Suppr超能文献

快速 AI 和 Viz.ai 软件在评估急性缺血性脑卒中的 CT 灌注输出比较。

A Comparison of CT Perfusion Output of RapidAI and Viz.ai Software in the Evaluation of Acute Ischemic Stroke.

机构信息

From the Department of Neurology (S.B.), Texas Tech University Health Sciences Center, Lubbock, Texas.

Department of Neurology (A.E.H.), Valley Baptist Medical Center Harlingen (L.N., R.S., Y.D.A., Z.M.K.), Harlingten, Texas.

出版信息

AJNR Am J Neuroradiol. 2024 Jul 8;45(7):863-870. doi: 10.3174/ajnr.A8196.

Abstract

BACKGROUND AND PURPOSE

Automated CTP postprocessing packages have been developed for managing acute ischemic stroke. These packages use image processing techniques to identify the ischemic core and penumbra. This study aimed to investigate the agreement of decision-making rules and output derived from RapidAI and Viz.ai software packages in early and late time windows and to identify predictors of inadequate quality CTP studies.

MATERIALS AND METHODS

One hundred twenty-nine patients with acute ischemic stroke who had CTP performed on presentation were analyzed by RapidAI and Viz.ai. Volumetric outputs were compared between packages by performing Spearman rank-order correlation and Wilcoxon signed-rank tests with subanalysis performed at early (<6 hours) and extended (>6 hours) time windows. The concordance of selecting patients on the basis of DAWN and DEFUSE 3 eligibility criteria was assessed using the McNemar test.

RESULTS

One hundred eight of 129 patients were found to have adequate-quality studies. Spearman rank-order correlation coefficients were calculated on time-to-maximum >6-second volume, time-to-maximum >10-second volume, CBF <30% volume, mismatch volume, and mismatch ratio between both software packages with correlation coefficients of 0.82, 0.65, 0.77, 0.78, 0.59, respectively. The Wilcoxon signed-rank test was also performed on time-to-maximum >6-second volume, time-to-maximum >10-second volume, CBF <30% volume, mismatch volume, and mismatch ratio with values of .30, .016, <.001, .03, <.001, respectively. In a 1-sided test, CBF <30% was greater in Viz.ai (< .001). Although this finding resulted in statistically significant differences, it did not cause clinically significant differences when applied to the DAWN and DEFUSE 3 criteria. A lower ejection fraction predicted an inadequate study in both software packages (= .018; 95% CI, 0.01-0.113) and (= .024; 95% CI, 0.008-0.109) for RapidAI and Viz.ai, respectively.

CONCLUSIONS

Penumbra and infarct core predictions between Rapid and Viz.ai correlated but were statistically different and resulted in equivalent triage using DAWN and DEFUSE3 criteria. Viz.ai predicted higher ischemic core volumes than RapidAI. Viz.ai predicted lower combined core and penumbra values than RapidAI at lower volumes and higher estimates than RapidAI at higher volumes. Clinicians should be cautious when using different software packages for clinical decision-making.

摘要

背景与目的

已开发出用于管理急性缺血性脑卒中的自动化 CTP 后处理软件包。这些软件包使用图像处理技术来识别缺血核心区和半影区。本研究旨在探讨 RapidAI 和 Viz.ai 软件包在早期和晚期时间窗内决策规则和输出的一致性,并确定 CTP 研究质量不足的预测因素。

材料与方法

对 129 例就诊时行 CTP 的急性缺血性脑卒中患者进行分析,这些患者分别由 RapidAI 和 Viz.ai 进行分析。通过 Spearman 等级相关系数和 Wilcoxon 符号秩检验进行包间比较,亚组分析在早期(<6 小时)和延长时间窗(>6 小时)进行。使用 McNemar 检验评估基于 DAWN 和 DEFUSE 3 入选标准选择患者的一致性。

结果

129 例患者中有 108 例被认为是高质量的研究。RapidAI 和 Viz.ai 软件包之间的时间至最大 6 秒容积、时间至最大 10 秒容积、CBF<30%容积、不匹配容积和不匹配比的 Spearman 等级相关系数分别为 0.82、0.65、0.77、0.78 和 0.59。Wilcoxon 符号秩检验也在时间至最大 6 秒容积、时间至最大 10 秒容积、CBF<30%容积、不匹配容积和不匹配比上进行, 值分别为 0.30、0.016、<0.001、0.03 和 <0.001。单侧检验发现,Viz.ai 的 CBF<30%(<.001)更大。虽然这一发现导致了统计学上的显著差异,但在应用于 DAWN 和 DEFUSE 3 标准时并未导致临床显著差异。两种软件包的射血分数较低均预测研究结果不足(=0.018;95%CI,0.01-0.113;=0.024;95%CI,0.008-0.109)。

结论

RapidAI 和 Viz.ai 之间的半影区和梗死核心预测结果相关,但存在统计学差异,且使用 DAWN 和 DEFUSE3 标准进行分诊的结果等效。Viz.ai 预测的缺血核心体积大于 RapidAI。Viz.ai 在较低的容积时预测的核心和半影区总和值低于 RapidAI,在较高的容积时预测的估计值高于 RapidAI。临床医生在进行临床决策时应谨慎使用不同的软件包。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验