Association between the Perfusion/Diffusion and Diffusion/FLAIR Mismatch: Data from the AXIS2 Trial

Author:

Wouters Anke1,Dupont Patrick23,Ringelstein Erich B4,Norrving Bo5,Chamorro Angel6,Grond Martin7,Laage Rico8,Schneider Armin9,Wilms Guido10,Thomalla Götz11,Lemmens Robin11213,Thijs Vincent N1213

Affiliation:

1. Department of Neurosciences and Experimental Neurology, KULeuven, Leuven, Belgium

2. Laboratory for Cognitive Neurology, Division of Experimental Neurology, Department of Neurosciences, KULeuven, Leuven, Belgium

3. Medical Imaging Research Center, KULeuven, Leuven, Belgium

4. Department of Neurology, University of Münster, Münster, Germany

5. Section of Neurology, Department of Clinical Sciences, Lund University, Lund, Sweden

6. Stroke Centre, University of Barcelona, Barcelona, Spain

7. Kreisklinikum Siegen GmbH, Klinik für Neurologie, Siegen, Germany

8. GUIDED Development Heidelberg GmbH, Heidelberg, Germany

9. Sygnis Bioscience, Molecular Neurology, Heidelberg, Germany

10. Department of Radiology, University Hospitals Leuven, Leuven, Belgium

11. UKE Hamburg-Eppendorf, Klinik und Poliklinik für Neurologie, Kopf- und Neurozentrum, Hamburg, Germany

12. Department of Neurology, University Hospitals Leuven, Leuven, Belgium

13. Laboratory of Neurobiology, Vesalius Research Center, KULeuven, Leuven, Belgium

Abstract

The perfusion-/diffusion-weighted imaging (PWI/DWI) mismatch and the diffusion/fluid attenuated inversion recovery (DWI/FLAIR) mismatch are magnetic resonance imaging (MRI) markers of evolving brain ischemia. We examined whether the DWI/FLAIR mismatch was independently associated with the PWI/DWI mismatch. Furthermore, we determined whether the presence of the DWI/FLAIR mismatch in patients with the PWI/DWI mismatch would provide additional information regarding last seen normal time (LTM). We used data from the ‘AX200 for ischemic stroke’ trial (AXIS 2 study NCT00927836). We studied the association between the presence of the DWI/FLAIR and PWI/DWI mismatch, baseline National Institute of Health Stroke Scale (NIHSS), age, ischemic-core volume, gender, intravenous (IV) tissue plasminogen activator (tPA), and perfusion-mismatch volume in univariate analysis. Significant variables ( P < 0.05) were added into the final multivariate model. We analyzed 197 patients. Seventy-two (37%) had both the PWI/DWI and the DWI/FLAIR mismatch. Patients with the double mismatch pattern had a shorter LTM than patients with the PWI/DWI mismatch alone (Median difference 90 minutes, P < 0.01). Multivariate analysis confirmed the independent association between the two mismatch patterns (odds ratio (OR) 2.6, 95% confidence interval (CI) 1.2 to 5.4). Our study implies that the DWI/FLAIR mismatch and PWI/DWI mismatch are strongly associated, independent from LTM. Furthermore, in the presence of the PWI/DWI mismatch, the DWI/FLAIR pattern indicates a shorter LTM. This could have implications in selecting patients for reperfusion therapy.

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine,Clinical Neurology,Neurology

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