Abstract DP310: Dual Antiplatelet versus Anticoagulant-Plus-Antiplatelet Therapy in Symptomatic Intracranial Atherosclerosis: A Multicenter Comparative Study

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Authors: M. Aemaz Ur Rehman, Fahad Khan, Shadi R. Yaghi, Sami Al Kasab, Ahmad Abu Qdais, Sridhara Yaddanapudi, Sabiha Sultana, Muhib Khan, Maarij Malik, James P. Klaas, Christopher R. Leon Guerrero, Faddi Ghassan Saleh Vélez
+38 more Cameron D. Owens, Camila Pinto, Margy E. McCullough‐Hicks, Dawson C Cooper, Abhiram Parameswaran Pillai, Praveen Hariharan, Shaista Alam, Mirjam R. Heldner, Kateryna Antonenko, William Almiri, Aaron Rothstein, Balaji Krishnaiah, Cheran Elangovan, Ayush Agarwal, Michele Romoli, Nicola Marrone, Stefano Vozzi, Malik Ghannam, Mahmoud Dibas, João Pedro Marto, Mohammad AlMajali, Alexis Netis Simpkins, Diana Aguiar de Sousa, Mafalda Soares, Amanda Lima, James Ernest Siegler, Argyro Tountopoulou, SOFIA VASILOPOULOU, Adam de Havenon, Nils Henninger, Johanna Helenius, Mohammad W Khasawneh, Piers Klein, Liqi Shu, Pooja Khatri, Thanh Ngoc Nguyen, David S. Liebeskind, Ekaterina Bakradze
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Abstract

Introduction: Intracranial atherosclerosis (ICAS) is a leading cause of ischemic stroke (IS) worldwide and carries a high risk of recurrence. Current guidelines favor 90 days of dual antiplatelet therapy (DAPT) for severe symptomatic ICAS, but recurrence remain high. Limited data suggest possible benefit of single antiplatelet plus anticoagulation (SAPT+AC). We compared the effectiveness and safety of DAPT versus SAPT+AC. We hypothesized that DAPT would lower 90-day recurrent IS risk without significantly increasing bleeding. Methods: This substudy of the Biomarkers and Recurrence Risk in Symptomatic Intracranial Arterial Stenosis (BIORISK-ICAS) included patients from 35 centers (Jan 2019–Jun 2024) with symptomatic 50–99% ICAS in the intracranial internal carotid, vertebral, basilar, or M1 segment of the MCA, presenting ≤72 hours from last known well. The primary efficacy outcome was recurrent IS in the same vascular territory at 90 days; the primary safety outcome was severe bleeding (symptomatic intracranial hemorrhage or major extracranial bleeding). Categorical variables were compared using χ 2 and continuous variables with the Student's t test; multivariable Cox regression adjusted for key covariates. Results: Of 2050 BIORISK-ICAS patients, 1658 met criteria (DAPT n=1499; SAPT+AC n=159). Mean age was 67 vs. 73 years, and 44% were women. At 90 days, recurrent IS occurred in 121 DAPT patients (8.07%) vs. 13 SAPT+AC patients (8.17%); unadjusted HR 0.83 (95% CI, 0.50–1.36; p=0.46). After adjustment for age, diabetes, coronary heart disease, atrial fibrillation, active smoking, and borderzone infarct, the adjusted HR was 0.99 (95% CI, 0.52–1.86; p=0.97). Severe bleeding occurred in 34 DAPT patients (2.26%) and 5 SAPT+AC patients (3.14%); unadjusted HR 0.79 (95% CI, 0.28–1.85; p=0.50), adjusted HR 0.66 (95% CI, 0.21–2.09; p=0.47). Conclusions: In patients with symptomatic ICAS, DAPT and SAPT+AC were associated with similar risks of 90-day recurrent ischemic stroke and severe bleeding. Well-powered randomized trials are needed to determine the optimal antithrombotic regimen in this high-risk population.

Fields of Study & Subjects

Cerebrovascular and Carotid Artery Diseases Acute Ischemic Stroke Management Antiplatelet Therapy and Cardiovascular Diseases

Publication details

Journal / source
Stroke
Volume
57
Issue
Suppl_1
Publication date
29 January 2026
Language
EN