victor Weber, Marcel Sinning, Jan‐Malte Grube, Eberhard Adam, Matti Bakhtiary, Farhad Zimmer, Sebastian Baldus, Stephan Kelm, Malte Nickenig, Georg Sedaghat, Alexander Clin Cardiol Clinical Investigations BACKGROUND: Despite major advances, transcatheter aortic valve replacement (TAVR) is still associated with procedure‐specific complications. Although previous studies reported lower bleeding rates in patients receiving protamine for heparin reversal, the optimal protamine‐to‐heparin dosing ratio is unknown. HYPOTHESIS: The aim of this study was a comparison of two different heparin antagonization regimens for the prevention of bleeding complications after TAVR. METHODS: The study included 1446 patients undergoing TAVR, of whom 623 received partial and 823 full heparin antagonization. The primary endpoint was a composite of 30‐day mortality, life‐threatening, and major bleeding. Safety endpoints included stroke and myocardial infarction at 30 days. RESULTS: Full antagonization of heparin resulted in lower rates of the primary endpoint as compared to partial heparin reversal (5.6% vs. 10.4%, p < .01), which was mainly driven by lower rates of life‐threatening (0.5% vs. 1.6%, p = .05) and major bleeding (3.2% vs. 7.5%, p < .01). Moreover, the incidence of major vascular complications was significantly lower in patients with full heparin reversal (3.5% vs. 7.5%, p < .01). The need for red‐blood‐cell transfusion was lower in patients receiving full as compared to partial heparin antagonization (10.4% vs. 15.9%, p < .01). No differences were observed in the incidence of stroke and myocardial infarction between patients with full and partial heparin reversal (2.2% vs. 2.6%, p = .73 and 0.2% vs. 0.4%, p = .64, respectively). CONCLUSIONS: Full heparin antagonization resulted in significantly lower rates of life‐threatening and major bleeding after TAVR as compared to partial heparin reversal. The occurrence of stroke and myocardial infarction was low and comparable between both groups. John Wiley and Sons Inc. 2022-10-19 /pmc/articles/PMC9849438/ /pubmed/36259730 http://dx.doi.org/10.1002/clc.23936 Text en © 2022 The Authors. Clinical Cardiology published by Wiley Periodicals, LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Investigations Al‐Kassou, Baravan Veulemans, Verena Shamekhi, Jasmin Maier, Oliver Piayda, Kerstin Zeus, Tobias Aksoy, Adem Zietzer, Andreas Meertens, Max Mauri, Victor Weber, Marcel Sinning, Jan‐Malte Grube, Eberhard Adam, Matti Bakhtiary, Farhad Zimmer, Sebastian Baldus, Stephan Kelm, Malte Nickenig, Georg Sedaghat, Alexander Optimal protamine‐to‐heparin dosing ratio for the prevention of bleeding complications in patients undergoing TAVR—A multicenter experience |
title | Optimal protamine‐to‐heparin dosing ratio for the prevention of bleeding complications in patients undergoing TAVR—A multicenter experience |
title_full | Optimal protamine‐to‐heparin dosing ratio for the prevention of bleeding complications in patients undergoing TAVR—A multicenter experience |
title_fullStr | Optimal protamine‐to‐heparin dosing ratio for the prevention of bleeding complications in patients undergoing TAVR—A multicenter experience |
title_full_unstemmed | Optimal protamine‐to‐heparin dosing ratio for the prevention of bleeding complications in patients undergoing TAVR—A multicenter experience |
title_short | Optimal protamine‐to‐heparin dosing ratio for the prevention of bleeding complications in patients undergoing TAVR—A multicenter experience |
title_sort | optimal protamine‐to‐heparin dosing ratio for the prevention of bleeding complications in patients undergoing tavr—a multicenter experience |
topic | Clinical Investigations |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9849438/ https://www.ncbi.nlm.nih.gov/pubmed/36259730 http://dx.doi.org/10.1002/clc.23936 |
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