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数字化乳腺钼靶筛查:平均腺体剂量及首次性能参数

Digital mammography screening: average glandular dose and first performance parameters.

作者信息

Weigel S, Girnus R, Czwoydzinski J, Decker T, Spital S, Heindel W

机构信息

Institut für Klinische Radiologie und Referenzzentrum Mammografie mit Screening-Einheit Münster-Nord, Universitätsklinikum Münster.

出版信息

Rofo. 2007 Sep;179(9):892-5. doi: 10.1055/s-2007-963387.

Abstract

PURPOSE

The Radiation Protection Commission demanded structured implementation of digital mammography screening in Germany. The main requirements were the installation of digital reference centers and separate evaluation of the fully digitized screening units. Digital mammography screening must meet the quality standards of the European guidelines and must be compared to analog screening results. We analyzed early surrogate indicators of effective screening and dosage levels for the first German digital screening unit in a routine setting after the first half of the initial screening round.

MATERIALS AND METHODS

We used three digital mammography screening units (one full-field digital scanner [DR] and two computed radiography systems [CR]). Each system has been proven to fulfill the requirements of the National and European guidelines. The radiation exposure levels, the medical workflow and the histological results were documented in a central electronic screening record.

RESULTS

In the first year 11,413 women were screened (participation rate 57.5 %). The parenchymal dosages for the three mammographic X-ray systems, averaged for the different breast sizes, were 0.7 (DR), 1.3 (CR), 1.5 (CR) mGy. 7 % of the screened women needed to undergo further examinations. The total number of screen-detected cancers was 129 (detection rate 1.1 %). 21 % of the carcinomas were classified as ductal carcinomas in situ, 40 % of the invasive carcinomas had a histological size <or= 10 mm and 61 % < 15 mm. The frequency distribution of pT-categories of screen-detected cancer was as follows: pTis 20.9 %, pT1 61.2 %, pT2 14.7 %, pT3 2.3 %, pT4 0.8 %. 73 % of the invasive carcinomas were node-negative.

CONCLUSION

The average glandular dose for all three digital screening units was below the AGD of the analog mammography screening units (1.7 mGy) used in the German trial projects. Nevertheless, the performance indicators of the European guidelines were fulfilled with respect to the prevalent tumor detection rate and tumor size distribution while meeting an acceptable recall rate. This first evaluation of a digital screening unit in Germany demonstrates that the quality standards are met at lower radiation dosage levels than in screen-film mammography.

摘要

目的

德国辐射防护委员会要求在德国有组织地实施数字化乳腺钼靶筛查。主要要求是设立数字参考中心,并对全数字化筛查设备进行单独评估。数字化乳腺钼靶筛查必须符合欧洲指南的质量标准,并且必须与传统筛查结果进行比较。我们分析了德国首个数字化筛查设备在首轮筛查上半年后的常规环境中有效筛查和剂量水平的早期替代指标。

材料与方法

我们使用了三台数字化乳腺钼靶筛查设备(一台全场数字化扫描仪[DR]和两台计算机X线摄影系统[CR])。每个系统均已证明符合国家和欧洲指南的要求。辐射暴露水平、医疗工作流程和组织学结果记录在中央电子筛查记录中。

结果

第一年筛查了11413名女性(参与率57.5%)。三种乳腺钼靶X线系统针对不同乳房大小的平均实质剂量分别为0.7(DR)、1.3(CR)、1.5(CR)mGy。7%的筛查女性需要进一步检查。筛查出的癌症总数为129例(检出率1.1%)。21%的癌被分类为原位导管癌,40%的浸润性癌组织学大小≤10mm,61%<15mm。筛查出的癌症pT分期的频率分布如下:pTis 20.9%,pT1 61.2%,pT2 14.7%,pT3 2.3%,pT4 0.8%。73%的浸润性癌无淋巴结转移。

结论

所有三台数字化筛查设备的平均腺体剂量低于德国试验项目中使用的传统乳腺钼靶筛查设备的平均腺体剂量(1.7mGy)。然而,在满足可接受召回率的同时,欧洲指南的性能指标在流行肿瘤检出率和肿瘤大小分布方面得到了满足。德国首个数字化筛查设备的这一首次评估表明,在比屏-片乳腺钼靶更低的辐射剂量水平下也能达到质量标准。

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