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Evaluations of UltraiQ software for objective ultrasound image quality assessment using images from a commercial scanner

机译:使用来自商用扫描仪的图像对用于客观超声图像质量评估的UltraiQ软件进行评估

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摘要

We evaluated a commercially available software package that uses B‐mode images to semi‐automatically measure quantitative metrics of ultrasound image quality, such as contrast response, depth of penetration (DOP), and spatial resolution (lateral, axial, and elevational). Since measurement of elevational resolution is not a part of the software package, we achieved it by acquiring phantom images with transducers tilted at 45 degrees relative to the phantom. Each measurement was assessed in terms of measurement stability, sensitivity, repeatability, and semi‐automated measurement success rate. All assessments were performed on a GE Logiq E9 ultrasound system with linear (9L or 11L), curved (C1‐5), and sector (S1‐5) transducers, using a CIRS model 040GSE phantom. In stability tests, the measurements of contrast, DOP, and spatial resolution remained within a ±10% variation threshold in 90%, 100%, and 69% of cases, respectively. In sensitivity tests, contrast, DOP, and spatial resolution measurements followed the expected behavior in 100%, 100%, and 72% of cases, respectively. In repeatability testing, intra‐ and inter‐individual coefficients of variations were equal to or less than 3.2%, 1.3%, and 4.4% for contrast, DOP, and spatial resolution (lateral and axial), respectively. The coefficients of variation corresponding to the elevational resolution test were all within 9.5%. Overall, in our assessment, the evaluated package performed well for objective and quantitative assessment of the above‐mentioned image qualities under well‐controlled acquisition conditions. We are finding it to be useful for various clinical ultrasound applications including performance comparison between scanners from different vendors.
机译:我们评估了一种商用软件包,该软件包使用B模式图像半自动测量超声图像质量的定量指标,例如对比度响应,穿透深度(DOP)和空间分辨率(横向,轴向和仰角)。由于高程分辨率的测量不是软件包的一部分,因此我们通过使用相对于幻像倾斜45度的换能器获取幻像来实现它。每次测量均根据测量稳定性,灵敏度,可重复性和半自动测量成功率进行评估。所有评估均使用CIRS 040GSE型幻象在具有线性(9L或11L),弯曲(C1-5)和扇形(S1-5)换能器的GE Logiq E9超声系统上进行。在稳定性测试中,分别在90%,100%和69%的情况下,对比度,DOP和空间分辨率的测量值保持在±10%的变化阈值内。在敏感性测试中,分别在100%,100%和72%的情况下,遵循预期的行为进行对比度,DOP和空间分辨率的测量。在可重复性测试中,对比度,DOP和空间分辨率(横向和轴向)的个体内和个体间变异系数分别等于或小于3.2%,1.3%和4.4%。与海拔分辨率测试相对应的变异系数均在9.5%以内。总体而言,在我们的评估中,评估套件在良好控制的采集条件下,对于上述图像质量的客观和定量评估表现良好。我们发现它可用于各种临床超声应用,包括不同供应商的扫描仪之间的性能比较。

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