Dual antiplatelet therapy with aspirin (acetylsalicylic acid) and clopidogrel is widely used in order to prevent recurrent ischaemic events in patients undergoing percutaneous coronary intervention. The goal is to achieve an optimal platelet inhibition, providing clear clinical benefit in most patients. However, a wide inter-individual variability exists in the response to antiplatelet drugs. Several factors, such as genetic, cellular and clinical factors, may contribute to determine fluctuation in platelet reactivity even within the individual patient. Patients with high post-treatment platelet reactivity are at higher risk of ischaemic events in both the short term (during or shortly after percutaneous coronary intervention) and the long term. Several methodologies and devices have been developed to monitor individual response to antiplatelet treatment assessing different pathways of platelet activation and aggregation. In these patients, more aggressive antithrombotic strategies and new generation drugs may be beneficial in order to reduce ischaemic complications after percutaneous coronary intervention. © 2010 Adis Data Information BV. All rights reserved.

Individual variability of response to antiplatelet therapy is an important determinant of adverse clinical outcome / Mangiacapra, F.; Barbato, Emanuele. - In: HIGH BLOOD PRESSURE & CARDIOVASCULAR PREVENTION. - ISSN 1120-9879. - 17:3(2010), pp. 121-130. [10.2165/11311890-000000000-00000]

Individual variability of response to antiplatelet therapy is an important determinant of adverse clinical outcome

BARBATO, EMANUELE
2010

Abstract

Dual antiplatelet therapy with aspirin (acetylsalicylic acid) and clopidogrel is widely used in order to prevent recurrent ischaemic events in patients undergoing percutaneous coronary intervention. The goal is to achieve an optimal platelet inhibition, providing clear clinical benefit in most patients. However, a wide inter-individual variability exists in the response to antiplatelet drugs. Several factors, such as genetic, cellular and clinical factors, may contribute to determine fluctuation in platelet reactivity even within the individual patient. Patients with high post-treatment platelet reactivity are at higher risk of ischaemic events in both the short term (during or shortly after percutaneous coronary intervention) and the long term. Several methodologies and devices have been developed to monitor individual response to antiplatelet treatment assessing different pathways of platelet activation and aggregation. In these patients, more aggressive antithrombotic strategies and new generation drugs may be beneficial in order to reduce ischaemic complications after percutaneous coronary intervention. © 2010 Adis Data Information BV. All rights reserved.
2010
acetylsalicylic acid; adenosine diphosphate; atorvastatin; biological marker; clopidogrel; omeprazole; prasugrel; purinergic P2Y12 receptor; ticagrelor; acute coronary syndrome; bleeding; blood clot lysis; DNA polymorphism; drug dose increase; drug eluting stent; drug megadose; drug response; drug safety; endothelial dysfunction; fibrinolytic therapy; gene mutation; heart infarction; human; loading drug dose; percutaneous coronary intervention; postoperative thrombosis; priority journal; review; ST segment elevation myocardial infarction; stent thrombosis; thrombocyte adhesion; thrombocyte aggregation; treatment outcome; Aspirin; therapeutic use; Clopidogrel; therapeutic use; Platelet-aggregation
01 Pubblicazione su rivista::01a Articolo in rivista
Individual variability of response to antiplatelet therapy is an important determinant of adverse clinical outcome / Mangiacapra, F.; Barbato, Emanuele. - In: HIGH BLOOD PRESSURE & CARDIOVASCULAR PREVENTION. - ISSN 1120-9879. - 17:3(2010), pp. 121-130. [10.2165/11311890-000000000-00000]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1660349
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