Silverman Isaac E, Beland Dawn K, Chhabra Jyoti, McCullough Louise D
Stroke Center, Hartford Hospital, University of Connecticut School of Medicine, CT, USA.
Conn Med. 2005 Nov-Dec;69(10):613-20.
Acute stroke therapy with intravenous (IV) tissue plasminogen activator (t-PA) is vastly underutilized. Increasingly, patients are being started on IV t-PA and being transferred to regional Stroke Center programs, where additional therapies can be offered in a multimodal format. We describe our experience at the Stroke Center at Hartford Hospital with interhospital patient transfers who received IV t-PA prior to transfer to our medical center.
A retrospective analysis of our Acute Stroke Therapies database was undertaken, encompassing the intial four-year period of our Stroke Center program (May 1, 2001 to April 30, 2005). We evaluated the patient characteristics, clinical outcomes, and adjunctive therapies of patients who were started on IV t-PA at referring hospitals prior to their emergent transfer to our Stroke Center.
From a total of 229 patients who received IV and/or IA thrombolysis and newer catheter-delivered devices or clinical trials at our Stroke Center, a total of 33 (14.4%) were started on IV t-PA at an outside hospital prior to transfer. Symptomatic hemorrhage occurred in one of the 33 patients (3.0%), and in-hospital mortality rate for these patients was 6.1%. A total of 26 patients (78.8%) had a positive outcome in that they were discharged either to home or to acute rehabilitation.
Use of IV t-PA in a "drip-and-ship" approach is growing at the regional Stroke Center at Hartford Hospital. This protocol is safe and offers several advances for the care of patients with AIS: (a) empowering emergency physicians and neurologists at outside hospitals, via access to a 24/7 Acute Stroke Hotline, to treat patients with AIS; (b) facilitating the early initiation of IV t-PA; and (c) offering adjunctive therapeutic approaches, following arrival at our facility, for patients not sufficiently improving with IV t-PA alone.
静脉注射组织纤溶酶原激活剂(t-PA)进行急性卒中治疗的应用严重不足。越来越多的患者开始接受静脉注射t-PA治疗,并被转至区域卒中中心项目,在那里可以以多模式形式提供额外的治疗。我们描述了哈特福德医院卒中中心对在转至我们医疗中心之前接受静脉注射t-PA的院间患者转运的经验。
对我们的急性卒中治疗数据库进行回顾性分析,涵盖卒中中心项目的最初四年(2001年5月1日至2005年4月30日)。我们评估了在转诊至我们的卒中中心之前在转诊医院开始接受静脉注射t-PA治疗的患者的特征、临床结局和辅助治疗。
在我们卒中中心接受静脉注射和/或动脉内溶栓以及更新的导管输送装置或临床试验的229例患者中,共有33例(14.4%)在转院之前在外部医院开始接受静脉注射t-PA治疗。33例患者中有1例(3.0%)发生症状性出血,这些患者的院内死亡率为6.1%。共有26例患者(78.8%)预后良好,即出院回家或接受急性康复治疗。
在哈特福德医院区域卒中中心,采用“边滴注边转运”方式使用静脉注射t-PA的情况正在增加。该方案是安全的,为急性缺血性卒中(AIS)患者的护理带来了多项进展:(a)通过接入全天候急性卒中热线,使外部医院的急诊医生和神经科医生能够治疗AIS患者;(b)促进静脉注射t-PA的早期启动;(c)对于仅接受静脉注射t-PA治疗效果不佳的患者,在到达我们的机构后提供辅助治疗方法。