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. 2025 Dec 12.
doi: 10.1007/s00062-025-01603-7. Online ahead of print.

Clinical Outcomes and Factors Associated with Reocclusion after Endovascular Therapy for Intracranial Atherothrombotic Stroke with Large Vessel Occlusion

Affiliations

Clinical Outcomes and Factors Associated with Reocclusion after Endovascular Therapy for Intracranial Atherothrombotic Stroke with Large Vessel Occlusion

Hiroyuki Ikeda et al. Clin Neuroradiol. .

Abstract

Purpose: Reocclusion after endovascular therapy (EVT) may worsen the clinical outcome of patients undergoing EVT for intracranial atherothrombotic stroke with large vessel occlusion (AT-LVO), but the details and risk factors have not been fully investigated.

Methods: Patients with intracranial AT-LVO were enrolled in a multicenter retrospective registry study conducted at 51 centers in Japan and were divided into two groups based on whether reocclusion occurred within 90 days after recanalization of intracranial AT-LVO with EVT: the reocclusion group and the patent group. The primary outcome was a modified Rankin Scale score of 0-2 at 90 days after EVT. Risk factors for reocclusion were also assessed.

Results: A total of 461 patients were enrolled, 66 (14.3%) in the reocclusion group and 395 (85.7%) in the patent group. Intracranial stenting and differences in antithrombotic regimens were not associated with reocclusion. The rate of patients with the primary outcome was significantly lower in the reocclusion group than in the patent group (15.4% vs. 46.4%, adjusted odds ratio 0.15 [95% confidence interval 0.06-0.33], P < 0.001). Reocclusion was associated with recurrent ischemic stroke, additional EVT or surgery, symptomatic intracranial hemorrhage, and all-cause death. Direct aspiration and vessel perforation were independent factors for reocclusion (adjusted odds ratio 1.82 [95% confidence interval 1.02-3.25], P = 0.043; adjusted odds ratio 5.91 [95% confidence interval 1.005-35.35], P = 0.049, respectively).

Conclusions: Reocclusion after EVT was associated with recurrent ischemic stroke, additional EVT or surgery, symptomatic intracranial hemorrhage, and poor clinical outcome at 90 days. Direct aspiration and vessel perforation were independent risk factors for reocclusion after EVT.

Keywords: Angioplasty; Aspiration catheter; Atherosclerosis; Recanalization; Stent; Thrombectomy.

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Conflict of interest statement

Declarations. Conflict of interest: H. Ikeda received lecture fees from Medtronic, Daiichi Sankyo, Johnson & Johnson, and Terumo. K. Uchida reports lecturer’s fees from Daiichi Sankyo, Bristol-Myers Squibb, Stryker, and Medtronic. H. Yamagami discloses lecturer’s fees from Stryker, Medtronic, Johnson & Johnson, Daiichi-Sankyo, Otsuka Pharmaceutical, and Bristol-Myers Squibb. N. Sakai reports a research grant from Japan Lifeline, Kaneka, Medtronic, Terumo, and TG Medical, lecturer’s fees from Asahi Intecc, Kaneka, Medtronic, Stryker, and Terumo, membership on the advisory boards for Johnson & Johnson, Medtronic, and Terumo outside the submitted work. M. Shirakawa received lecturer fees from Stryker, Medtronic, Terumo, Johnson & Johnson, and Kaneka. M. Beppu received manuscript fees from Medicus Shuppan. K. Toyoda reports lecture’s fees from Bayer, Daiichi Sankyo, Otsuka, Janssen, and Bristol Myers Squibb. Y. Matsumaru received lecture fees from Medtronic, Stryker, Terumo, Johnson and Johnson, Kaneka, and Jimro. Y. Matsumoto received lecturer fees from Kaneka, Medico’s Hirata, Fuji Systems, GE Healthcare, Otsuka, Takeda, Century Medical, Terumo, Medtronic, and Stryker. K. Todo received lecture fees from Pfizer, Bristol-Myers Squibb, Daiichi Sankyo, Bayer, Stryker, Medtronic, AstraZeneca, Otsuka Pharmaceutical, Kyowa Kirin, Takeda Pharmaceutical, and Amgen. S. Shindo received lecture fees from Medtronic, Kaneka, Stryker, Daiichi Sankyo, Asahi Intecc, Eisai, Bayer, Abbot Medical, Medicos Hirata, and Johnson & Johnson. M. Takeuchi received lecturer fees from Stryker, Daiichi Sankyo, Terumo, Asahi Intecc, and Johnson & Johnson. H. Imamura reports the lecturer’s fees from Medtronic, Daiichi Sankyo., Stryker, Terumo, Johnson & Johnson, and Asahi Intecc. K. Tanaka received lecturer’s fee from Stryker. H. Ishihara received lecture fees from Daiichi Sakyo and Stryker. T. Sano received lecture fees from Stryker. H. Araki received lecture fees from Pfizer, Bristol-Myers Squibb, Daiichi Sankyo, Johnson & Johnson, Medico’s Hirata, Asahi Intecc, and Medtronic. T. Nomura reports lecture’s fee from Oben, Daiici Sankyo, Bayer, Wakamoto Seiyaku, Idorsia Pharma, Stryker, Medtronic, Kaneka, and Johnson & Johnson. F. Sakakibara received manuscript fees from Medicus Shuppan. S. Yoshimura received research grants from Medico’s Hirata, Medtronic, and Terumo and lecture fees from Medtronic, Kaneka, Stryker, Daiichi Sankyo, Bristol Meyers Squibb, and Johnson & Johnson. M. Kinosada, M. Uezato, M. Chin, M. Hayakawa, S. Ota, M. Morimoto, and H. Kakita declare that they have no conflict of interest. Ethical standards: The study protocol was approved by the Institutional Review Board of Hyogo College of Medicine (approval number 3727) and all participating hospitals.

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