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
Objective: To investigate whether the location and extent of the CT hyperdense artery sign (HAS) at ...
Intravenous thrombolysis with alteplase is the only approved treatment for acute ischemic stroke, bu...
OBJECTIVE: To investigate whether the location and extent of the CT hyperdense artery sign (HAS) at ...
Alteplase was non-significantly associated with lower infarct growth and significantly associated wi...
to test whether alteplase given 3-6 h after stroke onset promotes reperfusion and attenuates infarct...
Objective To determine whether alteplase alters the development of ischemic lesions on brain imaging...
OBJECTIVE: To determine whether alteplase alters the development of ischemic lesions on brain imagin...
Thrombolytic therapy with intravenous alteplase within 4.5 hours of ischemic stroke onset increases ...
BACKGROUND: Thrombolytic therapy with intravenous alteplase within 4.5 hours of ischemic stroke ons...
Intravenous thrombolysis with alteplase is the only approved treatment for acute ischemic stroke, bu...
Background: Intravenous thrombolysis with alteplase is the only approved treatment for acute ischemi...
Background: Alteplase given within 4•5 hours of onset is the only approved medical treatment in acut...
Background Intravenous thrombolysis with alteplase is the only approved treatment for acute ischem...
when using coregistration techniques to determine the presence of mismatch at study entry, alteplase...
Intravenous thrombolysis with alteplase (Genentech; San Francisco, CA) is the only FDA approved trea...
Objective: To investigate whether the location and extent of the CT hyperdense artery sign (HAS) at ...
Intravenous thrombolysis with alteplase is the only approved treatment for acute ischemic stroke, bu...
OBJECTIVE: To investigate whether the location and extent of the CT hyperdense artery sign (HAS) at ...
Alteplase was non-significantly associated with lower infarct growth and significantly associated wi...
to test whether alteplase given 3-6 h after stroke onset promotes reperfusion and attenuates infarct...
Objective To determine whether alteplase alters the development of ischemic lesions on brain imaging...
OBJECTIVE: To determine whether alteplase alters the development of ischemic lesions on brain imagin...
Thrombolytic therapy with intravenous alteplase within 4.5 hours of ischemic stroke onset increases ...
BACKGROUND: Thrombolytic therapy with intravenous alteplase within 4.5 hours of ischemic stroke ons...
Intravenous thrombolysis with alteplase is the only approved treatment for acute ischemic stroke, bu...
Background: Intravenous thrombolysis with alteplase is the only approved treatment for acute ischemi...
Background: Alteplase given within 4•5 hours of onset is the only approved medical treatment in acut...
Background Intravenous thrombolysis with alteplase is the only approved treatment for acute ischem...
when using coregistration techniques to determine the presence of mismatch at study entry, alteplase...
Intravenous thrombolysis with alteplase (Genentech; San Francisco, CA) is the only FDA approved trea...
Objective: To investigate whether the location and extent of the CT hyperdense artery sign (HAS) at ...
Intravenous thrombolysis with alteplase is the only approved treatment for acute ischemic stroke, bu...
OBJECTIVE: To investigate whether the location and extent of the CT hyperdense artery sign (HAS) at ...