Impact of reconstruction kernel variability on segmentation consistency in low-dose thoracic CT.

Eléanor Liard, Aravind R Krishnan, Fabien Maldonado, Kim Sandler, Yuankai Huo, Lianrui Zuo, Bennett A Landman
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Abstract

Structural thoracic segmentation with computed tomography (CT) has become a ubiquitous step in medical image processing. Several tools-including TotalSegmentator-now provide efficient, open methods for labeling regions of interest (ROI) in CT. However, variability in CT reconstruction kernels, especially between soft and hard kernels, can affect image characteristics and potentially impact automatic segmentation, downstream analysis, and clinical decisions. Yet, this variability and its impact on downstream analysis have not been fully investigated in a systematic way. To address this, we examine the consistency of thoracic region segmentations produced by TotalSegmentator when applied to 9,529 CT images reconstructed with paired soft and hard kernels from the National Lung Screening Trial (NLST) dataset. It includes 9,529 CT scan pairs from 9,519 subjects (5,733 men, 3,796 women; ages 43-74), with each subject contributing one scan session, including data from multiple vendors (Siemens, Philips and GE Medical Systems) and reconstruction kernels, drawn from the Lung Screening Study (LSS) (n=6,794), American College of Radiology Imaging Network (ACRIN) with biomarkers (n=1,488), and ACRIN without biomarkers (n=1,247), with 10 duplicated subjects treated as separate individuals. We quantified kernel-induced variability using Dice similarity coefficient, volumetric and intensity differences across 84 thoracic regions. We evaluated the relationship between the average and difference of volumes, Hounsfield Units (HU) and standard deviation of HU of ROI. Additionally, we assessed manufacturer-specific differences in segmentation consistency between Philips, Siemens and GE Medical Systems. Graphical representations with Bland-Altman plots show that some thoracic regions (e.g. heart) are more robust to kernel variation than others (e.g. thyroid gland), and Siemens scanners show the lowest segmentation variability between kernel types. These findings provide early insights into when kernel-induced variability affects automatic segmentation performance differently across the body in clinical and research workflows, therefore emphasizing the need for consistent CT reconstruction or kernel harmonization.

重建核变异性对低剂量胸部CT分割一致性的影响。
利用计算机断层扫描(CT)进行胸部结构分割已成为医学图像处理中普遍存在的步骤。包括totalsegmentator在内的一些工具现在提供了高效、开放的方法来标记CT中的感兴趣区域(ROI)。然而,CT重建核的可变性,特别是软核和硬核之间的可变性,会影响图像特征,并可能影响自动分割、下游分析和临床决策。然而,这种可变性及其对下游分析的影响尚未得到系统的充分研究。为了解决这个问题,我们检查了TotalSegmentator产生的胸部区域分割的一致性,并将其应用于9529张使用国家肺筛查试验(NLST)数据集的配对软核和硬核重建的CT图像。该研究包括9519名受试者(5733名男性,3796名女性,年龄43-74岁)的9529对CT扫描,每个受试者贡献一次扫描,包括来自多个供应商(西门子,飞利浦和GE医疗系统)和重建核的数据,这些数据来自肺筛查研究(LSS) (n= 6794)、美国放射学院成像网络(ACRIN) (n= 1488)和不含生物标志物的ACRIN (n= 1247),其中10名重复受试者作为单独的个体处理。我们使用Dice相似系数、84个胸部区域的体积和强度差异来量化核诱导的变异性。我们评估了ROI的体积平均值和差值、Hounsfield单位(HU)和HU标准差之间的关系。此外,我们还评估了飞利浦、西门子和GE医疗系统在细分一致性方面的制造商特定差异。Bland-Altman图的图形表示表明,某些胸部区域(如心脏)比其他区域(如甲状腺)对核变异的鲁棒性更强,西门子扫描仪显示核类型之间的分割变异性最低。这些发现为临床和研究工作流程中核诱发的变异性对全身自动分割性能的影响提供了早期见解,因此强调了一致CT重建或核协调的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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