Qureshi A I, Ezzeddine M A, Nasar A, Suri M F K, Kirmani J F, Janjua N, Divani A A
Clinical Trials Division, Zeenat Qureshi Stroke Research Center, Department of Neurology and Neurosciences, University of Medicine and Dentistry of New Jersey, Newark, NJ, USA.
Neurology. 2006 Apr 25;66(8):1171-4. doi: 10.1212/01.wnl.0000208407.69544.5a.
To evaluate the effect of IV recombinant tissue plasminogen activator (rt-PA) in patients with hyperdense artery sign (HAS) on initial CT scan.
The authors determined the differential effect of IV rt-PA (0.9 mg/kg) in patients with HAS by testing the interaction of rt-PA and HAS in a logistic regression model after adjusting for age, sex, initial NIH Stroke Scale score (NIHSSS), time to randomization, systolic blood pressure, serum glucose, body temperature, and rt-PA in 616 patients treated within 3 hours of symptom onset. Outcomes evaluated included intracranial hemorrhage, modified Rankin scale (mRS) 0-1, Barthel Index (BI) of > or = 95, Glasgow Outcome Scale (GOS) of 0-1, NIHSSS 0-1, and death at 90 days.
HAS was detected on the initial CT scan in 91 (15%) of the 616 patients by an independent neuroradiologist. Significantly lower rates of mRS 0-1, BI > or = 95, GOS of 0-1, or NIHSSS 0-1 at 90 days were observed among patients with HAS. IV rt-PA significantly increased the rates of mRS 0-1, BI > or = 95, GOS of 0-1, or NIHSSS 0-1 at 90 days after adjusting for potential confounders without any significant modifying effect (interaction) of HAS. Among the 91 patients with HAS, rt-PA use demonstrated a trend or significance for increased adjusted rates of favorable outcomes by mRS (p = 0.04), BI (p = 0.1), GOS (p = 0.03), and NIHSSS (p = 0.01).
Although hyperdense artery sign is associated with poor outcome, IV recombinant tissue plasminogen activator may be beneficial in this subgroup of patients with ischemic stroke.
评估静脉注射重组组织型纤溶酶原激活剂(rt-PA)对初始CT扫描显示为高密度动脉征(HAS)患者的疗效。
作者通过在逻辑回归模型中测试rt-PA与HAS的相互作用,在调整年龄、性别、初始美国国立卫生研究院卒中量表评分(NIHSSS)、随机分组时间、收缩压、血糖、体温和rt-PA后,确定静脉注射rt-PA(0.9mg/kg)对HAS患者的不同影响。对616例症状发作3小时内接受治疗的患者进行评估,评估的结局包括颅内出血、改良Rankin量表(mRS)评分为0 - 1、Barthel指数(BI)≥95、格拉斯哥预后量表(GOS)评分为0 - 1、NIHSSS评分为0 - 1以及90天时的死亡情况。
616例患者中,有91例(15%)经独立神经放射科医生在初始CT扫描时检测到HAS。在90天时,HAS患者中mRS评分为0 - 1、BI≥95、GOS评分为0 - 1或NIHSSS评分为0 - 1的比例显著较低。在调整潜在混杂因素后,静脉注射rt-PA显著提高了90天时mRS评分为0 - 1、BI≥95、GOS评分为0 - 1或NIHSSS评分为0 - 1的比例,且HAS无任何显著的修正作用(相互作用)。在91例HAS患者中,使用rt-PA显示出mRS(p = 0.04)、BI(p = 0.1)、GOS(p = 0.03)和NIHSSS(p = 0.01)调整后良好结局率增加的趋势或显著性。
尽管高密度动脉征与不良结局相关,但静脉注射重组组织型纤溶酶原激活剂可能对该组缺血性卒中患者有益。