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Effect and safety of antithrombotic therapies for secondary prevention after acute coronary syndrome: a network meta-analysis

BACKGROUND: Dual antiplatelet therapy is a standard protocol for secondary prevention after acute coronary syndrome, but despite a variety of new dual antithrombotic strategies, there is a dearth of studies evaluating the effects and safety of some popular therapies. This study used a network meta-a...

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Autores principales: Mo, Fanrui, Li, Juan, Yan, Yuluan, Wu, Weifeng, Lai, Shayi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6207225/
https://www.ncbi.nlm.nih.gov/pubmed/30498334
http://dx.doi.org/10.2147/DDDT.S166544
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author Mo, Fanrui
Li, Juan
Yan, Yuluan
Wu, Weifeng
Lai, Shayi
author_facet Mo, Fanrui
Li, Juan
Yan, Yuluan
Wu, Weifeng
Lai, Shayi
author_sort Mo, Fanrui
collection PubMed
description BACKGROUND: Dual antiplatelet therapy is a standard protocol for secondary prevention after acute coronary syndrome, but despite a variety of new dual antithrombotic strategies, there is a dearth of studies evaluating the effects and safety of some popular therapies. This study used a network meta-analysis to compare the efficacy and safety of all available antithrombotic therapies. METHODS: PubMed, MEDLINE, and Cochrane library databases were searched for randomized controlled trials, published up to July 1, 2017, that evaluated the efficacy of antithrombotic therapy in acute coronary syndrome treatment. The primary endpoints were clinically significant bleeding and major bleeding and secondary endpoints were major cardiovascular events, all-cause deaths, cardiac deaths, and myocardial infarction. RESULTS: Compared with treatment with aspirin + new P2Y12 inhibitor, treatment with aspirin + new P2Y12 inhibitor converted to clopidogrel clinically reduced the risk of major cardiovascular events or significant bleeding (OR: 0.30, 95% credibility interval: 0.12–0.75). Both myocardial infarction risk (OR: 0.82, 95% credibility interval: 0.62–1.09) and major bleeding risk (OR: 0.18, 95% credibility interval: 0.01–1.68) were not significantly different between treatment regimens. There were no significant differences in major cardiovascular events, all-cause deaths, cardiac deaths, myocardial infarction, clinically significant bleeding, and major bleeding risk with rivaroxaban + new P2Y12 inhibitor therapy when compared with aspirin + new P2Y12 inhibitor. Compared with aspirin + clopidogrel, the conversion therapy further reduced the risk of myocardial infarction (OR: 1.81, 95%, credibility interval: 1.01–1.34) without an increased clinical risk of significant bleeding (OR: 0.41, 95%, credibility interval: 0.15–1.07). Treatment with aspirin + new P2Y12 inhibitors reduced all-cause deaths (OR: 0.91, 95% credibility interval: 0.84–0.98) and cardiac death risk (OR: 0.86, 95% credibility interval: 0.79–0.93). CONCLUSION: We concluded the following from our study: 1) an aspirin + new P2Y12 inhibitor/ clopidogrel conversion treatment strategy was not inferior to aspirin + new P2Y12 inhibitor; 2) compared with aspirin + clopidogrel, the conversion strategy may further reduce the risk of myocardial infarction without increasing the risk of bleeding; and 3) compared with aspirin + clopidogrel, treatment with aspirin + new P2Y12 inhibitors may result in reduced risk of death.
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spelling pubmed-62072252018-11-29 Effect and safety of antithrombotic therapies for secondary prevention after acute coronary syndrome: a network meta-analysis Mo, Fanrui Li, Juan Yan, Yuluan Wu, Weifeng Lai, Shayi Drug Des Devel Ther Original Research BACKGROUND: Dual antiplatelet therapy is a standard protocol for secondary prevention after acute coronary syndrome, but despite a variety of new dual antithrombotic strategies, there is a dearth of studies evaluating the effects and safety of some popular therapies. This study used a network meta-analysis to compare the efficacy and safety of all available antithrombotic therapies. METHODS: PubMed, MEDLINE, and Cochrane library databases were searched for randomized controlled trials, published up to July 1, 2017, that evaluated the efficacy of antithrombotic therapy in acute coronary syndrome treatment. The primary endpoints were clinically significant bleeding and major bleeding and secondary endpoints were major cardiovascular events, all-cause deaths, cardiac deaths, and myocardial infarction. RESULTS: Compared with treatment with aspirin + new P2Y12 inhibitor, treatment with aspirin + new P2Y12 inhibitor converted to clopidogrel clinically reduced the risk of major cardiovascular events or significant bleeding (OR: 0.30, 95% credibility interval: 0.12–0.75). Both myocardial infarction risk (OR: 0.82, 95% credibility interval: 0.62–1.09) and major bleeding risk (OR: 0.18, 95% credibility interval: 0.01–1.68) were not significantly different between treatment regimens. There were no significant differences in major cardiovascular events, all-cause deaths, cardiac deaths, myocardial infarction, clinically significant bleeding, and major bleeding risk with rivaroxaban + new P2Y12 inhibitor therapy when compared with aspirin + new P2Y12 inhibitor. Compared with aspirin + clopidogrel, the conversion therapy further reduced the risk of myocardial infarction (OR: 1.81, 95%, credibility interval: 1.01–1.34) without an increased clinical risk of significant bleeding (OR: 0.41, 95%, credibility interval: 0.15–1.07). Treatment with aspirin + new P2Y12 inhibitors reduced all-cause deaths (OR: 0.91, 95% credibility interval: 0.84–0.98) and cardiac death risk (OR: 0.86, 95% credibility interval: 0.79–0.93). CONCLUSION: We concluded the following from our study: 1) an aspirin + new P2Y12 inhibitor/ clopidogrel conversion treatment strategy was not inferior to aspirin + new P2Y12 inhibitor; 2) compared with aspirin + clopidogrel, the conversion strategy may further reduce the risk of myocardial infarction without increasing the risk of bleeding; and 3) compared with aspirin + clopidogrel, treatment with aspirin + new P2Y12 inhibitors may result in reduced risk of death. Dove Medical Press 2018-10-25 /pmc/articles/PMC6207225/ /pubmed/30498334 http://dx.doi.org/10.2147/DDDT.S166544 Text en © 2018 Mo et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Mo, Fanrui
Li, Juan
Yan, Yuluan
Wu, Weifeng
Lai, Shayi
Effect and safety of antithrombotic therapies for secondary prevention after acute coronary syndrome: a network meta-analysis
title Effect and safety of antithrombotic therapies for secondary prevention after acute coronary syndrome: a network meta-analysis
title_full Effect and safety of antithrombotic therapies for secondary prevention after acute coronary syndrome: a network meta-analysis
title_fullStr Effect and safety of antithrombotic therapies for secondary prevention after acute coronary syndrome: a network meta-analysis
title_full_unstemmed Effect and safety of antithrombotic therapies for secondary prevention after acute coronary syndrome: a network meta-analysis
title_short Effect and safety of antithrombotic therapies for secondary prevention after acute coronary syndrome: a network meta-analysis
title_sort effect and safety of antithrombotic therapies for secondary prevention after acute coronary syndrome: a network meta-analysis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6207225/
https://www.ncbi.nlm.nih.gov/pubmed/30498334
http://dx.doi.org/10.2147/DDDT.S166544
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