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Updated: May 21, 2025

Interventional Diagnostic Procedure: A Practical Guide for the Assessment of Coronary Vascular Function
Published on: March 15, 2022
Guided Antiplatelet Therapy for Stent-Treated Intracranial Aneurysms: A Cluster-Randomized Trial
Yangyang Zhou1,2, Jun Wang3, Wenqiang Li1,2
1Department of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, No. 119 South Fourth Ring West Road, Fengtai District, Beijing 100070, China.
Insights
Platelet function test-guided antiplatelet therapy significantly reduced ischemic events in patients undergoing intracranial aneurysm treatment. This approach, including ticagrelor, proved safe and effective, lowering event incidence without increasing bleeding risks.
Area of Science:
- Neurointerventional Surgery
- Cardiology
- Pharmacology
Background:
- Poor antiplatelet drug response during neurointerventions for intracranial aneurysms (IAs) elevates ischemic event (IE) risk.
- Ticagrelor may offer a safer alternative to clopidogrel in managing antiplatelet therapy.
- Standard dual antiplatelet therapy (SDAT) involves aspirin and clopidogrel.
Purpose of the Study:
- To evaluate if platelet function test (PFT)-guided antiplatelet therapy reduces IE incidence compared to SDAT in IA patients.
- To assess the efficacy and safety of PFT-guided therapy in neurointerventional procedures.
Main Methods:
- A prospective, multicenter, cluster-randomized trial involving 16 neurointerventional teams.
- Test group: PFT-guided therapy with dose adjustment or switch to ticagrelor for poor responders.
- Control group: SDAT. Primary outcome: cerebral IE within 30 days.
Main Results:
- Lower IE incidence in the PFT-guided group (6.8%) vs. SDAT group (13.2%) within 30 days (OR, 0.54; P=.03).
- Reduced IE incidence within 7 days (4.1% vs. 10.8%; OR, 0.48; P=.02).
- No significant difference in modified Rankin Scale scores or all-cause mortality; bleeding event incidence was similar between groups.
Conclusions:
- PFT-guided antiplatelet therapy is associated with a reduced incidence of ischemic events in patients undergoing endovascular treatment for IAs.
- Switching to ticagrelor as part of PFT-guided therapy did not increase the risk of bleeding events.
Abstract:
Background During neurointerventional treatment of intracranial aneurysms (IAs), poor antiplatelet drug response increases the risk of a cerebral ischemic event (IE). Replacing clopidogrel with ticagrelor may reduce this risk. Purpose To determine whether platelet function test (PFT)-guided antiplatelet therapy reduces incidence of IEs compared with standard dual antiplatelet therapy (SDAT; daily oral aspirin and clopidogrel, 100 mg and 75 mg, respectively) in patients undergoing endovascular intervention for IAs. Materials and Methods In this prospective, multicenter, cluster-randomized trial, 16 neurointerventional teams were randomly allocated to eight test and eight control clusters. Between May and August 2023, test group participants underwent PFT. Test group participants who showed poor antiplatelet response were administered an increased aspirin dose or were switched from clopidogrel to ticagrelor. The control group was administered SDAT. The primary outcome was any cerebral IE within 30 days after the procedure. The exploratory outcomes were any IE within 7 days, modified Rankin Scale score, and all-cause mortality within 30 days. The safety outcome measure was any bleeding event within 30 days. All outcome analyses were performed using generalized linear mixed-effects models. Results A total of 590 participants were included (median age, 58 years; 374 women). IE incidence within 30 days was lower in the test group than in the control group (6.8% [20 of 295] vs 13.2% [39 of 295]; odds ratio [OR], 0.54; 95% CI: 0.31, 0.94; P = .03) and within 7 days (4.1% [12 of 295] vs 10.8% [32 of 295]; OR, 0.48; 95% CI: 0.25, 0.89; P = .02) after undergoing the procedure. There was no evidence of a difference between the test group and the control group in modified Rankin Scale scores (0.33 vs 0.49, respectively; P = .11) or mortality (0.3% [one of 295] vs 2.0% [six of 295], respectively; P = .54). Furthermore, there was no evidence of a between-group difference in bleeding event incidence (24.1% [71 of 295] vs 31.2% [92 of 295]; OR, 0.67; 95% CI: 0.30, 1.5; P = .32). Conclusion PFT-guided antiplatelet therapy was associated with reduced IE incidence. Administration of 60 mg of ticagrelor did not increase bleeding event incidence. Clinicaltrials.gov Identifier: NCT05825391 © RSNA, 2025 Supplemental material is available for this article. See also the editorial by Kallmes and Altschul in this issue.
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