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对于脑卒中患者的轻度缺陷,是否有理由使用静脉注射组织型纤溶酶原激活剂?

Does mild deficit for patients with stroke justify the use of intravenous tissue plasminogen activator?

机构信息

University of Medicine and Dentistry of New Jersey, Newark, New Jersey 07103, USA.

出版信息

J Stroke Cerebrovasc Dis. 2010 Mar;19(2):116-20. doi: 10.1016/j.jstrokecerebrovasdis.2009.03.019.

Abstract

Intravenous (IV) tissue plasminogen activator (t-PA) is an effective medication currently used to treat acute ischemic stroke within 3 hours of symptom onset in patients with an identifiable clinical deficit measured using the National Institutes of Health Stroke Scale (NIHSS). Some reports suggest that patients with milder acute ischemic stroke may improve spontaneously and may not benefit additionally from IV thrombolysis. The objective of this retrospective study was to assess the outcomes of patients at our stroke center who received IV t-PA treatment for acute ischemic stroke, within 3 hours of symptom onset, outside the setting of a clinical trial and had a NIHSS score of less than or equal to 10 compared with historic control subjects. There were 52 patients who received IV t-PA for acute ischemic stroke. Of those, 31 (male 44% [n = 14]) had a NIHSS score of 10 or less (mean NIHSS score 6 +/- 2). The mean age was 61 +/- 14 years, the mean NIHSS score was 6 +/- 2, and the mean modified Rankin scale (mRS) score was 1.4 +/- 1.5. We identified 98 patients (male 74% [n = 73]) in the National Institute of Neurological Disorders and Stroke IV recombinant t-PA study placebo group. The mean age was 65 +/- 13 years, the mean NIHSS score was 7 +/- 2, and the mean mRS score was 2.5 +/- 1.7. Assuming equal variances, the mRS score at discharge, for the IV t-PA-treated group, demonstrated a better clinical outcome that was statistically significant (P < .009). This retrospective study demonstrates that administering IV t-PA to patients with a mild stroke, measuring 10 or less by the NIHSS, can lead to improved clinical outcome when compared with patients with similar NIHSS score who have not received similar treatment.

摘要

静脉内(IV)组织型纤溶酶原激活物(t-PA)是一种有效的药物,目前用于治疗症状发作后 3 小时内出现可识别的临床缺陷的急性缺血性脑卒中患者,使用国立卫生研究院卒中量表(NIHSS)进行测量。一些报告表明,轻度急性缺血性脑卒中患者可能会自发改善,并且可能不会从 IV 溶栓治疗中额外获益。本回顾性研究的目的是评估我们卒中中心的患者的结局,这些患者在临床试验之外,症状发作后 3 小时内接受了 IV t-PA 治疗急性缺血性脑卒中,NIHSS 评分小于或等于 10 分,与历史对照患者相比。有 52 名患者因急性缺血性脑卒中接受了 IV t-PA 治疗。其中 31 名(男性 44%[n=14])的 NIHSS 评分为 10 分或更低(平均 NIHSS 评分 6+/-2)。平均年龄为 61+/-14 岁,平均 NIHSS 评分为 6+/-2,平均改良 Rankin 量表(mRS)评分为 1.4+/-1.5。我们在国立神经病学与卒中研究所 IV 重组 t-PA 研究安慰剂组中确定了 98 名患者(男性 74%[n=73])。平均年龄为 65+/-13 岁,平均 NIHSS 评分为 7+/-2,平均 mRS 评分为 2.5+/-1.7。假设方差相等,IV t-PA 治疗组出院时的 mRS 评分显示出更好的临床结局,具有统计学意义(P<.009)。本回顾性研究表明,与未接受类似治疗的 NIHSS 评分相似但未接受类似治疗的患者相比,对 NIHSS 评分为 10 或更低的轻度脑卒中患者给予 IV t-PA 治疗可导致临床结局改善。

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