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(Stroke. 2005;36:1083.)
© 2005 American Heart Association, Inc.
Research Report |
From the Department of Neurology (O.O.Z., J.I.S., D.M.D.L.), Case Western Reserve University, Cleveland, Ohio; the Departments of Radiology (O.O.Z., M.J.A, T.P.S, D.S.E) and Neurosurgery (M.J.A.), Duke University and Medical Center, Durham, NC; and the Departments of Neurology (M.Y, A.P.S) and Radiology (G.A.C), Ohio State University, Columbus.
Correspondence to Osama O. Zaidat, MD, Duke University and Medical Center, Box 3808, Durham, NC 27710. E-mail ozaidat{at}hotmail.com
| Abstract |
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Methods A retrospective study was performed involving 3 university hospitals. All peri-CA IAT-treated cases were identified. Patient demographics, stroke severity, angiographic findings, thrombolytic use, modified Rankin Scale (mRS), ICH, and mortality were determined.
Results A total of 21 patients with postleft CA stroke were treated with IAT (mean age 71.8±12.3 years). Arterial occlusion was found in 14 (66.7%) and 7 (33.3%) of the anterior and posterior circulation, respectively. Mean time-to-therapy was 36±12 minutes from the time the neurological deficit was noted. mRS
2 occurred in 10 of 21 (48%) patients. Patients with younger age and shorter time-to-IAT had more complete arterial recanalization and clinical recovery. Symptomatic ICH occurred in 3 (14%) cases, and 4 (19%) patients died.
Conclusions Peri-CA IAT appears to be feasible and safe without increased risk of symptomatic ICH and death when compared with the previously reported IAT literature.
Key Words: cardiac catheterization cerebrovascular disorders stroke tissue plasminogen activator thrombolysis
| Introduction |
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Peri-CA stroke represents a unique opportunity for immediate stroke interventional therapy with intravenous, catheter-based intra-arterial thrombolysis (IAT) or combined therapy using recombinant tissue plasminogen activator (rtPA), pro-urokinase, or urokinase (UK)24 because of very short time-to-treatment and readily available resources. We report multicenter experience of IAT of peri-CA stroke.
| Subjects and Methods |
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4 points on NIHSS with well-defined hematoma on head CT.
Statistics
Analysis was performed with StatView 5.0 (SAS Institute). Bivariable comparisons were performed using Fishers exact test. Multivariable analysis with multiple comparison adjustment was performed.
| Results |
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Head CT evidence of early ischemia was present in 3 (12.5%) patients: 1 with reduced white-gray matter differentiation and 2 with loss of insular ribbon. All patients had activated clotting time between 250 and 300 seconds.
The occluded vessel was M1middle cerebral artery (MCA) in 3 (14%) patients, M2-MCA branch in 2 (10%), posterior cerebral artery in 4 (19%), basilar artery (BA) in 1(5%), vertebral artery in 2 (10%), and occlusion in 2 anterior circulation branches (MCA, anterior cerebral artery, or both) in 9 (43%).
Mean time-to-therapy was 106.7±38.3 minutes from last documented normal patient examination and 36±12 minutes from the time symptoms were initially observed. rtPA was used in 9 (43%) and UK in 12 (57%) patients. Median rtPA dose was 23 mg (range 12 to 34). Median UK dose was 1 000 000 U (range 50 000 to 1 500 000). No heparin was allowed for 24 hours after IAT. Recanalization (TIMI 1, 2, and 3) occurred in 14 (66.7%) patients: complete (TIMI 3) in 5 (24%) and partial (TIMI 1 and 2) in 9 (43%); no recanalization (TIMI 0) occurred in 7 (33.3%) patients.
Ten patients (48%) had good outcome at discharge, defined by mRS
2. Symptomatic ICH occurred in 3 (14%) patients, which was not related to intraprocedure anticoagulation. Four (19%) patients died: 1 related to ICH, 1 to large stroke, and 2 to CAD.
Younger age, shorter time-to-treatment, and lack of ICH showed a trend for improved outcome (Table). There was no statistically significant difference with regard to gender, race, thrombolytic agent used, or NIHSS, although patients with good outcome had numerically lower median NIHSS score than patients with bad outcome (15 versus 18). Multivariable analysis showed an association between age and time-to-treatment with better outcome (P value of 0.06 and 0.05, respectively; R-square 0.34).
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| Discussion |
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In our study, all centers had well-established brain attack protocol, with an experienced team of stroke neurologists and neurointerventionalists. All patients received full neurological evaluation, coagulation profile, and head CT scan. IAT was performed by experienced neurointerventionalists in specialized cerebral angiography suites. Ascertaining patients neurological status to be related to acute ischemic stroke rather than seizure, medication or hemodynamic compromise is of paramount significance before exposing patients to IAT.
Good outcome in our series may be related to rapid initiation of IAT. Other factors may include younger age and initial NIHSS. Our small sample size could not allow further exploration. Overall recanalization rate of 67% in our study was comparable to previous IAT studies. Complete recanalization occurred in 24%, which may be related to various types of clot and multiple distal small vessels occlusion that may be technically difficult to reach.
The rate of symptomatic ICH in our study was 14%, similar to other IAT studies,24 despite having aggressive anticoagulation in our study population for their CA intervention. Our mortality rate was 19%: 2 were related to ICH or stroke, and 2 were related to underlying CAD. This mortality rate is within the range of the previously published stroke thrombolysis literature, although considering that many of our patients had several comorbidities and some had acute MI.
In conclusion, IAT is a valid therapeutic option for peri-CA stroke. Symptomatic ICH and mortality were similar or lower than reported previously in IAT trials. Time-to-therapy, younger age, and initial NIHSS may influence clinical outcome.
Received January 20, 2005; accepted January 21, 2005.
| References |
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2. Furlan A, Higashida R, Wechsler L, Gent M, Rowley H, Kase C, Pessin M, Ahuja A, Callahan F, Clark WM, Silver F, Rivera F. Intra-arterial prourokinase for acute ischemic stroke. The PROACT II study: a randomized controlled trial. Prolyse in Acute Cerebral Thromboembolism. J Am Med Assoc. 1999; 282: 20032011.
3. IMS-Study Investigators. Combined intravenous and intra-arterial recanalization for acute ischemic stroke: the Interventional Management of Stroke Study. Stroke. 2004; 35: 904911.
4. Zaidat OO, Suarez JI, Santillan C, Sunshine JL, Tarr RW, Paras VH, Selman WR, Landis DM. Intra-arterial and combined intravenous and intra-arterial thrombolytic therapy for distal carotid artery occlusion. Stroke. 2002; 33: 18281833.
5. Sandoval AE, Laufer N. Thromboembolic stroke complicating coronary intervention: acute evaluation and management in the cardiac catheterization laboratory. Cathet Cardiovasc Diagn. 1998; 44: 412414.[Medline] [Order article via Infotrieve]
6. Oezbek C, Heisel A, Voelk M, Bay W, Berg G, Sen S, Schieffer H. Management of stroke complicating cardiac catheterization with recombinant tissue-type plasminogen activator. Am J Cardiol. 1995; 76: 733735.[Medline] [Order article via Infotrieve]
7. Kumar KP, Rao JS, Deb PS, Rao PS. Complete thrombolysis for acute embolic stroke during coronary angiography. Indian Heart J. 1999; 51: 429431.[Medline] [Order article via Infotrieve]
8. Battikh K, Rihani R, Lemahieu JM, Mokahal M, Houchaymi Z, Cornaert P, Dutoit A. Intra-arterial thrombolysis of a basilar vascular accident during coronary angiography. Arch Mal Coeur Vaiss. 2001; 94: 10251027.[Medline] [Order article via Infotrieve]
9. Al-Mubarak N, Vitek J, Mousa I, Iyer SS, Mgaieth S, Moses J, Roubin GS. Immediate catheter-based neurovascular rescue for acute stroke complicating coronary procedures. Am J Cardiol. 2002; 90: 173176.[Medline] [Order article via Infotrieve]
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