ntravenous tissue plasminogen activator (rt-PA) remains the only approved therapy for acute ischemic stroke with demonstrated effectiveness in phase 3 clinical trials. 1 Unfortunately, the utilization of this treatment is limited by a 6% risk of symptomatic brain hemorrhage 2 and a brief 3-hour time window of efficacy from symptom onset to treatment. 3Furthermore, its effectiveness is limited for several reasons; intravenously administered rt-PA often fails to lyse large clots, 4,5 arteries reocclude in about a third of cases, 5 flow may remain stagnant in the microcirculation despite clot lysis, 6,7 and cellular injury may continue despite reperfusion.
No takes yet. Share an insight, caveat, or question.
James C. Grotta (2003) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: