Samei Ehsan, Badano Aldo, Chakraborty Dev, Compton Ken, Cornelius Craig, Corrigan Kevin, Flynn Michael J, Hemminger Bradley, Hangiandreou Nick, Johnson Jeffrey, Moxley-Stevens Donna M, Pavlicek William, Roehrig Hans, Rutz Lois, Shepard Jeffrey, Uzenoff Robert A, Wang Jihong, Willis Charles E
Duke Advanced Imaging Laboratories, Department of Radiology, Duke University, DUMC 3302, Durham, North Carolina 27710, USA.
Med Phys. 2005 Apr;32(4):1205-25. doi: 10.1118/1.1861159.
Digital imaging provides an effective means to electronically acquire, archive, distribute, and view medical images. Medical imaging display stations are an integral part of these operations. Therefore, it is vitally important to assure that electronic display devices do not compromise image quality and ultimately patient care. The AAPM Task Group 18 (TG18) recently published guidelines and acceptance criteria for acceptance testing and quality control of medical display devices. This paper is an executive summary of the TG18 report. TG18 guidelines include visual, quantitative, and advanced testing methodologies for primary and secondary class display devices. The characteristics, tested in conjunction with specially designed test patterns (i.e., TG18 patterns), include reflection, geometric distortion, luminance, the spatial and angular dependencies of luminance, resolution, noise, glare, chromaticity, and display artifacts. Geometric distortions are evaluated by linear measurements of the TG18-QC test pattern, which should render distortion coefficients less than 2%/5% for primary/secondary displays, respectively. Reflection measurements include specular and diffuse reflection coefficients from which the maximum allowable ambient lighting is determined such that contrast degradation due to display reflection remains below a 20% limit and the level of ambient luminance (Lamb) does not unduly compromise luminance ratio (LR) and contrast at low luminance levels. Luminance evaluation relies on visual assessment of low contrast features in the TG18-CT and TG18-MP test patterns, or quantitative measurements at 18 distinct luminance levels of the TG18-LN test patterns. The major acceptable criteria for primary/ secondary displays are maximum luminance of greater than 170/100 cd/m2, LR of greater than 250/100, and contrast conformance to that of the grayscale standard display function (GSDF) of better than 10%/20%, respectively. The angular response is tested to ascertain the viewing cone within which contrast conformance to the GSDF is better than 30%/60% and LR is greater than 175/70 for primary/secondary displays, or alternatively, within which the on-axis contrast thresholds of the TG18-CT test pattern remain discernible. The evaluation of luminance spatial uniformity at two distinct luminance levels across the display faceplate using TG18-UNL test patterns should yield nonuniformity coefficients smaller than 30%. The resolution evaluation includes the visual scoring of the CX test target in the TG18-QC or TG18-CX test patterns, which should yield scores greater than 4/6 for primary/secondary displays. Noise evaluation includes visual evaluation of the contrast threshold in the TG18-AFC test pattern, which should yield a minimum of 3/2 targets visible for primary/secondary displays. The guidelines also include methodologies for more quantitative resolution and noise measurements based on MTF and NPS analyses. The display glare test, based on the visibility of the low-contrast targets of the TG18-GV test pattern or the measurement of the glare ratio (GR), is expected to yield scores greater than 3/1 and GRs greater than 400/150 for primary/secondary displays. Chromaticity, measured across a display faceplate or between two display devices, is expected to render a u',v' color separation of less than 0.01 for primary displays. The report offers further descriptions of prior standardization efforts, current display technologies, testing prerequisites, streamlined procedures and timelines, and TG18 test patterns.
数字成像提供了一种以电子方式获取、存档、分发和查看医学图像的有效手段。医学成像显示工作站是这些操作中不可或缺的一部分。因此,确保电子显示设备不会损害图像质量并最终影响患者护理至关重要。美国医学物理学会任务组18(TG18)最近发布了医学显示设备验收测试和质量控制的指南及验收标准。本文是TG18报告的执行摘要。TG18指南包括针对一级和二级显示设备的视觉、定量和高级测试方法。结合专门设计的测试图案(即TG18图案)进行测试的特性包括反射、几何失真、亮度、亮度的空间和角度依赖性、分辨率、噪声、眩光、色度和显示伪像。几何失真通过TG18-QC测试图案的线性测量来评估,一级/二级显示器的失真系数应分别小于2%/5%。反射测量包括镜面反射和漫反射系数,据此确定最大允许环境光照,以使由于显示反射导致的对比度下降保持在20%的限值以下,并且环境亮度(Lamb)水平不会在低亮度水平下过度损害亮度比(LR)和对比度。亮度评估依赖于对TG18-CT和TG18-MP测试图案中低对比度特征的视觉评估,或对TG18-LN测试图案18个不同亮度水平的定量测量。一级/二级显示器的主要可接受标准分别为最大亮度大于170/100 cd/m²、LR大于250/100以及对比度符合灰度标准显示功能(GSDF)优于10%/20%。测试角度响应以确定对于一级/二级显示器,对比度符合GSDF优于30%/60%且LR大于175/70的视角范围,或者确定TG18-CT测试图案的轴上对比度阈值仍可辨别的视角范围。使用TG18-UNL测试图案在显示器面板上两个不同亮度水平评估亮度空间均匀性应得出不均匀系数小于30%。分辨率评估包括对TG18-QC或TG18-CX测试图案中CX测试目标的视觉评分,一级/二级显示器的评分应大于4/6。噪声评估包括对TG18-AFC测试图案中对比度阈值的视觉评估,一级/二级显示器应至少有3/2个目标可见。该指南还包括基于调制传递函数(MTF)和噪声功率谱(NPS)分析进行更定量的分辨率和噪声测量的方法。基于TG18-GV测试图案低对比度目标的可见性或眩光率(GR)测量的显示眩光测试,一级/二级显示器的得分应大于3/1且GR大于400/150。在显示器面板上或两个显示设备之间测量的色度,一级显示器的u',v'颜色分离应小于0.01。该报告进一步描述了先前的标准化工作、当前的显示技术、测试前提条件、简化程序和时间表以及TG18测试图案。