Duration of Dual Antiplatelet Therapy After Coronary Stenting: A Review of the Evidence.
Identifieur interne : 002E96 ( Main/Exploration ); précédent : 002E95; suivant : 002E97Duration of Dual Antiplatelet Therapy After Coronary Stenting: A Review of the Evidence.
Auteurs : Gilles Montalescot [France] ; David Brieger [Australie] ; Anthony J. Dalby [Afrique du Sud] ; Seung-Jung Park [Corée du Sud] ; Roxana Mehran [États-Unis]Source :
- Journal of the American College of Cardiology [ 1558-3597 ] ; 2015.
Descripteurs français
- KwdFr :
- Antagonistes des récepteurs purinergiques P2Y (administration et posologie), Antiagrégants plaquettaires (administration et posologie), Endoprothèses à élution de substances (tendances), Essais contrôlés randomisés comme sujet (tendances), Facteurs temps, Humains, Intervention coronarienne percutanée (tendances), Resténose coronaire (), Resténose coronaire (diagnostic).
- MESH :
- administration et posologie : Antagonistes des récepteurs purinergiques P2Y, Antiagrégants plaquettaires.
- diagnostic : Resténose coronaire.
- tendances : Endoprothèses à élution de substances, Essais contrôlés randomisés comme sujet, Intervention coronarienne percutanée.
- Facteurs temps, Humains, Resténose coronaire.
English descriptors
- KwdEn :
- Coronary Restenosis (diagnosis), Coronary Restenosis (prevention & control), Drug-Eluting Stents (trends), Humans, Percutaneous Coronary Intervention (trends), Platelet Aggregation Inhibitors (administration & dosage), Purinergic P2Y Receptor Antagonists (administration & dosage), Randomized Controlled Trials as Topic (trends), Time Factors.
- MESH :
- chemical , administration & dosage : Platelet Aggregation Inhibitors, Purinergic P2Y Receptor Antagonists.
- diagnosis : Coronary Restenosis.
- prevention & control : Coronary Restenosis.
- trends : Drug-Eluting Stents, Percutaneous Coronary Intervention, Randomized Controlled Trials as Topic.
- Humans, Time Factors.
Abstract
The duration of dual antiplatelet therapy (DAPT) after coronary stenting has been evaluated in randomized studies with apparently conflicting results. Although longer exposure associates with more bleeding complications, late stent thrombosis (ST) and myocardial infarction are reduced. In addition, as new drug-eluting stents carry a lower risk of ST compared with the first-generation drug-eluting stents and possibly even bare-metal stents, a shift toward better protection from ST may have an effect on the duration and intensity of DAPT. Whether the duration of DAPT should be shorter or longer than the currently recommended 6 to 12 months is analyzed in this review, drawing on lessons from the most recent studies.
DOI: 10.1016/j.jacc.2015.05.053
PubMed: 26271067
Affiliations:
- Afrique du Sud, Australie, Corée du Sud, France, États-Unis
- Nouvelle-Galles du Sud, Région capitale de Séoul, État de New York, Île-de-France
- Paris, Sydney, Séoul
- Université de Sydney
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Le document en format XML
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<term>Drug-Eluting Stents (trends)</term>
<term>Humans</term>
<term>Percutaneous Coronary Intervention (trends)</term>
<term>Platelet Aggregation Inhibitors (administration & dosage)</term>
<term>Purinergic P2Y Receptor Antagonists (administration & dosage)</term>
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<term>Endoprothèses à élution de substances (tendances)</term>
<term>Essais contrôlés randomisés comme sujet (tendances)</term>
<term>Facteurs temps</term>
<term>Humains</term>
<term>Intervention coronarienne percutanée (tendances)</term>
<term>Resténose coronaire ()</term>
<term>Resténose coronaire (diagnostic)</term>
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<term>Resténose coronaire</term>
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<front><div type="abstract" xml:lang="en">The duration of dual antiplatelet therapy (DAPT) after coronary stenting has been evaluated in randomized studies with apparently conflicting results. Although longer exposure associates with more bleeding complications, late stent thrombosis (ST) and myocardial infarction are reduced. In addition, as new drug-eluting stents carry a lower risk of ST compared with the first-generation drug-eluting stents and possibly even bare-metal stents, a shift toward better protection from ST may have an effect on the duration and intensity of DAPT. Whether the duration of DAPT should be shorter or longer than the currently recommended 6 to 12 months is analyzed in this review, drawing on lessons from the most recent studies.</div>
</front>
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