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Vol 18, No 6 (2011)
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Published online: 2011-11-23
Submitted: 2013-01-14
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Post percutaneous coronary intervention antiplatelet therapy: Current perceptions, prospects and perplexity

Sadip Pant, Pritam Neupane, Ramesh KC, Murari Barakoti
Cardiol J 2011;18(6):712-717.

open access

Vol 18, No 6 (2011)
How to do
Published online: 2011-11-23
Submitted: 2013-01-14

Abstract

Dual antiplatelet therapy (DAT) has become standard care for patients undergoing percutaneous coronary intervention (PCI). Following balloon injury and stent placement, the intima at the site is distressed, resulting in the activation of coagulation cascade and platelets. In the case of bare metal stents (BMS), it takes six to eight weeks for the stent surface to be covered with neointima. However, in the case of a drug-eluting stent (DES), the process of healing is delayed and neointima may not form for months or even years. To prevent the formation of platelet thrombi, dual antiplatelet therapy is given as a combination of aspirin and clopidogrel for three months in a case of BMS and for a minimum of one year in a case of DES. A prolonged duration of therapy is often required for a subset of patients who are highly prone to thrombus formation. During most non-cardiac surgeries, dual antiplatelet therapy should be continued if bleeding can be directly controlled and excessive bleeding will have no adverse effect on the outcome of surgery. Prasugrel, another thienopyridine, is more potent and faster acting than clopidogrel, and is therefore of great value in cases of acute coronary syndrome during PCI, particularly in diabetics. Triple drug therapy, by adding cilastozol, is reserved for some selected thrombotic lesions. Ticagrelor and cangrelor are two new antiplatelet agents undergoing various clinical trials. (Cardiol J 2011; 18, 6: 712–717)

Abstract

Dual antiplatelet therapy (DAT) has become standard care for patients undergoing percutaneous coronary intervention (PCI). Following balloon injury and stent placement, the intima at the site is distressed, resulting in the activation of coagulation cascade and platelets. In the case of bare metal stents (BMS), it takes six to eight weeks for the stent surface to be covered with neointima. However, in the case of a drug-eluting stent (DES), the process of healing is delayed and neointima may not form for months or even years. To prevent the formation of platelet thrombi, dual antiplatelet therapy is given as a combination of aspirin and clopidogrel for three months in a case of BMS and for a minimum of one year in a case of DES. A prolonged duration of therapy is often required for a subset of patients who are highly prone to thrombus formation. During most non-cardiac surgeries, dual antiplatelet therapy should be continued if bleeding can be directly controlled and excessive bleeding will have no adverse effect on the outcome of surgery. Prasugrel, another thienopyridine, is more potent and faster acting than clopidogrel, and is therefore of great value in cases of acute coronary syndrome during PCI, particularly in diabetics. Triple drug therapy, by adding cilastozol, is reserved for some selected thrombotic lesions. Ticagrelor and cangrelor are two new antiplatelet agents undergoing various clinical trials. (Cardiol J 2011; 18, 6: 712–717)
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Keywords

percutaneous coronary intervention; dual antiplatelet therapy; restenosis

About this article
Title

Post percutaneous coronary intervention antiplatelet therapy: Current perceptions, prospects and perplexity

Journal

Cardiology Journal

Issue

Vol 18, No 6 (2011)

Pages

712-717

Published online

2011-11-23

Bibliographic record

Cardiol J 2011;18(6):712-717.

Keywords

percutaneous coronary intervention
dual antiplatelet therapy
restenosis

Authors

Sadip Pant
Pritam Neupane
Ramesh KC
Murari Barakoti

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