Albers G W, Bates V E, Clark W M, Bell R, Verro P, Hamilton S A
Stanford Stroke Center, Stanford University Medical Center, Palo Alto, Calif 94304-1705, USA.
JAMA. 2000 Mar 1;283(9):1145-50. doi: 10.1001/jama.283.9.1145.
Tissue-type plasminogen activator (tPA) is the only therapy for acute ischemic stroke approved by the Food and Drug Administration.
To assess the safety profile and to document clinical outcomes and adverse events in patients treated with intravenous tPA for acute stroke in clinical practice.
Prospective, multicenter study of consecutive patients enrolled between February 1997 and December 1998 at 57 medical centers in the United States (24 academic and 33 community).
Intravenous tPA (recombinant alteplase).
Three hundred eighty-nine patients with a mean age of 69 years (range, 28-100 years); 55% were men.
Time intervals between stroke symptom onset, hospital arrival, and treatment with tPA; pretreatment computed tomographic scan results, intracerebral hemorrhage, and major systemic bleeding. The modified Rankin Scale score was used to assess clinical outcomes at 30 days.
Median time from stroke onset to treatment was 2 hours 44 minutes, and the median baseline National Institutes of Health Stroke Scale score was 13. The 30-day mortality rate was 13%. At 30 days after treatment, 35% of patients had very favorable outcomes (modified Rankin score, 0-1) and 43% were functionally independent (modified Rankin score, 0-2). Thirteen patients (3.3%) experienced symptomatic intracerebral hemorrhage, including 7 who died. Twenty-eight patients (8.2%) had asymptomatic intracerebral hemorrhage within 3 days of treatment with tPA. Protocol violations were reported for 127 patients (32.6%), and included treatment with tPA more than 3 hours after symptom onset in 13.4%, treatment with anticoagulants within 24 hours of tPA administration in 9.3%, and tPA administration despite systolic blood pressure exceeding 185 mm Hg in 6.7%. A multivariate analysis found predictors of favorable outcome to be a less severe baseline National Institutes of Health Stroke Scale score, absence of specific abnormalities (effacement or hypodensity of >33% of the middle cerebral artery territory or a hyperdense middle cerebral artery) on the baseline computed tomographic scan, an age of 85 years or younger, and a lower mean arterial pressure at baseline.
This study, conducted at multiple institutions throughout the United States, suggests that favorable clinical outcomes and low rates of symptomatic intracerebral hemorrhage can be achieved using tPA for stroke treatment.
组织型纤溶酶原激活剂(tPA)是美国食品药品监督管理局批准的唯一用于急性缺血性中风的治疗方法。
评估静脉注射tPA治疗急性中风患者的安全性,并记录临床结局和不良事件。
对1997年2月至1998年12月在美国57个医疗中心(24个学术中心和33个社区中心)连续入组的患者进行的前瞻性多中心研究。
静脉注射tPA(重组阿替普酶)。
389例患者,平均年龄69岁(范围28 - 100岁);55%为男性。
中风症状发作、入院和tPA治疗之间的时间间隔;治疗前计算机断层扫描结果、颅内出血和严重全身性出血。采用改良Rankin量表评分评估30天时的临床结局。
从中风发作到治疗的中位时间为2小时44分钟,基线美国国立卫生研究院卒中量表中位评分为13分。30天死亡率为13%。治疗后30天,35%的患者预后非常良好(改良Rankin评分0 - 1),43%的患者功能独立(改良Rankin评分0 - 2)。13例患者(3.3%)发生有症状性颅内出血,其中7例死亡。28例患者(8.2%)在tPA治疗后3天内有无症状性颅内出血。报告有127例患者(32.6%)违反方案,包括症状发作后3小时以上接受tPA治疗(13.4%)、tPA给药后24小时内使用抗凝剂(9.3%)以及收缩压超过185 mmHg时仍给予tPA治疗(6.7%)。多因素分析发现,预后良好的预测因素为基线美国国立卫生研究院卒中量表评分较轻、基线计算机断层扫描无特定异常(大脑中动脉区域>33%的脑沟消失或低密度或大脑中动脉高密度影)、年龄85岁及以下以及基线平均动脉压较低。
这项在美国多个机构开展的研究表明,使用tPA治疗中风可实现良好的临床结局和较低的有症状性颅内出血发生率。