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

Authors :
Enomoto Y
Matsubara H
Ishihara T
Shoda K
Mizutani D
Egashira Y
Ishii A
Sakamoto M
Sumita K
Nakagawa I
Higashi T
Yoshimura S
Source :
Journal of neurointerventional surgery [J Neurointerv Surg] 2024 Apr 23; Vol. 16 (5), pp. 491-497. Date of Electronic Publication: 2024 Apr 23.
Publication Year :
2024

Abstract

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.<br />Objective: To determine the optimal DAPT duration in patients with SAC/FD.<br />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.<br />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.<br />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.<br />Trial Registration Number: UMIN000044122 :https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000050384.<br />Competing Interests: Competing interests: YEn received a research grant from Sysmex; a lecture fee from Stryker, Medtronic, Johnson and Johnson, Daiichi-Sankyo and Otsuka Pharmaceutical. AI received a lecture fee feom Medtronic, Stryker, Terumo, Johnson and Johnson, Medico's Hirata, Kaneka, Daiichi-Sankyo and Otsuka Pharmaceutical; a research glant from Fuji film. MS received a lecture fee from Medtronic. KSu received a lecture fee from Stryker and Daiichi-Sankyo. IN received a lecture fee from Terumo, Kaneka and Daiichi-Sankyo. TH received a lecture fee from Stryker, Medtronic, Johnson and Johnson, Daiichi-Sankyo and Abbott; a research grant from Stryker, Medtronic, Asahi Intec, Kaneka, Medico's Hirata, Boehringer Ingelheim and Eisai. SY recieved a research grant from Asahi Intec, Biomedical Solution, Medico's Hirata, Medtronic, Otsuka Pharmaceutical, Stryker and Terumo; a lecture fee from Stryker, Medtronic, Johnson and Johnson, Kaneka, Daiichi-Sankyo, Bayer and Bristol-Meyers Squibb.<br /> (© Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.)

Details

Language :
English
ISSN :
1759-8486
Volume :
16
Issue :
5
Database :
MEDLINE
Journal :
Journal of neurointerventional surgery
Publication Type :
Academic Journal
Accession number :
37344176
Full Text :
https://doi.org/10.1136/jnis-2023-020285