| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
(Stroke. 2008;39:1171.)
© 2008 American Heart Association, Inc.
Original Contributions |
From the Stroke Service, Department of Neurology (H.A., A.B.S.) and A.A. Martinos Center for Biomedical Imaging (H.A., E.M.A., M.V., B.O., M.Z., O.W., A.G.S.), Department of Radiology, Massachusetts General Hospital, Harvard Medical School, Boston, Mass; and the National Institute of Neurological Disorders and Stroke (W.J.K.), NIH, Bethesda, Md.
Correspondence to Hakan Ay, MD, A.A. Martinos Center for Biomedical Imaging and Stroke Service, Departments of Neurology and Radiology, Massachusetts General Hospital, Harvard Medical School, 149 13th Street, Room 2301, Charlestown MA 02129. E-mail hay{at}partners.org
Background and Purpose— The measurement of ischemic lesion volume on diffusion- (DWI) and perfusion-weighted MRI (PWI) is examiner dependent. We sought to quantify the variance imposed by measurement error in DWI and PWI lesion volume measurements in ischemic stroke.
Methods— Fifty-eight consecutive patients with DWI and PWI within 12 hours of symptom onset and follow-up MRI on
day-5 were studied. Two radiologists blinded to each other measured lesion volumes by manual outlining on each image. Interexaminer reliability was evaluated by intraclass correlation coefficients (ICC) and relative paired difference or RPD (ratio of difference between 2 measurements to their mean). The ratio of between-examiner variability to between-subject variability (variance ratio) was calculated for each imaging parameter.
Results— The correlation (ICC) between examiners ranged from 0.93 to 0.99. The median RPD was 10.0% for DWI, 14.1% for mean transit time, 18.9% for cerebral blood flow, 21.0% for cerebral blood volume, 16.8% for DWI/MTT mismatch, and 6.3% for chronic T2-weighted images. There was negative correlation between RPD and lesion volume in all but chronic T2-weighted images. The variance ratio ranged between 0.02 and 0.10.
Conclusion— Despite high correlation between volume measurements of abnormal regions on DWI and PWI by different examiners, substantial differences in individual measurements can still occur. The magnitude of variance from measurement error is primarily determined by the type of imaging and lesion volume. Minimizing this source of variance will better enable imaging to deliver on its promise of smaller sample size.
Key Words: acute stroke diffusion-weighted imaging MRI neuroradiology
|
Stroke Home | Subscriptions | Archives | Feedback | Authors | Help | AHA Journals Home | Search Copyright © 2008 American Heart Association, Inc. All rights reserved. Unauthorized use prohibited. |