by Kenneth A. Fetterly MS, Nicholas J. Hangiandreou PhD, Steve G. Langer PhD
Devising an enterprise-wide quality control program for PACS monitors is critical in an electronic environment.
Kenneth A. Fetterly, MS
|
The goals of a monitor quality control (QC) program are to ensure
consistent display performance (thus allowing optimal image
display), to identify and resolve problems before they become
clinically relevant, and to make monitor use and support as
efficient as possible. In addition to the monitor itself, the
electronic image display system consists of a video card and cable,
gray-scalecalibration software, and clinical image display
software. Environmental factors, such as ambient light and stray
radio-frequency signals, also contribute to image display
performance.
Nicholas J. Hangiandreou, PhD
|
Major image-quality considerations for monitor QC include
contrast, resolution, artifacts, and noise. It is especially
important to the quality of diagnostic image interpretation (and,
therefore, to patient care) to ensure that monitors have
appropriate contrast throughout the full video range and that all
monitors attached to a single workstation have the same grayscale
response. The luminance range of the monitors should also meet the
vendor's specifications, the recommendations of professional
radiology societies, and the predetermined policies of the health
care enterprise.
PROGRAM COMPONENTS
Steve G. Langer, PhD
|
A basic monitor QC program requires five primary tools: a
predefined set of QC procedures, a set of appropriate test images,
control limits, a database for tracking program activities and
assets, and a photometer. Written QC procedures must be thorough,
concise, and accurate.1
An organized QC program has administrative advantages over
crisis-based maintenance, but regular attention also improves the
performance of monitors (Figure 1). For example, the ability to
prevent the steady loss of cathode ray tube (CRT) luminance over
time is of benefit. Several other common display problems can also
be detected and corrected with an effective QC program. These
include degraded sharpness, poor contrast, horizontal tearing,
phosphor burn-in, and other problems typical of electronic
displays.
Figure 1. Luminance degradation over time in monitors with and without regular maintenance.
|
Prior to performing QC procedures, the technician must first
clean the monitor face and verify that viewing conditions are
normal. In addition, he or she should verify that the screen saver
is active, since this is an important factor in conserving monitor
electronics and in preventing CRT phosphor burn-in problems. Note
that implementation of a screen saver in conjunction with a flat
panel liquid crystal display (LCD) would not be expected to
lengthen its life-cycle because the back light will remain fully
activated.
Our QC image series contains window patterns of 0%, 50%, and
100% luminance; a Society of Motion Picture and Television
Engineers (SMPTE) pattern (Figure 2, page 50); a 100% uniform field
pattern; and standard clinical images. Objective measurements from
the 0% and 100% video level images are obtained and the brightness
and contrast of the monitors are adjusted accordingly to ensure an
appropriate grayscale luminance range. After adjustment, the
luminance of a 50% video level is measured to verify that the
overall contrast of the monitors is appropriate. Subjective
observations of whether the 5% and 95% SMPTE patches are visible,
the image geometry is square, the images are spatially stable, and
image flickering is minimal are also verified and recorded. Further
subjective observations include evaluations of text sharpness,
bar-pattern contrast, tearing at vertical edges, phosphor burn-in,
and clinical image display.
Figure 2. A society of Motion Picture and Television Engineers test pattern used to monitor quality control.
|
All measurements have associated control limits that are based
on clinical use, vendor specifications, and human perception.
Subjective evaluations are based largely on experience. We
implemented a three point scale of like-new, adequate, and
inadequate for the subjective tests.
Several more advanced monitor test patterns can also be used to
assess display performance. The Briggs Pattern2 (Figure 3a, page
52) or a Contrast-Detail Pattern can be used as a combined measure
of monitor sharpness, noise, and contrast; the Cx Pattern3 (Figure
3b, page 52) evaluates sharpness alone. Recently, Task Group 18 of
the American Association of Physicists in Medicine has made
available recommended monitor evaluation procedures, including
appropriate test patterns4 (Figure 3d, page 52). It is recommended
that new monitor quality control programs be based on the work of
this group. More advanced monitor characterization can be performed
using a CCD camera.5-7 Resolution measurements may be achievable
with high-end consumer grade CCD cameras; however, measurements of
monitor noise will require a scientific grade CCD camera.
Figure 3. A sample of monitor test patterns used to gauge various quality benchmarks includes (a) Briggs Pattern, used to assess sharpness, noise, and contrast; (b) Cx Pattern, used to assess sharpness; (c) Contrast-Detail Pattern, used to assess sharpness, noise, and contrast; and (d) TG18-QC Pattern(s) (American Association of Physicists in Medicine TG-18), used to assess geometric distortion, sharpness, noise, contrast, and contrast resolution.
|
Acceptance testing upon the arrival of a new monitor is an
important part of a monitor QC program. This process not only
ensures that the new monitor is working as well as it should, but
also allows the technician to record baseline data for later
comparison during periodic QC visits. At our institution, the
objective measurements performed during acceptance testing include
the standard QC measurements as well as static artifact evaluation
of the glass and phosphor,8 and measurement of luminance overhead.
Also, it is appropriate to verify that the vendor's specifications
of monitor performance are met.
The ability to accurately record and recall QC measurements is
also important. This will allow comparison of a monitor's QC data
with previous measurements and comparison to the performance of
other monitors. A database of QC results has been found to be very
valuable for these purposes. Implementation of the database on a
laptop computer provides a convenient means to enter data and
perform real-time comparison to control limits in the field.
PROGRAM EXPERIENCE
Our formal QC program for monitors has been in place for 5
years. Covered by the program are 10 clinical quality assurance
workstations with 10 monitors, 10 grayscale diagnostic workstations
with 30 monitors, and 50 grayscale review workstations with 90
monitors.
Acceptance testing is performed prior to the installation of a
new CRT monitor and QC is performed after a week, a month, and
every 3 months thereafter. These QC intervals have been found to
be appropriate for our current CRT display technology; however,
customization of these intervals dependent upon display type is
appropriate. A monitor QC program can be planned using a staff-time
estimate of 20 minutes per monitor per visit. This allows time for
QC procedures (including luminance adjustments), travel between
workstations, and data recording. For monitors on a quarterly QC
protocol, this requires 80 minutes per year. We have found that CRT
displays require additional maintenance after they are initially
installed and that the life-cycle of the displays is approximately
2 years. Therefore, an overall estimate of approximately 3 hours of
staff time per monitor per year is realistic for planning purposes.
Given the purchase cost of electronic displays, it is appropriate
to actively maintain these devices to ensure optimal performance
and maximum life. The costs associated with active support have
been estimated to be a relatively small fraction (5-10%) of the
overall cost of ownership of CRT displays.
NEW TECHNOLOGIES
The introduction of new display technologies will likely result
in changes to QC procedures for electronic displays. As flat-panel
liquid crystal displays continue to replace CRTs, the QC program
and its resources will need to be adjusted accordingly. Improved
luminance stability is expected from LCDs and image sharpness is
expected to remain static. Often, automatic control of the
luminance response is built into the display. It can be reasonably
anticipated that LCDs will not require as much support effort as
CRT displays. The decreased effort required to support LCDs will
likely not offset the higher purchase price of these displays.
However, LCDs may prove to be cost-effective if their life-cycles
are appropriately long.
CONCLUSION
For a monitor QC program to be effective, it must take into
account the capabilities and limitations of the entire display
chain. This requires that technicians be familiar with all of an
enterprise's monitors, video cards, calibration software, and
image-display software, as well as with external equipment that
might create image display problems. Working relationships that
foster the best possible support for monitor users must be
established along with appropriate QC procedures. It has been our
experience that the superior performance and increased life-cycle
of monitors that are actively supported as part of a QC program
justify the effort and resources expended.
Kenneth A. Fetterly, MS, Nicholas J. Hangiandreou, PhD, and
Steve G. Langer, PhD, are medical physicists at Mayo Clinic,
Rochester, Minn. This article has been adapted from Developing an
Enterprise-Wide Monitor QC Program, which Mr Fetterly presented at
the annual meeting of the Society for Computer Applications in
Radiology in Salt Lake City, May 2002.
Further Reading
National Institute of Display Technologies. Technology center.
Available at: http://www.nidl.org/tech_mstr.htm.
Accessed March 5, 2003.
Video Electronics Standards Association. Standards. Available
at: http://www.vesa.org/standards.htm.
Accessed March 5, 2003.
References:
- Groth DA, Bernatz SN, Fetterly KA, Hangiandreou NJ. Cathode ray tube quality control and acceptance testing program: initial results for clinical PACS displays. RadioGraphics. 2001;21:719-732.
- Briggs SJ. Softcopy display of electro-optical imagery. Proc SPIE. 1987;762.
- Kohm KS, Cameron AW, Van Metter RL. Visual CRT sharpness estimation using a fiducial marker set. Proc SPIE. 2001;4319:286-297.
- American Association of Physicists in Medicine Task Group 18. Assessment of display performance for medical imaging systems (draft). Available at: http://deckard.mc.duke.edu/~samei/tg18. Accessed March 5, 2003.
- Roehrig H. The monochrome cathode ray tube display and its performance. In: Kim Y, Horii SC, eds. Handbook of Medical Imaging. Vol 3. Bellingham, Wash: SPIE Press; 2000:155-220.
- Kruger RL, Fetterly KA, Hangiandreou NJ, Van Metter RL Determining the sharpness of electronic displays: an evaluation of three methods. J Digital Imaging. 2001;2:83-91.
- Samei E, Flynn MJ. A method for in-field evaluation of the modulation transfer function of electronic display devices. Proc SPIE. 2001;4319:596-607.
- Copeland JF, Helhus CS, Horton R, Venkatakrishnan V, Zamenhof RG, Mendel JB. Practical quality control standards for digital display monitors. Proc SPIE. 2000;3976:315-323.
- Flynn MJ, Badano A. Image quality degradation by light scattering in display devices. J Digital Imaging. 1999; 2:50-59.