Egan R, Lutsep H L, Clark W M, Quinn J, Kearns K, Lockfeld A, Ireland S, Goins S, Buchholz G
J Stroke Cerebrovasc Dis. 1999 Sep-Oct;8(5):287-90. doi: 10.1016/s1052-3057(99)80001-9.
Tissue plasminogen activator (t-PA) is the first effective treatment for stroke. This study sought to explore the outcome of patients treated with t-PA in the community after approval of its use in the treatment of stroke in June, 1996.
All patients with acute stroke within the 6-hospital Oregon Stroke Center network were screened for potential t-PA treatment. Baseline and 24-hour outcome assessments were performed with the use of the National Institutes of Health Stroke Scale (NIHSS) and computed tomography (CT); 3-month outcome was evaluated by using the Modified Rankin scale.
Thirty-three patients who met the criteria for t-PA therapy were treated within 3 hours of symptom onset. All but 2 strokes were in the anterior circulation; 48.5% were cardioembolic. The NIHSS scores at 24 hours after administration of t-PA (mean, 14.7) showed modest gains from baseline NIHSS scores (mean, 16.6). Twelve patients (36%) had minimal or no deficits at 3 months. Three patients (9%), all of whom had baseline NIHSS scores of 20 or more, had symptomatic intracranial hemorrhages, 2 of which were fatal (6%).
This study shows the feasibility of treating acute stroke with t-PA in the community. The percentage of fully recovered patients at 3 months mirrored those in the National Institute of Neurologic Disorders and Stroke (NINDS) trial.
组织型纤溶酶原激活剂(t-PA)是治疗中风的首个有效药物。本研究旨在探讨1996年6月t-PA被批准用于治疗中风后,社区中接受t-PA治疗的患者的治疗结果。
对俄勒冈州中风中心网络内6家医院的所有急性中风患者进行筛查,以确定其是否适合接受t-PA治疗。使用美国国立卫生研究院卒中量表(NIHSS)和计算机断层扫描(CT)进行基线和24小时预后评估;使用改良Rankin量表评估3个月时的预后。
33例符合t-PA治疗标准的患者在症状出现后3小时内接受了治疗。除2例中风外,其余均发生在前循环;48.5%为心源性栓塞。t-PA给药后24小时的NIHSS评分(平均14.7)较基线NIHSS评分(平均16.6)有适度改善。12例患者(36%)在3个月时几乎没有或没有残疾。3例患者(9%)出现症状性颅内出血,所有患者的基线NIHSS评分均为20或更高,其中2例死亡(6%)。
本研究表明在社区中使用t-PA治疗急性中风是可行的。3个月时完全康复患者的比例与国立神经疾病和中风研究所(NINDS)试验中的比例相当。