Parr L F, Anderson A L, Glennon B K, Fetherston P
Naval Medical Center, Portsmouth, VA, USA.
J Digit Imaging. 2001 Jun;14(2 Suppl 1):22-6. doi: 10.1007/BF03190289.
Previous literature indicates a need for more data collection in the area of quality control of high-resolution diagnostic monitors. Throughout acceptance testing, which began in June 2000, stability of monitor calibration was analyzed. Although image quality on all monitors was found to be acceptable upon initial acceptance testing using VeriLUM software by Image Smiths, Inc (Germantown, MD), it was determined to be unacceptable during the clinical phase of acceptance testing. High-resolution monitors were evaluated for quality assurance on a weekly basis from installation through acceptance testing and beyond. During clinical utilization determination (CUD), monitor calibration was identified as a problem and the manufacturer returned and recalibrated all workstations. From that time through final acceptance testing, high-resolution monitor calibration and monitor failure rate remained a problem. The monitor vendor then returned to the site to address these areas. Monitor defocus was still noticeable and calibration checks were increased to three times per week. White and black level drift on medium-resolution monitors had been attributed to raster size settings. Measurements of white and black level at several different size settings were taken to determine the effect of size on white and black level settings. Black level remained steady with size change. White level appeared to increase by 2.0 cd/m2 for every 0.1 inches decrease in horizontal raster size. This was determined not to be the cause of the observed brightness drift. Frequency of calibration/testing is an issue in a clinical environment. The increased frequency required at our site cannot be sustained. The medical physics division cannot provide dedicated personnel to conduct the quality-assurance testing on all monitors at this interval due to other physics commitments throughout the hospital. Monitor access is also an issue due to radiologists' need to read images. Some workstations are in use 7 AM to 11 PM daily. An appropriate monitor calibration frequency must be established during acceptance testing to ensure unacceptable drift is not masked by excessive calibration frequency. Standards for acceptable black level and white level drift also need to be determined. The monitor vendor and hospital staff agree that currently, very small printed text is an acceptable method of determining monitor blur, however, a better method of determining monitor blur is being pursued. Although monitors may show acceptable quality during initial acceptance testing, they need to show sustained quality during the clinical acceptance-testing phase. Defocus, black level, and white level are image quality concerns, which need to be evaluated during the clinical phase of acceptance testing. Image quality deficiencies can have a negative impact on patient care and raise serious medical-legal concerns. The attention to quality control required of the hospital staff needs to be realistic and not have a significant impact on radiology workflow.
以往文献表明,在高分辨率诊断监视器的质量控制领域需要更多的数据收集。在2000年6月开始的验收测试过程中,对监视器校准的稳定性进行了分析。尽管在使用Image Smiths公司(马里兰州日耳曼敦)的VeriLUM软件进行初始验收测试时,发现所有监视器的图像质量都可以接受,但在验收测试的临床阶段却被判定为不可接受。从安装到验收测试及之后,每周都会对高分辨率监视器进行质量保证评估。在临床使用判定(CUD)期间,监视器校准被确定为一个问题,制造商返回并重新校准了所有工作站。从那时到最终验收测试,高分辨率监视器校准和监视器故障率仍然是个问题。然后监视器供应商返回现场处理这些问题。监视器散焦仍然很明显,校准检查增加到每周三次。中分辨率监视器的白电平与黑电平漂移归因于光栅尺寸设置。在几个不同尺寸设置下对白电平与黑电平进行测量,以确定尺寸对白电平与黑电平设置的影响。黑电平随尺寸变化保持稳定。水平光栅尺寸每减小0.1英寸,白电平似乎增加2.0 cd/m²。经判定,这不是观察到的亮度漂移的原因。校准/测试频率在临床环境中是一个问题。我们现场所需的增加后的频率无法持续。由于医院内其他物理工作的任务安排,医学物理部门无法在此间隔为所有监视器提供专门人员进行质量保证测试。由于放射科医生需要读取图像,监视器的使用权限也是一个问题。一些工作站每天从上午7点到晚上11点都在使用。必须在验收测试期间确定合适的监视器校准频率,以确保不可接受的漂移不会被过高的校准频率掩盖。还需要确定可接受的黑电平与白电平漂移标准。监视器供应商和医院工作人员一致认为,目前,非常小的印刷文本是确定监视器模糊度的一种可接受方法,然而,正在寻求一种更好的确定监视器模糊度的方法。尽管监视器在初始验收测试期间可能显示出可接受的质量,但在临床验收测试阶段它们需要显示出持续的质量。散焦、黑电平与白电平是图像质量问题,在验收测试的临床阶段需要对其进行评估。图像质量缺陷可能对患者护理产生负面影响,并引发严重的医疗法律问题。医院工作人员对质量控制的关注需要切合实际,并且不会对放射科工作流程产生重大影响。