Donate Help Contact The AHA Sign In Home
American Heart Association
Stroke
Search: search_blue_button Advanced Search
Stroke. 2009;40:3245-3251
Published online before print August 13, 2009, doi: 10.1161/STROKEAHA.109.558635
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
40/10/3245    most recent
STROKEAHA.109.558635v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Olivot, J.-M.
Right arrow Articles by Albers, G. W.
PubMed
Right arrow PubMed Citation
Right arrow Articles by Olivot, J.-M.
Right arrow Articles by Albers, G. W.
Right arrowPubmed/NCBI databases
Medline Plus Health Information
*Stroke
Related Collections
Right arrow CT and MRI
Right arrow Acute Cerebral Infarction
Right arrow Thrombolysis

(Stroke. 2009;40:3245.)
© 2009 American Heart Association, Inc.


Original Contributions

Geography, Structure, and Evolution of Diffusion and Perfusion Lesions in Diffusion and Perfusion Imaging Evaluation For Understanding Stroke Evolution (DEFUSE)

Jean-Marc Olivot, MD, PhD; Michael Mlynash, MD, MS; Vincent N. Thijs, MD, PhD; Archana Purushotham, MBBS, PhD; Stephanie Kemp, BS; Maarten G. Lansberg, MD, PhD; Lawrence Wechsler, MD; Garry E. Gold, MD, PhD; Roland Bammer, PhD; Michael P. Marks, MD Gregory W. Albers, MD

From the Department of Neurology (J-M.O., M.M., A.P., S.K., M.G.L., G.W.A.), Neurological Sciences and the Stanford Stroke Center, Stanford University Medical Center, Stanford, Calif; the Department of Neurology (V.N.T.), University Hospitals Leuven, Leuven, Belgium, and Vesalius Research Center, VIB, Leuven, Belgium; UMPC Stroke Institute and Department of Neurology (L.W.), University of Pittsburgh, Pittsburgh, Pa; and the Department of Radiology and the Stanford Stroke Center (G.E.G., R.B., M.P.M.), Stanford University Medical Center, Stanford, Calif.

Correspondence to Jean-Marc Olivot, MD, PhD, Department of Neurology and Neurological Sciences and the Stanford Stroke Center, Stanford University Medical Center, 701 Welch Road, Suite 325, Palo Alto, CA 94304. E-mail jmolivot{at}stanford.edu

Background and Purpose— The classical representation of acute ischemic lesions on MRI is a central diffusion-weighted imaging (DWI) lesion embedded in a perfusion-weighted imaging (PWI) lesion. We investigated spatial relationships between final infarcts and early DWI/PWI lesions before and after intravenous thrombolysis in the Diffusion and perfusion imaging Evaluation For Understanding Stroke Evolution (DEFUSE) study.

Methods— Baseline and follow-up DWI and PWI lesions and 30-day fluid-attenuated inversion recovery scans of 32 patients were coregistered. Lesion geography was defined by the proportion of the DWI lesion superimposed by a Tmax (time when the residue function reaches its maximum) >4 seconds PWI lesion; Type 1: >50% overlap and Type 2: ≤50% overlap. Three-dimensional structure was dichotomized into a single lesion (one DWI and one PWI lesion) versus multiple lesions. Lesion reversal was defined by the percentage of the baseline DWI or PWI lesion not superimposed by the early follow-up DWI or PWI lesion. Final infarct prediction was estimated by the proportion of the final infarct superimposed on the union of the DWI and PWI lesions.

Results— Single lesion structure with Type 1 geography was present in only 9 patients (28%) at baseline and 4 (12%) on early follow-up. In these patients, PWI and DWI lesions were more likely to correspond with the final infarcts. DWI reversal was greater among patients with Type 2 geography at baseline. Patients with multiple lesions and Type 2 geography at early follow-up were more likely to have early reperfusion.

Conclusion— Before thrombolytic therapy in the 3- to 6-hour time window, Type 2 geography is predominant and is associated with DWI reversal. After thrombolysis, both Type 2 geography and multiple lesion structure are associated with reperfusion.


Key Words: brain infarction • magnetic resonance • thrombolysis