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When is the Best Time for the Second Antiplatelet Agent in Non-St Elevation Acute Coronary Syndrome?

Dual antiplatelet therapy is a well-established treatment in patients with non-ST elevation acute coronary syndrome (NSTE-ACS), with class I of recommendation (level of evidence A) in current national and international guidelines. Nonetheless, these guidelines are not precise or consensual regarding...

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Autores principales: Silva, Pedro Gabriel Melo de Barros e, Ribeiro, Henrique Barbosa, Baruzzi, Antônio Claudio do Amaral, da Silva, Expedito Eustáquio Ribeiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Cardiologia - SBC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4811279/
https://www.ncbi.nlm.nih.gov/pubmed/27027367
http://dx.doi.org/10.5935/abc.20160042
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author Silva, Pedro Gabriel Melo de Barros e
Ribeiro, Henrique Barbosa
Baruzzi, Antônio Claudio do Amaral
da Silva, Expedito Eustáquio Ribeiro
author_facet Silva, Pedro Gabriel Melo de Barros e
Ribeiro, Henrique Barbosa
Baruzzi, Antônio Claudio do Amaral
da Silva, Expedito Eustáquio Ribeiro
author_sort Silva, Pedro Gabriel Melo de Barros e
collection PubMed
description Dual antiplatelet therapy is a well-established treatment in patients with non-ST elevation acute coronary syndrome (NSTE-ACS), with class I of recommendation (level of evidence A) in current national and international guidelines. Nonetheless, these guidelines are not precise or consensual regarding the best time to start the second antiplatelet agent. The evidences are conflicting, and after more than a decade using clopidogrel in this scenario, benefits from the routine pretreatment, i.e. without knowing the coronary anatomy, with dual antiplatelet therapy remain uncertain. The recommendation for the upfront treatment with clopidogrel in NSTE-ACS is based on the reduction of non-fatal events in studies that used the conservative strategy with eventual invasive stratification, after many days of the acute event. This approach is different from the current management of these patients, considering the established benefits from the early invasive strategy, especially in moderate to high-risk patients. The only randomized study to date that specifically tested the pretreatment in NSTE-ACS in the context of early invasive strategy, used prasugrel, and it did not show any benefit in reducing ischemic events with pretreatment. On the contrary, its administration increased the risk of bleeding events. This study has brought the pretreatment again into discussion, and led to changes in recent guidelines of the American and European cardiology societies. In this paper, the authors review the main evidence of the pretreatment with dual antiplatelet therapy in NSTE-ACS.
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spelling pubmed-48112792016-04-01 When is the Best Time for the Second Antiplatelet Agent in Non-St Elevation Acute Coronary Syndrome? Silva, Pedro Gabriel Melo de Barros e Ribeiro, Henrique Barbosa Baruzzi, Antônio Claudio do Amaral da Silva, Expedito Eustáquio Ribeiro Arq Bras Cardiol Review Article Dual antiplatelet therapy is a well-established treatment in patients with non-ST elevation acute coronary syndrome (NSTE-ACS), with class I of recommendation (level of evidence A) in current national and international guidelines. Nonetheless, these guidelines are not precise or consensual regarding the best time to start the second antiplatelet agent. The evidences are conflicting, and after more than a decade using clopidogrel in this scenario, benefits from the routine pretreatment, i.e. without knowing the coronary anatomy, with dual antiplatelet therapy remain uncertain. The recommendation for the upfront treatment with clopidogrel in NSTE-ACS is based on the reduction of non-fatal events in studies that used the conservative strategy with eventual invasive stratification, after many days of the acute event. This approach is different from the current management of these patients, considering the established benefits from the early invasive strategy, especially in moderate to high-risk patients. The only randomized study to date that specifically tested the pretreatment in NSTE-ACS in the context of early invasive strategy, used prasugrel, and it did not show any benefit in reducing ischemic events with pretreatment. On the contrary, its administration increased the risk of bleeding events. This study has brought the pretreatment again into discussion, and led to changes in recent guidelines of the American and European cardiology societies. In this paper, the authors review the main evidence of the pretreatment with dual antiplatelet therapy in NSTE-ACS. Sociedade Brasileira de Cardiologia - SBC 2016-03 /pmc/articles/PMC4811279/ /pubmed/27027367 http://dx.doi.org/10.5935/abc.20160042 Text en http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Silva, Pedro Gabriel Melo de Barros e
Ribeiro, Henrique Barbosa
Baruzzi, Antônio Claudio do Amaral
da Silva, Expedito Eustáquio Ribeiro
When is the Best Time for the Second Antiplatelet Agent in Non-St Elevation Acute Coronary Syndrome?
title When is the Best Time for the Second Antiplatelet Agent in Non-St Elevation Acute Coronary Syndrome?
title_full When is the Best Time for the Second Antiplatelet Agent in Non-St Elevation Acute Coronary Syndrome?
title_fullStr When is the Best Time for the Second Antiplatelet Agent in Non-St Elevation Acute Coronary Syndrome?
title_full_unstemmed When is the Best Time for the Second Antiplatelet Agent in Non-St Elevation Acute Coronary Syndrome?
title_short When is the Best Time for the Second Antiplatelet Agent in Non-St Elevation Acute Coronary Syndrome?
title_sort when is the best time for the second antiplatelet agent in non-st elevation acute coronary syndrome?
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4811279/
https://www.ncbi.nlm.nih.gov/pubmed/27027367
http://dx.doi.org/10.5935/abc.20160042
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