Modified ASPECTS for DWI including deep white matter lesions predicts subsequent intracranial hemorrhage

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Abstract

We hypothesized that extensive early ischemic changes increase subsequent intracranial hemorrhage (ICH) in patients within 3 h of onset regardless of intravenous tPA (IV-tPA). We have established a modified scoring method, ASPECTS?W, including deep white matter lesions on DWI (DWI-W) in addition to the original ASPECTS regions. We aimed to elucidate whether CTASPECTS, DWI-ASPECTS, and ASPECTS?W could be useful tools in helping to predict subsequent ICH in acute ischemic stroke. One-hundred sixty-four consecutive patients with anterior circulation ischemic stroke were enrolled. All patients underwent both MRI and CT within 3 h of onset. ASPECTS?W was defined as an 11-point method combining the ten ASPECTS regions and DWI-W. The relationships of CT-ASPECTS, DWI-ASPECTS, and ASPECTS?W with ICH within the initial 36 h were assessed. Thirty-six patients (22%) were treated with IVtPA. Follow-up CT was obtained in 159 patients, and 19 (12%) developed ICH. Patients with ICH had higher baseline NIHSS scores (median, 25 vs. 13, p = 0.010), a higher rate of IV-tPA (42 vs. 20%, p = 0.041), lower CTASPECTS (median, 7 vs. 10, p = 0.008), lower DWIASPECTS (6 vs. 9, p = 0.001), lower ASPECTS?W (6 vs. 9, p = 0.001), and higher DWI-W lesions (74 vs. 47%, p = 0.048) than those without ICH. ICA or M1 proximal occlusion was more frequently seen in patients with ICH (68 vs. 32%, p = 0.004) than in those without ICH. On multivariate regression analysis, lower ASPECTS?W (OR 0.75, 95% CI 0.58-0.96, p = 0.027) and administration of IV-tPA (OR 9.13, 95% CI 2.15-46.21, p = 0.004) independently predicted ICH development. In conclusion, ASPECTS?W is a useful tool for predicting ICH development independent of IV-tPA. © Springer-Verlag 2012.

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Kawano, H., Hirano, T., Nakajima, M., Inatomi, Y., Yonehara, T., & Uchino, M. (2012). Modified ASPECTS for DWI including deep white matter lesions predicts subsequent intracranial hemorrhage. Journal of Neurology, 259(10), 2045–2052. https://doi.org/10.1007/s00415-012-6446-1

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