Dual antiplatelet therapy with cilostazol in stroke patients with extracranial arterial stenosis or without arterial stenosis: A subgroup analysis of the CSPS.com trial

Author:

Uchiyama Shinichiro1ORCID,Toyoda Kazunori2ORCID,Okamura Satomi3,Omae Katsuhiro3,Hoshino Haruhiko4ORCID,Kimura Kazumi5ORCID,Kitagawa Kazuo6ORCID,Minematsu Kazuo7ORCID,Yamaguchi Takenori2

Affiliation:

1. Clinical Research Center for Medicine, International University of Health and Welfare, Center for Brain and Cerebral Vessels, Sanno Medical Center, Tokyo, Japan

2. Department of Cerebrovascular Medicine, National Cerebral and Cardiovascular Center, Suita, Japan

3. Department of Data Science, National Cerebral and Cardiovascular Center, Suita, Japan

4. Department of Neurology, Tokyo Saiseikai Central Hospital, Tokyo, Japan

5. Department of Neurology, Nippon Medical School, Tokyo, Japan

6. Department of Neurology, Tokyo Women’s Medical University, Tokyo, Japan

7. Medical Corporation Iseikai, Osaka, Japan

Abstract

Background: We previously reported that dual antiplatelet therapy (DAPT) with cilostazol was superior to aspirin or clopidogrel for the prevention of recurrent stroke and vascular events in a subgroup analysis of intracranial arterial stenosis in the Cilostazol Stroke Prevention Study for Antiplatelet Combination ( CSPS.com ), a randomized controlled trial. Aims: We conducted another subgroup analysis to investigate the benefit of DAPT with cilostazol in patients with extracranial arterial stenosis (ECAS) and those without arterial stenosis. Methods: We compared the risk of recurrent ischemic stroke, vascular events, and major bleeding between DAPT with cilostazol plus aspirin or clopidogrel and aspirin or clopidogrel alone in patients with ischemic stroke between 8 and 180 days before starting trial treatment and ECAS or without arterial stenosis. Results: The median follow-up period was 1.4 years. The risk of recurrent ischemic stroke (hazard ratio (HR): 1.04, 95% confidence interval (CI): 0.42–2.57) and vascular events (HR: 0.97, 95% CI: 0.42–2.24) did not differ between the two groups for the 253 patients with ECAS, whereas they were lower (HR: 0.36, 95% CI: 0.18–0.74 and HR: 0.47, 95% CI: 0.26–0.85, respectively) in the DAPT group for the 944 patients without arterial stenosis. The risk of major bleeding did not differ between the groups in patients with ECAS (HR: 0.58, 95% CI: 0.05–6.39) or without arterial stenosis (HR: 0.79, 95% CI: 0.27–2.26). Conclusion: DAPT with cilostazol might be beneficial for prevention of recurrent stroke and vascular events in patients without arterial stenosis but not in those with ECAS. Data access statement: We will make the deidentified participant data from this research available to the scientific community with as few restrictions as feasible, while retaining exclusive use until the publication of major output.

Funder

Japan Agency for Medical Research and Development

otsuka pharmaceutical

Publisher

SAGE Publications

Subject

Neurology

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