Adjunct Intraarterial or Intravenous Tirofiban Versus No Tirofiban After Successful Recanalization of Basilar Artery Occlusion Stroke: The BASILAR Registry

Author:

Li Huagang1,Ju Dongsheng2,Tao Zhaojun3,Wang Jiayin3,Nguyen Thanh N.4ORCID,Saver Jeffrey L.5ORCID,Nogueira Raul G.6ORCID,Liu Chang7ORCID,Yang Qingwu7ORCID,Qiu Zhongming37ORCID,Yin Congguo8,Sun Dong1,Liu Shudong9ORCID

Affiliation:

1. Department of Neurology, Zhongnan Hospital Wuhan University Wuhan China

2. Department of Neurology Songyuan Jilin Oilfield Hospital Songyuan China

3. Department of Neurology The 903rd Hospital of The People’s Liberation Army Hangzhou China

4. Department of Neurology and Radiology Boston Medical Center Boston MA USA

5. Department of Neurology David Geffen School of Medicine at University of California at Los Angeles Los Angeles CA USA

6. Department of Neurology, UPMC Stroke Institute University of Pittsburgh School of Medicine Pittsburgh PA USA

7. Department of Neurology Xinqiao Hospital and The Second Affiliated Hospital, Army Medical University (Third Military Medical University) Chongqing China

8. Department of Neurology, Affiliated Hangzhou First People’s Hospital Zhejiang University School of Medicine Hangzhou China

9. Department of Neurology Yongchuan Hospital of Chongqing Medical University, Chongqing Key Laboratory of Cerebrovascular Disease Research Chongqing China

Abstract

Background Approximately half of patients who achieve successful reperfusion do not achieve functional independence. The present study sought to investigate the clinical outcomes and safety of intraarterial or intravenous tirofiban as adjunct therapy in patients with acute basilar artery occlusion who had achieved successful recanalization with endovascular treatment. Methods and Results In the national, prospective BASILAR (Endovascular Treatment for Acute Basilar Artery Occlusion Study) registry, 458 patients who met inclusion criteria were divided into 3 groups based on tirofiban administration (no tirofiban, n=262; intravenous tirofiban, n=101; intraarterial+intravenous tirofiban, n=95). Their clinical outcomes were compared with 90‐day modified Rankin Scale scores. Adjusted odds ratios (aORs) and 95% CIs were obtained by logistic regression models and propensity score matching. Safety outcomes included any intracranial hemorrhage (ICH), symptomatic ICH, and mortality. Among 458 included patients, 184 (40.2%) achieved a favorable outcome (modified Rankin Scale score 0–3). There were no differences between the intravenous tirofiban group and the no tirofiban group in terms of safety and clinical outcomes (all P >0.05). Compared with the no tirofiban group, the intraarterial+intravenous tirofiban group had higher odds of 90‐day modified Rankin Scale score 0 to 3 (aOR, 2.44 [95% CI, 1.30–4.64], P =0.006) and lower 3‐month mortality (aOR, 0.38 [95% CI, 0.19–0.71], P =0.002) without an increase in any ICH (aOR, 0.34 [95% CI, 0.09–1.01], P =0.07) or symptomatic ICH (aOR, 0.23 [95% CI, 0.03–0.90], P =0.05). Similar results of intraarterial+intravenous tirofiban on improving clinical outcomes were detected in novel cohorts constructed by propensity score matching. Conclusions Intraarterial+intravenous rather than intravenous tirofiban improved clinical outcomes without increasing the frequency of symptomatic ICH among patients with basilar artery occlusion after successful endovascular treatment. Further studies are needed to delineate the roles of intraarterial+intravenous tirofiban in patients with basilar artery occlusion receiving endovascular treatment.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Endovascular Treatment for Basilar Artery Occlusion;Journal of Clinical Medicine;2024-07-16

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