NEMA MITA WP 1-2017 Computed Tomography Image Quality (CTIQ) Low-Contrast Detectability (LCD) Assessment When Using Dose Reduction Technology.pdf
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1、NEMA Standards PublicationNational Electrical Manufacturers AssociationNEMA/MITA WP 1-2017Computed Tomography Image Quality (CTIQ):Low-Contrast Detectability (LCD) Assessment When Using Dose Reduction TechnologyNEMA/MITA WP 1-2017 Page i 2017 National Electrical Manufacturers Association A NEMA Medi
2、cal Imaging b. No ROI will come to within 5 mm of any other rod; and c. No ROI will come to within 10 mm of the edge of the phantom. Figure 4 shows ROI size for LU and LK and ROI positions for each rod with respect to other ROIs. Figure 4 Illustrates ROI Sizes and How Far They Can Move for Each Rod.
3、 During initial testing, it was seen that the choice of rod sizes was acceptable for body protocols, but had too much contrast for useful testing with head protocols with ROC testing. That is, the AUC seen with typical head exams and no body ring was close to 0.99, which does not allow useful compar
4、isons. Two alternatives have been considered. The first is to use LROC testing with head protocols. By adding a localization parameter to the design, results allowed comparative testing. The second alternative was to create a second head phantom, with lower contrast rods. After working with the phan
5、tom manufacturer, a second phantom (head phantom) was created for testing head protocols, with the following sizes of rods, at the same positions as for the body phantom. Manufacturers were able to achieve good results with the second phantom (head phantom), but depending on the clinical protocol/po
6、pulation alternative head phantoms, such as a 16 cm phantom with a Teflon annulus to simulate bone, could be considered. NEMA/MITA WP 1-2017 Page 8 2017 National Electrical Manufacturers Association Table 1 Rod Diameters and Contrasts for Body and Head Phantoms Rod Body Phantom Head Phantom Diameter
7、 (mm) Contrast (HU) Diameter (mm) Contrast (HU) 1 3 14 2 9 2 5 7 3 5 3 7 5 4 4 4 10 3 5 3 A second concern raised during the initial testing of the phantom was quality control. Some vendors saw very different contrast (i.e., more than HU) in the rods than specified by the supplier. To help evaluate
8、the contrast, four rods were added to each phantom, with length 10 mm, but diameter 15 mm, for easier measurement of CT number. However, these rods showed a variation in CT number compared to the small rods. Therefore, follow-up work is being conducted with the phantom manufacturer with respect to t
9、he 15 mm rods. The initial version of the phantom had a 20 mm blank section, which made it difficult to get a sufficient number of blank images from a single helical scan. The second version had a 40 mm blank section, allowing more blank images to compare with a rod image. A limitation on the use of
10、 this phantom is that the contrast difference is created almost entirely by differences in density of the rod materials, rather than different rod compositions. This means that the contrast difference is relatively insensitive to changes in tube voltage. Clinically, lowering tube voltage allows impr
11、oved low-contrast detectability, since the tissues inside the body are comprised of different chemical compositions. NEMA/MITA WP 1-2017 Page 9 2017 National Electrical Manufacturers Association 6 Sample ROC Curves The following figures represent sample ROC curves with the head and body phantoms, wh
12、ich evaluate performance of images generated on actual systems. Figure 5 ROC Curve Examples. Left: 3 Mm 14 Hu Object without Body Ring. Right: 5 mm 7 Hu Object with Body Ring (Courtesy of GE Healthcare) Figure 6 LROC Curve Examples. Left: 10 Mm 3 Hu Object without Body Ring Right: 7 Mm 5 Hu Object w
13、ith Body Ring (Courtesy of GE Healthcare) NEMA/MITA WP 1-2017 Page 10 2017 National Electrical Manufacturers Association Figure 7 ROC Curve for Head Phantom (courtesy of Toshiba) 7 Conclusion The use of task-based observers to quantify low-contrast detectability as a function of dose reduction provi
14、des a practical, repeatable method for measuring performance of both FBP and IR. The phantom designed by MITA, in consultation with the FDA, is an effective tool for conducting observer studies that yields meaningful data in a manner precise enough for regulatory purposes. NEMA/MITA WP 1-2017 Page 1
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