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Published on: March 15, 2022
Clopidogrel discontinuation and platelet reactivity following coronary stenting
D Mylotte1, A J Peace, A T Tedesco
1Department of Molecular and Cellular Therapeutics, The Royal College of Surgeons in Ireland, Dublin, Ireland.
Insights
Discontinuing clopidogrel after drug-eluting stent implantation may cause a temporary increase in platelet reactivity. This rebound effect, observed one month after stopping clopidogrel, could explain post-discontinuation thrombotic events.
Area of Science:
- Cardiology
- Pharmacology
- Hematology
Background:
- Dual antiplatelet therapy (DAPT) with aspirin and clopidogrel is standard for one year post-drug-eluting stent (DES) or myocardial infarction.
- Concerns exist regarding ischemic events clustering within 90 days of clopidogrel withdrawal.
Purpose of the Study:
- To investigate a potential transient 'rebound' increase in platelet reactivity after clopidogrel discontinuation.
- To explore the hypothesis that platelet function is altered within three months of stopping clopidogrel.
Main Methods:
- Prospective study of 32 patients on DAPT for at least one year post-DES.
- Platelet aggregation assessed via light transmission aggregometry using multiple agonists (ADP, epinephrine, arachidonic acid, TRAP, collagen).
- Platelet function measured one week, one month, and three months after clopidogrel cessation.
Main Results:
- Clopidogrel discontinuation increased platelet aggregation to most agonists, excluding arachidonic acid.
- Significantly higher platelet aggregation to ADP and epinephrine occurred at one month versus three months post-clopidogrel withdrawal.
- A transient increase in platelet reactivity to ADP and epinephrine was observed one month after clopidogrel cessation.
Conclusions:
- A transient increase in platelet reactivity occurs one month after clopidogrel withdrawal.
- This rebound phenomenon may contribute to the observed clustering of thrombotic events post-clopidogrel discontinuation.
- Further validation in larger patient cohorts is warranted.
Aims:
Antiplatelet therapy with aspirin and clopidogrel is recommended for 1 year after drug-eluting stent (DES) implantation or myocardial infarction. However, the discontinuation of antiplatelet therapy has become an important issue as recent studies have suggested a clustering of ischemic events within 90 days of clopidogrel withdrawal. The objective of this investigation was to explore the hypothesis that there is a transient 'rebound' increase in platelet reactivity within 3 months of clopidogrel discontinuation.
Methods And Results:
In this prospective study, platelet function was assessed in patients taking aspirin and clopidogrel for at least 1 year following DES implantation. Platelet aggregation was measured using a modification of light transmission aggregometry in response to multiple concentrations of adenosine diphosphate (ADP), epinephrine, arachidonic acid, thrombin receptor activating peptide and collagen. Clopidogrel was stopped and platelet function was reassessed 1 week, 1 month and 3 months later. Thirty-two patients on dual antiplatelet therapy were recruited. Discontinuation of clopidogrel increased platelet aggregation to all agonists, except arachidonic acid. Platelet aggregation in response to ADP (2.5, 5, 10, and 20 μm) and epinephrine (5 and 20 μm) was significantly increased at 1 month compared with 3 months following clopidogrel withdrawal. Thus, a transient period of increased platelet reactivity to both ADP and epinephrine was observed 1 month after clopidogrel discontinuation.
Conclusions:
This study demonstrates a transient increase in platelet reactivity 1 month after clopidogrel withdrawal. This phenomenon may, in part, explain the known clustering of thrombotic events observed after clopidogrel discontinuation. This observation requires confirmation in larger populations.
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