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Published online before print July 22, 2008, 10.1148/radiol.2483071602

(Radiology 2008;248:979.)

A more recent version of this article appeared on September 1, 2008
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© RSNA, 2008

Neuroradiology

T2' Imaging Predicts Infarct Growth beyond the Acute Diffusion-weighted Imaging Lesion in Acute Stroke1

Susanne Siemonsen, Thies Fitting, MD, Götz Thomalla, MD, Peter Horn, MD, Jürgen Finsterbusch, PhD, Paul Summers, MD, Christian Saager, MD, Thomas Kucinski, MD, and Jens Fiehler, MD

1 From the Departments of Neuroradiology (S.S., T.F., P.H., C.S., J. Fiehler) and Neurology (G.T., J. Finsterbusch), University Medical Center Hamburg–Eppendorf, Martinistrasse 52, 20246 Hamburg, Germany; Department of Biomedical Sciences, University of Modena, Modena, Italy (P.S.); and Roentgenkliniken Huddinge, Karolinska University Hospital, Stockholm, Sweden (T.K.). Received September 11, 2007; revision requested December 21; revision received January 29, 2008; accepted March 27; final version accepted April 15. Supported in part by Else-Kröner-Fresenius Stiftung (C.S.) and by the European Union Proposal/Contract 027294-I-Know-STREP (S.S.). Address correspondence to S.S. (e-mail: s.siemonsen{at}uke.uni-hamburg.de).

Purpose: To show that measurement of the transverse relaxation time that characterizes signal loss caused by local susceptibilities (T2') is sensitive to an increased deoxyhemoglobin concentration in the brain, indicating tissue at risk for infarction.

Materials and Methods: The study was approved by the local institutional review board; patients or their guardians provided informed consent. Magnetic resonance (MR) imaging was performed within 6 hours of symptom onset and again 1–11 days thereafter in 100 consecutive stroke patients, all of whom received intravenous thrombolytic therapy (mean age, 67 years). The MR imaging protocol included diffusion- and perfusion-weighted imaging for determination of apparent diffusion coefficient (ADC) and time to peak (TTP), along with quantitative T2 and T2* imaging. T2' maps were calculated and visually compared with ADC and TTP lesions by two independent observers.

Results: A T2'>ADC mismatch was observed by reader 1 in 73 (73%) of 100 patients, and by reader 2 in 65 (65%) patients. Respective sensitivities of T2'>ADC and of TTP>ADC mismatches for later infarct growth were 0.87 and 0.98 for reader 1 and 0.78 and 0.98 for reader 2, with respective specificities of 0.42 and 0.04 for reader 1 and 0.46 and 0.04 for reader 2. The odds ratios for infarct growth in the presence of a T2' > ADC mismatch were 4.59 (reader 1 P = .002) and 3.10 (reader 2 P = .012), while the odds ratios for TTP>ADC mismatch were 2.22 (reader 1 P = .606) and 1.73 (reader 2 P > .999).

Conclusion: The presence of a T2' > ADC mismatch is a more specific predictor of infarct growth than is TTP>ADC mismatch and hence may be of clinical value in patient selection for acute stroke therapies in the future.

© RSNA, 2008







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