Ly Catherine Kim
Edward B. Singleton Diagnostic Imaging Services, Texas Children's Hospital, Houston 77030-2399, USA.
J Digit Imaging. 2002;15 Suppl 1:33-40. doi: 10.1007/s10278-002-5027-8. Epub 2002 Mar 21.
With growing dependence on picture archiving and communication systems for viewing images, a quality assurance program to monitor the condition of workstation displays has become increasingly important. At present there is no universally accepted program for PACS, but there are groups such as DICOM Working Group 11 of the ACR-NEMA and AAPM Task Group 18 that are working on image quality guidelines for interpretation from soft-copy displays. Texas Children's Hospital (TCH) is developing our own quality assurance program. Data is being collected to determine the appropriate frequency of calibration, the useful life of the displays, appropriate manufacturers, and model-dependent limits on maximum and minimum luminance (black level), symptoms of degradation, and monitor cleanliness. Our system includes a variety of monitors manufactured by Sun, AFP, Siemens, Image Systems, Barco, and Orwin. We are presently collecting data on individual monitor luminance functions but have not yet initiated service calls based on deviation from the DICOM Part 14 Grayscale Display Function (GSDF). The GSDF was intended to produce a grayscale in which driving levels produce changes in luminance that are perceptually equivalent throughout the entire luminance range for a specific test target. Our data is based on measurements of luminance from a digital Society of Motion Picture and Television Engineers (SMPTE) test pattern, which is a standard used by many other institutions. TCH's biomedical engineer measures luminance data each month from the display of the SMPTE pattern and record the results in a spreadsheet. The engineer also makes subjective evaluations of sharpness, geometric distortion, and artifacts. When a monitor's luminance falls outside of arbitrary 10% limits of maximum or minimum luminance, then a service call is placed to the vendor. The luminance check by the biomedical engineer is used to verify both routine and unscheduled calibrations. In addition to the monthly monitor checks, the vendor calibrates the monitor every three months. The vendor checks the following: width and height of display, focus and position of image, SMPTE test pattern, and a graph of the GSDF Index produced by an automatic calibration software by the video driver card. Monitors are also cleaned occasionally for dust, fingerprints, ink, and pencil marks, which accumulate with routine use. This paper reports data collected to date on luminance drift, as well as conclusions on appropriate frequency of test and calibration, and our experience with monitor useful life.
随着对用于查看图像的图像存档与通信系统的依赖日益增加,用于监测工作站显示器状况的质量保证计划变得越发重要。目前尚无适用于PACS的普遍接受的计划,但诸如美国放射学会(ACR)-美国国家电子制造商协会(NEMA)的DICOM第11工作组和美国医学物理学家协会(AAPM)任务组18等团体正在制定关于从软拷贝显示器进行解读的图像质量指南。德克萨斯儿童医院(TCH)正在制定我们自己的质量保证计划。正在收集数据以确定校准的适当频率、显示器的使用寿命、合适的制造商以及与型号相关的最大和最小亮度(黑电平)限制、退化症状和显示器清洁度。我们的系统包括由太阳公司、AFP、西门子、图像系统公司、巴可公司和奥温公司生产的各种显示器。我们目前正在收集关于各个显示器亮度功能的数据,但尚未基于与DICOM第14部分灰度显示功能(GSDF)的偏差发起服务呼叫。GSDF旨在生成一种灰度,其中驱动电平在整个亮度范围内针对特定测试目标产生在感知上等效的亮度变化。我们的数据基于对数字电影与电视工程师协会(SMPTE)测试图案的亮度测量,这是许多其他机构使用的标准。TCH的生物医学工程师每月从SMPTE图案的显示器测量亮度数据,并将结果记录在电子表格中。工程师还对清晰度、几何失真和伪影进行主观评估。当显示器的亮度超出最大或最小亮度的任意10%限制时,就会向供应商发出服务呼叫。生物医学工程师进行的亮度检查用于验证常规和不定期校准。除了每月对显示器进行检查外,供应商每三个月对显示器进行一次校准。供应商检查以下内容:显示器的宽度和高度、图像的焦点和位置、SMPTE测试图案以及由视频驱动卡的自动校准软件生成的GSDF指数图。显示器也会偶尔清洁灰尘、指纹、墨水和铅笔痕迹,这些会在日常使用中积累。本文报告了迄今为止收集到的关于亮度漂移的数据,以及关于测试和校准的适当频率的结论,还有我们对显示器使用寿命的经验。