Focal Spot, Winter 2006/2007

https://digitalcommons.wustl.edu/focal_spot_archives/1104/thumbnail.jp

An investigation into the use of charge-coupled devices for digital mammography

This thesis describes the design, optimisation, construction and evaluation of a laboratory based digital mammography system which uses phosphor coated charge-coupled devices (CCDs) for x-ray detection. The size mismatch between the breast and the CCD is overcome by operating the CCD in time delay and integration (TDI) mode and scanning across the breast. Multiparameter optimisations have been carried out for a wide range of digital mammography system configurations and requirements, with the aim of optimising the image quality for a given patient dose. The influence of slot width, exposure time, focal spot size, detector resolution and noise level, dose restrictions, patient thickness and x- ray tube target on the system configuration to give optimum image quality is examined. The system is fully characterised in terms of responsivity, dark current, modulation transfer functions (MTFs), noise power spectra (NPS) and spatial frequency dependent detective quantum efficiency (DQE(f)). Direct interactions of x-rays with the CCD are shown to give a significant increase in the high frequency values of the MTF. These interactions also act as a source of noise and act to significantly reduce the DQE(f) at all frequencies. A subjective comparison of images produced with the optimised prototype system with those produced using a conventional film-screen detector shows that these interactions must be removed if the prototype system is to produce images of equal quality to those currently produced using film-screen combinations. Other improvements to the system are suggested

The effects of stereo shift angle, geometric magnification and display zoom on depth measurements in digital stereomammography

Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/134800/1/mp7615.pd

Large field of view, fast and low dose multimodal phase-contrast imaging at high x-ray energy

X-ray phase contrast imaging (XPCI) is an innovative imaging technique which extends the contrast capabilities of ‘conventional’ absorption based x-ray systems. However, so far all XPCI implementations have suffered from one or more of the following limitations: low x-ray energies, small field of view (FOV) and long acquisition times. Those limitations relegated XPCI to a ‘research-only’ technique with an uncertain future in terms of large scale, high impact applications. We recently succeeded in designing, realizing and testing an XPCI system, which achieves significant steps toward simultaneously overcoming these limitations. Our system combines, for the first time, large FOV, high energy and fast scanning. Importantly, it is capable of providing high image quality at low x-ray doses, compatible with or even below those currently used in medical imaging. This extends the use of XPCI to areas which were unpractical or even inaccessible to previous XPCI solutions. We expect this will enable a long overdue translation into application fields such as security screening, industrial inspections and large FOV medical radiography – all with the inherent advantages of the XPCI multimodality

Development of a flat-panel x-ray source

A novel flat-panel transmission type X-ray source was developed for both medical and industrial use. Depending on the geometry of the given situation, the flat-panel X-ray source could be used in tomography, radiography or tomosynthesis. Furthermore, the unit could be used as a portable X-ray scanner or an integral part of an existing detection system. The design incorporates a field emission cathode made of ultra-nanocrystalline diamonds (UNCD) doped with nitrogen. These field emitters show good electron output at low power and can be deposited over large areas as is the case with carbon nanotube forest (CNT) cathodes. This work presents the first generation of the UNCD based FEA prototype which was manufactured at the Center of Nanoscale Material, within Argonne National Laboratory, with standard microfabrication techniques. The prototype is a 3 x 3 pixel field emission array (FEA), with a pixel size of 225 µm by 225 µm and a pitch of 500 µm. The fabricated cathode was developed using a microfabrication process which allows for individual electrically addressable UNCD gated arrays on-chip which demonstrated monolithic integration of the electron extraction grid. The transmission target consists of tungsten for X-ray generation, which is sputtered directly upon a thin aluminum sheet as an X-ray filter. A low voltage power supply allows for electron extraction between the cathode and the grid; while a high voltage power supply accelerates the electrons towards the anode. A low energy X-ray high purity germanium detector (HPGe) is mounted outside of the vacuum chamber for X-ray detection and measurement --Abstract, page iii

Review of Methods for Intraoperative Margin Detection for Breast Conserving Surgery

Breast conserving surgery (BCS) is an effective treatment for early-stage cancers as long as the margins of the resected tissue are free of disease according to consensus guidelines for patient management. However, 15% to 35% of patients undergo a second surgery since malignant cells are found close to or at the margins of the original resection specimen. This review highlights imaging approaches being investigated to reduce the rate of positive margins, and they are reviewed with the assumption that a new system would need high sensitivity near 95% and specificity near 85%. The problem appears to be twofold. The first is for complete, fast surface scanning for cellular, structural, and/or molecular features of cancer, in a lumpectomy volume, which is variable in size, but can be large, irregular, and amorphous. A second is for full, volumetric imaging of the specimen at high spatial resolution, to better guide internal radiologic decision-making about the spiculations and duct tracks, which may inform that surfaces are involved. These two demands are not easily solved by a single tool. Optical methods that scan large surfaces quickly are needed with cellular/molecular sensitivity to solve the first problem, but volumetric imaging with high spatial resolution for soft tissues is largely outside of the optical realm and requires x-ray, micro-CT, or magnetic resonance imaging if they can be achieved efficiently. In summary, it appears that a combination of systems into hybrid platforms may be the optimal solution for these two very different problems. This concept must be cost-effective, image specimens within minutes and be coupled to decision-making tools that help a surgeon without adding to the procedure. The potential for optical systems to be involved in this problem is emerging and clinical trials are underway in several of these technologies to see if they could reduce positive margin rates in BCS

Focal Spot, Spring 1991

https://digitalcommons.wustl.edu/focal_spot_archives/1057/thumbnail.jp

Virtual clinical trials in medical imaging: a review

The accelerating complexity and variety of medical imaging devices and methods have outpaced the ability to evaluate and optimize their design and clinical use. This is a significant and increasing challenge for both scientific investigations and clinical applications. Evaluations would ideally be done using clinical imaging trials. These experiments, however, are often not practical due to ethical limitations, expense, time requirements, or lack of ground truth. Virtual clinical trials (VCTs) (also known as in silico imaging trials or virtual imaging trials) offer an alternative means to efficiently evaluate medical imaging technologies virtually. They do so by simulating the patients, imaging systems, and interpreters. The field of VCTs has been constantly advanced over the past decades in multiple areas. We summarize the major developments and current status of the field of VCTs in medical imaging. We review the core components of a VCT: computational phantoms, simulators of different imaging modalities, and interpretation models. We also highlight some of the applications of VCTs across various imaging modalities

Focal Spot, Summer 1988

https://digitalcommons.wustl.edu/focal_spot_archives/1049/thumbnail.jp

Improved Diagnostics by Assessing the Micromorphology of Breast Calcifications via X-Ray Dark-Field Radiography

Breast microcalcifications play an essential role in the detection and evaluation of early breast cancer in clinical diagnostics. However, in digital mammography, microcalcifications are merely graded with respect to their global appearance within the mammogram, while their interior microstructure remains spatially unresolved and therefore not considered in cancer risk stratification. In this article, we exploit the sub-pixel resolution sensitivity of X-ray dark-field contrast for clinical microcalcification assessment. We demonstrate that the micromorphology, rather than chemical composition of microcalcification clusters (as hypothesised by recent literature), determines their absorption and small-angle scattering characteristics. We show that a quantitative classification of the inherent microstructure as ultra-fine, fine, pleomorphic and coarse textured is possible. Insights underlying the micromorphological nature of breast calcifications are verified by comprehensive high-resolution micro-CT measurements. We test the determined microtexture of microcalcifications as an indicator for malignancy and demonstrate its potential to improve breast cancer diagnosis, by providing a non-invasive tool for sub-resolution microcalcification assessment. Our results indicate that dark-field imaging of microcalcifications may enhance the diagnostic validity of current microcalcification analysis and reduce the number of invasive procedures