Interexaminer Difference in Infarct Volume Measurements on MRI

Author:

Ay Hakan1,Arsava E. Murat1,Vangel Mark1,Oner Banu1,Zhu Mingwang1,Wu Ona1,Singhal Aneesh1,Koroshetz Walter J.1,Sorensen A. Gregory1

Affiliation:

1. 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.

Abstract

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.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Advanced and Specialized Nursing,Cardiology and Cardiovascular Medicine,Neurology (clinical)

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