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DOI:10.2214/AJR.04.1713
AJR 2006; 187:1492-1498
© American Roentgen Ray Society


Original Research

Full-Field Digital Mammography on LCD Versus CRT Monitors

Margarita L. Zuley1, Kathleen M. Willison1, Ermelinda Bonaccio2, David P. Miller3, David L. Leong4,5,6, Posy J. Seifert1, Patricia Somerville1 and Stamatia Destounis1

1 Department of Radiology, The Elizabeth Wende Breast Clinic, 170 Sawgrass Dr., Rochester, NY 14620.
2 Department of Radiology, Roswell Park Cancer Institute, Buffalo, NY.
3 Ovation Research Group, Highland Park, IL.
4 Digital Radiography Systems Division, Analogic Corporation, Peabody, MA.
5 UCD School of Medicine and Medical Sciences, Dublin, Ireland.
6 Department of Mathematics and Statistics, University of New Hampshire, Durham, NH.

Received November 5, 2004; accepted after revision September 18, 2005.

 
Address correspondence to M. L. Zuley.


Abstract
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
OBJECTIVE. Our purpose was to determine if the display of full-field digital mammograms on a 5-megapixel liquid crystal display (LCD) monitor is at least equivalent to the display of the same on a 5-megapixel cathode ray tube (CRT) monitor.

MATERIALS AND METHODS. Five radiologists evaluated normal anatomy and features of 61 abnormalities in 48 full-field digital mammograms. A 9-point Likert scale was used to compare images on two identical soft-copy review workstations, one equipped with two 5-megapixel CRTs and the other with two 5-megapixel LCDs. Outcomes were evaluated using a random-effects analysis of variance model. Means and SEs were reported. Ninety-five percent confidence intervals and p values were calculated.

RESULTS. The two systems were equivalent for most features. The LCDs were rated better for the sharpness of mass margins (p = 0.011) and mass conspicuity (p = 0.050). For calcium features, the LCDs were rated better than the CRTs for lesion conspicuity (p = 0.010) and number of calcifications (p = 0.043). For architectural distortions, there was no statistically significant difference between the monitors in any of the features evaluated. For display characteristics, the LCDs were better for luminance (p = 0.021). The CRTs were significantly better for image noise (p = 0.001). In the overall ratings, there was no statistically significant difference between the two displays.

CONCLUSION. The 5-megapixel monochrome active-matrix LCD is equivalent to and in some respects better than the 5-megapixel CRT display for full-field digital mammograms over a range of normal and abnormal findings.

Keywords: breast • breast cancer • mammography • PACS


Introduction
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
The widespread implementation of full-field digital mammography has naturally raised questions about the optimal display, storage, and retrieval of images. Today, primary interpretation of digital mammography is typically performed on the soft-copy review workstation, which is purchased with the acquisition unit. Integral in the approved soft-copy review workstation are two 5-megapixel (MP) (2,048 x 2,560 pixels) cathode ray tube (CRT) monitors. Simultaneously, the rest of radiology is moving away from CRT monitors for several reasons. CRTs typically have a low luminance (300 cd/m2), requiring ambient light levels to be so low that the inevitable comparison with prior studies on an alternator or viewbox is difficult because the average luminance from alternators or viewboxes is approximately 2,000 cd/m2. CRTs also have a short life expectancy (with slow degradation of display quality over time) of approximately 36 months (about 30,000 hours), requiring replacement rather than repair. For optimal function in a standard reviewing room, CRTs are typically set at their highest luminance levels, which further decreases the life of the monitor.

Eye fatigue is also a problem because CRTs require the screen to be constantly refreshed, or repainted, because the image on the screen relies on light emitted from phosphors that fade quickly. Despite improvements in refresh-rate standards from 60 to 75 MHz by Video Electronics Standards Association (VESA) standards, eye fatigue is still an issue for the radiologist. In addition, the emissive nature of the CRT results in blooming of the focused beam at the periphery of the monitor, which degrades resolution in these areas. This emissive nature also creates veiling glare (unwanted scattered light), which results in degradation of the overall contrast resolution. CRTs are heavy ({approx} 40 lb [18 kg] each); they have a large, cumbersome footprint; and they have a high heat output, which requires additional air conditioning. For these and other reasons, liquid crystal display (LCD) monitors are coming into favor.

LCD monitors are lightweight (< 15 lb [7 kg]), have a small footprint, and are becoming less cost-prohibitive. They have a long life expectancy, with minimal cost impact of replacing the fluorescent lamp backlight. Refresh rates are not a concern with LCD monitors because they virtually hold a charge until updated. The design of the LCD does not require a focused beam to produce an image. Instead, an electronic current is applied to a thin-film transistor (TFT), rendering the entire surface of the LCD a uniform resolution. Moreover, the flat-panel design provides a better overall resolution for a given display matrix as illustrated in a study comparing the clinical impact of 3-MP LCD with 5-MP CRT for lung nodules (Siegel E et al., presented at the 2002 annual meeting of the International Society for Optical Engineering). Monitor luminance has been shown to be at least as important as monitor resolution [1-3], and with superior luminance of approximately 700 cd/m2—nearly double the luminance of the CRT—LCDs are an attractive alternative to CRTs. To date, some studies have shown equivalence between LCDs and CRTs in the display of radiographic abnormalities [4].

Our study was designed to determine if the display of full-field digital mammograms on a 5-MP LCD monitor was at least equivalent to the display of the same on a 5-MP CRT monitor. This study was performed in the context of trying to determine the optimal display of full-field digital mammography images and represents just one of many small steps necessary to be able to integrate the display, storage, and retrieval of digital mammography into PACS systems, which so many of us already use.


Materials and Methods
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
Study Design
The study involved a comparison of mammographic and display features viewed on two identical soft-copy review workstations using a 9-point Likert scale. On one of these workstations, reviewers used two 5-MP CRTs; on the other workstation, reviewers used two 5-MP active matrix LCDs.

Case Selection
The reports of all screening mammograms performed on one full-field digital mammography unit (SenoScan, Fischer Imaging) from March 2003 to November 2003 were reviewed (n = 2,500). The hardcopy images of all cases that were given a BI-RADS category of 2 or 0 were evaluated (n =331) by the study coordinator in medical record number order to obtain as random a sample as possible. We then enriched the data set with missing lesion types and breast densities. This was done with the intention of representing the spectrum and frequency of mammographic abnormalities to include mass; calcium; mass with calcium; and architectural distortion in dense, heterogeneously dense, scattered, and adipose-replaced tissue types. The resultant data set consisted of 48 cases containing 61 abnormalities including 30 mass lesions, 21 calcium lesions, and 10 architectural distortions. Asymmetric densities were grouped in the mass category. Two of the 48 cases had a calcified mass. The calcium and mass features for these two cases were evaluated separately by the reviewers and the results included in the mass and calcium numbers. Tables 1 and 2 show the distribution of lesion features, breast density, and size. In addition, five normal cases were chosen across the four tissue types.


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TABLE 1: Case Distribution of Features

 

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TABLE 2: Lesion Size and Distribution of Breast Densities

 


Figure 1
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Fig. 1 Images were viewed on paired monitors, with 5-megapixel (MP) liquid crystal display (LCD) monitors in center immediately adjacent to each other and 5-MP cathode ray tube (CRT) monitors flanking LCDs. Note that image difference is photographic effect, not an indication of monitor capacity or limitations.

 
Scale Development
A 9-point, non-forced-choice Likert scale was designed to evaluate the anatomic and pathologic mammographic features listed in Appendix 1 and the thickness and conspicuity of the skin line and subcutaneous tissue. Soft-copy display characteristics, including luminance, dynamic range, sharpness, background homogeneity, image distortion, display noise, image size, and image noise, were also included in the Likert scale. For computing a mean for each characteristic, the 9-point Likert scale was constructed with text anchors indicating that each end of the scale corresponded to one monitor system being 100% better (dramatically better) than the other and the middle value corresponded to equality. The other intermediary values were 75% better (significantly better), 50% better (moderately better), and 25% better (slightly better) in one direction or the other. Thus, the completed 1-9 Likert scale was easily transformed to a comparative performance scale of negative 100% to positive 100%, in which positive values indicate a preference for the LCD and negative values indicate a preference for the CRT. From this, the mean preference of the reviewers for each characteristic was computed. Positive or negative values were not assigned to either system during reviewer sessions.


APPENDIX 1: Mammographic Features Evaluated on the Likert Scale


Abnormality

Feature
Mass Shape
Margin sharpness
Density
Conspicuity
Calcium Number
Shape
Sharpness of edges
Distribution
Conspicuity
Architectural distortion Spiculation
Density
Parenchymal edge distortion
Overall conspicuity
Mass with calcifications

Features of both mass and calcium

The Likert scale design was based on the mammographic features detailed and defined by the American College of Radiology BI-RADS [5], which is familiar to all radiologists and quite complete in detailing mammographically found features. Five test cases were then reviewed by two board-certified radiologists who are fellowship trained in mammography. Based on this test cohort, the scale was adjusted for the full study group analysis.

Reviewer Training
Before starting the evaluations, the three radiologists who were not involved in the Likert scale development participated in a training session to become familiar with the scale, the definitions, and the image display protocols. The test set of five mammograms that were initially used to refine the Likert scale was also used for this reviewer training session.

Case Analysis
The study group was evaluated independently by the five radiologists. The reviewers had an average of 8 years (range, 5-12 years) of experience in screen-film mammography and 1 year of experience in soft-copy reviewing of digital mammography. Each radiologist interprets approximately 30,000 mammograms per year in our practice. The evaluations were done with the cases displayed in random order as to tissue type and abnormality. Because the study was not done to evaluate each radiologist's interpretation skills, and to avoid the possibility of inadvertent evaluation of the wrong lesion, the radiologist was directed to the lesion of interest with a lesion-specific data form that indicated the type and geographic location of the lesion of interest. Four mass features were assessed: shape, margin sharpness, density, and conspicuity. The calcium features analyzed were number, shape, and sharpness of edges; distribution; and conspicuity. Four architectural distortion features were evaluated: spiculation, density, parenchymal edge distortion, and conspicuity. For all cases, including the five normal cases, the skin was evaluated for thickness, subcutaneous tissue visibility, and overall conspicuity. In addition, display characteristics, including luminance, dynamic range, image sharpness, background homogeneity, image distortion, display noise, and image size, were compared (see Appendix 2 for definitions). Last, for each mammogram, the reviewers were asked to provide an overall assessment of the CRTs and LCDs from zero to 100% better for either monitor, with zero being equivalent. This overall assessment was not tied to any word anchors, allowing the reviewer to choose from the full range of the scale.


APPENDIX 2: Definitions and Guidelines Used in the Likert Scale Evaluation


Display Characteristic

Guideline
Luminance Maximum brightness of the display. Does the image appear brighter on one monitor?
Dynamic range Total amount of gray-scale information that is visible on the display. Do you see more shades of gray on one monitor versus the other? Picking a very dark, very bright, and midgray location, look at the same location of an image on both monitors. Is the difference in minimum, maximum, and midgray noticeable? Remember that the very bright area is the same as luminance.
Sharpness Edge detail or crispness of the image on the display. Are the edges of objects easier to see? Are calcifications better defined on one monitor? Look at the image in the center and at the corners of the image.
Background homogeneity Defined as the perception of color change (rainbow-like ripple) evident in the background of the monitor.
Image distortion Geometric nonuniformity in the display. Does the image appear to be distorted? Do straight lines appear curved? Look at the image in the center and at the corners of the image.
Display noise Noise that is seen in the displayed image that will vary with time. Does the image appear noisier in one monitor versus the other? Look at the image in the center and at the corners of the image. Display noise changes with time; X-ray quantum noise will not change. Wavy lines or moving streaks are considered noise.
Image size The physical size of the displayed image. Does the display size on one monitor versus the other affect your ability to detect and classify masses, calcifications, and architectural distortions?
Image noise

An overall grainy appearance throughout the image on the liquid crystal display (LCD) monitors. Does the structured noise in the LCD display affect your ability to assess the image and lesion features?

The Monitors
Two identical soft-copy review workstations were used to conduct the study. One was equipped with and optimized for two 5-MP CRTs (MGD521M, Barco) with Dome R5 (5-MP) display controllers (Planar Systems), and the other was equipped with and optimized for two 5-MP monochrome active-matrix LCDs (Dome C5i with Dome DX [5-MP] display controllers, Planar Systems). Images were sent simultaneously to both workstations for display. Both monitor systems were set to accept 8-bit images and display at 8 bits. Target monitor luminance was chosen by the vendor and calibrated as would be typical in the clinical setting, with the CRT pair set at 300 cd/m2, and the LCD pair set at 550 cd/m2. Before each session, quality assurance testing was performed as specified by the vendor.

Full-Field Digital Mammograms
The full-field digital mammography images were acquired using the SenoScan. This system acquires images at 12 bits and then performs a 12- to 8-bit transformation on the data before sending the images to the soft-copy review workstation for display. This process is standard for this unit. The acquisition and display bit depth were not altered for this study.

Data Collection
Two 1-hour reviewing sessions were arranged for each radiologist to evaluate the 53 cases (five normal and 48 with abnormalities). The reviewers were blinded to the other reviewers' results. During each session, the research assistant filled in all the data on the Likert scales. The cases were reviewed by acquisition-date order so that they were random with respect to tissue and lesion type. The images were viewed on paired monitors, with the 5-MP LCDs in the center immediately adjacent to each other and the 5-MP CRTs flanking the LCDs (Fig. 1). The radiologists had the ability to put any pair of monitors in black-screen mode if the light was limiting evaluation of the other pair. The images were always first displayed with identical window and level parameters on both sets of monitors; however, the radiologist could change the window and level of any of the images during the study. The cases were interpreted in a standard reviewing room without ambient light. A definition and guideline sheet of each item to be assessed was prepared and provided to the reviewers (Appendix 2). Once the session was over, the radiologist could not change any responses.

Hanging Protocol
The hanging protocols between comparison components were matched. The cases were displayed on each set of monitors with the following hanging protocol: four-view mammogram, four views were hung on one monitor; bilateral craniocaudal (CC) views were hung simultaneously, one each on the right and left monitor of each set of monitors followed by bilateral mediolateral oblique (MLO) images displayed in the same way. Finally, the two views of each breast (CC and MLO views) were displayed again at full resolution, one on each monitor. The monitors were all turned slightly toward the midline so that the reviewer had as close to a perpendicular viewing angle to the face of each monitor as possible.

Statistical Analysis
All outcomes were evaluated using a random effects analysis of variance model in which both reviewer and case are treated as random effects. The advantage of this model is that the p values and confidence intervals are calculated in a way that takes into account the likely clustering of ratings for the same case reviewed by multiple reviewers and the likely clustering of ratings for the same reviewers in their reviews of multiple cases. In this way, the results may be projected to a new reviewer interpreting a new case. For each outcome, the mean and model-based SEs were reported. A 95% confidence interval and the p value were calculated for each characteristic for which all the reviewers did not rate the monitors as equivalent.

Interobserver variability for the five reviewers was reported when the difference between systems was statistically significant. In these instances, the range of individual reviewer averages was reported. Intraobserver variability could not be truly evaluated because each reviewer interpreted each case only once. However, intraobserver variability was addressed by presenting ranges of individual case averages across reviewers. This is the case variability, which is defined as the average preference that the reviewers had for each case given any particular feature. This is important to illustrate that the results were not skewed by any one case but also shows the extent to which the level of preference did differ over cases.


Results
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
Mass Features
The LCD and CRT displays were both statistically and clinically equivalent with respect to the ratings of most mass features (Table 3). The largest difference in display was present for margin sharpness, which was rated on average 3.6% better on the LCD monitors (p = 0.011), with individual reviewer averages for the five reviewers ranging from 0.8% better to 8.6% better. The reviewers preferred the LCDs for mass conspicuity (1.3% on average; variation in reviewer averages, 0.8-1.7%; variation in case averages, -5% to 25%), but the preference was on the border of being statistically significant (p = 0.05) because the upper and lower bounds of the 95% confidence limits suggest that the difference is unlikely to be more than 5% favoring one monitor or the other.


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TABLE 3: Results of Feature Comparison for Mass

 

Calcium Features
The LCD monitors were either equivalent or better than the CRTs with respect to calcium features (Table 4). In particular, reviewers favored the LCD for conspicuity (6.2% better, p = 0.010; variation in reviewer averages, 0-10.7% better; variation in case averages, 5.0% worse to 25.0% better). Reviewers also favored the LCDs for number of calcifications (2.4%, p = 0.043; variation in reviewer averages, 0-6.0% better; variation in case averages, 0-15.0% better). The LCD and CRT displays did not differ with respect to shape, sharpness of edges, or distribution of calcifications.


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TABLE 4: Results of Feature Comparison for Calcium

 

Architectural Distortion Features
The two displays did not differ significantly for architectural distortion features (Table 5). The observed differences favoring the LCD system fell well short of statistical significance (p = 0.588 for spiculation, p = 0.323 for parenchymal edge distortion, and p = 0.802 for conspicuity). A rating of "no difference" was given by every reviewer for every case for the density feature of architectural distortion, so no SE or inferential statistics could be computed; however, the consistent rating of zero is clearly strong evidence in favor of equivalence.


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TABLE 5: Results of Feature Comparison for Architectural Distortion

 

Evaluation of Display Features for All Cases, Including the Normal Set
In the evaluation of display features, which included both the normal cases and the cases containing abnormalities (Table 6), the LCDs were significantly better with respect to luminance (14.3%, p = 0.021). Individual reviewer averages ranged from 2.2% to 26.5% better for luminance. The CRTs had a significant advantage for image noise (2.8%, p < 0.001; variation in reviewer averages, 0.5-4.8% better; variation in case averages, 0-10% better). The two displays did not significantly differ for dynamic range, skin thickness, subcutaneous tissue, conspicuity of the skin and subcutaneous tissues, image distortion, display noise, or image size.


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TABLE 6: Results of Display Feature Comparison for All Cases, Including Normal Cases

 

Overall
In addition to the feature-by-feature rating, an overall rating was provided on a continuous 100% to 100% scale (Table 7). The LCD and CRT displays were both statistically and clinically equivalent for evaluation of all features included.


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TABLE 7: Results of Overall Rating Stratified by Primary Lesion Type

 


Discussion
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
The demanding nature of mammographic imaging has delayed its entry into the digital age. Even with the recent regulatory approval of full-field digital mammography units, the road to digital mammography has been fraught with transitional issues, not the least of which is the cost of implementing a digital mammography program. However, the initial cost of the full-field digital mammography acquisition unit is just one aspect. In order for digital mammography to be included in whole-department PACS systems, issues such as archiving, universal soft-copy review workstations, and monitor choices are all critical. As directed by the United States Food and Drug Administration, each vendor of full-field digital mammography units has provided a package for digital mammography from acquisition to display to storage. As we move out of the research arena with digital mammography and into the high-volume use of this technology, it is imperative that we work to make this technique fit into our preexisting PACS systems. In doing so, we will help control the overall costs of the systems both in dollars spent and in interpretation time. Because LCD monitors are now widely used for the primary interpretation of other techniques, it seemed logical to evaluate their use for mammography.

This study showed that the 5-MP LCD display is equivalent to and in some respects better than the 5-MP CRT display for full-field digital mammograms over a range of mammography cases. We found that the LCD monitors showed improved calcium conspicuity. Likely, these results are at least in part due to the fixed matrix of the LCDs. This fixed matrix creates a crisper image compared with a CRT because each pixel in the LCD matrix remains constant over time in both location and size. In contrast, each pixel in the matrix of the CRT varies over time in both location and size, producing an inherent slight blurring of pixel edges. The light source of the CRT is fired thousands of times per second to create the resultant image. This constant refreshing of each pixel is minutely variable in location rather than fixed. Further, because the technology is based on a fired light source, there is slight divergence of the light beam as it travels through space, producing a slight blur.

These two aspects of the CRT result in a slightly smoother display than the LCD, but one that is less sharp. The fixed matrix of the LCD produces a more grainy display. Image noise was the only characteristic that was found to be statistically superior on the CRT. However, in our study this image noise, or graininess, did not affect the radiologists' ability to evaluate lesion features. The structured noise inherent in the design of the TFTs likely accounts for the noise seen on the LCDs in this study. Newer TFT designs are eliminating this problem. Background homogeneity was also rated superior on the CRTs but fell short of statistical significance. The reduction of background homogeneity on the LCDs is due to the limitations of the viewing angle and luminance falloff from off-axis viewing with the LCDs. One way to limit this problem is to carefully maintain a viewing angle as close to 0° as possible (straight-on viewing or perpendicular to the screen). Further, CRTs typically have a blacker background than LCDs. It is our opinion that the increased luminance and wider dynamic range of the LCDs more than compensate for this difference and that this difference did not affect our ability to assess lesion features.

Among the lesion features for which differences were identified between systems, there was limited interreviewer variability. In these instances, all five reviewer averages showed either no preference or a preference for the same system. Case variability was somewhat greater. However, there was no outlier case that skewed the data in favor of one system or another for any of the features. For example, the CRT was not preferred for any single case or by any reviewer for number of calcifications, and the LCD was not preferred for any single case or by any reviewer for image noise. Finally, in the overall assessment of the two monitors, no statistically significant difference was noted.

There are several limitations of this study. The comparison was done with an 8-bit display system using images that are intended to be displayed at 8 bits. Some full-field digital mammography manufacturers display at 10 bits. The industry standard for display of digital radiography has historically been set at 8 bits based on research showing that the human eye can realistically see approximately 256 shades of gray (or 8 bits). The monitors evaluated in this study have an 8-bit control card and 8-bit display. It has not yet been shown that 8-bit display is the most optimal bit-depth display for digital mammography. In fact, there is some controversy among digital mammography manufacturers regarding the optimal bit depth for acquisition or display of digital mammograms. Full-field digital mammography images are typically acquired at a predetermined bit depth (12-14 bits) and then undergo processing to transform the images to 8-12 bits for transfer. Finally, the images that arrive at the soft-copy review workstation may require that the display control card perform another transformation for final display at 8-10 bits. Users should understand the acquisition bit depth, the hardware that performs this processing, and the display bit depth of the system they are using. The work to determine the optimal bit depth for display of full-field digital mammography still needs to be done.

The physical setup of placing the LCDs in the center flanked by the CRTs may also have presented a potential bias. This setup was chosen to eliminate problems with off-angle viewing on the LCDs. We tested the arrangement of the LCDs flanking the CRTs before starting the study. The luminance falloff and "rainbow" effect resulting from this arrangement caused a significant loss in perceptible image quality of the LCDs, so this arrangement was not used in the trial. Conversely, because all of the reviewers had significant previous experience interpreting full-field digital mammograms on CRTs, a potential bias existed toward that with which the radiologists were already comfortable, namely, the CRTs. Unfortunately, in this study design, it is impossible to eliminate all bias because it is readily apparent which monitor is which.

We considered these potential biases unavoidable for a direct side-by-side comparison of the images. An alternative design would have been to evaluate the monitors in different reviewing sessions, but because we were using the CRTs as the gold standard and the details of mammographic lesions are so subtle, we thought the most accurate comparison would be side by side so that these subtle differences could be detected and evaluated.

In summary, we found that 5-MP flat-panel monitors are at least equivalent to and in some aspects superior to 5-MP CRTs in the display of full-field digital mammographic images.


References
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
 

  1. Herron JM, Bender TM, Campbell WL, Sumkin JH, Rockette HE, Gur D. Effects of luminance and resolution on observer performance with chest radiographs. Radiology 2000;215 : 169-174[Abstract/Free Full Text]
  2. Ikeda M, Ishigaki T, Shimamoto K, et al. Influence of monitor luminance change on observer performance for detection of abnormalities depicted on chest radiographs. Invest Radiol2003; 38:57 -63[CrossRef][Medline]
  3. Kimme-Smith C, Haus AG, DeBruhl N, Basset LW. Effects of ambient light and view box luminance on the detection of calcifications in mammography. AJR 1997;168 : 775-778[Abstract/Free Full Text]
  4. Krupinski EA, Johnson J, Roehrig H, Nafziger J, Fan J, Lubin J. Use of a human visual system model to predict observer performance with CRT vs LCD display of images. J Digit Imaging 2004;17 : 258-263[CrossRef][Medline]
  5. American College of Radiology. Breast imaging reporting and data system atlas (BI-RADS—mammography), 4th ed. Reston, VA: American College of Radiology, 2003

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