LAUSR

Objective The aim of this study was to evaluate visual and quantitative differences of delay-sensitive (singular value deconvolution [SVD]) and delay-insensitive (SVD+) computed tomography perfusion (CTP) postprocessing methods in acute ischemic stroke patients and their variability according to location of critical stenosis. Methods The CTPs of 45 patients were retrospectively processed with 2 different methods. Comparing with the contralateral normal hemisphere, relative and difference of metrics were calculated (relative cerebral blood volume, relative cerebral blood flow [rCBF], relative mean transite time [rMTT], and difference mean transite time [dMTT]). Patients were categorized into 5 groups according to superiority in visual assessment of penumbra between postprocessing methods. Locations of critical stenosis and their percentages in each group were identified and compared. Results Differences were formulated as (rCBF/1.4, rMTT × 1.4, dMTT/3.8) SVD = (rCBF, rMTT, dMTT) SVD+. In group 1, penumbra was noted in SVD, whereas pseudohyperperfusion was noted in SVD+. In groups 2 and 3, penumbra was better distinguished in SVD than in SVD+ in decreasing easiness, respectively. In group 4, penumbra assessment was similar in both. In group 5, penumbra was better distinguished in SVD+. Groups 1 and 5 were the groups in which the frequency of critical distal stenosis was 100%. Groups 2, 3, and 4 were the groups having high rates of proximal critical stenosis in decreasing proportions, respectively (90%, 87%, and 77%). Conclusions In both CTP methods, the most prominent difference was found in dMTT. Visually, penumbra was better distinguished by SVD in proximal critical stenosis, whereas was better distinguished by SVD+ in distal critical stenosis. In cases having both ipsilateral critical proximal and distal stenoses, penumbra was noted in SVD but pseudohyperperfusion in SVD+. This finding showed that extraction of contrast delay in the SVD+ method might cause false results in cases of ipsilateral critical proximal and distal stenoses.