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Meta-analysis comparing direct oral anticoagulants versus vitamin K antagonists in patients with left ventricular thrombus
Current American College of Cardiology/American Heart Association guidelines for stroke or ST-elevation myocardial infarction recommend the use of oral vitamin K antagonists (VKAs) as a first-line anticoagulant. Although several studies have compared the use of direct oral anticoagulants (DOACs) to...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8177531/ https://www.ncbi.nlm.nih.gov/pubmed/34086768 http://dx.doi.org/10.1371/journal.pone.0252549 |
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author | Kido, Kazuhiko Ghaffar, Yasir Abdul Lee, James C. Bianco, Christopher Shimizu, Mikiko Shiga, Tsuyoshi Hashiguchi, Masayuki |
author_facet | Kido, Kazuhiko Ghaffar, Yasir Abdul Lee, James C. Bianco, Christopher Shimizu, Mikiko Shiga, Tsuyoshi Hashiguchi, Masayuki |
author_sort | Kido, Kazuhiko |
collection | PubMed |
description | Current American College of Cardiology/American Heart Association guidelines for stroke or ST-elevation myocardial infarction recommend the use of oral vitamin K antagonists (VKAs) as a first-line anticoagulant. Although several studies have compared the use of direct oral anticoagulants (DOACs) to VKAs for left ventricular thrombus (LVT) anticoagulation therapy, they are small scale and have produced conflicting results. Thus, this meta-analysis was performed to aggregate these studies to better compare the efficacy and safety of DOACs with VKAs in patients with LVT. Cochrane Library, Google Scholar, MEDLINE, and Web of Science database searches through January 10, 2021 were performed. Eight studies evaluating stroke or systemic embolism (SSE), six studies for LVT resolution, and five studies for bleeding were included. There were no statistically significant differences in SSE (OR 0.89; 95% CI 0.46, 1.71; p = 0.73; I(2) = 45%) and LVT resolution (OR 1.13; 95% CI 0.75, 1.71; p = 0.56; I(2) = 1%) between DOAC and VKA (reference group) therapy. DOAC use was significantly associated with lower bleeding event rates compared to VKA use (OR 0.61; 95% CI 0.40, 0.93; p = 0.02; I(2) = 0%). DOACs may be feasible alternative anticoagulants to vitamin K antagonists for LV thrombus treatment. Randomized controlled trials directly comparing DOACs with VKAs are needed. |
format | Online Article Text |
id | pubmed-8177531 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-81775312021-06-07 Meta-analysis comparing direct oral anticoagulants versus vitamin K antagonists in patients with left ventricular thrombus Kido, Kazuhiko Ghaffar, Yasir Abdul Lee, James C. Bianco, Christopher Shimizu, Mikiko Shiga, Tsuyoshi Hashiguchi, Masayuki PLoS One Research Article Current American College of Cardiology/American Heart Association guidelines for stroke or ST-elevation myocardial infarction recommend the use of oral vitamin K antagonists (VKAs) as a first-line anticoagulant. Although several studies have compared the use of direct oral anticoagulants (DOACs) to VKAs for left ventricular thrombus (LVT) anticoagulation therapy, they are small scale and have produced conflicting results. Thus, this meta-analysis was performed to aggregate these studies to better compare the efficacy and safety of DOACs with VKAs in patients with LVT. Cochrane Library, Google Scholar, MEDLINE, and Web of Science database searches through January 10, 2021 were performed. Eight studies evaluating stroke or systemic embolism (SSE), six studies for LVT resolution, and five studies for bleeding were included. There were no statistically significant differences in SSE (OR 0.89; 95% CI 0.46, 1.71; p = 0.73; I(2) = 45%) and LVT resolution (OR 1.13; 95% CI 0.75, 1.71; p = 0.56; I(2) = 1%) between DOAC and VKA (reference group) therapy. DOAC use was significantly associated with lower bleeding event rates compared to VKA use (OR 0.61; 95% CI 0.40, 0.93; p = 0.02; I(2) = 0%). DOACs may be feasible alternative anticoagulants to vitamin K antagonists for LV thrombus treatment. Randomized controlled trials directly comparing DOACs with VKAs are needed. Public Library of Science 2021-06-04 /pmc/articles/PMC8177531/ /pubmed/34086768 http://dx.doi.org/10.1371/journal.pone.0252549 Text en © 2021 Kido et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Kido, Kazuhiko Ghaffar, Yasir Abdul Lee, James C. Bianco, Christopher Shimizu, Mikiko Shiga, Tsuyoshi Hashiguchi, Masayuki Meta-analysis comparing direct oral anticoagulants versus vitamin K antagonists in patients with left ventricular thrombus |
title | Meta-analysis comparing direct oral anticoagulants versus vitamin K antagonists in patients with left ventricular thrombus |
title_full | Meta-analysis comparing direct oral anticoagulants versus vitamin K antagonists in patients with left ventricular thrombus |
title_fullStr | Meta-analysis comparing direct oral anticoagulants versus vitamin K antagonists in patients with left ventricular thrombus |
title_full_unstemmed | Meta-analysis comparing direct oral anticoagulants versus vitamin K antagonists in patients with left ventricular thrombus |
title_short | Meta-analysis comparing direct oral anticoagulants versus vitamin K antagonists in patients with left ventricular thrombus |
title_sort | meta-analysis comparing direct oral anticoagulants versus vitamin k antagonists in patients with left ventricular thrombus |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8177531/ https://www.ncbi.nlm.nih.gov/pubmed/34086768 http://dx.doi.org/10.1371/journal.pone.0252549 |
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