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Antithrombotic therapy in peripheral arterial disease
BACKGROUND: Patients with peripheral arterial disease (PAD) are at increased risk for major adverse cardiovascular events (MACE) such as cardiovascular death, myocardial infarction, and stroke as well as major adverse limb events (MALE) such as amputation and acute limb ischemia. Therefore, preventi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9606411/ https://www.ncbi.nlm.nih.gov/pubmed/36312276 http://dx.doi.org/10.3389/fcvm.2022.927645 |
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author | Espinola-Klein, Christine Weißer, Gerhard Schmitt, Volker Schwaderlapp, Melanie Munzel, Thomas |
author_facet | Espinola-Klein, Christine Weißer, Gerhard Schmitt, Volker Schwaderlapp, Melanie Munzel, Thomas |
author_sort | Espinola-Klein, Christine |
collection | PubMed |
description | BACKGROUND: Patients with peripheral arterial disease (PAD) are at increased risk for major adverse cardiovascular events (MACE) such as cardiovascular death, myocardial infarction, and stroke as well as major adverse limb events (MALE) such as amputation and acute limb ischemia. Therefore, prevention of thrombotic events is crucial to improve the prognosis of PAD patients. This review article concludes current evidence and guideline recommendations about antithrombotic therapy in PAD patients. Antithrombotic therapy is highly effective to reduce MACE and MALE events in PAD patients. Recently, the concept of dual pathway inhibition (low-dose rivaroxaban plus acetylic salicylic acid (ASA) has been tested in the COMPASS and VOYAGER-PAD trial. Compared to ASA alone dual pathway inhibition was superior to prevent MACE and MALE. After peripheral revascularization, in particular the risk for acute limb ischemia was reduced. In contrast, the risk for major bleeding is increased. Therefore, current guidelines recommend the combination of low-dose rivaroxaban and ASA in PAD patients with low bleeding risk. In patients with high bleeding risk, a single antiplatelet drug (preferable clopidogrel) is indicated. In patients with atherosclerotic vascular disease and indication for oral anticoagulation, no additional antiplatelet drug is necessary, as this would increase the risk of bleeding without improving the prognosis. CONCLUSION: Antithrombotic treatment reduces MACE and MALE and is recommended in all patients with PAD. Individual bleeding risk should always be considered based on the current data situation and an individual benefit-risk assessment must be carried out. |
format | Online Article Text |
id | pubmed-9606411 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-96064112022-10-28 Antithrombotic therapy in peripheral arterial disease Espinola-Klein, Christine Weißer, Gerhard Schmitt, Volker Schwaderlapp, Melanie Munzel, Thomas Front Cardiovasc Med Cardiovascular Medicine BACKGROUND: Patients with peripheral arterial disease (PAD) are at increased risk for major adverse cardiovascular events (MACE) such as cardiovascular death, myocardial infarction, and stroke as well as major adverse limb events (MALE) such as amputation and acute limb ischemia. Therefore, prevention of thrombotic events is crucial to improve the prognosis of PAD patients. This review article concludes current evidence and guideline recommendations about antithrombotic therapy in PAD patients. Antithrombotic therapy is highly effective to reduce MACE and MALE events in PAD patients. Recently, the concept of dual pathway inhibition (low-dose rivaroxaban plus acetylic salicylic acid (ASA) has been tested in the COMPASS and VOYAGER-PAD trial. Compared to ASA alone dual pathway inhibition was superior to prevent MACE and MALE. After peripheral revascularization, in particular the risk for acute limb ischemia was reduced. In contrast, the risk for major bleeding is increased. Therefore, current guidelines recommend the combination of low-dose rivaroxaban and ASA in PAD patients with low bleeding risk. In patients with high bleeding risk, a single antiplatelet drug (preferable clopidogrel) is indicated. In patients with atherosclerotic vascular disease and indication for oral anticoagulation, no additional antiplatelet drug is necessary, as this would increase the risk of bleeding without improving the prognosis. CONCLUSION: Antithrombotic treatment reduces MACE and MALE and is recommended in all patients with PAD. Individual bleeding risk should always be considered based on the current data situation and an individual benefit-risk assessment must be carried out. Frontiers Media S.A. 2022-10-13 /pmc/articles/PMC9606411/ /pubmed/36312276 http://dx.doi.org/10.3389/fcvm.2022.927645 Text en Copyright © 2022 Espinola-Klein, Weißer, Schmitt, Schwaderlapp and Munzel. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cardiovascular Medicine Espinola-Klein, Christine Weißer, Gerhard Schmitt, Volker Schwaderlapp, Melanie Munzel, Thomas Antithrombotic therapy in peripheral arterial disease |
title | Antithrombotic therapy in peripheral arterial disease |
title_full | Antithrombotic therapy in peripheral arterial disease |
title_fullStr | Antithrombotic therapy in peripheral arterial disease |
title_full_unstemmed | Antithrombotic therapy in peripheral arterial disease |
title_short | Antithrombotic therapy in peripheral arterial disease |
title_sort | antithrombotic therapy in peripheral arterial disease |
topic | Cardiovascular Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9606411/ https://www.ncbi.nlm.nih.gov/pubmed/36312276 http://dx.doi.org/10.3389/fcvm.2022.927645 |
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