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(Stroke. 2007;38:313.)
© 2007 American Heart Association, Inc.
Original Contributions |
From Klinik und Poliklinik für Neurologie (G.T., A.K., M.R.), Neuro-Zentrum; Neuroradiologische Abteilung (J.F., T.K.), Klinik und Poliklinik für Radiologie, Universitätsklinikum Hamburg-Eppendorf, Hamburg, Germany; Klinik und Poliklinik für Neurologie der Universität zu Köln (J.S., O.Z.W.), Köln, Germany; Neurologische Klinik (M.K., P.D.S.), Universitätsklinikum Erlangen, Erlangen, Germany; Klinik und Poliklinik für Neurologie, Charité- Universitätsmedizin Berlin, Berlin, Germany (J.B.F.); Neurologische Klinik (J.R.), Klinikum Minden, Minden, Germany.
Correspondence to Götz Thomalla, Neuro-Zentrum, Klinik und Poliklinik für Neurologie, Universitätsklinikum Hamburg-Eppendorf, Martinistraße 52, D-20246 Hamburg, Germany. E-mail thomalla{at}uke.uni-hamburg.de
Background and Purpose Intracerebral hemorrhage represents the most feared complication of treatment with intravenous tissue plasminogen activator. We studied whether perfusion-weighted imaging and diffusion-weighted imaging has the potential to identify patients at risk of severe intracerebral hemorrhage after treatment with intravenous tissue plasminogen activator.
Methods We analyzed data of prospectively studied MRI selected acute ischemic stroke patients treated with intravenous tissue plasminogen activator within 6 hours. All patients were examined by perfusion- and diffusion-weighted imaging
6 hours. Perfusion- and diffusion-weighted imaging lesion volumes were calculated. Hemorrhagic transformation was assessed on follow-up CT or MRI and diagnosed as hemorrhagic transformation, parenchymal hemorrhage, or symptomatic intracerebral hemorrhage according to ECASS II criteria.
Results Of 152 patients, hemorrhagic transformation was seen in 60 (39.5%), parenchymal hemorrhage in 15 (9.9%), and symptomatic intracerebral hemorrhage in 4 (2.6%). Multiple logistic regression analysis identified onset to treatment time after 3 to 6 hours (P<0.001), a larger perfusion-weighted imaging lesion volume (P=0.002), and, as a tendency, a higher score on the National Institutes of Health Stroke Scale on admission (P=0.068) as independent predictors of hemorrhagic transformation. Neither MRI lesion volumes nor severity of symptoms, but rather only an older age tended to be associated with parenchymal hemorrhage (P=0.087).
Conclusion Our results further support the concept of a different pathogenesis for hemorrhagic transformation and parenchymal hemorrhage. Whereas hemorrhagic transformation should be regarded as a clinically irrelevant epiphenomenon of ischemic damage and reperfusion, parenchymal hemorrhage appears to be related to biologic effects of tissue plasminogen activator and other pre-existing pathologic conditions, which deserve further investigation.
Key Words: magnetic resonance imaging, diffusion-weighted magnetic resonance imaging, perfusion-weighted outcome stroke, acute thrombolytic therapy tissue plasminogen activator
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