From the Departments of Neurology (I.R., S.A., N.R., L.S.), Radiology (W.C., M.L.), and Emergency Medicine (J.G., J.M.), Massachusetts General Hospital, Harvard Medical School, Boston, MA.
Stroke. 2014 Feb;45(2):504-8. doi: 10.1161/STROKEAHA.113.004073. Epub 2014 Jan 7.
National guidelines recommend imaging within 25 minutes of emergency department arrival and intravenous tissue-type plasminogen activator within 60 minutes of emergency department arrival for patients with acute stroke. In 2007, we implemented a new institutional acute stroke care model to include 10 best practices and evaluated the effect of this intervention on improving door-to-computed tomography (CT) and door-to-needle (DTN) times at our hospital.
We compared patients who presented directly to our hospital with acute ischemic stroke in the preintervention (2003-2006) and postintervention (2008-2011) periods. We did not include 2007, the year that the new protocol was established. Predictors of DTN ≤60 minutes before and after the intervention were assessed using χ(2) for categorical variables, and t test and Wilcoxon signed-rank test for continuous variables.
Among 2595 patients with acute stroke, 284 (11%) received intravenous tissue-type plasminogen activator. For patients arriving within an intravenous tissue-type plasminogen activator window, door-to-CT <25 improved from 26.7% pre intervention to 52.3% post intervention (P<0.001). Similarly, the percentage of patients with DTN <60 doubled from 32.4% to 70.3% (P<0.001). Patients with DTN ≤60 did not differ significantly with respect to demographics, comorbidities, or National Institutes of Health Stroke Scale score in comparison with those treated after 60 minutes.
Door-to-CT and DTN times improved dramatically after applying 10 best practices, all of which were later incorporated into the Target Stroke Guidelines created by the American Heart Association. The only factor that significantly affected DTN60 was the intervention itself, indicating that these best practices can result in improved DTN times.
国家指南建议,对于急性脑卒中患者,在急诊科到达后 25 分钟内进行影像学检查,在急诊科到达后 60 分钟内给予静脉组织型纤溶酶原激活剂。2007 年,我们实施了一种新的院内急性脑卒中治疗模式,包含 10 项最佳实践,并评估了这种干预对改善我院患者的门到计算机断层扫描(CT)时间和门到针时间(DTN)的效果。
我们比较了干预前(2003-2006 年)和干预后(2008-2011 年)直接来我院就诊的急性缺血性脑卒中患者。我们未将 2007 年(新方案建立的那一年)纳入其中。使用卡方检验比较干预前后 DTN≤60 分钟的预测因素,使用 t 检验和 Wilcoxon 符号秩检验比较连续变量。
在 2595 例急性脑卒中患者中,284 例(11%)接受了静脉组织型纤溶酶原激活剂治疗。对于符合静脉组织型纤溶酶原激活剂治疗时间窗的患者,门到 CT<25 分钟的比例从干预前的 26.7%提高到了干预后的 52.3%(P<0.001)。同样,DTN<60 分钟的患者比例从 32.4%增加到了 70.3%(P<0.001)。与治疗时间超过 60 分钟的患者相比,DTN≤60 分钟的患者在人口统计学特征、合并症或美国国立卫生研究院卒中量表评分方面无显著差异。
应用 10 项最佳实践后,门到 CT 和 DTN 时间显著缩短,这些最佳实践后来都被纳入美国心脏协会制定的《目标脑卒中指南》中。唯一显著影响 DTN60 的因素是干预本身,这表明这些最佳实践可以缩短 DTN 时间。