The impact of the DWI-FLAIR-mismatch in the ECASS-4 trial – A post hoc analysis

Author:

Pfaff Johannes AR1ORCID,Bendszus Martin1,Donnan Geoffrey2,Molina Carlos3,Leys Didier4ORCID,Schellinger Peter D5,Schwab Stefan6,Toni Danilo7,Wahlgren Nils7,Hacke Werner8,Ringleb Peter Arthur8

Affiliation:

1. Heidelberg University Hospital, Department of Neuroradiology, Heidelberg, Germany

2. National Stroke Research Institute, Neurosciences Bldg, Heidelberg Heights, Australia

3. Hospital Universitari Vall d’Hebron, Department of Neurosciences, Barcelona, Spain

4. Hopital Roger Salengro, Service de neurologie et pathologie neurovasculaire, Lille Cedex, France

5. University Hospital Erlangen, Department of Neurology, Erlangen, Germany

6. Hospital Policlinico Umberto I, Emergency Department Stroke Unit, Rome, Italy

7. Karolinska Institutet, Department of Clinical Neurosciences, Stockholm, Sweden

8. Heidelberg University Hospital, Department of Neurology, Heidelberg, Germany

Abstract

Introduction To investigate the impact of a mismatch between diffusion-weighted imaging (DWI) and fluid attenuated inversion recovery (FLAIR) on functional outcome in patients with acute stroke in a prolonged time window or unknown time of symptom onset randomized to intravenous thrombolysis or placebo. Patients and Methods We performed a post-hoc analysis of the European Cooperative Acute Stroke Study-4 (ECASS-4) trial. ECASS-4 was an investigator driven, phase 3, multi-center, double-blind, placebo-controlled study which randomized ischemic stroke patients presenting within 4.5 and 9h of stroke onset or unknown time-window to either rt-PA or placebo after MR-imaging. Two subgroups “no mismatch” (nMM) and “any mismatch” (aMM) were created by applying a DWI-FLAIR-mismatch criterion. We calculated frequency of nMM and aMM and performed a univariate analysis (Fisher's Test) for excellent clinical outcome (mRS 0-1) and mortality (mRS=6). Results MR-Imaging of n=111/119 (93.2%) patients was suitable for this analysis. DWI-FLAIR mismatch was found in 49 patients (44.1%). Proportions of mismatch nMM and aMM were comparable in treatment-groups (aMM: Placebo 46.3%, Alteplase 42.1%; p=0.70). Patients with nMM showed no benefit of rt-PA-treatment (OR (95%CI) mRS 0-1: 0.95 (0.29-3.17)). Patients with aMM showed a point estimate of the odds ratio in favour of a treatment benefit of rt-PA (mRS 0-1: OR (95%CI) 2.62 (0.68-11.1)). Mortality within 90 days was not different in patients treated with rt-PA if nMM (15.2%) or aMM (12.5%) was present. Discussion In this analysis no significant evidence, but subtle indication towards patients treated with rt-PA in a prolonged time window reaching an excellent clinical outcome if a DWI-FLAIR-mismatch is present on initial stroke MR-imaging. Conclusion A DWI-FLAIR mismatch in the region of ischemia as imaging based surrogate parameter for patient selection for i.v. rt-PA should be strongly pursued.

Funder

Boehringer Ingelheim

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine,Neurology (clinical)

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