Donate Help Contact The AHA Sign In Home
American Heart Association
Stroke
Search: search_blue_button Advanced Search
Published Online
on September 27, 2007

Stroke. 2007
Published online before print September 27, 2007, doi: 10.1161/STROKEAHA.107.485995
A more recent version of this article appeared on November 1, 2007
This Article
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
38/11/2919    most recent
STROKEAHA.107.485995v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
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
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Merino, J. G.
Right arrow Articles by Warach, S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Merino, J. G.
Right arrow Articles by Warach, S.
Right arrowPubmed/NCBI databases
*Substance via MeSH
Medline Plus Health Information
*MRI Scans
Related Collections
Right arrow CT and MRI
Right arrow Acute Cerebral Infarction
Right arrow Computerized tomography and Magnetic Resonance Imaging
Right arrow Thrombolysis

Submitted on February 22, 2007
Revised on April 25, 2007
Accepted on April 26, 2007

Lesion Volume Change After Treatment With Tissue Plasminogen Activator Can Discriminate Clinical Responders From Nonresponders

José G. Merino MD, MPhil*; Lawrence L. Latour PhD; Jason W. Todd MD; Marie Luby PhD; Peter D. Schellinger MD, PhD; Dong-Wha Kang MD; and Steven Warach MD, PhD

From the Section on Stroke Diagnostics and Therapeutics (J.G.M., L.L.L., J.W.T., M.L., P.D.S., D.-W.K., S.W.), National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Md; NorthEast Neurology (J.W.T.), NorthEast Medical Center, Concord, NC; Neurologische Klinik (P.D.S.), Universitätsklinikum Erlangen, Erlangen, Germany; and the Department of Neurology (D.-W.K.), Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.

* To whom correspondence should be addressed. E-mail: merinoj{at}ninds.nih.gov.

Background and Purpose—A change in acute-to-chronic lesion volume has been proposed as a biomarker for stroke therapies. The objectives of this study were to determine the magnitude of lesion volume change after standard treatment with tissue plasminogen activator and to determine whether specific volume change thresholds can discriminate clinical responders from nonresponders.

Methods—We measured lesion volume on diffusion weighted at baseline and on 90-day fluid attenuated inversion recovery MRI and scored 3-month modified Rankin Scale in consecutive patients treated with tissue plasminogen activator. We identified variables associated with excellent (modified Rankin Scale 0 to 1) and independent (modified Rankin Scale 0 to 2) outcomes.

Results—We included 53 patients (mean age 69 years, median baseline National Institutes of Health Stroke Scale score 7). The mean acute-to-chronic lesion volume increase was 11.7 (±7.7) cm3. In 23 patients, the chronic lesion was smaller than the baseline lesion. At 3 months, 32 patients had an excellent clinical outcome. Dichotomous volume change variables associated with outcome included decrease in volume ≥30% (P=0.004) and volume increase ≥5 cm3 (P=0.002).

Conclusions—In patients given standard tissue plasminogen activator therapy, changes in lesion volume are associated with clinical outcome, and threshold lesion volumes can differentiate excellent and poor outcome, suggesting these as a potential marker of outcome.


Key words: acute stroke • brain imaging • brain infarction • MRI • thrombolysis • thrombolytic RX