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(Stroke. 2004;35:1139.)
© 2004 American Heart Association, Inc.
Original Contributions |
Neurologische Universitätsklinik, Heidelberg, Germany
An extract of the first 250 words of the full text is provided, because this article has no abstract. |
To treat, or not to treat: that is the question: Whether tis nobler in the mind to suffer The uncertainties rendered by open case series, Or to take arms against a sea of troubles, And by performing adequate trials end them? Modified from William Shakespeares Hamlet (III, i)
At present, only intravenous thrombolysis (IVT) with recombinant tissue plasminogen activator (rt-PA) administered within 3 hours after symptom onset is proven to be effective for the treatment of acute stroke. Based on level I evidence from the NINDS trial and several meta-analyses, rt-PA has been approved in many countries around the world, including the USA, Canada, Australia, and most of Europe. A recent meta-analysis (Marler et al, Lancet 2004, in press) also demonstrates a significant effect of rt-PA in the 3- to 4.5-hour window, albeit that has not changed approval regulations. National and international committees and guidelines name IVT with rt-PA within the 3-hour time window as the first-line treatment of choice. In specific, the European Stroke Initiative (EUSI) states "intravenous rt-PA (0.9 mg/kg, maximum 90 mg), with 10% of the dose given as a bolus followed by an infusion lasting 60 minutes, is the recommended treatment within 3 hours of onset of ischemic stroke (level I)" and "the benefit from the use of intravenous rt-PA for acute ischemic stroke beyond 3 hours after onset of the symptoms is smaller, but present up to 4.5 hours (level I)."1 The American Stroke Association (ASA) guidelines state: "intravenous rt-PA (0.9 mg/kg, maximum dose
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