PT  - JOURNAL ARTICLE
AU  - Amira R. Al-Buhairi
AU  - Mohammed M. Jan
TI  - Recombinant tissue plasminogen activator for acute ischemic stroke
DP  - 2002 Jan 01
TA  - Saudi Medical Journal
PG  - 13--19
VI  - 23
IP  - 1
4099  - http://smj.org.sa/content/23/1/13.short
4100  - http://smj.org.sa/content/23/1/13.full
SO  - Saudi Med J2002 Jan 01; 23
AB  - Stroke is a leading cause of serious and long-term disability and death worlwide, with approximately 750,000 strokes occuring annually in the United States of America. The risk of stroke doubles each decade for people over 55 years. Cerebral angiography conducted soon after the onset of stroke demonstrates arterial occlusion in 70%-80% of cases. Recanalization of an occluded cerebral artery may assist in the recovery of reversibly ischemic tissue and limit the neurological disability. In June 1996, the recombinant tissue plasminogen activator was approved as a safe and an effective intravenous treatment for acute ischemic stroke, especially if given within 3 hours of onset of symptoms. Since approval, less than 5% of all stroke patients are receiving recombinant tissue plasminogen activator. In this review we try to answer the question of whether recombinant tissue plasminogen activator therapy should be the first-line treatment for acute ischemic stroke. The result of major recombinant tissue plasminogen activator trials will be summarized and reviewed critically.