Is there a sense of unjustified prejudice in digital X-ray
imaging? This segment of radiographic imaging has experienced
double-digit market growth during the past decade, and there is an
expanding, diverse range of technology available. But are these
emerging devices inappropriately classified based on preconceived
notions? Is it time to reexamine our perceptions and to consider a
logical means of understanding, describing, and using future
digital projection radiography technologies?
As a modality, digital radiography (DR) has been segregated into
systems labeled
DR
,
computed radiography
(CR),
digital
,
direct
, and
indirect
, as well as other names. Unfortunately, these labels often
increase confusion. Within these broad labels, there is a great
diversity of technology, with specific strengths and weaknesses.
For instance, a variety of detectors are used within the category
of DR and, within CR, different imaging plates and scanning methods
are used. Using these labels, assumptions have been made as to
imaging performance, diagnostic capabilities, and workflow
efficiencies. Instead, each system should be evaluated on its own
merits. Perhaps it is time to take a step back and begin an
open-minded discussion of the realities of this technology.
This supplement to
Applied Radiology
contributes to such a discussion. These informative articles
present a range of material on the evolution of DR, distinctions in
the teminology and technology, how to select systems to meet an
institution's needs, and what the future may hold for digital
imaging.
In supporting this publication, it is our hope that readers will
explore the evolution of digital X-ray terms and categories, which
will help them to better understand the differences and
similarities between the technologies. It is important for
radiologists and radiology administrators to consider, evaluate,
and categorize digital X-ray systems based on how they actually
address and satisfy their departments' needs.
John B. Strauss
Director of Marketing, Imaging Systems
FUJIFILM Medical Systems USA, Inc.
Stamford, CT
Dr. Seibert
is a Professor of Radiology, University of California, Davis
Medical Center, Sacramento, CA.
Categorizing digital radiography systems is no longer as simple
as "computed radiography" (CR) and "direct and/or digital
radiography" (DR). The more technology changes, the more it
changes. The CR versus DR issue is no exception, where historical
boundaries of CR (with passive, cassette-based image acquisition
and detector handling with offline processing) and the fully
integrated DR system (with automatic processing and display) are
now converging. Historically, CR has referred to the implementation
of a cassette-based photostimulable storage phosphor (PSP) imaging
plate reader and quality-control workstation that are packaged as
an add-on system to existing X-ray devices using screen-film
detectors. In contrast, DR has been touted as a totally integrated
X-ray source-generator-detector solution with images displayed for
review within the room shortly after the X-ray exposure. Now, "CR"
technology (specifically using PSP converters) has been developed
into integrated X-ray systems and has completely automated
acquisition, display, and processing. Now "DR" technology has
cassette-based detectors available for situations requiring more
flexibility in positioning and multiple uses in conventional X-ray
cassette trays and bedside portable radiography.
Computed radiography uses a PSP that transiently stores a latent
image in the form of electrons in semistable traps within the
phosphor structure, with subsequent data extraction using a
stimulating point laser beam that scans the phosphor surface point
by point. Line scan laser sources coupled to an array of microlens
and photodiode light detectors stimulate and acquire data in
parallel, reducing the readout time of a PSP imaging plate from
about a minute to ≤10 seconds, which is comparable to other digital
radiography detectors known for readout speed.
In its current definition,
DR
describes a multitude of digital X-ray detection systems that
immediately process the absorbed X-ray signal after exposure and
produce the image for viewing with no further user interaction.
This fact has resulted in the use of the term
direct radiography
by many manufacturers, which has added to the nomenclature
confusion, because of another use of
direct
that describes the conversion of X-rays into charge, which is
described later. In terms of CR versus DR, inclusion of automated
CR systems would fall into the DR category, along with optically
coupled scintillator to charge-coupled device (CCD) camera systems,
fiberoptically coupled rectangular CCD array slot-scan detector
systems, complementary metal-oxide semiconductor (CMOS) detector
systems, thin-film-transistor (TFT) flat-panel detector systems,
and slot-scan photon counting detectors, which were recently
introduced. The
CR
and
DR
acronyms no longer define the essence of digital radiography
detector attributes, since distinct classification into these 2
broad categories is no longer possible and, in fact, often leads to
confusion and "marketeering" claims and counterclaims.
In a recent publication by a multi-societal effort (including
the American College of Radiology, the American Association of
Physicists in Medicine, and the Society of Imaging Informatics in
Medicine) to determine practice guidelines for the use of CR and DR
in the clinical environment,
1
a consensus to title the work
Practice Guidelines for Digital Radiography
2
was made to be inclusive of all types of digital radiographic
systems, in recognition of the issues explained above. Likewise, in
this article, the term
digital radiography
refers to all types of digital radiographic systems, including both
those that had been historically termed
CR
and those historically termed
DR
.
So, how should one categorize current state-of-the-art digital
radiography technology? One method promoted in this article
considers 3 characteristics: 1) detector form factor; 2) image
acquisition geometry; and 3) X-ray signal conversion method, as
explained below. Various digital radiography detectors and
attributes are listed in Table 1.
Detector form factor considers aspects such as "cassette" versus
"cassetteless" (Figure 1) and "passive" versus "active" operation.
A majority of cassette-based digital detectors are based on PSP
technology as a direct replacement for screen-film, thus providing
a cost-effective means to achieve digital image acquisition, while
at the same time allowing great positioning flexibility. Passive
operation allows an asynchronous coupling of the X-ray exposure and
storage of the image signal on the phosphor. Subsequent processing
is performed by physically inserting the cassette/ phosphor plate
into an image "reader" to render the radiograph. Multiplexing of
several rooms to 1 reader is possible but is also time-ineffi-cient
and potentially limiting in busy, high-throughput rooms. An
alternative is a cassette-based TFT-array detector for use with
portable radiography examinations and as a "drop-in" to cassette
trays in general radiographic rooms. This detector uses a wired
electronic connection to the X-ray generator to actively integrate
and read out the X-ray image after exposure. A CMOS detector in a
cassette configuration for mammography is available as a
replacement for screen-film mammography. Wireless interfaces will
likely soon appear on such detector systems. Image display shortly
after the exposure and good positioning flexibility are benefits;
damage to the detector by unintentional mishandling is a
potentially costly drawback.
Cassetteless digital detectors are part of an integrated X-ray
generator, X-ray tube, and detector system. The basic meaning of
"cassetteless" indicates that the image is acquired and
subsequently displayed at the in-room technologist console for
review and manipulation with minimal user interaction. The earliest
"cassetteless" systems had PSP plate changers with automated
acquisition, point-scan laser readout, image processing, and
display, with individual processing times on the order of a minute.
Recent introduction of line-scan laser excitation of the PSP
imaging plate reduces readout time of a large 35 × 43-cm
field-of-view (FOV) detector in as few as 5 seconds, with automatic
processing and display. This is comparable to many large FOV
optically coupled CCD and flat-panel TFT arrays, which comprise the
majority of cassetteless digital radiography systems. In the
extreme are "real-time" flat-panel systems specifically
manufactured for fluoroscopic imaging that also provide
radiographic capabilities. Other cassetteless radiographic systems
include slot-scan acquisition devices in which the image is
produced by scanning a collimated beam and detector array across
the FOV over a time span of seconds.
Image acquisition geometry distinguishes instantaneous
acquisition of a large-area digital image with a short exposure
time versus a sequential, long exposure time acquisition of a
slot-scan device. Most digital detectors for radiography use a
large-area FOV geometry, which allows short exposure times to
decrease the probability of patient motion. However, detected
scatter from the patient reduces image contrast and consumes a
fraction of the digital range of the detector with essentially
useless information. Thus, an antiscatter grid is often used with
thicker body parts (it is used in essentially all adult imaging
except extremity examinations) and in-curs a relatively large dose
penalty (typically double the patient dose) because of the loss of
primary radiation. The slot-scan geometry with pre-and post-patient
collimation produces a narrow fan-beam incident on a scintillator
coupled to a time-delay-integrate CCD photodetector array.
3
Since at any instant only a small fraction of the patient volume is
irradiated, the amount of scatter is reduced to low levels, and the
amount of detected scatter is extremely low because of postpatient
collimation and a small detector area. Grids are not required,
which results in good dose utilization; image acquisition times,
however, are extended into seconds, and the detector/collimator
configuration makes positioning a challenge for nonstandard imaging
protocols.
X-ray signal conversion is described by indirect, direct, or
photon-counting methods. All digital detectors produce an output
signal, usually in the form of electrons or holes (positive ions),
which represent a quantity of charge that is proportional to the
number of Xrays ab-sorbed at a specific detector element (del)
position. The magnitude of the charge is converted to a voltage and
then to a digital value for storage in the image matrix at the
corresponding del location in the detector plane.
Indirect
refers to the conversion of X-rays into secondary information
carriers, such as absorbed X-ray energy to light energy conversion
in a scintillator, or to stored electrons in semistable traps
within a storage phosphor and subsequent stimulation with a laser
and light emission. For each X-ray photon absorbed, a large
amplification of light photon carriers is produced on account of
the large energy difference of X-rays (keV) versus light (eV) or
energy required to trap electrons in a storage phosphor (eV).
Regardless of the method by which secondary light photons are
formed, the large numbers are directed to a wavelength-matched
sensitive photodiode-TFT array via direct optical coupling, to a
CCD area detector by lens-optical coupling, or via a light-guide
pickup to a photomultiplier tube in a PSP reader device. Charge
amplitude is generated in response to the amplitude of light
intensity (and thus X-ray intensity). A proportional voltage is
produced and digitized to form the digital gray-scale image. Thus,
scintillator-based TFT arrays, optically coupled CCD camera
systems, and fiberoptically coupled CCD slot-scan systems as well
as all PSP systems are classified as indirect acquisition
devices.
Direct
, in the context of this article (unlike the use of this term by
many manufacturers that produce indirect acquisition DR devices),
refers to the method of ac-quisition and conversion of absorbed
X-ray energy into electron/hole pairs (charge) using semiconductor
converters such as amorphous selenium (
a
-Se), solid-state silicon, or high-pressure gas. These direct
acquisition detectors have a voltage applied to electrodes on
opposite surfaces of the absorber/semiconductor material to
separate and collect the generated electrons and holes. A small
amount of energy (on the order of 50 eV) is needed to produce an
ion pair for
a
-Se; for a 50-keV absorbed X-ray, hundreds of charge information
carriers are generated. Similar amplification of charge per
absorbed X-ray photon occurs in other direct converters as well.
Electric field lines direct the ion pairs to the collection
electrodes without lateral spreading, thus providing high intrinsic
resolution by accurately mapping the X-ray photon absorption event
to the corresponding del position.
Photon-counting detectors are currently configured in slot-scan
geometry, composed of either high-pressure gas or solid-state
silicon. These detectors measure absorbed X-ray photon events
individually as counts instead of energy integration like all other
detectors.
4
Since a count will be tallied independent of the photon energy, a
signal-to-noise ratio advantage of up to 40% is achieved for the
same number of X-ray photons absorbed in the detector compared with
energy integration detectors, as there is no bias toward higher
energy photons, and elimination of other noise sources accompanying
an energy-integrator detector is possible. A limitation is the
maximum count rate that can be sustained.
So, what is the "best" digital radiography detector? There is no
straightforward answer, as advantages and disadvantages are based
upon multiple comparisons of the following characteristics:
detective quantum efficiency (DQE), spatial resolution, contrast
resolution, dose efficiency, acquisition and display speed,
radiographic positioning flexibility, image quality, ability to use
existing radiographic equipment, integration with information
systems and electronic networks, system costs, service costs,
detector longevity, and survival in a hostile environment (eg,
trauma imaging), among many other benchmarks. Matching an
appropriate digital radiography device with its intended clinical
purpose is an exercise in determining actual needs and patient
throughput requirements prior to evaluating the type of DR system
that will best meet those needs in a cost-effective and efficient
manner.
5,6
Conclusion
The terms
CR
and
DR
will continue to be used, but collectively we must think beyond the
traditional CR versus DR comparisons, past the issues of X-ray
converter materials, to clinical relevance, cost-effectiveness,
dose efficiency, image processing functionality, overall image
quality, proper use of digital radiography attributes (eg, variable
speed characteristics and dose index values), quality-control
phantoms and automated computer routines to verify proper function,
patient throughput, uptime, reliability, longevity, service,
and
optimization in the clinical arena. Insisting on DR systems that
can self-monitor and verify optimal performance through the
automated analysis of quality-control phantom images will move the
industry toward providing these important tools.
Finally, while dose efficiency is important, it shouldn't be the
overriding consideration in determining the type of imaging system
that best meets a specific clinical need, as all DR systems that
are approved by the U.S. Food and Drug Administration must
demonstrate a reasonable image quality over a typical range of
incident exposures for clinical procedures. More important is an
understanding and use of exposure index values that describe the
"effective speed" of the detector to ensure that overexposures that
are otherwise difficult to discern do not become the standard of
practice as a result of complacency and/or ignorance.
REFERENCES
- Williams MB, Krupinski EA, Strauss KJ, et al. Digital
radiography image quality: Image acquisition. J Am Coll
Radiol.2007;4:371-388.
- ACR Practice Guideline for Digital Radiography. Approved May
2007. Available on the American College of Radiology Web site at:
http://www.acr.org/
SecondaryMainMenuCategories/quality_safety/guidelines/MedicalPhysics.aspx.
Accessed August 8, 2007.
- Samei E, Lo JY, Yoshizumi TT, et al. Comparative scatter and
dose performance of slot-scan and full-field digital chest
radiography systems. Radiology. 2005; 235:940-949.
- Pisano ED, Yaffe MJ. Digital
mammography.Radiology.2005;234:353-362.
- Reiner BI, Siegel EL, Hooper FJ, et al. Multi-institutional
analysis of computed and direct radiography: Part I. Technologist
productivity. Radiology.2005;236: 413-419.
- Reiner BI, Salkever D, Siegel EL, et al. Multi-institutional
analysis of computed and direct radiography: Part II. Economic
analysis. Radiology.2005;236:420-426.
Mr. Romlein
is a Managing Partner of Qualiteering Labs LLP, Thurmont,
MD.
In 1990, projection radiography comprised roughly 70% of the
total imaging workload of radiology departments; currently it
accounts for just over 50%. Computed radiography (CR) was the first
large-scale technology to support digital projection radiography,
but it has now been complemented by digital radiography (DR). One
key underlying reason for the different names was originally based
upon the use of either cassette-based photostimulable phosphor
imaging plates (CR) or integrated solid state devices (DR) as the
X-ray image receptors. While there were clear distinctions in early
CR and DR, the two technologies have grown toward each other in
their efforts to satisfy the needs of the projection radiography
workflow, throughput, and feature requirements.
Over time, there has been constant market pressure in the
development of the two modalities to make improvements in what was
seen to be the shortcomings of both CR and DR. These gradual design
changes caused the differences between the 2 technologies to begin
to disappear as they each moved toward becoming a better and more
versatile modality in support of the projection radiography
marketplace.
Blurred lines of distinction
A key early distinction between CR and DR was the use of
centralized versus decentralized workflow. As originally
implemented, CR was a cassette-based, centralized system that
mimicked the workflow model of a conventional film-based radiology
department using a daylight loading film processor. The centralized
design was a good fit for the existing layout of the radiology work
cores, which allowed for an easy transition of the film processing
spaces and, even more importantly, the cassette-based CR design
required no modification of the X-ray machines themselves.
The concept of a decentralized workflow, in which image
acquisition, image inspection and adjustment, and transfer to the
picture archiving and communication system (PACS) could be
accomplished by the technologist without ever leaving the X-ray
room, was not even a consideration in the early days. Such a
workflow model was never available for general radiology
applications in the film-based era; it would have required a
daylight loader in each room. The closest approximation to a
decentralized film-based system was the dedicated chest room with
an automatic film changer.
On the other hand, DR, in the form in which it was originally
implemented, required, and still requires a decentralized workflow.
The DR detector was permanently associated with the X-ray generator
and tube head. Each DR room operated as an independent system. Each
system was associated with a single-operator console from which the
images are acquired, assembled into a completed study, adjusted as
necessary, and transferred to either the PACS or a laser film
printer.
Distinctions and blur factors
The following paragraphs list a series of commonly believed
distinctions between CR and DR technologies and offer a description
of how that distinction has been blurred by changes in the
technologies or their applications.
Distinction:
Cassette-based systems require that the technologist transport
cassettes to a centralized processing location because the physical
facility cannot accommodate a decentralized workflow.
Blur factor:
CR cassette readers have decreased in size and cost and have
increased in speed, so that it is now feasible to have a dedicated
reader inside each X-ray room or control booth, which enables a
decentralized workflow that is very similar to a DR system.
Distinction:
CR systems all use cassette-based photostimulable phosphor (PSP)
detector image capture with associated human transport to a
centralized CR reader, image processing, and DICOM transfer
station.
Blur factor:
Current cassetteless PSP-based X-ray systems incorporate the image
receptor into the design of the X-ray systems with no human
transport of the image receptor required.
Distinction:
CR is required to obtain digital radiographs from portable X-ray
systems.
Blur factor:
Portable X-ray units are now available with an integrated
"tethered" DR detector that requires no human transport to a CR
reader and processing station following the exposure.
Distinction:
The integrated DR detector on a portable X-ray unit has the
advantage over CR of giving the technologist feedback on
positioning and image quality while still at bedside.
Blur factor:
Portable X-ray units are now available with integrated CR cassette
readers that approach this same functionality and require minimal
human transport.
Distinction:
Certain projections are difficult to obtain on DR systems due to
the bulk of the DR detector/bucky and the physical limitations of
the detector suspension systems.
Blur factor 1:
DR rooms can now be configured as hybrid systems with both
suspended bucky detectors and tethered flat-panel detectors. This
provides the additional freedom to use the tethered detector as a
free cassette for difficult positioning situations.
Blur factor 2:
A cassetteless PSP integrated X-ray system could exhibit the same
positioning limitations as a DR-integrated X-ray system.
Distinction:
Research has shown significant differences in total study
performance time principally because of the human transport of the
CR cassettes and postprocessing workflow.
1
Blur factor:
While this is true for most cassette-based, centrally organized CR
systems, the PSP-integrated X-ray systems eliminate all human
transport requirements, use high-speed line-scanning technology for
image acquisition, and consolidate the inspection, processing, and
DICOM transmission functions into the X-ray control area, thus
reducing or eliminating the workflow time differences.
Detectors
Several different digital detectors have emerged and have been
put into production for different digital imaging uses. For the
most part, there is little the consumer can do to influence which
detector type is used in any given device, but some basic
understanding of the differences is helpful.
CR generally implies the use of PSP detectors, which are
typically used in cassette-based imaging applications and are now
found in cassetteless digital imaging systems. Commercial detectors
have been introduced based on PSP compounds including but not
limited to: rubidium chloride (RbCl), and a variety of barium
flourohalides doped with europium (BaFBr:Eu
2
, BaF(Br,I):Eu
2
, and BaFI:Eu). These are unstructured phosphors that are scanned
in a raster pattern using laser light of a specific wavelength. The
resulting light emissions escaping from the phosphor are
concurrently collected and measured by either a moving photo
detector or a light collection circuit that feeds a stationary
photo detector. The collected light signals are proportional to
X-rays captured on the imaging plate and so have the relative
spatial and contrast information required to reconstruct the X-ray
image. This scanning methodology and BaFBr imaging plates are used
in cassette-based readers and have been incorporated into some
cassetteless X-ray systems. These cassetteless systems also
incorporate a rapid imaging plate (IP) changing mechanism to rotate
between multiple installed IPs. This technique makes a blank IP
rapidly available for the next exposure while scanning the IP that
was last exposed to X-rays.
Cesium bromide doped with europium (CsBr:Eu) is a newer phosphor
that is sometimes referred to as a needle phosphor because of its
needlelike structure. This PSP is more efficient in its return of
signal per unit of X-ray dose and can be scanned by a line-scanning
mechanism, which reduces the image acquisition cycle to <10
seconds. CsBr receptors work well in cassetteless X-ray systems
because of the very high image transfer rate.
DR generally implies the use of solid-state detectors that were
initially integrated into a cassetteless relationship with an X-ray
source, generator, and control station. The use of solid-state
imaging systems in cassette-based image receptors has recently been
introduced but is limited to a subset of detector types and imaging
systems. DR systems use arrays or flat panels that are made up of
thin-film transistor (TFT) arrays or of other detector materials.
The structure of the array must accommodate either the direct or
indirect X-ray conversion properties of each detector material to
produce electrical output signals proportional to the received
X-ray image.
General radiography and digital mammography systems use the
widest variety of digital detectors including, but not limited to,
the following types: amorphous silicon TFT (a-Si TFT), amorphous
selenium TFT (a-Se TFT), charge-coupled device (CCD), and
complementary metal oxide semiconductors (CMOS). All but one (a-Se
TFT) of these detector types use indirect conversion processes to
change received X-rays into electrical signal. Digital detectors
that are typically used for acquiring fluoroscopic imagery include
a-Si TFT and a-Se TFT. Digital detectors made of Gd
2
O
2
S photodiode TFT arrays and CMOS detectors are exceptions, as they
have been used in cassette-based systems.
In general, these arrays are made up of discrete detector
elements (dels) arranged into a flat panel. Each del, either
directly or indirectly, builds up an electrical charge that is
proportional to the amount of X-rays striking it. Each del is also
directly addressable via the imbedded circuitry of the flat panel
and can be read following the X-ray exposure. Reading out the
electrical signals sequentially in lines and rows reproduces the
spatial arrangement of the flat panel and delivers an image matrix
of discrete picture elements (pixels), each of which is
proportional to a small portion of the X-ray image.
Spatial resolution
Spatial resolution is dependent on several factors. In DR
receptors, the actual size of the dels in the image receptor matrix
coupled with the geometry of the X-ray system and the patient
establishes a spatial relationship to the anatomy being imaged. The
closer the centers of the dels are, the higher the spatial
resolution. In arrays that use indirect DR detectors, the amount of
light spread during the X-ray-to-light conversion process has a
negative effect on spatial resolution. To limit this, some
manufacturers use structured converters that contain the emitted
light and reflect it toward a single del. PSP receptors do not have
physical image elements and instead rely on photo detectors being
rapidly sampled during the motion of the IP through the detector
mechanism. The faster the sample rate, the higher the resulting
spatial resolution, as long as the signal-to-noise ratio remains
acceptable.
Motion-related artifacts
A key difference between PSP detectors and most digital
detectors is that PSP image acquisition and erasure is accomplished
by some form of relative motion between the image phosphor and the
light collection and erasure circuitry. This relative motion can be
the source of artifacts for a variety of reasons.
2
Most solid-state detectors (with the exception of the slot-scanned
detectors used in some applications) do not use any moving parts to
acquire the images from the receptors or to perform erasures and
are, therefore, free of this source of artifact.
DR receptor artifacts
The solid-state image receptors have a set of issues that PSP
receptors do not. All dels must be periodically equalized to
provide the same base state for an image to be built upon.
Additionally, some dels will fail to respond for one reason or
another and must be masked from their surrounding dels to prevent
dead pixels from appearing in the displayed image. While masking
methods vary, the general process is to create a map of all failed
dels and upon image processing, paint the image pixels that
correspond to the failed dels with approximations of the signals
from their surrounding pixels, thus masking the failing dels.
Exposure indicators
Film-screen quality control operations monitored X-ray exposure
as it was indexed to the optical density (OD) of processed films.
While most CR manufacturers provide an indicator of how much X-ray
exposure arrived at the imaging receptor, there is no consistency
in the methods used or in the scale of the indicators. For the most
part, DR manufacturers do not express exposure index at all. The
American Association of Physicists in Medicine (AAPM) Task group
116 has begun work on this issue and has recommended a uniform
exposure indicator for digital imaging. This recommendation has not
yet been implemented in the industry.
Consistency versus best of breed
In the analog film/screen days, we usually worked with a
standard film/ screen combination throughout the de-partment, in
order to have a consistent appearance. There is an advantage to
keeping each diagnostic modality area on similar imaging platforms;
this preserves the consistency of workflow functionality and the
look and feel of images. Such consistency reduces mistakes and
retakes and optimizes the comparison of images over time. The
best-of-breed approach for selecting CR and DR imaging systems
often mixes systems of different types and adds confusion and
inconsistency to an imaging section's operations and the resulting
imagery.
Conclusion
In the ongoing discussion of DR versus CR, while there are
differences in the underlying technologies, there is a growing
overlap in their functionality and performance levels. The use of
the term "digital radiography" to mean both DR and CR makes sense,
given that digital imaging operations are so similar and must be
addressed collectively as well as individually.
Adding the terms "cassetteless" and "cassette-based" to the
conversation (as is suggested by the American College of Radiology,
3
AAPM, and the Society for Imaging Informatics in Medicine) adds
even more clarity. Understanding and retaining the details of the
actual acquisition devices and their image receptors is, of course,
important for a variety of reasons. These include performing valid
acceptance testing and quality control and retaining a valid
history and audit trail in our libraries, technical documentation,
and imaging archives. Additionally, while the lines between DR and
CR have been blurred, the study of underlying technologies
associated with each exposes their differences, such as motion
artifacts and lack of exposure indices, which should be understood
and managed in order to optimize imaging operations. Finally, the
overmixing of imaging devices with different technologies into a
single workflow center can lead to confusion, errors, waste, and
inconsistent imagery.
REFERENCES
- Reiner BI, Siegel EL, Hooper FJ, et al. Multi-institutional
analysis of computed and direct radiography: Part 1. Technologist
productivity. Radiology. 2005;236:413-419.
- Willis CE, Thompson SK, Shepard SJ. Artifacts and
misadventures in digital radiography.Appl
Radiol.2004:33(1):11-20.
- ACR. Practice Guideline for Digital Radiography. (Res. 42)
October 1, 2007. Reston, VA: American College of Radiology.
2007:23-35. Available in pdf format at
www.acr.org/SecondaryMainMenuCategories/quality_safety/guidelines/dx/digital_radiography.aspx.
Accessed October 3, 2007.
Ms. Dallessio
is the Technology Correspondent for
Applied Radiology.
As radiology workloads continue to increase and the staffing
shortage shows no signs of abating, the choice of X-ray and other
imaging equipment becomes an important factor in determining how
effectively and productively a radiology department can function.
When purchasing new equipment, the stakeholders in the imaging
department must carefully consider many factors, including
workflow, image quality and consistency, ease of use, connectivity,
quality assurance, service, maintenance, and acquisition and usage
costs.
"In any equipment purchase, you need to look at the clinical
utility of what you are trying to achieve. Then you must brace that
against the quality of the product and the quality of the outcome
you are trying to achieve: in this case, images and imaging," said
Steven Metcalf, BS, CRA, Manager of Radiology Services, Altru
Health System, Grand Forks, ND.
"In our department, when it came time to purchase new X-ray
equipment, we weighed the image quality versus the utility of the
equipment versus the overall cost of the equipment. Then, given our
budgetary restraints, we decided what would make the most sense,"
said Russell E. McWey, MD, Chief of Medical Imaging, Virginia
Hospital Center, Arlington, VA. "Then we made on-site visits and
looked at the individual pieces of equipment to help us decide what
we liked and did not like."
Workflow efficiencies
For many radiology departments, workflow efficiency is the
primary consideration when purchasing new X-ray equipment.
"Generally, workload trends are always on the increase in
radiology. I do not think that is unique to my service. It is a
well-identified national trend," said Metcalf. "In addition, I
believe the radiologist shortage will continue to plague us for
some time to come. Certainly, the implementation of digital
technology and picture archiving and communications systems (PACS)
is a benefit because of the way they improve efficiency."
The issue of workflow was also an important consideration for
Radiology Manager Mark Brown, BA, RT(R)(M) and his coworkers when
they were asked to purchase X-ray equipment for Memorial Health
Systems' new Memorial Hospital North in Colorado Springs, CO. "The
first consideration was how we could decrease the number of
full-time equivalents (FTEs) and still offer state-of-the-art
imaging," said Brown, "because I knew we were going to have a
limited number of FTEs available for the new hospital."
"In today's digital world," said Metcalf, "there are
efficiencies that a particular product may bring to your
department, and with digital radiology (DR) products that is
certainly a factor. Workflow is a major concern, particularly as it
relates to the implementation of DR, specifically what this
technology can do based on the fact that the user is not handling
cassettes and the technologist does not need to be involved in
processing images."
"With DR," explained Brown, "the technologist does not have to
touch the cassette or process anything. The machine does it
automatically. The images are immediately transferred to a monitor,
where the user can manipulate them and prepare them for the
radiologist. DR gives you all the information at one time. The
technologist can position the patient on the table, take the
exposure, and, by the time he or she is ready to position the
patient for the next exposure, the first exposure is ready to be
reviewed and manipulated."
Connectivity
How well the new equipment interacts with a facility's
information infrastructure is critical to the purchasing decision.
"Connectivity was a huge issue for us as well," said Brown. "With
our last system, we had several connectivity issues and concerns.
The biggest factor in this is the PACS because it is system-wide
and everyone is affected by it. When we first implemented PACS in
2000, connectivity was a nightmare. We ended up buying black boxes
to place everywhere when we had been under the assumption that the
system was just 'plug and play.'"
"The implementation of PACS was a driver in our purchasing
decision," added Metcalf. "In the PACS world, you want to move all
equipment into the digital modality. With radiographic services,
that means the implementation of computed radiography (CR) or DR.
In our facilities, we used a combination of CR and DR and placed DR
systems into each of our 3 main facilities where we have the
highest volume. In the other locations, it made more sense for us
to put in CR. In our main hospital, we have a DR suite, as well as
single-plate reader systems in our intensive care unit (ICU) and
other high-usage areas among the nursing floors."
The issue of connectivity was also very important at Virginia
Hospital Center, according to McWey. He noted that they considered
how the data would be processed and stored and which processing
algorithms can be applied to the image at the reading station when
it is retrieved on the PACS.
Learning curve and the user interface
Along with connectivity, when migrating to digital systems, the
consistency of the user interface and the learning curve should be
considered. It takes time for technologists to become proficient
with a new system. "When you move the technologist from the
traditional world of analog imaging to digital, it's not as easy a
transition as people think it might be," explained Brown. "It is
important to be sure that the technologists are prepared for the
change," he advised. "If the new system takes them out of their
comfort zone, then they will be a bit more apprehensive. There is a
large learning curve that can't be ignored." When the user
interface is consistent and familiar, the transition can be easier
and, said Metcalf, "your staff training is more uniform, and you
have fewer errors with those functions."
"When we switched to DR at our institution, there was certainly
a learning curve in understanding the exposure differences between
analog imaging and DR and CR," said Metcalf, "but the technologists
transitioned quite smoothly."
"I think it was easier since the interfaces were similar to what
the technologists had been using before," added McWey. "So even
though it was a new product and had to be learned, our new DR
system has the same look as the old CR systems in terms of how
patient information is input and the protocols are selected."
For Brown, the opening of a new campus was an opportunity to
bring in new technologists and train them immediately on the new
technology. "All of the diagnostic radiology equipment at our
outpatient facilities is DR-based," he explained. "So I thought
this was a great opportunity for us to go totally DR at the new
campus and to move the newly hired technologists to DR from the
start. That way we wouldn't have to retrain them on DR once we
upgraded."
Image quality and consistency
The main function of any radiology department is to provide
clear, easy-to-read images that help the physician make an accurate
diagnosis. Therefore, the quality and consistency of the images
produced should be of prime importance when choosing new radiology
equipment. "Image resolution is extremely important," said
McWey.
One of the advantages of DR in terms of image quality, he noted,
is the fact that DR is a closed system; therefore, the risk of
artifacts due to contamination with dirt or dust is reduced. "Since
DR is a contained system," he said, "there are very few issues with
artifact contamination."
"There is not a lot of Quality Assurance (QA) work required for
this system," continued McWey. "It's all integrated in the system.
The only maintenance we perform is to erase the receptors daily.
Routine maintenance is performed by the manufacturer."
"In the applications training process for the technologists,
quality control was addressed," added Metcalf. "The technologists
were taught how to ensure--by looking at the data screens when they
capture an image--that they have the correct exposure and that the
image is of proper quality."
At Memorial Hospital North, they decided to institute a new QA
program when they installed their new DR system. "Every morning we
image a phantom to make sure that when the radiologists pull images
up, they are consistent," explained Brown. "We use the same
technique, the same density, and the same resolution to be able to
check the images."
Cost and service concerns
"There are other factors that also come into play when choosing
new equipment," said Metcalf, "including the support of your
regional sales and service force and costs. Certainly a lower cost
was important to us, although it wasn't a huge issue."
"For us, service was a huge concern," said Brown. "If the
manufacturer doesn't have adequate service, it doesn't do us any
good. We can't function effectively if the machine goes down."
In addition to the acquisition cost, the ongoing cost of
consumables is also a consideration in choosing the right equipment
for your facility. With DR, there are fewer consumable costs than
with analog equipment. "You don't have to purchase film or the
chemistry products and equipment that are needed to process the
film," said Metcalf. "In addition, there are no cassettes to be
replaced either."
Making the right decision
When it comes to making the final purchase decision, all of the
stakeholders in the process should be involved. "At our facility,
the radiologists were very involved when it came to the PACS
decision, primarily from the aspect of selecting the workstations
and understanding the functionality of the workstations, because
they are their tools," said Metcalf. "The DR decision, on the other
hand, was pretty much left to the technical staff. For vendor
selection, we primarily used our technical staff and technical
supervisors," explained Metcalf. "I was more involved in the
financial analysis and assessing quotes and bids to ensure that
they were competitive in the market."
"We have a committee that made the final decision regarding
which PACS system we purchased," said Brown. "After that, the
radiology management team sat down and decided which equipment
would fit best in the areas we manage. Most of the time, it's a
team effort through which we poll the staff to see what they need.
Then the managers and directors have their input. No single
individual makes the final decision."
In Virginia, the decision was made by McWey and the radiology
administrator. "We had some input from the general radiologists,
but it was primarily the two of us, our PACS administrator, and our
radiology information system (RIS) administrator who were involved
in the decision-making process."
"We narrowed the choice down to 2 or 3 vendors," concluded
Metcalf. "The FUJI SpeedSuite (FUJIFILM Medical Systems USA,
Stamford, CT) was a very attractive product for us in that it
bridged the gap when it came to comparing CR to DR in the workflow.
It also bridged the gap for us in relation to the cost comparison
with the more traditional type of DR system with the amorphous
flat-panel silicone detector. In fact, when we began our selection
process," he said, "we did not think we were going to choose DR. We
expected to implement CR throughout the facility. However, this
particular product gave us the opportunity to think about our DR
decision again. The decisive factor was that we could improve our
workflow process with DR in our 3 high-volume areas. Once we
realized that, it became a very good and obvious choice for
us."
Dr. Seibert
is a Professor of Radiology, University of California, Davis
Medical Center, Sacramento, CA.
Categorizing digital radiography systems is no longer as simple
as "computed radiography" (CR) and "direct and/or digital
radiography" (DR). The more technology changes, the more it
changes. The CR versus DR issue is no exception, where historical
boundaries of CR (with passive, cassette-based image acquisition
and detector handling with offline processing) and the fully
integrated DR system (with automatic processing and display) are
now converging. Historically, CR has referred to the implementation
of a cassette-based photostimulable storage phosphor (PSP) imaging
plate reader and quality-control workstation that are packaged as
an add-on system to existing X-ray devices using screen-film
detectors. In contrast, DR has been touted as a totally integrated
X-ray source-generator-detector solution with images displayed for
review within the room shortly after the X-ray exposure. Now, "CR"
technology (specifically using PSP converters) has been developed
into integrated X-ray systems and has completely automated
acquisition, display, and processing. Now "DR" technology has
cassette-based detectors available for situations requiring more
flexibility in positioning and multiple uses in conventional X-ray
cassette trays and bedside portable radiography.
Computed radiography uses a PSP that transiently stores a latent
image in the form of electrons in semistable traps within the
phosphor structure, with subsequent data extraction using a
stimulating point laser beam that scans the phosphor surface point
by point. Line scan laser sources coupled to an array of microlens
and photodiode light detectors stimulate and acquire data in
parallel, reducing the readout time of a PSP imaging plate from
about a minute to ≤10 seconds, which is comparable to other digital
radiography detectors known for readout speed.
In its current definition,
DR
describes a multitude of digital X-ray detection systems that
immediately process the absorbed X-ray signal after exposure and
produce the image for viewing with no further user interaction.
This fact has resulted in the use of the term
direct radiography
by many manufacturers, which has added to the nomenclature
confusion, because of another use of
direct
that describes the conversion of X-rays into charge, which is
described later. In terms of CR versus DR, inclusion of automated
CR systems would fall into the DR category, along with optically
coupled scintillator to charge-coupled device (CCD) camera systems,
fiberoptically coupled rectangular CCD array slot-scan detector
systems, complementary metal-oxide semiconductor (CMOS) detector
systems, thin-film-transistor (TFT) flat-panel detector systems,
and slot-scan photon counting detectors, which were recently
introduced. The
CR
and
DR
acronyms no longer define the essence of digital radiography
detector attributes, since distinct classification into these 2
broad categories is no longer possible and, in fact, often leads to
confusion and "marketeering" claims and counterclaims.
In a recent publication by a multi-societal effort (including
the American College of Radiology, the American Association of
Physicists in Medicine, and the Society of Imaging Informatics in
Medicine) to determine practice guidelines for the use of CR and DR
in the clinical environment,
1
a consensus to title the work
Practice Guidelines for Digital Radiography
2
was made to be inclusive of all types of digital radiographic
systems, in recognition of the issues explained above. Likewise, in
this article, the term
digital radiography
refers to all types of digital radiographic systems, including both
those that had been historically termed
CR
and those historically termed
DR
.
So, how should one categorize current state-of-the-art digital
radiography technology? One method promoted in this article
considers 3 characteristics: 1) detector form factor; 2) image
acquisition geometry; and 3) X-ray signal conversion method, as
explained below. Various digital radiography detectors and
attributes are listed in Table 1.
Detector form factor considers aspects such as "cassette" versus
"cassetteless" (Figure 1) and "passive" versus "active" operation.
A majority of cassette-based digital detectors are based on PSP
technology as a direct replacement for screen-film, thus providing
a cost-effective means to achieve digital image acquisition, while
at the same time allowing great positioning flexibility. Passive
operation allows an asynchronous coupling of the X-ray exposure and
storage of the image signal on the phosphor. Subsequent processing
is performed by physically inserting the cassette/ phosphor plate
into an image "reader" to render the radiograph. Multiplexing of
several rooms to 1 reader is possible but is also time-ineffi-cient
and potentially limiting in busy, high-throughput rooms. An
alternative is a cassette-based TFT-array detector for use with
portable radiography examinations and as a "drop-in" to cassette
trays in general radiographic rooms. This detector uses a wired
electronic connection to the X-ray generator to actively integrate
and read out the X-ray image after exposure. A CMOS detector in a
cassette configuration for mammography is available as a
replacement for screen-film mammography. Wireless interfaces will
likely soon appear on such detector systems. Image display shortly
after the exposure and good positioning flexibility are benefits;
damage to the detector by unintentional mishandling is a
potentially costly drawback.
Cassetteless digital detectors are part of an integrated X-ray
generator, X-ray tube, and detector system. The basic meaning of
"cassetteless" indicates that the image is acquired and
subsequently displayed at the in-room technologist console for
review and manipulation with minimal user interaction. The earliest
"cassetteless" systems had PSP plate changers with automated
acquisition, point-scan laser readout, image processing, and
display, with individual processing times on the order of a minute.
Recent introduction of line-scan laser excitation of the PSP
imaging plate reduces readout time of a large 35 × 43-cm
field-of-view (FOV) detector in as few as 5 seconds, with automatic
processing and display. This is comparable to many large FOV
optically coupled CCD and flat-panel TFT arrays, which comprise the
majority of cassetteless digital radiography systems. In the
extreme are "real-time" flat-panel systems specifically
manufactured for fluoroscopic imaging that also provide
radiographic capabilities. Other cassetteless radiographic systems
include slot-scan acquisition devices in which the image is
produced by scanning a collimated beam and detector array across
the FOV over a time span of seconds.
Image acquisition geometry distinguishes instantaneous
acquisition of a large-area digital image with a short exposure
time versus a sequential, long exposure time acquisition of a
slot-scan device. Most digital detectors for radiography use a
large-area FOV geometry, which allows short exposure times to
decrease the probability of patient motion. However, detected
scatter from the patient reduces image contrast and consumes a
fraction of the digital range of the detector with essentially
useless information. Thus, an antiscatter grid is often used with
thicker body parts (it is used in essentially all adult imaging
except extremity examinations) and in-curs a relatively large dose
penalty (typically double the patient dose) because of the loss of
primary radiation. The slot-scan geometry with pre-and post-patient
collimation produces a narrow fan-beam incident on a scintillator
coupled to a time-delay-integrate CCD photodetector array.
3
Since at any instant only a small fraction of the patient volume is
irradiated, the amount of scatter is reduced to low levels, and the
amount of detected scatter is extremely low because of postpatient
collimation and a small detector area. Grids are not required,
which results in good dose utilization; image acquisition times,
however, are extended into seconds, and the detector/collimator
configuration makes positioning a challenge for nonstandard imaging
protocols.
X-ray signal conversion is described by indirect, direct, or
photon-counting methods. All digital detectors produce an output
signal, usually in the form of electrons or holes (positive ions),
which represent a quantity of charge that is proportional to the
number of Xrays ab-sorbed at a specific detector element (del)
position. The magnitude of the charge is converted to a voltage and
then to a digital value for storage in the image matrix at the
corresponding del location in the detector plane.
Indirect
refers to the conversion of X-rays into secondary information
carriers, such as absorbed X-ray energy to light energy conversion
in a scintillator, or to stored electrons in semistable traps
within a storage phosphor and subsequent stimulation with a laser
and light emission. For each X-ray photon absorbed, a large
amplification of light photon carriers is produced on account of
the large energy difference of X-rays (keV) versus light (eV) or
energy required to trap electrons in a storage phosphor (eV).
Regardless of the method by which secondary light photons are
formed, the large numbers are directed to a wavelength-matched
sensitive photodiode-TFT array via direct optical coupling, to a
CCD area detector by lens-optical coupling, or via a light-guide
pickup to a photomultiplier tube in a PSP reader device. Charge
amplitude is generated in response to the amplitude of light
intensity (and thus X-ray intensity). A proportional voltage is
produced and digitized to form the digital gray-scale image. Thus,
scintillator-based TFT arrays, optically coupled CCD camera
systems, and fiberoptically coupled CCD slot-scan systems as well
as all PSP systems are classified as indirect acquisition
devices.
Direct
, in the context of this article (unlike the use of this term by
many manufacturers that produce indirect acquisition DR devices),
refers to the method of ac-quisition and conversion of absorbed
X-ray energy into electron/hole pairs (charge) using semiconductor
converters such as amorphous selenium (
a
-Se), solid-state silicon, or high-pressure gas. These direct
acquisition detectors have a voltage applied to electrodes on
opposite surfaces of the absorber/semiconductor material to
separate and collect the generated electrons and holes. A small
amount of energy (on the order of 50 eV) is needed to produce an
ion pair for
a
-Se; for a 50-keV absorbed X-ray, hundreds of charge information
carriers are generated. Similar amplification of charge per
absorbed X-ray photon occurs in other direct converters as well.
Electric field lines direct the ion pairs to the collection
electrodes without lateral spreading, thus providing high intrinsic
resolution by accurately mapping the X-ray photon absorption event
to the corresponding del position.
Photon-counting detectors are currently configured in slot-scan
geometry, composed of either high-pressure gas or solid-state
silicon. These detectors measure absorbed X-ray photon events
individually as counts instead of energy integration like all other
detectors.
4
Since a count will be tallied independent of the photon energy, a
signal-to-noise ratio advantage of up to 40% is achieved for the
same number of X-ray photons absorbed in the detector compared with
energy integration detectors, as there is no bias toward higher
energy photons, and elimination of other noise sources accompanying
an energy-integrator detector is possible. A limitation is the
maximum count rate that can be sustained.
So, what is the "best" digital radiography detector? There is no
straightforward answer, as advantages and disadvantages are based
upon multiple comparisons of the following characteristics:
detective quantum efficiency (DQE), spatial resolution, contrast
resolution, dose efficiency, acquisition and display speed,
radiographic positioning flexibility, image quality, ability to use
existing radiographic equipment, integration with information
systems and electronic networks, system costs, service costs,
detector longevity, and survival in a hostile environment (eg,
trauma imaging), among many other benchmarks. Matching an
appropriate digital radiography device with its intended clinical
purpose is an exercise in determining actual needs and patient
throughput requirements prior to evaluating the type of DR system
that will best meet those needs in a cost-effective and efficient
manner.
5,6
Conclusion
The terms
CR
and
DR
will continue to be used, but collectively we must think beyond the
traditional CR versus DR comparisons, past the issues of X-ray
converter materials, to clinical relevance, cost-effectiveness,
dose efficiency, image processing functionality, overall image
quality, proper use of digital radiography attributes (eg, variable
speed characteristics and dose index values), quality-control
phantoms and automated computer routines to verify proper function,
patient throughput, uptime, reliability, longevity, service,
and
optimization in the clinical arena. Insisting on DR systems that
can self-monitor and verify optimal performance through the
automated analysis of quality-control phantom images will move the
industry toward providing these important tools.
Finally, while dose efficiency is important, it shouldn't be the
overriding consideration in determining the type of imaging system
that best meets a specific clinical need, as all DR systems that
are approved by the U.S. Food and Drug Administration must
demonstrate a reasonable image quality over a typical range of
incident exposures for clinical procedures. More important is an
understanding and use of exposure index values that describe the
"effective speed" of the detector to ensure that overexposures that
are otherwise difficult to discern do not become the standard of
practice as a result of complacency and/or ignorance.
REFERENCES
- Williams MB, Krupinski EA, Strauss KJ, et al. Digital
radiography image quality: Image acquisition. J Am Coll
Radiol.2007;4:371-388.
- ACR Practice Guideline for Digital Radiography. Approved May
2007. Available on the American College of Radiology Web site at:
http://www.acr.org/
SecondaryMainMenuCategories/quality_safety/guidelines/MedicalPhysics.aspx.
Accessed August 8, 2007.
- Samei E, Lo JY, Yoshizumi TT, et al. Comparative scatter and
dose performance of slot-scan and full-field digital chest
radiography systems. Radiology. 2005; 235:940-949.
- Pisano ED, Yaffe MJ. Digital
mammography.Radiology.2005;234:353-362.
- Reiner BI, Siegel EL, Hooper FJ, et al. Multi-institutional
analysis of computed and direct radiography: Part I. Technologist
productivity. Radiology.2005;236: 413-419.
- Reiner BI, Salkever D, Siegel EL, et al. Multi-institutional
analysis of computed and direct radiography: Part II. Economic
analysis. Radiology.2005;236:420-426.
Dr. Siegel
is a Professor of Diagnostic Radiology and the Radiology
Associate Vice Chairman for Informatics, Diagnostic Imaging,
University of Maryland Medical Center; and the Director,
Baltimore Veterans Affairs Medical Center, Baltimore, MD. He is
also a member of the editorial board of this journal.
Digital radiography, despite its fascinating technology, its
tremendous potential, and the fact that it remains the primary and
dominant diagnostic imaging screening modality, is not considered
by most radiologists to be "sexy." No major conferences for
radiologists are currently dedicated to digital radiography, and
the number of abstracts and papers about the technology is
Lilliputian compared with those about multidetector computed
tomography (CT), positron emission tomography/ CT, and magnetic
resonance imaging (MRI). General radiography is arguably in danger
of becoming a lost art. A thoracic radiologist trained before the
use of picture archiving communications systems (PACS) recently
lamented the fact that today's radiology residents seem to pay
scant attention to "plain films"; they immediately ask for a CT
study when shown a chest radiograph at the American Board of
Radiology examinations in Louisville, KY. This seems unfortunate
and ironic, not only because the roots of diagnostic radiology are
in conventional radiography but also because this continues to be
the most common type of imaging study performed in the United
States and throughout the world. Conventional radiology continues
to represent an important and fundamental diagnostic tool.
Digital radiography was originally conceived and marketed in the
1980s and early 1990s as a way to improve the image quality of film
by taking advantage of an innovative detector (photostimulable
plate) that had a substantially wider dynamic range than had been
possible using film, performing image processing to extract the
most clinically important imaging information, and printing this
image to film. Initial versions of this system printed 2 images on
a single film, each processed differently to present 2 perspectives
of the radiograph.
By the early 1990s, however, it seemed increasingly clear that
film's days were numbered. The substantial increases in computer
workstation speed, network performance, and storage capacity (along
with major reductions in prices) finally made it possible to create
a practical filmless radiology department and healthcare
enterprise. Conventional radiography was the one remaining
nondigital modality in most departments, and digital radiography
became an enabling technology not only for film-based image
enhancement but for entirely filmless operation. Digital X-ray
technology and options have expanded dramatically over the past
several years (as has ambiguity about the terminology used to
describe these options).
Current state-of-the-art digital X-ray systems offer excellent
dynamic range with similar or reduced quantum detection efficiency
(permitting dose reduction with equivalent image quality) and,
along with image processing, offer significant potential to
substantially improve on the image quality that is typically
achieved with film. These systems combine the advantages of digital
imaging, such as image processing, direct transfer to PACS, and
elimination of film and associated chemicals, with the advantages
of conventional X-ray, such as low cost, portability, flexibility
in positioning, and very low radiation dose (typically <5% of
the dose that is required for CT).
However, the overall quality of digital radiography studies in
actual practice has not met the potential of the technology to
improve on conventional film radiography and, in many cases, has
actually fallen behind the quality achieved on film. This is the
result of a combination of the increased complexity of digital
radiography, limited training for technologists in digital X-ray
techniques, relatively low interest by radiologists in the
modality, and a general lack of understanding about digital image
processing and the artifacts and pitfalls associated with it.
1,2
Despite initial reports by our group and others about decreased
retake rates due to the improved dynamic range of digital
radiography, image retake rates are still unacceptably high and
image quality is too frequently suboptimal.
3
The mantra of PACS has been to have images available at any time
and any place to anyone who needs to review them. The mantra of
digital radiography must be to be able to acquire images any time
and any place, make these images available immediately for quality
review, and then send them to a PACS for near real-time display.
This can be achieved either by having a cassette reader available
in every hospital area in which studies are obtained or,
alternatively, by using a technology that reads/processes the
images immediately and then displays them for evaluation by the
technologist and simultaneously sends them to the PACS. This type
of immediate read/processing digital system has been introduced
within the past few years and will continue to become faster,
lighter, more rugged, and more affordable over time.
Portable digital radiography is currently the area with the
greatest potential for improvement in digital radiography and will
continue to be for the foreseeable future. Challenges for optimal
or even adequate image quality include the following: portable
generators with limited power; difficulties in positioning
critically ill, unstable, or fragile patients for standard views;
challenges with the use of grids in portable studies; limited time
to obtain the study; and inability to visualize the image during
the examination to determine whether the study was adequate.
Another problem is the required trade-off between performing
multiple studies and having to wait a relatively long time to
process images, as well as the inefficiencies associated with
taking plates down to the main department.
Additional clinical challenges include the need for improved
productivity because of staff shortages and space limitations; the
need to reduce costs to enable digital imaging solutions in
lower-volume imaging locations, such as family practice,
orthopedic, podiatric, and chiropractic settings; and the need to
improve image quality and image acquisition and transmission times
for remote locations (such as the intensive care unit, emergency
department, and operating rooms), particularly in settings where
patient positioning is challenging. Productivity can be enhanced by
evaluating and redesigning workflow processes. Technologists should
spend a higher percentage of their time performing studies than
they do performing the clerical/manual steps typically required by
many digital radiographic systems today. Multi-institution
time/motion studies evaluated by our research team have documented
that technologists spend >40% of their time on clerical and
image quality assurance steps. Improving this imbalance will
require integration of digital X-ray systems into the radiology and
hospital information systems as well as additional automation of
the technologists' workflow.
Despite major advances in digital radiography, the basic way in
which images are obtained has not fundamentally changed during the
past 100 years. In order to achieve a major advance in the
evolution of digital radiography, we need to take advantage of the
unique capabilities of digital X-ray technology, rather than using
it as a mere substitute for film. For example, digital detectors
have a different "k-edge" from that of film, giving us flexibility
in rethinking the energy of the radiation in addition to dose.
Digital systems make image subtraction relatively simple, and we
can take advantage of this by utilizing dual-energy subtraction. We
have made the transition to dual-energy subtraction for all
outpatient examinations at our facility and have found that this
improves sensitivity and specificity for lung nodules and other
pathology as well as for bony lesions in the chest. We plan to
perform research on this technology in other areas of the body.
Dual-energy technology may give way to multienergy X-ray and
photon-counting devices that, in the future, could provide even
greater contrast and spatial resolution at reduced doses. Digital
X-ray may bring a renaissance in the use of tomography and
tomosynthesis because of the relative ease of computer processing
of multiple images using technology developed for CT. This could
produce much higher contrast images than are possible with planar
X-ray techniques, with far lower doses than are achievable using
CT. Digital image acquisition also facilitates the use of
computer-aided detection of lung nodules, microcalcifications and
masses on a mammogram, and detection of interstitial lung disease
and life support lines in ways that would be difficult to achieve
with film.
Conclusion
Despite the sometimes astonishing advances in CT, MRI, and
optical and molecular imaging, the good news is that radiology's
mainstay--conventional radiography--is making exciting and
innovative advances. The challenge is to engage and educate the
diagnostic imaging community about the very real advantages and
potential that digital radiology is bringing to our most
time-honored imaging modality.
REFERENCES
- Willis CE, Thommpson SK, Shepard SJ. Artifacts and
misadventures in digital radiography.Appl
Radiol.2004;33(1):11-20.
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