Safety and Efficacy of Low-Dose Eptifibatide for Tandem Occlusions in Acute Ischemic Stroke

IF 3.2 Q2 CLINICAL NEUROLOGY Neurology International Pub Date : 2024-02-09 DOI:10.3390/neurolint16010017
P. Latacz, Tadeusz Popiela, P. Brzegowy, B. Lasocha, Krzysztof Kwiecień, M. Simka
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Abstract

Objectives: The optimal treatment strategy for ischemic stroke in patients presenting with tandem occlusions of the internal carotid artery remains controversial. Several studies have demonstrated better clinical outcomes after eptifibatide, which is a short half-life antiplatelet agent. This retrospective analysis focused on the safety and efficacy of low-dose eptifibatide administration in stroke patients with tandem lesions. Methods: We evaluated the results of endovascular treatment in 148 stroke patients with tandem lesions. Patients in whom balloon angioplasty alone resulted in satisfactory cerebral flow did not receive eptifibatide (33 patients); others received this drug together with stent implantation (115 patients). Eptifibatide was given as an intravenous bolus of 180 μg/kg and then in a modified low dose of 1 μg/kg/min for 24 hours. Results: There were no statistically significant differences between both groups regarding 30-day mortality, frequency of thrombotic events, or hemorrhagic complications. An analysis of clinical status at 30-day follow-up revealed that the administration of eptifibatide was associated with a statistically significant better outcome: a higher rate of either no neurological symptoms or only mild symptoms (4 NIHSS points maximally). Conclusions: The administration of eptifibatide in stroke patients presenting with tandem lesions is relatively safe. Moreover, treatment with this drug can improve clinical outcomes in these challenging patients.
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小剂量埃菲巴特治疗急性缺血性卒中串联闭塞的安全性和有效性
目的:颈内动脉串联闭塞患者缺血性中风的最佳治疗策略仍存在争议。有几项研究表明,使用短半衰期抗血小板药物埃替巴肽可获得更好的临床疗效。这项回顾性分析的重点是对有串联病变的中风患者使用小剂量依菲巴特的安全性和有效性。方法:我们评估了 148 例有串联病变的脑卒中患者的血管内治疗效果。仅通过球囊血管成形术获得满意脑血流的患者未接受依菲巴特治疗(33 例),其他患者在接受支架植入术的同时接受了依菲巴特治疗(115 例)。依普替巴肽的静脉注射剂量为 180 μg/kg,然后以 1 μg/kg/min 的改良低剂量持续 24 小时。结果显示两组患者在 30 天死亡率、血栓事件发生频率或出血并发症方面均无明显统计学差异。对随访 30 天的临床状况进行分析后发现,使用依菲巴特的结果在统计学上明显更好:无神经系统症状或仅有轻微症状(NIHSS 最大值为 4 分)的比例更高。结论是对出现串联病变的脑卒中患者使用依菲巴特相对安全。此外,使用该药物治疗可改善这些具有挑战性的患者的临床预后。
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来源期刊
Neurology International
Neurology International CLINICAL NEUROLOGY-
CiteScore
3.70
自引率
3.30%
发文量
69
审稿时长
11 weeks
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