Pretreatment Diffusion- and Perfusion-MR Lesion Volumes Have a Crucial Influence on Clinical Response to Stroke Thrombolysis

Author:

Parsons Mark W1,Christensen Soren2,McElduff Patrick1,Levi Christopher R1,Butcher Ken S3,De Silva Deidre A4,Ebinger Martin5,Barber P Alan6,Bladin Christopher7,Donnan Geoffrey A8,Davis Stephen M9,

Affiliation:

1. Department of Neurology, Hunter Medical Research Institute Centre for Brain and Mental Health Research, John Hunter Hospital, University of Newcastle, Newcastle, New South Wales, Australia

2. Department of Radiology, Royal Melbourne Hospital, University of Melbourne, Parkville, Victoria, Australia

3. Department of Neurology, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Alberta, Canada

4. Department of Neurology, Singapore General Hospital, Singapore

5. The Center for Stroke Research Berlin, Charité—Universitätsmedizin Berlin, Germany

6. Department of Medicine, Auckland Hospital, University of Auckland, Auckland, New Zealand

7. Eastern Health Melbourne Neurosciences, Box Hill, Victoria, Australia

8. National Stroke Research Institute, Austin Health, Melbourne, Victoria, Australia

9. Department of Neurology, Royal Melbourne Hospital, University of Melbourne, Parkville, Victoria, Australia

Abstract

We hypothesized that pretreatment magnetic resonance imaging (MRI) diffusion-weighted imaging (DWI) and perfusion-weighted imaging (PWI) lesion volumes may have influenced clinical response to thrombolysis in the Echoplanar Imaging Thrombolytic Evaluation Trial (EPITHET). In 98 patients randomized to intravenous (IV) tissue plasminogen activator (tPA) or placebo 3 to 6 h after stroke onset, we examined increasing acute DWI and PWI lesion volumes (Tmax—with 2-sec delay increments), and increasing PWI/DWI mismatch ratios, on the odds of both excellent (modified Rankin Scale (mRS): 0 to 1) and poor (mRS: 5 to 6) clinical outcome. Patients with very large PWI lesions (most had internal carotid artery occlusion) had increased odds ratio (OR) of poor outcome with IV-tPA (58% versus 25% placebo; OR=4.13, P=0.032 for Tmax +2-sec volume >190 mL). Excellent outcome from tPA treatment was substantially increased in patients with DWI lesions <18 mL (77% versus 18% placebo, OR=15.0, P<0.001). Benefit from tPA was also seen with DWI lesions up to 25 mL (69% versus 29% placebo, OR=5.5, P=0.03), but not for DWI lesions >25 mL. In contrast, increasing mismatch ratios did not influence the odds of excellent outcome with tPA. Clinical responsiveness to IV-tPA, and stroke outcome, depends more on baseline DWI and PWI lesion volumes than the extent of perfusion–diffusion mismatch.

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine,Neurology (clinical),Neurology

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