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Updated: Jul 16, 2025

Interventional Diagnostic Procedure: A Practical Guide for the Assessment of Coronary Vascular Function
Published on: March 15, 2022
Strokes and Transient Ischemic Attacks Occurrence During Annual Dual Antiplatelet Therapy
Victor L Serebruany1, Jean-Francois Tanguay2, Milana L Gurvich3
1Department of Neurology, Johns Hopkins University, Baltimore, MD.
Background:
The incidence of stroke/TIA during annual dual antiplatelet therapy (ADAPT) for acute coronary syndrome (ACS) remains high. Some evidence suggests that shorter than ADAPT may diminish such risk, still providing adequate vascular protection. However, the precise timing of strokes/TIA occurrences during ADAPT is unclear but may be important for determining optimal preventive treatment duration.
Study Question:
The precise timing of secondary cerebrovascular events over ADAPT.
Study Design:
Access was gained to the FDA-issued Platelet Inhibition and Outcomes (PLATO) trial data set on which post hoc analyses of stroke/TIA timing after ticagrelor and clopidogrel on top of aspirin was explored.
Measures And Outcomes:
Events were counted and plotted over time from day 1 till day 365 after the index ACS event.
Results:
Among 18,624 enrollees, 252 strokes and 49 TIAs were reported. After the exclusion of entries with missing dates, unclear randomization codes, and events beyond 1-year follow-up, 238 strokes and 45 TIAs were analyzed. Overall, most frequent strokes/TIAs occurred within the first day after qualifying ACS, with the gradual declines after day 7 and day 40 reaching background counts thereafter. The strokes/TIAs patterns did not differ much between P 2 Y12 inhibitors except for twice more events at day 1 and excess exclusions after day 365 in the ticagrelor arm.
Conclusions:
Most cerebrovascular events emerged very early after ACS despite ADAPT. This large hypothesis-generating evidence may justify shorter than the ADAPT duration after ACS. Twice more events at day 1 and excess late ticagrelor exclusions in PLATO deserve further scrutiny.
Registration:
URL: https://www.clinicaltrials.gov ; Unique identifier: NCT00391872.
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