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Assessment of non‐vitamin K antagonist oral anticoagulants for the management of left ventricular thrombus

Although several studies have assessed the effect of non‐vitamin K antagonist oral anticoagulants (NOACs) relative to that of vitamin K antagonists (VKAs) in patients with left ventricular thrombus, the results remain controversial. Herein, a meta‐analysis was performed to compare the effectiveness...

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Autores principales: Li, Shunhui, Deng, Yuqing, Tong, Yifan, Xiong, Qiangzhen, Hu, Jing, Jiang, Xiaojie, He, Tao, Liu, Liyun, Chen, Hui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wiley Periodicals, Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8207971/
https://www.ncbi.nlm.nih.gov/pubmed/33797773
http://dx.doi.org/10.1002/clc.23553
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author Li, Shunhui
Deng, Yuqing
Tong, Yifan
Xiong, Qiangzhen
Hu, Jing
Jiang, Xiaojie
He, Tao
Liu, Liyun
Chen, Hui
author_facet Li, Shunhui
Deng, Yuqing
Tong, Yifan
Xiong, Qiangzhen
Hu, Jing
Jiang, Xiaojie
He, Tao
Liu, Liyun
Chen, Hui
author_sort Li, Shunhui
collection PubMed
description Although several studies have assessed the effect of non‐vitamin K antagonist oral anticoagulants (NOACs) relative to that of vitamin K antagonists (VKAs) in patients with left ventricular thrombus, the results remain controversial. Herein, a meta‐analysis was performed to compare the effectiveness and safety of NOACs versus VKAs for the treatment of left ventricular thrombus. We systematically searched the Cochrane Library, PubMed and Embase databases until November 2020 for studies that compared the effects of NOACs versus VKAs in patients with left ventricular thrombus. The treatment effects were expressed as odds ratios (ORs) with 95% confidence intervals (CIs) and pooled by a random‐effects model. Seven retrospective studies involving 865 patients with left ventricular thrombus (266 NOAC and 599 VKA users) were included. The pooled analysis suggested no difference in the rate of thrombus resolution between the NOAC and VKA groups (OR = 0.83, 95% CI 0.61–1.13). There were also no differences in the rates of stroke or systemic embolism (OR = 0.62, 95% CI 0.20–1.97), bleeding events (OR = 0.73, 95% CI 0.37–1.45), or all‐cause death (OR = 0.92, 95% CI 0.50–1.69) between patients treated with NOACs and those treated with VKAs. In addition, the rates of thrombus resolution, stroke or systemic embolism, bleeding events, and all‐cause death between NOAC‐ and warfarin‐treated patients were also similar. Our current evidence suggested that NOAC and VKA users had similar rates of thrombus resolution and clinical outcomes among patients with left ventricular thrombus. Further large‐scale prospective studies should confirm our results.
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spelling pubmed-82079712021-06-25 Assessment of non‐vitamin K antagonist oral anticoagulants for the management of left ventricular thrombus Li, Shunhui Deng, Yuqing Tong, Yifan Xiong, Qiangzhen Hu, Jing Jiang, Xiaojie He, Tao Liu, Liyun Chen, Hui Clin Cardiol Reviews Although several studies have assessed the effect of non‐vitamin K antagonist oral anticoagulants (NOACs) relative to that of vitamin K antagonists (VKAs) in patients with left ventricular thrombus, the results remain controversial. Herein, a meta‐analysis was performed to compare the effectiveness and safety of NOACs versus VKAs for the treatment of left ventricular thrombus. We systematically searched the Cochrane Library, PubMed and Embase databases until November 2020 for studies that compared the effects of NOACs versus VKAs in patients with left ventricular thrombus. The treatment effects were expressed as odds ratios (ORs) with 95% confidence intervals (CIs) and pooled by a random‐effects model. Seven retrospective studies involving 865 patients with left ventricular thrombus (266 NOAC and 599 VKA users) were included. The pooled analysis suggested no difference in the rate of thrombus resolution between the NOAC and VKA groups (OR = 0.83, 95% CI 0.61–1.13). There were also no differences in the rates of stroke or systemic embolism (OR = 0.62, 95% CI 0.20–1.97), bleeding events (OR = 0.73, 95% CI 0.37–1.45), or all‐cause death (OR = 0.92, 95% CI 0.50–1.69) between patients treated with NOACs and those treated with VKAs. In addition, the rates of thrombus resolution, stroke or systemic embolism, bleeding events, and all‐cause death between NOAC‐ and warfarin‐treated patients were also similar. Our current evidence suggested that NOAC and VKA users had similar rates of thrombus resolution and clinical outcomes among patients with left ventricular thrombus. Further large‐scale prospective studies should confirm our results. Wiley Periodicals, Inc. 2021-04-02 /pmc/articles/PMC8207971/ /pubmed/33797773 http://dx.doi.org/10.1002/clc.23553 Text en © 2021 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 Reviews
Li, Shunhui
Deng, Yuqing
Tong, Yifan
Xiong, Qiangzhen
Hu, Jing
Jiang, Xiaojie
He, Tao
Liu, Liyun
Chen, Hui
Assessment of non‐vitamin K antagonist oral anticoagulants for the management of left ventricular thrombus
title Assessment of non‐vitamin K antagonist oral anticoagulants for the management of left ventricular thrombus
title_full Assessment of non‐vitamin K antagonist oral anticoagulants for the management of left ventricular thrombus
title_fullStr Assessment of non‐vitamin K antagonist oral anticoagulants for the management of left ventricular thrombus
title_full_unstemmed Assessment of non‐vitamin K antagonist oral anticoagulants for the management of left ventricular thrombus
title_short Assessment of non‐vitamin K antagonist oral anticoagulants for the management of left ventricular thrombus
title_sort assessment of non‐vitamin k antagonist oral anticoagulants for the management of left ventricular thrombus
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8207971/
https://www.ncbi.nlm.nih.gov/pubmed/33797773
http://dx.doi.org/10.1002/clc.23553
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