The emergency room is the front line in the battle against stroke. In 2007 the results of 2 phase III international stroke trials were announced: DIAS-2 evaluated IV recombinant tissue plasminogen activator (rtPA) within an expanded time window based on the demonstration of MR perfusion-diffusion mismatch, and FAST was designed to confirm the clinical benefits of early hemostatic therapy with recombinant activated factor VII (rFVIIa) for intracerebral hemorrhage (ICH). These trials promised to usher in a new era of therapy for thousands of acute stroke victims in our emergency departments. Unfortunately, both trials were negative. On the brighter side, however, a meta-analysis of 3 European hemicraniectomy trials for middle cerebral artery (MCA) infarction showed a powerful mortality reduction. These studies have established hemicraniectomy with duroplasty as the treatment of choice for younger patients (<60 years) admitted to intensive care with medically refractory edema and intracranial pressure related to MCA infarction. ICH is widely recognized as the deadliest and least treatable form of stroke. Thus, it was with great anticipation that the results of the FAST trial were announced at the European Stroke Congress in Glasgow in the spring of 2007. FAST was designed to confirm the strikingly positive results of an earlier phase IIB trial investigating the effects of rFVIIa on hematoma expansion in the acute phase of ICH. In addition to an approximate 50% reduction in ICH volume growth, 3 doses of rFVIIa (40, 80, and 160 μg/kg) were collectively associated with a statistically significant 38% mortality reduction, as well as improved functional outcomes according to the modified Rankin scale (mRS).1 In FAST, the experiment was repeated with the exact same inclusion and exclusion criteria (no upper limit on baseline ICH volume), time window (up to 4 hours), and clinical outcome measure (the frequency of death or severe …