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Randomized Controlled Trial
. 2024 Oct 1;81(10):1043-1050.
doi: 10.1001/jamaneurol.2024.2652.

Endovascular vs Medical Management of Acute Basilar Artery Occlusion: A Secondary Analysis of a Randomized Clinical Trial

Collaborators, Affiliations
Randomized Controlled Trial

Endovascular vs Medical Management of Acute Basilar Artery Occlusion: A Secondary Analysis of a Randomized Clinical Trial

Rui Li et al. JAMA Neurol. .

Erratum in

  • Error in Figure.
    [No authors listed] [No authors listed] JAMA Neurol. 2024 Oct 1;81(10):1103. doi: 10.1001/jamaneurol.2024.3566. JAMA Neurol. 2024. PMID: 39401027 Free PMC article. No abstract available.

Abstract

Importance: In several randomized clinical trials, endovascular thrombectomy led to better functional outcomes than conventional treatment at 90 days poststroke in patients with acute basilar artery occlusion. However, the long-term clinical outcomes of these patients have not been well delineated.

Objective: To evaluate 1-year clinical outcomes in patients with acute basilar artery occlusion following endovascular thrombectomy vs control.

Design, setting, and participants: This study is an extension of the ATTENTION trial, a multicenter, randomized clinical trial. Patients were included between February 2021 and January 2022, with 1-year follow-up through April 2023. This multicenter, population-based study was conducted at 36 comprehensive stroke sites. Patients with acute basilar artery occlusion within 12 hours of estimated symptom onset were included. Of the 342 patients randomized in the ATTENTION trial, 330 (96.5%) had 1-year follow-up information available.

Exposures: Endovascular thrombectomy (thrombectomy group) vs best medical treatment (control group).

Main outcomes and measures: The primary outcome was defined as a score of 0 to 3 on the modified Rankin Scale (mRS) at 1 year. Secondary outcomes were functional independence (mRS score 0-2), excellent outcome (mRS score 0-1), level of disability (distribution of all 7 mRS scores), mortality, and health-related quality of life at 1 year.

Results: Among 330 patients who had 1-year follow-up data, 227 (68.8%) were male, and the mean (SD) age was 67.0 (10.7) years. An mRS score 0 to 3 at 1 year was achieved by 99 of 222 patients (44.6%) in the thrombectomy group and 21 of 108 (19.4%) in the control group (adjusted rate ratio, 2.23; 95% CI, 1.51-3.29). Mortality at 1 year compared with 90 days was more frequent in both the thrombectomy group (101 of 222 [45.5%] vs 83 of 226 [36.7%]) and the control group (69 of 108 [63.9%] vs 63 of 114 [55.3%]). Excellent outcome (mRS score 0-1) at 1 year compared with 90 days increased in the thrombectomy group (62 of 222 [27.9%] vs 45 of 226 [19.9%]) but not in the control group (9 of 108 [8.3%] vs 9 of 114 [7.9%]) resulting in a magnified treatment benefit.

Conclusions and relevance: Among patients with basilar artery occlusion within 12 hours of onset, the benefits of endovascular thrombectomy at 1 year compared with 90 days were sustained for favorable (mRS score 0-3) outcome and enhanced for excellent (mRS score 0-1) outcome.

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Conflict of interest statement

Conflict of Interest Disclosures: Dr Nguyen reported serving as associate editor of Stroke and on advisory boards for Aruna Bio and Brainomix outside the submitted work. Dr Saver reported personal fees from Medtronic, Biogen, Roche, Genentech, Boehringer Ingelheim, and Bayer outside the submitted work. Dr Nogueira reported consulting fees for advisory roles with Anaconda, Biogen, Cerenovus, Genentech, Philips, Hybernia, Hyperfine, Imperative Care, Medtronic, Phenox, Philips, Prolong Pharmaceuticals, Stryker Neurovascular, Shanghai Wallaby, and Synchron and stock options for advisory roles with Astrocyte, Brainomix, Cerebrotech, Ceretrieve, Corindus Vascular Robotics, CrestecBio, Euphrates Vascular, Vesalio, Viz-AI, RapidPulse, and Perfuze; in addition, Dr Nogueira is one of the principal investigators of the Endovascular Therapy for Low NIHSS Ischemic Strokes (ENDOLOW) trial, funding for which is provided by Cerenovus; the principal investigator of the Combined Thrombectomy for Distal MediUm Vessel Occlusion StroKe (DUSK) trial, funding for which is provided by Stryker Neurovascular; and is an investor in Viz-AI, Perfuze, Cerebrotech, Reist/Q’Apel Medical, Truvic, Tulavi Therapeutics, Vastrax, Piraeus Medical, Brain4Care, Quantanosis AI, and Viseon. No other disclosures were reported.

Figures

Figure 1.
Figure 1.. Distribution of the Modified Rankin Scale Scores at 1 Year (Intention-to-Treat Population)
The scores range from 0 to 6, with each score representing a specific level of disability: 0, no symptoms; 1, no clinically significant disability; 2, slight disability (patients are able to look after their own affairs without assistance but are unable to carry out all previous activities); 3, moderate disability (patients require some help but are able to walk unassisted); 4, moderately severe disability (patients are unable to attend to bodily needs without assistance and are unable to walk unassisted); 5, severe disability (patients require constant nursing care and attention); 6, death. The adjusted common odds ratio was 2.55 (95% CI, 1.60-4.08) toward a better outcome with the thrombectomy group at 1 year.
Figure 2.
Figure 2.. Kaplan-Meier Estimates of Mortality During the 1-Year Follow-Up After Randomization
Compared to the control group, the adjusted hazard ratio for death at 1 year in the thrombectomy group was 0.62 (95% CI, 0.45-0.84).
Figure 3.
Figure 3.. Subgroup Analyses of Primary Outcome at 1 Year
BAO indicates basilar artery occlusion; ICAD, intracranial atherosclerotic disease; NIHSS, National Institutes of Health Stroke Scale; OTR, estimated time of basilar artery occlusion to randomization; PC-ASPECTS, posterior circulation Acute Stroke Prognosis Early Computed Tomography Score; RR, rate ratio.

References

    1. Tao C, Nogueira RG, Zhu Y, et al. ; ATTENTION Investigators . Trial of endovascular treatment of acute basilar-artery occlusion. N Engl J Med. 2022;387(15):1361-1372. doi: 10.1056/NEJMoa2206317 - DOI - PubMed
    1. Jovin TG, Li C, Wu L, et al. ; BAOCHE Investigators . Trial of thrombectomy 6 to 24 hours after stroke due to basilar-artery occlusion. N Engl J Med. 2022;387(15):1373-1384. doi: 10.1056/NEJMoa2207576 - DOI - PubMed
    1. Langezaal LCM, van der Hoeven EJRJ, Mont’Alverne FJA, et al. ; BASICS Study Group . Endovascular therapy for stroke due to basilar-artery occlusion. N Engl J Med. 2021;384(20):1910-1920. doi: 10.1056/NEJMoa2030297 - DOI - PubMed
    1. Liu X, Dai Q, Ye R, et al. ; BEST Trial Investigators . Endovascular treatment versus standard medical treatment for vertebrobasilar artery occlusion (BEST): an open-label, randomised controlled trial. Lancet Neurol. 2020;19(2):115-122. doi: 10.1016/S1474-4422(19)30395-3 - DOI - PubMed
    1. Abdalkader M, Finitsis S, Li C, et al. ; BasilaR Artery Ischemia Network STudy of Endovascular versus Medical Management (BRAINSTEM) Group . Endovascular versus medical management of acute basilar artery occlusion: a systematic review and meta-analysis of the randomized controlled trials. J Stroke. 2023;25(1):81-91. doi: 10.5853/jos.2022.03755 - DOI - PMC - PubMed

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