The Potential Impact of Maintaining a 3-Hour IV Thrombolysis Window: How Many More Patients can we Safely Treat?

BACKGROUND: In 2008, the European Cooperative Acute Stroke Study-3 (ECASS-3) demonstrated that intravenous-tissue plasminogen activator could be safely administered for acute stroke patients presenting between 3 and 4.5 hours from symptom onset. Recently, the Food and Drug Administration rejected ex...

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Detaylı Bibliyografya
Asıl Yazarlar: Lyerly, Michael J., Albright, Karen C., Boehme, Amelia K., Shahripour, Reza Bavarsad, Houston, James T., Rawal, Pawan V., Kapoor, Niren, Alvi, Muhammad, Sisson, April, Alexandrov, Anne W., Alexandrov, Andrei V.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2013
Konular:
Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3901990/
https://ncbi.nlm.nih.gov/pubmed/24471140
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