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Circulation. 2006;113:e64-e66
doi: 10.1161/CIRCULATIONAHA.105.552802
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(Circulation. 2006;113:e64-e66.)
© 2006 American Heart Association, Inc.


Images in Cardiovascular Medicine

Intra-Arterial Thrombolysis for Left Middle Cerebral Artery Embolic Stroke During Coronary Angiography

Patrizia Presbitero, MD; Gabriele L. Gasparini, MD; Paolo Pagnotta, MD

From the Department of Invasive Cardiology, Istituto Clinico Humanitas, Rozzano, Italy.

Correspondence to Dr Patrizia Presbitero, Department of Invasive Cardiology, Istituto Clinico Humanitas, Via Manzoni 56, 20089 Rozzano (Milan), Italy. E-mail patrizia.presbitero{at}humanitas.it

Cerebral thromboembolism is an uncommon but serious complication of cardiac catheterization. Early diagnosis and rapid treatment by reperfusion techniques have been shown to prevent long-term neurological morbidity. We report 2 consecutive cases of successful local intra-arterial thrombolysis (LIT) for embolic stroke of the middle cerebral artery (MCA) during diagnostic coronary angiography that resulted in complete neurological recovery.

A 77-year-old woman with severe valvular aortic stenosis was admitted to our catheterization laboratory for a preoperative coronary angiography. Performed from the femoral approach, it showed a normal angiographic pattern. Immediately after the procedure, the patient became stuporous with right hemiplegia and global aphasia. She was hemodynamically stable.

The left carotid digital subtraction angiography that was performed immediately revealed total occlusion of the M2 part of the left MCA. There was no extravasation of contrast (Figure 1). We decided to administer selective intra-arterial urokinase infusion. After systemic heparinization (bolus of 5000 UI), a 6F Amplatz Right Guide catheter was placed in the left internal carotid artery. Using an infusion catheter (Ultrafuse 3.6 F) that was advanced to the upper end of the cervical part of the internal carotid artery, we performed LIT with urokinase (total dose, 700 000 U) near the proximal end of the occluding thrombus. Twenty minutes after LIT (2 hours after the clinical onset of occlusion), a control angiogram showed complete recanalization of the vessel (Figure 2). The patient’s neurological status improved immediately. The next day, neurological evaluation revealed no deficits. Computed tomography performed 4 days later did not show any signs of infarction. Ten days later, the patient underwent successful aortic valve replacement.


Figure 1
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Figure 1. First patient with severe calcified aortic valve stenosis. The carotid angiogram, performed immediately after coronary angiography at the beginning of cerebral symptoms, reveals total embolic occlusion of the M2 part of the left MCA with TIMI 0 flow (arrow).


Figure 2
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Figure 2. First patient. Recanalized left MCA after 700 000 U intra-arterial urokinase infusion, with total disappearance of the occlusion with normal anterograde flow (arrow).

A 72-year-old man with a congestive heart failure was admitted for cardiac catheterization. Coronary angiography, performed from the femoral approach with 6F catheters, excluded coronary artery disease. Two hours after the procedure, the patient was found stuporous with global aphasia. Ischemic stroke resulting from a left MCA occlusion was confirmed by a left carotid digital subtraction angiography. There was no extravasation of contrast (Figure 3).


Figure 3
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Figure 3. Second patient with dilated cardiomyopathy. The carotid angiogram, performed 2 hours after coronary angiography at the beginning of cerebral symptoms, reveals total embolic occlusion of the M2 part of the left MCA with TIMI 0 flow (see arrow).

We again administered intra-arterial urokinase as previously described. Five minutes after LIT (total urokinase dose, 500 000 U), a control angiogram showed complete recanalization of the left MCA (3 hours after the clinical onset of occlusion) (Figure 4). The patient’s neurological status improved immediately. Computed tomography performed the next day was normal, and neurological evaluation did not reveal any deficit. The patient was discharged 3 days later.


Figure 4
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Figure 4. Second patient. Recanalized left MCA after 500 000 U intra-arterial urokinase, with total disappearance of the occlusion with normal anterograde flow (arrow).

Catheterization-related strokes are rare (0.07% to 0.38%)1,2 and almost always are of embolic origin. Emboli can originate from dislodgement of material from plaque rupture, calcium from aortic cusps, or thrombus formation in the catheters or on the guides.3–5 Furthermore, the apposition of thrombus to the embolic material may be an important component of cerebral artery occlusion. Computed tomography scan and magnetic resonance imaging seem to be unnecessary because they do not add anything to the diagnosis and treatment. An immediate carotid angiogram to assess cerebral artery occlusion appears to be the best and least time-consuming approach. Hemorrhagic stroke can be recognized by extravasation or late persistence of contrast. Recent studies comparing intra-arterial and intravenous thrombolytic therapy in thromboembolic stroke have shown a higher rate of revascularization with intra-arterial thrombolysis.6,7 Previous trials have shown the safety and efficacy of intra-arterial thrombolysis with urokinase.8,9 The reperfusion rate is &70% in atherosclerotic strokes within the first 6 hours and ≥75% within the first 3 hours.10 Cerebral bleeding was noted in 10% of patients who had successful thrombolysis.9 The major constraints for a wide application of intra-arterial thrombolysis in embolic stroke are the narrow period of efficacy (first 3 hours)10,11 and the availability of facilities for catheterization and experienced personnel. Therefore, in an interventional setting, intra-arterial thrombolysis seems to be the most effective and least time-consuming approach. To the best of our knowledge, intra-arterial thrombolysis was never reported in the treatment of stroke as a complication of coronary angiography. The excellent angiographic and clinical results obtained in these 2 cases lead us to advise this treatment as the first choice for treating embolic stroke during cardiac catheterization.


*    Disclosures
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*Disclosures
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None.


*    References
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1. Kennedy JW. Complications associated with cardiac catheterization and angiography. Cathet Cardiovasc Diagn. 1982; 8: 5–11.[Medline] [Order article via Infotrieve]

2. Fuchas S, Stabile E, Kinnaird TD, Mintz GS, Gruberg L, Canos DA, Pinnow EE, Kornoswki R, Suddath WO, Satler LF, Pichard AD, Kent KM, Weissman NJ. Stroke complicating percutaneous coronary interventions: incidence, predictors, and prognostic implications. Circulation. 2002; 106: 86–91.[Abstract/Free Full Text]

3. Tunick PA, Rosenzweig BP, Katz ES, Freedberg RS, Perez JL, Kronzon I. High risk for vascular events in patients with protruding aortic atheromas: a prospective study. J Am Coll Cardiol. 1994; 23: 1085–1090.[Abstract]

4. Khatibzadeh M, Mitush R, Stierle U, Gromoll B, Sheikhzadeh A. Aortic atherosclerotic plaque as a source of systemic emboli. J Am Coll Cardiol. 1996; 27: 664–669.[Abstract]

5. Keeley EC, Grines CL. Scraping of aortic debris by coronary guiding catheters: a prospective evaluation of 1.000 cases. J Am Coll Cardiol. 1998; 32: 1861–1895.[Abstract/Free Full Text]

6. Pessin M, Del Zeppo G, Furlan A. Thrombolytic treatment in acute stroke. In: Moskowitz M, Caplan LR, eds. Cerebrovascular Diseases: Nineteenth Princeton Stroke Conference. Boston, Mass: ButterWorth-Heinemann; 1995: 409–418.

7. Ng PP, Higashida RT, Cullen SP, Malek R, Dowed CF, Halbach VV. Intraarterial thrombolysis trials in acute ischemic stroke. J Vasc Interv Radiol. 2004; 15: S77–S85.[Medline] [Order article via Infotrieve]

8. Del Zoppo GJ, Higashida RT, Furlan AJ, Pessin MS, Rowley HA, Gent M. PROACT: a phase II randomized trial of recombinant pro-urokinase by direct arterial delivery in acute middle cerebral artery stroke. Stroke. 1998; 29: 4–11.[Abstract/Free Full Text]

9. Furlan AJ, Higashida RT, 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. JAMA. 1999; 282: 2003–2011.[Abstract/Free Full Text]

10. Bourekas EC, Slivka AP, Shah R, Sunshine J, Suarez JI. Intraarterial thrombolytic therapy within 3 hours of the onset of ischemic stroke. Neurosurgery. 2004; 54: 39–46.[Medline] [Order article via Infotrieve]

11. Schellinger PD, Warach S. Therapeutic time window of thrombolytic therapy following stroke. Curr Atheroscler Rep. 2004; 6: 288–294.[Medline] [Order article via Infotrieve]


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