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(Stroke. 2002;33:493.)
© 2002 American Heart Association, Inc.
Original Contributions |
From Stanford University School of Medicine, Stanford, Calif (G.W.A., S.A.H.); Oregon Health Sciences University, Portland (W.M.C.); Marshfield Clinic, Marshfield, Wis (K.P.M.).
Correspondence to Gregory W. Albers, MD, Director, Stanford Stroke Center, 701 Welch Rd, Bldg B, Suite 325, Palo Alto, CA 94304.
Background and Purpose Only a single study has demonstrated beneficial effects of intravenous tissue plasminogen activator (tPA) in stroke patients.
Methods We evaluated the clinical outcomes of the 61 patients enrolled in the Alteplase Thrombolysis for Acute Noninterventional Therapy in Ischemic Stroke (ATLANTIS) study who were randomized to receive intravenous tPA or placebo within 3 hours of symptom onset.
Results Despite a significant increase in the rate of symptomatic intracranial hemorrhage, tPA-treated patients were more likely to have a very favorable outcome (score of
1) on the National Institutes of Health Stroke Scale at 90 days (P=0.01).
Conclusions These data support current recommendations to administer intravenous tPA to eligible ischemic stroke patients who can be treated within 3 hours of symptom onset.
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