Demeestere Jelle, Verhaaren Benjamin F J, Christensen Soren, Wouters Anke, Albers Gregory W, Lansberg Maarten G, Lemmens Robin
Leuven Brain Institute, Department of Neurosciences, Experimental Neurology, KU Leuven-University of Leuven, Belgium.
Department of Neurology, Leuven University Hospital, Belgium.
Neurology. 2025 Apr 8;104(7):e213439. doi: 10.1212/WNL.0000000000213439. Epub 2025 Mar 11.
It is unknown whether acute CT perfusion (CTP) core imaging may underestimate the follow-up infarct. We hypothesize that infarct underestimation occurs especially in late-presenting patients and that underestimated infarct can partially be detected on baseline noncontrast CT (NCCT).
We included patients with acute anterior circulation ischemic stroke who underwent baseline NCCT and CTP imaging, complete endovascular reperfusion, and follow-up MRI from the Endovascular Therapy Following Imaging Evaluation for Ischemic Stroke (DEFUSE 3) trial and a consecutive, monocenter cohort. We divided patients into early (<6 hours) and late (6-24 hours) presenters. We performed semiautomated segmentations of the acute ischemic lesion on NCCT using 5% relative density difference () and used the relative cerebral blood flow <30% to segment the CTP core. On coregistered images, we performed volumetric and voxel-based analyses to compare infarct estimations by imaging modality. Spatial accuracy for the follow-up infarct was assessed using the Dice similarity coefficient (DSC) and balanced accuracy.
We included 109 patients with a median age of 70 (interquartile range [IQR] 31-93) years of whom 52% were female. The follow-up infarct was underestimated by the CTP core (mean absolute volume difference [MAVD] = 14 mL [SD 36], < 0.001), but not by the union lesion (MAVD = 3 mL [SD 32], = 0.76). Infarct underestimation was greater in late presenters (median 17 mL [IQR 7-33] vs 7 mL [IQR 4-25] in early presenters, < 0.01) and in patients with poor collaterals (median 20 mL [IQR 8-56] vs 8 mL [IQR 4-20] in patients with good collaterals, < 0.01). Median 25% of the infarct missed by the CTP core could be detected on baseline rNCCT in late presenters (vs. median 3% in early presenters). The combined and CTP core lesion more accurately detected the follow-up infarct compared with the CTP core alone (median DSC 0.37 [IQR 0.06-0.55] vs 0.18 [IQR 0-0.42] and median balanced accuracy 0.67 [IQR 0.53-0.75] vs 0.56 [IQR 0.50-0.67], < 0.001 for both).
Underestimation of follow-up infarct by CTP is substantial and the follow-up infarct can partially be detected by baseline NCCT, especially in patients with stroke with delayed presentation. Combining and CTP increases the accuracy for predicting the follow-up infarct.
急性CT灌注(CTP)核心影像是否会低估随访梗死灶尚不清楚。我们推测梗死灶低估尤其发生在就诊较晚的患者中,且在基线非增强CT(NCCT)上可部分检测到被低估的梗死灶。
我们纳入了来自缺血性卒中影像评估后的血管内治疗(DEFUSE 3)试验及一个连续的单中心队列中,接受了基线NCCT和CTP成像、完全血管内再灌注及随访MRI的急性前循环缺血性卒中患者。我们将患者分为就诊早(<6小时)和就诊晚(6 - 24小时)两组。我们使用5%的相对密度差异在NCCT上对急性缺血性病变进行半自动分割,并使用相对脑血流量<30%来分割CTP核心区。在配准图像上,我们进行基于体积和体素的分析,以比较不同成像方式对梗死灶的估计。使用Dice相似系数(DSC)和平衡准确率评估随访梗死灶的空间准确性。
我们纳入了109例患者,中位年龄为70岁(四分位间距[IQR] 31 - 93),其中52%为女性。CTP核心区低估了随访梗死灶(平均绝对体积差异[MAVD] = 14 mL [标准差36],P < 0.001),但联合病变区未低估(MAVD = 3 mL [标准差32],P = 0.76)。就诊晚的患者梗死灶低估更严重(就诊晚患者中位数为17 mL [IQR 7 - 33],就诊早患者为7 mL [IQR 4 - 25],P < 0.01),侧支循环差的患者也是如此(侧支循环差的患者中位数为20 mL [IQR 8 - 56],侧支循环好的患者为8 mL [IQR 4 - 20],P < 0.01)。在就诊晚的患者中,CTP核心区遗漏的梗死灶中位数的25%可在基线rNCCT上检测到(就诊早的患者中为中位数3%)。与单独的CTP核心区相比,联合的NCCT和CTP核心区病变能更准确地检测随访梗死灶(中位数DSC 0.37 [IQR 0.06 - 0.55] 对比0.18 [IQR 0 - 0.42],中位数平衡准确率0.67 [IQR 0.53 - 0.75] 对比0.56 [IQR 0.50 - 0.67],两者P < 0.001)。
CTP对随访梗死灶的低估很显著,且随访梗死灶可部分通过基线NCCT检测到,尤其是在就诊延迟的卒中患者中。联合NCCT和CTP可提高预测随访梗死灶的准确性。