Sommer A, Schopphoven S, Land I, Blaser D, Sobczak T
Physical-technical quality assurance group, Reference Center Muenster for Mammography at the University Hospital Muenster;
Physical-technical quality assurance group, Reference Center for Mammography Southwest in Marburg;
Rofo. 2014 May;186(5):474-81. doi: 10.1055/s-0033-1356284. Epub 2014 Feb 20.
As part of the physico-technical quality assurance of the German breast cancer screening program, the threshold contrast visibility and the average glandular dose of every digital mammography system have to fulfill the requirements of the "European guidelines for quality assurance in breast cancer screening and diagnosis" (4th Edition). To accomplish uniform measurements in all federal states of Germany, the physical board of the reference centers developed a special guideline in 2009. Due to recent changes in the guidelines and standards, a second version of the guideline was developed by the reference centers. This guideline describes the determination of the average glandular dose as well as the CDMAM image acquisition and the CDMAM image evaluation. The determination of the threshold contrast visibility can be performed visually or automatically. The determination of the average glandular dose is based on DIN 6868 - 162 and the threshold contrast visibility test is based on the German "Quality Assurance Guideline".
作为德国乳腺癌筛查计划物理技术质量保证的一部分,每个数字乳腺摄影系统的阈值对比度可见度和平均腺体剂量必须符合《欧洲乳腺癌筛查与诊断质量保证指南》(第4版)的要求。为了在德国所有联邦州进行统一测量,参考中心的物理委员会于2009年制定了一项特殊指南。由于指南和标准最近发生了变化,参考中心又制定了该指南的第二版。本指南描述了平均腺体剂量的测定以及CDMAM图像采集和CDMAM图像评估。阈值对比度可见度的测定可以通过视觉或自动方式进行。平均腺体剂量的测定基于DIN 6868 - 162,阈值对比度可见度测试基于德国的《质量保证指南》。