Mazya Michael V, Lees Kennedy R, Collas David, Rand Viiu-Marika, Mikulik Robert, Toni Danilo, Wahlgren Nils, Ahmed Niaz
From the Department of Neurology (M.V.M., N.W., N.A.), Karolinska University Hospital, Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden; Acute Stroke Unit & Cerebrovascular Clinic (K.R.L.), Institute of Cardiovascular & Medical Sciences, University of Glasgow; Stroke Unit (D.C.), Watford General Hospital, UK; Department of Neurology (V.-M.R.), North Estonia Medical Centre, Tallinn, Estonia; International Clinical Research Center and Department of Neurology (R.M.), St. Anne's University Hospital, Brno, Czech Republic; and Department of Neurology and Psychiatry (D.T.), Sapienza University of Rome, Italy.
Neurology. 2015 Dec 15;85(24):2098-106. doi: 10.1212/WNL.0000000000002199. Epub 2015 Nov 6.
To study the safety of off-label IV thrombolysis in patients with very severe stroke (NIH Stroke Scale [NIHSS] scores >25) compared with severe stroke (NIHSS scores 15-25), where treatment is within European regulations.
Data were analyzed from 57,247 patients with acute ischemic stroke receiving IV tissue plasminogen activator in 793 hospitals participating in the Safe Implementation of Thrombolysis in Stroke (SITS) International Stroke Thrombolysis Registry (2002-2013). Eight hundred sixty-eight patients (1.5%) had NIHSS scores >25 and 19,995 (34.9%) had NIHSS scores 15-25. Outcome measures were parenchymal hemorrhage, symptomatic intracerebral hemorrhage, mortality, and functional outcome.
Parenchymal hemorrhage occurred in 10.7% vs 11.0% (p = 0.79), symptomatic intracerebral hemorrhage per SITS-MOST (SITS-Monitoring Study) in 1.4% vs 2.5% (p = 0.052), death at 3 months in 50.4% vs 26.9% (p < 0.001), and functional independence at 3 months in 14.0% vs 29.0% (p < 0.001) of patients with NIHSS scores >25 and NIHSS scores 15-25, respectively. Multivariate adjustment did not change findings from univariate comparisons. Posterior circulation stroke was more common in patients with NIHSS scores >25 (36.2% vs 7.4%, p < 0.001), who were also more often obtunded or comatose on presentation (58.4% vs 7.1%, p < 0.001). Of patients with NIHSS scores >25, 26.2% were treated >3 hours from symptom onset vs 14.5% with NIHSS scores of 15-25.
Our data show no excess risk of cerebral hemorrhage in patients with NIHSS score >25 compared to score 15-25, suggesting that the European contraindication to IV tissue plasminogen activator treatment at NIHSS levels >25 may be unwarranted. Increased mortality and lower rates of functional independence in patients with NIHSS score >25 are explained by higher stroke severity, impaired consciousness on presentation due to posterior circulation ischemia, and longer treatment delays.
研究在欧洲规定范围内,与重度卒中(美国国立卫生研究院卒中量表[NIHSS]评分15 - 25分)患者相比,超说明书静脉溶栓治疗极重度卒中(NIHSS评分>25分)患者的安全性。
分析了参与卒中溶栓安全实施(SITS)国际卒中溶栓登记研究(2002 - 2013年)的793家医院中57247例接受静脉注射组织型纤溶酶原激活剂的急性缺血性卒中患者的数据。868例患者(1.5%)NIHSS评分>25分,19995例患者(34.9%)NIHSS评分15 - 25分。观察指标为脑实质出血、症状性脑出血、死亡率和功能转归。
NIHSS评分>25分的患者脑实质出血发生率为10.7%,NIHSS评分15 - 25分的患者为11.0%(p = 0.79);根据SITS - MOST(SITS监测研究)标准,症状性脑出血发生率分别为1.4%和2.5%(p = 0.052);3个月时死亡率分别为50.4%和26.9%(p < 0.001);3个月时功能独立率分别为14.0%和29.0%(p < 0.001)。多变量调整并未改变单变量比较的结果。后循环卒中在NIHSS评分>25分的患者中更常见(36.2%比7.4%,p < 0.001),这些患者就诊时也更常出现意识模糊或昏迷(58.4%比7.1%,p < 0.001)。NIHSS评分>25分的患者中,26.2%在症状发作后>3小时接受治疗,而NIHSS评分为15 - 25分的患者这一比例为14.5%。
我们的数据显示,与NIHSS评分15 - 25分的患者相比,NIHSS评分>25分的患者脑出血风险并未增加,这表明欧洲将NIHSS评分>25分作为静脉注射组织型纤溶酶原激活剂治疗的禁忌证可能没有依据。NIHSS评分>25分的患者死亡率增加和功能独立率较低,原因是卒中严重程度更高、因后循环缺血就诊时意识受损以及治疗延迟时间更长。