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Stroke. 2007;38:80-84
Published online before print November 22, 2006, doi: 10.1161/01.STR.0000251720.25337.b0
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(Stroke. 2007;38:80.)
© 2007 American Heart Association, Inc.


Original Contributions

Is Intra-Arterial Thrombolysis Safe After Full-Dose Intravenous Recombinant Tissue Plasminogen Activator for Acute Ischemic Stroke?

Hashem M. Shaltoni, MD; Karen C. Albright, DO, MPH; Nicole R. Gonzales, MD; Raymond U. Weir, MD; Aslam M. Khaja, MD; Rebecca M. Sugg, MD; Morgan S. Campbell, III, MD; Edwin D. Cacayorin, MD; James C. Grotta, MD Elizabeth A. Noser, MD

From the Departments of Neurology (H.M.S., K.C.A., N.R.G., A.M.K., R.M.S., J.C.G., E.A.N.) and Radiology (R.U.W., E.D.C.), University of Texas–Houston Medical School, Houston, Tex, and the Department of Neurology (M.S.C., III), Alabama Neurological Institute, Birmingham, Ala.

Correspondence to James C. Grotta, MD, Vascular Neurology Program, Department of Neurology, University of Texas Health Science Center–Houston, 6431 Fannin St, MSB 7.128, Houston, TX 77030. E-mail James.C.Grotta{at}uth.tmc.edu

Background and Purpose— The optimal approach for acute ischemic stroke patients who do not respond to intravenous recombinant tissue plasminogen activator (IV rt-PA) is uncertain. This study evaluated the safety and response to intra-arterial thrombolytics (IATs) in patients unresponsive to full-dose IV rt-PA.

Methods— A case series from a prospectively collected database on consecutive acute ischemic stroke patients treated with IATs after 0.9 mg/kg IV rt-PA during a 7-year interval was collected. Primary outcome measures included symptomatic intracranial hemorrhage and mortality. As indicators of response, secondary outcome measures were recanalization and discharge disposition.

Results— Sixty-nine patients (mean±SD age, 60±13 years; range, 26 to 85 years; 55% male) with a median pretreatment National Institutes of Health Stroke Scale score of 18 (range, 6 to 39) were included. IV rt-PA was started at 124±32 minutes (median, 120 minutes) and IAT, at 288±57 minutes (median, 285 minutes). IATs consisted of reteplase (n=56), alteplase (n=7), and urokinase (n=6), with an average total dosage of 2.8 U, 8.6 mg, and 700 000 U, respectively. Symptomatic intracranial hemorrhage occurred in 4 of 69 (5.8%) patients; 3 cases were fatal. Recanalization was achieved in 50 (72.5%) and a favorable outcome (home or inpatient rehabilitation) in 38 (55%).

Conclusions— IAT therapy after full-dose IV rt-PA in patients with persisting occlusion and/or lack of clinical improvement appears safe compared with IV rt-PA alone or low-dose IV rt-PA followed by IAT. A high rate of recanalization and favorable outcome can be achieved.


Key Words: acute stroke • endovascular treatment • intracranial hemorrhage • t-PA • thrombolysis




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