Wednesday, 27 June 2012

CR and DR Information from our sponsor iCRco

Click here Spreadsheet for Kodak CR reader data analysis if Exposure index
CR Basics

CR Introduction



CR uses an imaging plate coated with storage phosphors to capture x-rays as they pass through the patient. Trace amounts of impurities are added to the phosphor materials in a process called "doping," to alter their crystalline form and physical properties. When irradiated, the enhanced phosphors absorb and store x-ray energy in gaps in their altered crystal structure. This trapped energy comprises a latent image; when stimulated by additional light energy of the proper wavelength, the trapped energy is released.

In modern CR systems, storage phosphors commonly are stimulated with a low-energy laser to release visible light wherever x-rays have been absorbed. This light is captured and converted into an electrical signal, which is converted to data that can be transmitted to remote systems or locations, displayed on laser-printed films or softcopy workstations and stored digitally. An X-ray with Vision
Other than the absence of film and chemical processing, from the technician's and the patient's perspectives, computed radiography - including equipment for capture - works very much like conventional film-screen radiology. The difference is in the benefits.
Phosphor plates, like film, are stored in cassette format. In fact, existing analog equipment, from generators to x-ray tubes, examination tables and upright chest exam systems, can be used with a CR system. Technicians simply insert a CR cassette instead of a film cassette, take the x-ray, and then transfer the exposed cassette with x-ray images into the CR unit that scans and translates the contents into data, to be sent to soft copy display, archives, or hard copy print-out.
Compared to conventional film-screen capture, CR technology speeds image availability and can reduce image retakes and duplication costs, to boost workflow and productivity. CR also offers more options for displaying, sharing and storing images.
From the core precepts of storage phosphor-based image generation, improvements in phosphor screen coating, optics and scanning systems, and image data processing have increased the sophistication of computed radiography. Kodak scientists' contributions in many areas have helped make it possible for self-contained hardware and software systems to handle every step from image acquisition to display. In general, CR systems are getting smaller and faster, to handle heavy patient loads in tight spaces, such as emergency rooms or intensive care units.
The Next Step
Kodak experts are continuing to refine aspects of CR to address industry challenges including the types of exams possible, such as "long length" imaging. Not long ago, physicians requiring hip-to-foot, full spine or other "long length" images needed to use film-based image capture - along with attendant chemical processing and film handling. Kodak recently introduced fully automatic stitching software and cassette positioning system that delivers images up to 17 inches wide by 51 inches long (43 x 129 cm), with few, if any, visible seams. The results can be viewed in soft copy or printed on film using a Kodak DryView laser imager for viewbox display.
In an ongoing commitment to digital imaging, Kodak continues to refresh CR technology quickly, applying its innovation and expertise to meet the needs of hospital radiology centers and diagnostic facilities - whether they are high-traffic, cutting-edge teaching schools, or low-volume operations with specific cost requirements. Since 2000, Kodak has introduced three DirectView CR systems for single- or multi-plate image capture and high-volume image generation and processing, with additional new product offerings expected by the end of 2003.
Efficiency - better workflow and greater productivity - remains a top priority for healthcare providers. For those facilities that have adopted CR, further advances in system capacity and image processing capability contribute to quantity and quality of images, so that the time to produce images is reduced, and the number of radiography sessions completed is increased. Kodak pioneered remote operations panel display equipment that allows radiology technicians to perform most system functions while away from the main CR unit. Images may be reviewed or accessed from an examination room as if the technician were using the primary CR system itself. Other software makes it possible for demographic data to be entered by department administrative personnel, to make the best use of technician's time.
Advances in image science also make it possible for radiology centers to improve operations without huge capital investment; for example, Kodak recently introduced third-generation software for image enhancement and processing. Along with these improvements, the cost has come down, and CR systems with better functionality are available at half the price typical just five or six years ago. These changes further encourage adoption of CR by healthcare providers.
As CR was becoming more standard in hospitals and diagnostic centers, Kodak scientists began work several years ago on the next wave of radiographic imaging technology: Digital, or direct, radiography (DR). DR systems feature a detector that has the capability to produce images very quickly, either through a similar phosphor stimulation process or by a special material that converts x-ray energy directly to a charge that is read by a semiconductor. Indeed, adoption of Kodak CR technology could help customers more quickly embrace DR technology. Kodak is commercializing this next generation of radiography technology to leverage the familiar functional aspects of its CR systems, so that DR will be easy to incorporate into existing radiology practices and workflow.
© Eastman Kodak Company, 2003. Kodak, DirectView and DryView are trademarks.
http://www.kodak.com

CR v Film screen imaging - process



 
The Diagnostic Imaging Chain in CR

Compare this with the standard film screen Imaging Chain
Compare FS and CR Storage Phosphors
Advantages of CR over FS systems
Ref: Kodak Training CD


CR Storage phosphor screens a review of FS exposure



Comparison of CR / FS Screens
 

 
Take a look at the graph below, it shows the Kv sensitivity of different screen emulsions, the absorption at low energies i.e. those energies possessed by scattered radiation generally below 55-60Kv. the green line shows typical sensitivity of Lanex screens which primarily absorbs radiation above around 50 Kv the K edge absorption of Gadolinium. However the phosphor used in CR image plates is based on are europium-doped barium fluorohalide crystals have a K edge at 37 Kv making the receptors more sensitive to scattered radiation Kv values

With FS radiography we know that the image density and contrast is controlled by the Kv and mAS respectively

The range of subject densities affect the contrast of the organs on the image

The Exposure values set control where the subject density levels appear on the range of densities on the film and how squashed up or extended along the range of densities available on the film


Other factors effecting Contrast in FS radiography

The effect of scatter on an image

The graph below shows where the scattered energies appear on the graph of screen absorption - note the more scatter radiation energies falling below the K edge of the phosphor decreases the amount of image produced by the scatter



Exposure Techniques in CR



Having reviewed the exposure factor considerations we now need to look at the differences with CR. mA - It is no longer true that mAs controls image density, in FS where the same medium is used for detection and display the 2 are intimately linked. However in CR where detection and display are separate processes they are not linked. For a given CR image receptor mAS still determines the number of quanta that are absorbed and , therefore noise, the image processing controls the output signal and hence image density in CR.
kV - Kv still controls contrast BUT a linear response of CR (Exposure v density) means that matching the subject contrast to the Kv and film screen combination is much less important. The prime influence on contrast in CR comes from the "lookup tables" Kv along with tube filtration still controls the incident x-ray spectrum and therefore, subject contrast and scatter, image processing can partially compensate for loss of subject contrast.


This difference between Film Screen imaging and Computed radiography and the transition from FS to CR imaging is something radiographers find difficult and when  they produce a light or dark image are tempted to repeat the image using more or less exposure respectively in order to correct the image - this is the INCORRECT way to approach the problem, the method should be to check the Exposure index to see if enough exposure has been received by the imaging plate to permit image manipulation then check and adjust the image using the image processing functions of the system.
Scatter
As with FS systems scatter plays an important role - in fact scatter and its control is more important in CR than in FS radiography


CR Systems and Scatter
Here we compare the absorption spectra of FS screens (green line)  and CR image screens, (pink line) note the absorption peak (K edge) of CR screens to the considerably  lower due to the primary absorber Barium of CR compared with Gadolinium of FS screens,  hence the greater sensitivity to scattered radiation energies.

Now look at the primary and secondary or scatter spectra for a typicaly 80 Kv exposure, the scattered x-rays have lower energies than the primary beam, the storage phosphor CR absorbtion peak falls in the middle of the scattered engies range indicating that it will absorb a fair amount of these energies - compare this with the Lanex regular screen phosphor.
CR storage phosphor screens absorb more x-ray scatter than most conventional FS combinations under the same exposure conditions. This may explain observations that image quality of some images where there is a lot of scatter eg (Mediatinum in non grid chest images and the abdomen of large patients)  is lower with CR than conventional FS radiography.

Summary of Comparison of CR and FS phosphorus


Lookup table,
table allowing a display system to map pixel values into colours or grey scale values with a convenient range of brightness and contrast. Thus, a narrow range of input pixel intensities may be mapped onto the available range of output intensities. Rather than using the pixel values directly, the value is instead used as an address into a lookup table where the content of the table at that address defines the output  grey-scale value
.

The Imaging Cycle



Consider now the imaging cycle events
 
On x-ray exposure the latent image is formed by trapping electrons in the screen, half of the energy disappears immediately in the form of light, the remaining is trapped in metastable storage states in the screen.
When exposed to X-rays, the europium atoms in the phosphor crystalline lattice are ionized (converted from 2+ to 3+), liberating a valence electron. These electrons are raised to a higher energy state in the conduction band (see solid and photoconduction for an explanation of conduction band). Once in the conduction band, the electrons travel freely until they are trapped in a so-called F-centre in a metastable state with an energy level slightly below that of the conduction band, but higher than that of the valence band. The number of trapped electrons is proportional to the amount of X-rays absorbed locally. The trapped electrons constitute the latent image. Due to thermal motion, the electrons will slowly be liberated from the traps, and the latent image should therefore be read without too much delay. At room temperature, the image should, however, be readable up to 8 hours after exposure.
The wide-latitude response of the storage phosphors means that a high-quality image can be produced regardless of the relative amount of exposure to the plate. The laser beam in the CR reader scans across the imaging plate, the phosphors are excited and release the energy they have stored. This energy is emitted from the plate as a violet blue glow. The strength of this glow is directly proportional to the amount of radiation absorbed. The phosphor glow is captured in the scanner and converted into a digital image. Because visible (“photo”) light excites (“stimulates”) the phosphors to glow (“luminesce”), this process is known as photo stimulated luminescence and the phosphors are often called photostimulable phosphors or storage phosphors.

The laser scan does not extract all the energy stored in the crystals so the storage phosphor plate must be erased. After the plate is scanned it enters the eraser where it is flooded with bright fluorescent light. This intense light removes any residual energy remaining on the plate so that it can be used again. At the end of the erase cycle, the operator removes the storage phosphor plate from the eraser drawer and reloads it into a cassette. There is no evidence that the storage phosphors’ exposure or erasure response changes over time.
 

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