Thortveit E T, Bøe M G, Ljøstad U, Mygland A, Tveiten A
Department of Neurology, Sørlandet Sykehus, Kristiansand, Norway.
Acta Neurol Scand. 2014 Oct;130(4):248-52. doi: 10.1111/ane.12204. Epub 2013 Nov 21.
To assess time trends in intravenous thrombolytic (iv tPA) treatment in a general local hospital during a period with organizational changes, especially how movement of treatment start from the emergency room (ER) to the CT laboratory, and changing method of administration of acute antihypertensive medication influenced on door-to-needle time (DNT).
All stroke patients treated with iv tPA have been prospectively enrolled in the Safe Implementation of Treatments in Stroke (SITS) registry. Data from 2007 to 2011 were reviewed. Safety was evaluated by the incidence of symptomatic intracerebral hemorrhage (SICH). Predictors of DNT were assessed by multivariable regression.
Two hundred and forty-three patients were treated with iv tPA. The annual treatment rate reached 21.9% of patients with ischemic strokes admitted to the hospital. Median DNT decreased from 36 to 28 min (P ≤ 0.001). The incidence of SICH remained low and was throughout the period 2.5%. Treatment start in the CT laboratory vs in the ER was associated with a reduction in median DNT (P = 0.007). Acute antihypertensive treatment and treatment with warfarin were associated with increased DNT (P = 0.024 and P = 0.003, respectively). Age, gender, baseline NIHSS, onset-to-door time, comorbidity, and method of administration of acute antihypertensive treatment did not influence DNT significantly.
Streamlining of iv tPA logistics can reduce median DNT to <30 min in a general local hospital. Moving treatment start from the ER to the CT laboratory contributed to reduce DNT. Our organizational model was resistant to influence on DNT by patient age, gender, stroke severity, and time to hospital arrival. The incidence of SICH remained low.
评估在一家当地综合医院组织架构变革期间静脉溶栓(iv tPA)治疗的时间趋势,特别是治疗起始从急诊室(ER)转移至CT实验室的情况,以及急性抗高血压药物给药方式的改变对门到针时间(DNT)的影响。
所有接受iv tPA治疗的卒中患者均前瞻性纳入卒中治疗安全实施(SITS)登记系统。回顾了2007年至2011年的数据。通过症状性脑出血(SICH)的发生率评估安全性。通过多变量回归评估DNT的预测因素。
243例患者接受了iv tPA治疗。年治疗率达到入院缺血性卒中患者的21.9%。中位DNT从36分钟降至28分钟(P≤0.001)。SICH的发生率一直较低,整个期间为2.5%。在CT实验室而非急诊室开始治疗与中位DNT的降低相关(P = 0.007)。急性抗高血压治疗和华法林治疗与DNT增加相关(分别为P = 0.024和P = 0.003)。年龄、性别、基线美国国立卫生研究院卒中量表(NIHSS)评分、发病到入院时间、合并症以及急性抗高血压治疗的给药方式对DNT无显著影响。
在当地综合医院,优化iv tPA的后勤流程可将中位DNT降至<30分钟。将治疗起始从急诊室转移至CT实验室有助于缩短DNT。我们的组织模式对患者年龄、性别、卒中严重程度和入院时间对DNT的影响具有抗性。SICH的发生率一直较低。