The Effects of Alteplase 3 to 6 Hours After Stroke in the EPITHET–DEFUSE Combined Dataset

Author:

Ogata Toshiyasu1,Christensen Soren1,Nagakane Yoshinari1,Ma Henry1,Campbell Bruce C.V.1,Churilov Leonid1,Lansberg Maarten G.1,Straka Matus1,De Silva Deidre A.1,Mlynash Michael1,Bammer Roland1,Olivot Jean-Marc1,Desmond Patricia M.1,Albers Gregory W.1,Davis Stephen M.1,Donnan Geoffrey A.1,

Affiliation:

1. From the Florey Neuroscience Institutes, Austin Health, Melbourne, Australia (T.O., Y.N., H.M., L.C., G.A.D.); University of Melbourne, Melbourne, Australia (S.C., B.C.V.C., P.M.D., S.M.D., G.A.D.); Royal Melbourne Hospital, Melbourne, Australia (S.C., B.C.V.C., P.M.D., S.M.D.); Monash Medical Centre, Monash University, Melbourne, Australia (H.M.); Department of Mathematics and Statistics, University of Melbourne, Melbourne, Australia (L.C.); Department of Neurology, Neurological Sciences, and the...

Abstract

Background and Purpose— Two phase 2 studies of alteplase in acute ischemic stroke 3 to 6 hours after onset, Echoplanar Imaging Thrombolytic Evaluation Trial (EPITHET; a randomized, controlled, double-blinded trial), and Diffusion and Perfusion Imaging Evaluation for Understanding Stroke Evolution Study (DEFUSE; open-label, treatment only) using MR imaging-based outcomes have been conducted. We have pooled individual patient data from these to assess the response to alteplase. The primary hypothesis was that alteplase would significantly attenuate infarct growth compared with placebo in mismatch-selected patients using coregistration techniques. Methods— The EPITHET–DEFUSE study datasets were pooled while retaining the original inclusion and exclusion criteria. Significant hypoperfusion was defined as a Tmax delay >6 seconds), and coregistration techniques were used to define MR diffusion-weighted imaging/perfusion-weighted imaging mismatch. Neuroimaging, parameters including reperfusion, recanalization, symptomatic intracerebral hemorrhage, and clinical outcomes were assessed. Alteplase and placebo groups were compared for the primary outcome of infarct growth as well for secondary outcome measures. Results— From 165 patients with adequate MR scans in the EPITHET–DEFUSE pooled data, 121 patients (73.3%) were found to have mismatch. For the primary outcome analysis, 60 patients received alteplase and 41 placebo. Mismatch patients receiving alteplase had significantly attenuated infarct growth compared with placebo ( P =0.025). The reperfusion rate was also increased (62.7% vs 31.7%; P =0.003). Mortality and clinical outcomes were not different between groups. Conclusions— The data provide further evidence that alteplase significantly attenuates infarct growth and increases reperfusion compared with placebo in the 3- to 6- hour time window in patients selected based on MR penumbral imaging. Clinical Trial Registration— URL: http://www.clinicaltrials.gov . Unique identifier: NCT00238537

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Advanced and Specialized Nursing,Cardiology and Cardiovascular Medicine,Neurology (clinical)

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