Suppr超能文献

挪威替奈普酶溶栓治疗急性缺血性卒中试验(NOR-TEST)中的卒中模拟病例的安全性及其预测因素。

Safety and predictors of stroke mimics in The Norwegian Tenecteplase Stroke Trial (NOR-TEST).

机构信息

1 Center for Neurovascular Diseases, Haukeland University Hospital, Bergen, Norway.

2 Department of Clinical Medicine, University of Bergen, Bergen, Norway.

出版信息

Int J Stroke. 2019 Jul;14(5):508-516. doi: 10.1177/1747493018790015. Epub 2018 Jul 18.

Abstract

BACKGROUND

Stroke mimics are frequently treated with thrombolysis in clinical practice and thrombolytic trials. Although alteplase in stroke mimics has proven to be safe, safety of tenecteplase in stroke mimics has not been assessed in an ischemic stroke study setting. We aimed to assess clinical characteristics and safety of stroke mimics treated with thrombolysis in the Norwegian Tenecteplase Stroke Trial. We also aimed to identify possible predictors of stroke mimics as compared to patients with acute cerebral ischemia.

METHODS

Norwegian Tenecteplase Stroke Trial was a phase-3 trial investigating safety and efficacy of tenecteplase vs. alteplase in patients with suspected acute cerebral ischemia. Two groups were defined based on diagnose at discharge: patients with a different diagnose than ischemic stroke or transient ischemic attack (stroke mimics group) and patients diagnosed with ischemic stroke or transient ischemic attack (acute cerebral ischemia group). Logistic regression analyses were performed with stroke mimics vs. acute cerebral ischemia as dependent variable to identify predictors of stroke mimics.

RESULTS

Of 1091 randomized patients, 181 (16.6%) were stroke mimics. Migraine (22.2%) and peripheral vertigo (11.4%) were the two most frequent stroke mimic-diagnoses. There was no symptomatic intracerebral hemorrhage in the stroke mimics group. Stroke mimics were independently associated with age ≤60 years (OR 2.75, p < 0.001), female sex (OR 1.48, p = 0.026), no history of myocardial infarction (OR 2.03, p = 0.045), systolic BP ≤ 150 mmHg (OR 2.33, p < 0.001), NIHSS ≤ 6 points (OR 1.83, p = 0.011), sensory loss (OR 1.55, p = 0.015), and no facial paresis (OR 2.41, p < 0.001) on admission.

CONCLUSION

Thrombolysis with tenecteplase seems to be as safe as with alteplase in stroke mimics. Predictors were identified for stroke mimics which may contribute to differentiate stroke mimics from acute cerebral ischemia in future stroke trials.

摘要

背景

在临床实践和溶栓试验中,经常对卒中模拟患者进行溶栓治疗。虽然阿替普酶治疗卒中模拟患者已被证明是安全的,但在缺血性卒中研究环境中尚未评估替奈普酶治疗卒中模拟患者的安全性。我们旨在评估在挪威替奈普酶溶栓试验中接受溶栓治疗的卒中模拟患者的临床特征和安全性。我们还旨在确定与急性脑缺血患者相比,卒中模拟患者的可能预测因素。

方法

挪威替奈普酶溶栓试验是一项 3 期试验,旨在评估替奈普酶与阿替普酶治疗疑似急性脑缺血患者的安全性和有效性。根据出院时的诊断将患者分为两组:诊断为非缺血性卒中或短暂性脑缺血发作(卒中模拟组)和诊断为缺血性卒中或短暂性脑缺血发作(急性脑缺血组)。采用逻辑回归分析,将卒中模拟患者与急性脑缺血患者作为因变量,以确定卒中模拟患者的预测因素。

结果

在 1091 例随机患者中,有 181 例(16.6%)为卒中模拟患者。偏头痛(22.2%)和周围性眩晕(11.4%)是两种最常见的卒中模拟诊断。卒中模拟组无症状性颅内出血。年龄≤60 岁(OR 2.75,p<0.001)、女性(OR 1.48,p=0.026)、无心肌梗死史(OR 2.03,p=0.045)、收缩压≤150mmHg(OR 2.33,p<0.001)、NIHSS≤6 分(OR 1.83,p=0.011)、感觉丧失(OR 1.55,p=0.015)和无面瘫(OR 2.41,p<0.001)是卒中模拟患者的独立预测因素。

结论

替奈普酶溶栓与阿替普酶溶栓一样安全,可用于治疗卒中模拟患者。已经确定了卒中模拟患者的预测因素,这可能有助于在未来的卒中试验中区分卒中模拟患者和急性脑缺血患者。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验