Orlando Alessandro, Wagner Jeffrey C, Fanale Christopher V, Whaley Michelle, McCarthy Kathryn L, Bar-Or David
Swedish Medical Center, Englewood, Colorado.
Swedish Medical Center, Englewood, Colorado.
J Stroke Cerebrovasc Dis. 2016 Apr;25(4):969-76. doi: 10.1016/j.jstrokecerebrovasdis.2016.01.003. Epub 2016 Feb 5.
To describe the 4-year experience of symptomatic intracranial hemorrhage (sICH) rate at a high-volume comprehensive stroke center.
All admitted adult (≥18 years) patients presenting with an ischemic stroke from 2010 to 2013 were included in this study. The primary outcome was sICH, defined as any hemorrhage with neurological deterioration (change in National Institutes of Health Stroke Scale score ≥4) within 36 hours of intravenous tissue plasminogen activator (IV-tPA) treatment, or any hemorrhage resulting in death. Secondary outcomes were in-hospital mortality and having a favorable modified Rankin Scale (mRS) score (≤2).
A total of 1925 did not receive intravascular (IV) or intra-arterial (IA) therapy; only 451 received IV therapy; and 175 received both IV and IA therapies. In IV-only patients, the overall rate of sICH was 2.2%; in IV and IA patients, the rate was 5.7%; and in patients who received no therapy, the rate was .4%. The IV-only group had an sICH rate of .9% in 2013. There were no differences in the adjusted odds of dying in the hospital between the study groups. IV-only treatment offered significantly better odds of achieving a favorable functional outcome, compared to no therapy, among patients with moderate stroke severity, whereas IV and IA treatments offered significantly better odds among patients with severe strokes. The odds of achieving a favorable functional outcome by discharge were decreased by 97% if patients suffered an sICH (OR = .03, 95%CI = .004, .19).
Despite an increased risk of sICH with IV-tPA, treatment with IV-tPA continues to be associated with increased odds of a favorable discharge mRS.
描述一家大型综合卒中中心4年来有症状性颅内出血(sICH)发生率的情况。
本研究纳入了2010年至2013年期间所有因缺血性卒中入院的成年(≥18岁)患者。主要结局为sICH,定义为在静脉注射组织型纤溶酶原激活剂(IV-tPA)治疗36小时内出现任何伴有神经功能恶化(美国国立卫生研究院卒中量表评分变化≥4)的出血,或任何导致死亡的出血。次要结局为住院死亡率和获得良好的改良Rankin量表(mRS)评分(≤2)。
共有1925例患者未接受血管内(IV)或动脉内(IA)治疗;仅451例接受了IV治疗;175例接受了IV和IA治疗。仅接受IV治疗的患者中,sICH的总体发生率为2.2%;接受IV和IA治疗的患者中,发生率为5.7%;未接受治疗的患者中,发生率为0.4%。2013年,仅接受IV治疗的组sICH发生率为0.9%。各研究组之间在调整后的院内死亡几率方面没有差异。与未治疗相比,在中度卒中严重程度的患者中,仅接受IV治疗显著提高了获得良好功能结局的几率,而在重度卒中患者中,IV和IA治疗显著提高了获得良好结局的几率。如果患者发生sICH,出院时获得良好功能结局的几率降低了97%(比值比[OR]=0.03,95%置信区间[CI]=0.004,0.19)。
尽管使用IV-tPA会增加sICH的风险,但IV-tPA治疗仍然与出院时获得良好mRS评分的几率增加相关。