Optimal duration of dual antiplatelet therapy for stent-assisted coiling or flow diverter placement

医学 养生 外科 支架 人口 生存分析 队列 内科学 环境卫生
作者
Yukiko Enomoto,Hirofumi Matsubara,Takuma Ishihara,Kenji Shoda,Daisuke Mizutani,Yusuke Egashira,Akira Ishii,Makoto Sakamoto,Kazutaka Sumita,Ichiro Nakagawa,Toshio Higashi,Shinichi Yoshimura
出处
期刊:Journal of NeuroInterventional Surgery [BMJ]
卷期号:: jnis-020285 被引量:8
标识
DOI:10.1136/jnis-2023-020285
摘要

Background Dual antiplatelet therapy (DAPT) is necessary to prevent thromboembolic complications after stent-assisted coiling (SAC) or flow-diversion (FD) for cerebral aneurysms, but the optimal antiplatelet regimen remains unclear. Objective To determine the optimal DAPT duration in patients with SAC/FD. Methods This multicenter cohort study enrolled patients who received SAC/FD for cerebral aneurysms at seven Japanese institutions between January 2010 and December 2020. The primary outcome was the time from procedure to the occurrence of a composite of target vessel-related thromboembolic events, procedure-unrelated major bleeding events, or death. The cumulative event-free survival rates were analyzed using a Kaplan–Meier curve, and the differences in each outcome between the groups dichotomized by the duration of DAPT were analyzed using the log-rank test. Results Of 632 patients (median observational period, 646 days), primary outcome occurred in 63 patients (10.0%), most frequently within 30 days after the procedure. The cumulative event-free survival rates at 30 days, 1 year, and 2 years after the procedure were 93.3% (91.4 to 95.3%), 91.5% (89.3 to 93.7%), and 89.5% (87.0 to 92.0%), respectively. The cumulative event-free survival rates after switching to monotherapy were similar for the >91 and <90 days DAPT groups in the population limited to patients who were switched from DAPT to monotherapy without major clinical events. Conclusions Thromboembolic events rarely occurred beyond 30 days after SAC/FD. The duration of DAPT may be shortened if patients have a periprocedural period without events. Further prospective studies are warranted to determine the optimal duration of antiplatelet therapy. Trial registration number UMIN000044122 : https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000050384 .
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