Radiology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Abstract Freely available
Right arrow Figures Only
Right arrow Full Text (PDF)
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Samei, E.
Right arrow Articles by Eyler, W. R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Samei, E.
Right arrow Articles by Eyler, W. R.
(Radiology. 1999;213:727-734.)
© RSNA, 1999


Thoracic Imaging

Detection of Subtle Lung Nodules: Relative Influence of Quantum and Anatomic Noise on Chest Radiographs1

Ehsan Samei, PhD, Michael J. Flynn, PhD and William R. Eyler, MD

1 From the Department of Diagnostic Radiology, Henry Ford Health System, Detroit, Mich. Received November 23, 1998; revision requested February 11, 1999; revision received March 31; accepted July 1. Address reprint requests to M.J.F., Radiology Research (2F), Henry Ford Health System, 1 Ford Pl, Detroit, MI 48202 (e-mail: mikef@rad.hfh.edu).


    Abstract
 TOP
 Abstract
 Introduction
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 Appendix 1
 References
 
PURPOSE: To assess the relative influence of quantum mottle and structured lung patterns (anatomic noise) on the detection of subtle lung nodules on chest radiographs.

MATERIALS AND METHODS: Sixty 8 x 8-cm lung pattern images were extracted from digital chest radiographs in healthy individuals. Sixty quantum mottle images of the same size and quantum noise level were extracted from uniformly exposed digital radiographs. Simulated nodules with various peak contrast-diameter products (CD) that emulated subtle tissue-equivalent lung nodules were numerically superimposed at the center on three-fourths of the images. Printouts were independently viewed and scored by five experienced radiologists. The area under the receiver operating characteristic curve (Az) was estimated as a measure of the detectability of the nodules.

RESULTS: At a fixed observer performance level (eg, Az = 0.8), much smaller and lower-contrast nodules were detected on quantum mottle images (1-mm diameter, CD = 0.01 mm), compared with those on anatomic images (4.5-mm diameter, CD = 0.20 mm). The findings generally agreed with the signal-to-noise ratio calculations based on statistical observer models.

CONCLUSION: The detection of subtle lung nodules on chest radiographs is limited by anatomic noise.

Index terms: Diagnostic radiology, observer performance • Lung neoplasms, diagnosis, 60.1215, 60.31 • Lung, nodule, 60.1215, 60.281 • Radiography, digital, 60.1215 • Receiver operating characteristic (ROC) curve • Thorax, radiography, 60.1215


    Introduction
 TOP
 Abstract
 Introduction
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 Appendix 1
 References
 
The detection of subtle lung nodules on chest radiographs is one of the outstanding challenges in chest radiography. About 30% of lung nodules are missed at the first reading of chest radiographs, although they can be clearly identified retrospectively (1,2). Despite many technologic advances in the last 4 decades, this number has not improved (15).

The detection of abnormalities on medical images is generally understood to be limited by the amount of noise on the image. In the context of this article, noise is defined as the ensemble of all the variations (fluctuating intensities) present on the image that interfere with the detection of the "true" signal that is sought (nodule). (The term "noise" is used to describe "relative noise," or variations signal divided by the mean.)

On chest radiographs, there are two major sources of such variations: quantum noise (mottle), which reflects the variations due to the finite number of x-ray quanta that form the image, and anatomic noise, which reflects the highly "correlated" variations formed by the projection of anatomic features in the thorax, such as ribs, pulmonary vessels, and lung tissue.

The influence of quantum noise on the detection of low-contrast lesions, such as subtle lung nodules, is well understood (6,7). This influence can be minimized either by increasing the patient dose, an action that is generally discouraged, or by improving the detective quantum efficiency of the imaging system. However, substantial improvement in the detective quantum efficiency of imaging systems in the past few decades, which has reduced the level of quantum noise on chest radiographs, has led to no or little improvement in the detection of subtle lung nodules. The influence of anatomic noise on the detection of subtle lung nodules is well acknowledged in the clinical literature (812), but the processes by which this influence takes place are not well understood (13,14).

The goal of this study was to substantiate the relative influence of quantum and anatomic noise in the detection of subtle lung nodules on clinical chest radiographs. The objective was somewhat similar to that of a previous study (15) in which the detection of a single-size Gaussian nodule was assessed in the presence or absence of the anatomic pattern associated with a single chest radiograph with various levels of added noise. Noise on the radiograph was measured in the rib interspaces, and the nodule was similarly placed.

In the present study, in contrast, we used a larger number of images with different anatomic and quantum mottle backgrounds. We also used tissue-equivalent lesions of various sizes, which were placed at random locations in a highly controlled observer performance experiment. The aims were to establish the magnitude of difference in the detection thresholds for images with quantum noise and images with anatomic and quantum noise, at a clinically relevant level of quantum noise (exposure), and to compare the observer results with the theoretic expectations based on the noise characteristics of the images.


    MATERIALS AND METHODS
 TOP
 Abstract
 Introduction
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 Appendix 1
 References
 
Two separate observer performance experiments were performed to examine the detection of lung nodules against backgrounds of anatomic patterns and quantum mottle.

Acquisition of Anatomic Images
Twenty posteroanterior chest radiographs in 20 patients (10 men, 10 women; age range, 28–77 years; mean age, 41 years) were selected from our clinical database. According to the radiology reports, the patients were free from any acute pulmonary abnormalities. The images were acquired by using a digital storage phosphor radiographic system (FCR-9501-HQ; Fuji Medical Systems, Tokyo, Japan) and 35 x 43-cm standard-resolution phosphor screens (ST-Va; Fuji Medical Systems). A 115-kVp x-ray beam from a high-frequency generator (1050 HF; Acoma, Wheeling, Ill) and a 12:1, 59-lines-per-centimeter antiscatter grid (Gilardoni, Milan, Italy) were used for all acquisitions. All exposures were made by using an automatic exposure control that was calibrated to operate the system with a 22.7-mR entrance exposure for a standard 22-cm-thick Lucite slab. The phosphor screens were processed with the automatic Exposure Data Recognizer, or EDR, mode for the "Chest, General" protocol of the system.

The 10-bit, 4k (3,520 x 4,280) digital image data stored on a clinical workstation (HIC-654, Fuji Medical Systems) were transferred as 2k (1,760 x 2,140), 10 bits in logarithmic scale, to a research work-station (Sparc 2; Sun Microsystems, Palo Alto, Calif) through a small computer system interface, or SCSI, connection (DASM-FDLR, Analogic, Peabody, Mass). From each radiograph, three 400 x 400-pixel (8 x 8-cm) images were extracted at random locations within three general zones: upper left lung, upper right lung, and lower right lung. Thus, a total of 60 anatomic images were generated.

Acquisition of Quantum Mottle Images
Four storage phosphor radiographs of a 7.62-cm-thick Lucite slab placed at the detector were acquired by using the same x-ray tube, generator, antiscatter grid, and kVp as those used for the anatomic images. The semiautomatic Exposure Data Recognizer mode for the "Test, Contrast" protocol of the system with a fixed latitude of 2.0 was used for all four uniformly exposed radiographs. The acquired radiographs were transferred to our research workstation in a manner similar to that stated previously. Fifteen 400 x 400-pixel (8 x 8-cm) images were extracted from each radiograph, which generated a total of 60 quantum mottle images.

It was important to ensure that the level of quantum noise on the quantum mottle images was the same as that of the anatomic images. To do that, the average screen exposure for each anatomic image was determined from the average pixel value within a 128 x 128-pixel central area of the image by using the following equation:

where E is the average exposure to the screen in milliroentgens; L and S are the latitude and sensitivity values, respectively, that are uniquely specified for each image by the histogram analysis algorithm of the storage phosphor system; Q is the mean pixel value; and c0 is the calibration factor, which equaled 200 for an unfiltered 80-kVp x-ray beam (16,17). c0 is a strong function of beam quality (18); for this study, a value of 120 was used, which was estimated for a 115-kVp x-ray beam that was filtered with a 1.9-cm-thick slab of aluminum placed at the tube. The level of primary beam hardening associated with 1.9-cm aluminum filtration was similar to that of 22 cm of soft tissue.

Figure 1 illustrates the distribution of the average exposure values that were calculated for the anatomic images. The results show a broad distribution (mean, 1.02 mR; SD, 0.4 mR). In accordance with these results, the quantum mottle images were acquired with a screen exposure of 0.8 mR; this value was slightly lower than the mean value given previously. The quantum mottle images were acquired at 0.8 mR prior to the full verification of the calculated results. However, after verification, the level of exposure for the quantum mottle images was found to be sufficiently within the wide range of exposure levels on the anatomic images.



View larger version (17K):
[in this window]
[in a new window]
 
Figure 1. Plot shows the exposures to the storage phosphor screens that were calculated from the average pixel values in 128 x 128-central pixel blocks on anatomic images. The exposure value used to acquire the quantum mottle images (dashed line) is well within the distribution associated with the anatomic images.

 
Simulation of Nodules
Each set of 60 anatomic and quantum mottle images was randomized and was divided into four groups of 15. One group from each set was kept as the control set, with no nodules. Three simulated nodules with different contrasts and diameters were digitally superimposed on the centers of the images in the remaining three groups. The superpositioning was performed by subtracting a nodule mask from the image data in the logarithmic scale while taking into account the latitude and sensitivity of the image. The nodule masks were circular; the subject contrast profiles followed a mathematic function that was deduced from a database of real lung nodules (19,20), as follows:

where c(r) is the contrast c as a function of radial distance r and -0.6D <= r <= 0.6D; C is the peak contrast of the nodule (C = {Delta}E/E0 = ln[E0/E]); and D is the diameter of the nodule at the imaging plane, which is specified as the full-width-at-fifth-maximum of the profile (Fig 2).



View larger version (15K):
[in this window]
[in a new window]
 
Figure 2. Plot shows the universal contrast profile (solid line) used to simulate subtle lung nodules is normalized at the maximum and at one-fifth of the maximum. The Gaussian approximation of the profile (dashed line) used for the SNR calculations uses the same normalization points and closely resembles the nodular profile.

 
All simulated nodules used in the study had a peak contrast–to-diameter ratio of 0.0098 mm-1, corresponding to spherical, uniform, muscle-equivalent lesions within the lungs that were imaged with the 115-kVp x-ray beam. This ratio was calculated by using the following equation:

where {rho}n is the density of the nodule (assumed to be 1.0 g/mL); {rho}l is the density of the lung (assumed to be 0.3 g/mL); R is the ratio of the scatter to the primary signal intensity; and M is the contrast produced per unit thickness of nodular material, when no scattered radiation is present. For this study, R was assumed to be 0.68 on the basis of our measurements in a chest phantom. M was assumed to be 0.0235 mm-1 on the basis of findings from our prior work (table 3 from reference 20).

The values for peak contrast–diameter products (CDs) for the nodules were chosen to produce a range of observer responses from "probably not present" to "probably present," which bracketed the detection thresholds for each type of background. This was accomplished by performing two pilot studies in which the appearances of nodules of varying sizes and contrast were examined against anatomic and quantum mottle backgrounds by two experienced radiologists (including W.R.E.). From the results of the pilot studies, peak contrast and diameter for the actual study were chosen to bracket the detection thresholds. The images used in the pilot studies were not used in the actual study. For each type of background, three nodular diameters were identified, with three distinct CDs. Table 1 shows the CD values of the nodules used in the observer performance experiments.


View this table:
[in this window]
[in a new window]
 
TABLE 1. Peak Subject Contrast, Full-Width-at-Fifth-Maximum Diameter, and CDs of the Simulated Nodules Used in the Observer Performance Experiments
 
Printing of Images
After the insertion of the nodules onto the images, logarithmic-scale image data were transformed into optical density values by using a transformational method that was developed at our laboratory (21). This method was used to construct a Hurter and Driffield characteristic curve by using two Gaussian gradient components. For each gradient component, the maximum contrast, SD, and mean were specified. The cumulative integral of the gradient components was then calculated as the Hurter and Driffield curve. One of the advantages of this straightforward transformational method was that the influence of the gradient parameters on the overall transformation and the "look" of the image could be intuitively discerned.

For this study, we constructed and used a Hurter and Driffield curve similar to that of a conventional screen-film system for chest radiography (Ortho-C/Lanex; Eastman Kodak, Rochester, NY), as illustrated in Figure 3. The {gamma} values for this curve within the optical density range applicable to this study were similar to those of currently used screen-film systems (eg, InSight, Eastman Kodak). For each image, the average pixel value within a 128 x 128-pixel central area was used as the mean value for the main gradient component. Thus, the average level of contrast and optical density at the center of all images where nodules were superimposed were constant.



View larger version (13K):
[in this window]
[in a new window]
 
Figure 3. Plot shows the model used for the Hurter and Driffield transformation of the log of the signal data to optical density. A Hurter and Driffield curve (solid line) similar to that of a conventional screen-film system (OC/Lanex; Eastman Kodak) ({diamondsuit}) was generated by using two Gaussian gradient functions (dashed lines). The difference in the screen-film and model transformations is due to the baseline optical density. The gradient functions can be manipulated easily to construct various transformational curves.

 
The images were padded with 2.6-cm horizontal and 4.1-cm vertical margins of 1.8 constant optical density to create display characteristics (ie, eye adaptation and visual glare) similar to those of chest radiographs. Figure 4 shows two examples of images. Each group of 60 images was randomly assigned and was printed six-on-one on 10 sheets of film by using a laser printer (Ektascan model 2180; Eastman Kodak). The printer was calibrated before printing the images, and its linearity was independently verified in 0.1-density steps between optical densities of 0.1 and 3.0.



View larger version (151K):
[in this window]
[in a new window]
 
Figure 4a. Examples of (a) anatomic and (b) quantum mottle images used in the observer performance experiments show the nodules with CDs of 0.4 mm (6.4-mm diameter) and 0.0171 mm (1.32-mm diameter), respectively, superimposed at the centers of the images. Images were padded with 2.6-cm horizontal and 4.1-cm vertical margins, with a constant optical density of 1.8.

 


View larger version (130K):
[in this window]
[in a new window]
 
Figure 4b. Examples of (a) anatomic and (b) quantum mottle images used in the observer performance experiments show the nodules with CDs of 0.4 mm (6.4-mm diameter) and 0.0171 mm (1.32-mm diameter), respectively, superimposed at the centers of the images. Images were padded with 2.6-cm horizontal and 4.1-cm vertical margins, with a constant optical density of 1.8.

 
Observer Performance Experiments
The anatomic and quantum mottle images were independently viewed by five observers (including W.R.E.). Four observers had more than 20 years of experience as chest radiologists (W.R.E.), and one was a general radiologist. The anatomic and quantum mottle images were interpreted in separate sessions by each observer.

At the beginning of each session, the reading protocol was explained to the observer: The observer task was to discern whether a nodule was present at the center of the image and to indicate his confidence level by using a five-point grading scale (Table 2). Before the study began, the observer viewed two graded example hard-copy films; each contained six images of a background with six superimposed simulated nodules with increasing values. This was followed with the reading of two practice hard-copy films that were similar to those used for the actual study. The observer was subsequently provided with the expected answers so he could assess the visibility level of the nodules and adjust the grading. The observer was told that there was a 75% probability that a nodule was present on each image.


View this table:
[in this window]
[in a new window]
 
TABLE 2. Grading Scale Used to Score Findings on the Images
 
The viewing took place in a room with low ambient lighting, and the same viewing box was used for all reading sessions. No constraints on time or viewing distance were imposed. The reading session for each set of 10 hard-copy films (60 images) took about 20–30 minutes.

Data Analysis
A standard receiver operating characteristic analysis (2225) was used to process the results of the observer performance experiments. For each observer, the scores ascribed to the images that depicted nodules with a particular value and the scores ascribed to the control images that depicted no nodules were counted in separate data sets. These data were then processed by using ROCFIT (June 1993 version), a program developed by C. E. Metz of the University of Chicago, Ill, to estimate the maximum likelihood of a binomial receiver operating characteristic curve and its associated parameters from a set of categorical rating-scale data (26,27). The area under the receiver operating characteristic curve (Az) was obtained for each observer as a function of the CD of the nodule for each type of background. The data were averaged across observers. The accuracy of each averaged Az value was assessed by estimating the standard error (SE), as described by Swets and Pickett (25), by using the following equation:

where S2 values are variances associated with case sample c, between-reader br, and within-reader wr errors and where l is the number of observers. There were no repeated readings in this study. Therefore, the within-reader error was not independently measured, and its variance was not included in the error estimation for the standard error. This led to only a conservative overestimation in the resultant error (ie, the results were more accurate than those calculated in the study).

To relate the results of the observer performance experiments to the noise characteristics on the images, Az values were used to estimate the signal-to-noise ratios (SNRs) for the nodules by using the following equation (14,28):

where SNRm is the measured SNR. erf(u) is the error function, which is defined as follows:

The experimentally observed SNRs were then compared with the SNRs predicted with two observer models, the Hotelling model (which was used to perform the detection task by cross-correlating the image data with a template at the location of the nodule, taking into account the background variations), and a non-prewhitening model with a visual-response function (29) (which was used to perform the detection task by cross-correlating the image data with a modified version of the signal intensity as a template, not taking into account the background variation). The details of these calculations are provided in the Appendix.


    RESULTS
 TOP
 Abstract
 Introduction
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 Appendix 1
 References
 
Table 3 shows the observer results for nodules on anatomic images. The between-observer variability was notably large. Although the Az values for any given nodule varied across observers, a similar Az-CD dependence was evident for each observer. Figure 5 illustrates this dependence, averaged over all observers and readings. The Az value increased when the CD approached 1.0 at an extrapolated nodule CD value of approximately 0.44 mm (6.7-mm diameter).


View this table:
[in this window]
[in a new window]
 
TABLE 3. Az and Associated Case Sample and within-Reader Errors (Sc+wr) as a Function of the CDs of the Simulated Nodules on Anatomic Images
 


View larger version (14K):
[in this window]
[in a new window]
 
Figure 5. Plot shows the performance index Az, averaged over all observers and readings, as a function of the peak CD of the nodules that were superimposed on quantum mottle images (containing quantum noise) and anatomic images (containing anatomic and quantum noise) at a clinically relevant exposure level (200-speed detector system). Individual observer data are also plotted ({diamondsuit}). Error bars show the two-standard error intervals that were calculated by using the Swets method. The graph illustrates an order of magnitude difference in the CDs of the nodules for equal detectability against quantum and anatomic and backgrounds.

 
Table 4 shows the observer results for nodules on quantum mottle images. Figure 5 shows Az as a function of the CD averaged over all the observers and readings. The Az value approached a saturation of 1.0 at a nodule CD value of about 0.02 mm (1.44-mm diameter). A proportionality between Az and CD similar to that of the anatomic images may be discerned. In the case of nodules on quantum mottle images, however, the transition was much sharper. The average slope of the plot of Az versus the logarithm of the CD on anatomic images (0.596 mm-1) was about half that of the plot for quantum mottle images (1.123 mm-1). The difference was statistically significant (P = .003).


View this table:
[in this window]
[in a new window]
 
TABLE 4. Az and Associated Case Sample and within-Reader Errors (Sc+wr) as a Function of the CDs of the Simulated Nodules on Quantum Mottle Images
 
The most notable finding in Figure 5 is that to produce the same Az, the CD of a nodule placed on an anatomically structured background should be an order of magnitude higher than that of a nodule placed on a background that contains only the quantum noise component of the background. The observed differences in the CD for equivalent Az values were statistically significant (P = .001). If an Az value of 0.8 was to be considered the detection threshold, a tissue-equivalent nodule must have had a CD of about 0.2 mm (4.55-mm diameter) to be detected on an anatomic background that contained anatomic and quantum noise. The corresponding CD value on a background that contained only quantum noise was about 0.0135 mm (1.17-mm diameter).

Figure 6 illustrates the measured SNR as a function of the calculated SNR for anatomic and quantum mottle images from the non-prewhitening and the Hotelling observer models. The two observer models yielded similar results with both backgrounds. However, in both cases, model observer values were higher than those inferred by the Az values. The observer results for both backgrounds were in general agreement with those obtained with the two observer models; the results did not indicate which model was best.



View larger version (16K):
[in this window]
[in a new window]
 
Figure 6a. Plots of the measured SNRs versus computed SNRs for the anatomic and quantum mottle images obtained by using the (a) non-prewhitening (NPW) and (b) Hotelling observer models show both models yielded similar results for anatomic and quantum noise backgrounds. Both models indicated a higher SNR than that derived from the observer performance results.

 


View larger version (17K):
[in this window]
[in a new window]
 
Figure 6b. Plots of the measured SNRs versus computed SNRs for the anatomic and quantum mottle images obtained by using the (a) non-prewhitening (NPW) and (b) Hotelling observer models show both models yielded similar results for anatomic and quantum noise backgrounds. Both models indicated a higher SNR than that derived from the observer performance results.

 

    DISCUSSION
 TOP
 Abstract
 Introduction
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 Appendix 1
 References
 
The influence of quantum noise in limiting the detection of abnormalities on medical images is well recognized (6,7). This understanding has been an incentive for the quantitative assessment of noise and noise propagation in medical imaging and for the improvement of the quantum efficiency in imaging systems. Object variability, or anatomic noise, is also regarded as an important factor that limits the detectability of low-contrast objects (13,14). The relative contribution of these noise components depends on the imaging modality that is used (eg, nuclear medicine imaging, fluoroscopy) and on the particular diagnostic task that is performed (eg, the detection of low-contrast lesions in the lungs vs the detection in the less-penetrated mediastinal region on a chest radiograph). Consequently, some diagnostic tasks can be considered to be quantum-limited, whereas others are limited by object variability.

In this study, an attempt was made to quantitatively compare the relative influence of quantum and anatomic noise in the detection of low-contrast subtle lung nodules on chest radiographs. The results suggest that this diagnostic task is not quantum-limited. The detection of lung nodules is affected much more by the anatomic structured pattern of the thorax than by quantum noise.

As shown in Figure 5, for both types of backgrounds, the Az value increased with the CD of the nodule. The observed behavior can be explained in the context of signal detection theory and in terms of the underlying probability distribution functions for noise and for signal and noise (25,30). If these distribution functions are assumed to be Gaussian, the Az value is expected to increase with signal as the integral of a Gaussian distribution function (14), which creates a sigmoidal curve that becomes saturated at an Az of 1.0. The rate of the increase is dependent on the width of the Gaussian distribution function; a narrow width distribution function leads to a sharp saturation, and vice versa.

In our results, the uniform increase in the Az value with the CD of the nodule for both quantum mottle images and anatomic images seems to fit this description. For anatomic images, however, the slope was about half that of the quantum mottle images, which suggests a wider underlying probability distribution function for the backgrounds of anatomic patterns.

In this study, the position and characteristics of the target were clearly explained to the observers; thus, the observer experiments were of the type known as signal-known-exactly (31,32). In such studies, the detection performance is expected to be better than that of clinical studies in which the observers must find nodules at unknown locations. The use of a signal-known-exactly protocol was based on two rationales: (a) The statistical characteristics of signal-known-exactly protocols are well understood, and (b) the goal of the study was not to investigate the detection in absolute terms, but rather, to understand the relative differences associated with the backgrounds of quantum noise and quantum and anatomic noise under ideal circumstances.

To demonstrate the influence of knowing the possible location of a nodule, a comparison can be made between the findings in this study and those of an earlier study, in which observers were to detect similar kinds of simulated nodules that were randomly positioned on full-chest radiographs (19). The investigators found that a CD of at least 0.8 mm (9-mm diameter for a tissue-equivalent lesion) was necessary if a nodule was to be detected, whereas investigators in this study found a corresponding value (for Az = 0.8) of about 0.2 mm (4.55-mm diameter). This comparison clearly demonstrates the importance of localization in the detection of lung nodules.

The simulated nodular patterns used in this study were circular. Findings from studies on the etiologic and computed tomographic characteristics of lung nodules (33,34) showed a great variability in overall shape, outline irregularity, and in-homogeneity of these nodules, especially in cases of primary carcinoma. The perceived limitation of the nodular shapes used in our study, however, proved to be insubstantial for anatomic images. The projected circular images of simulated nodules over the anatomic backgrounds overlapped with the structured pattern of the backgrounds, and the conjoined images of the nodules had irregularities and spiculations that were very similar to those of real lung nodules.

In a previous study (19), we demonstrated that experienced observers were not able to distinguish real and simulated nodules of the type used in this study. It should be noted, however, that the irregularity in the shape of a nodule that is placed on a quantum mottle background may affect its detectability. If irregularity reduces the detectability of a nodule against such a background, this may suggest an overestimation of the influence of anatomic noise in our study; the magnitude remains to be determined in further research.

The results of this study suggest that anatomic noise associated with the background lung structure strongly limits the detection of subtle nodules in the lung. One of the implications of this finding is the potential for a reduction in the dose to the patient; since the relative quantum noise is inversely related to the square root of the dose to the patient and since the detection of lung nodules is not limited by quantum noise, it may be concluded that the exposure to the patient at chest examination can be reduced without a marked loss in the detectability of lung nodules. It should be noted, however, that this may adversely affect the detection of mediastinal lesions or the presentation of other features, such as interstitial lung disease; these tasks were not addressed in this study.



View larger version (29K):
[in this window]
[in a new window]
 
Figure a1a. Noise power spectra computed for the (a) anatomic and (b) quantum mottle images show the substantial variations among the noise power spectra for the anatomic images and show the markedly higher level of the noise spectrum at lower spatial frequencies on the anatomic images compared with those on the quantum mottle images. The means of these spectra were used for the SNR calculations outlined in the Appendix.

 



View larger version (14K):
[in this window]
[in a new window]
 
Figure a1b. Noise power spectra computed for the (a) anatomic and (b) quantum mottle images show the substantial variations among the noise power spectra for the anatomic images and show the markedly higher level of the noise spectrum at lower spatial frequencies on the anatomic images compared with those on the quantum mottle images. The means of these spectra were used for the SNR calculations outlined in the Appendix.

 


    Appendix 1
 TOP
 Abstract
 Introduction
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 Appendix 1
 References
 
The Hotelling SNR, or SNRhot, was calculated by using the following equation:

where f is the radial spatial frequency, fN is the Nyquist frequency (2.5 cycles per millimeter for 0.2-mm pixels), S(f) is the Fourier transform of the contrast profile for the nodule, and W(f) is the noise power spectrum on the background image.

The non-prewhitening SNR, or SNRnpw, was calculated by using the following equation:

where H(f) is the modulation transfer function of the imaging system. V(f) is the frequency-dependent visual-response function based on an approximation suggested by Burgess (29), as follows:

where c is a scale factor selected to yield the maximum of the function at 4 cycles per degree (29). With a 50-cm distance between the eye and the image, c was calculated to be 3.07 mm2 by using the differential of this equation.

For the signal term S(f), the contrast profile of the nodules was approximated by means of a two-dimensional Gaussian function that had a full-width-at-fifth-maximum diameter equivalent to that of the actual nodule profiles, as follows:

This function has a simple Fourier transform with the following form:

where C is the peak contrast of the nodule, D is the full-width-at-fifth-maximum diameter of the nodule, and {alpha} is a scaling factor equal to 0.148. Figure 2 illustrates the Gaussian approximation of the nodule profile.

H(f) and W(f) were measured experimentally. H(f) was measured by using a high-precision–edge testing device. The details of this measurement method are fully disclosed in a previous article (35). W(f) was assessed on the basis of Fourier analysis of the image data by using a method developed previously (21,36). Each image was divided into a 2 x 2 matrix with 128 x 128 subarrays (ie, four 2.56 x 2.56-cm blocks). Very-low-frequency trends within each subarray were removed by subtracting a second-order polynomial fit from the data.

The image data were then scaled to relative values and the power spectrum was computed within each subarray by using a two-dimensional fast Fourier transformational algorithm and a Hamming spectral estimation window. The estimates from all four subarrays were averaged to obtain the power spectrum for each image, and the data in each radial differential circle were averaged to obtain the radial power spectrum for all the images. Figure A1 shows the estimated noise power spectra. The spectral estimates for different images of each type were similar. The data for all 60 anatomic and all 60 quantum mottle images were averaged for the observer model calculations.


    Acknowledgments
 
The authors gratefully acknowledge the participation of Gordon Beute, MD, David Spizarny, MD, David Wang, MD, and Carl Zylak, MD, in the observer performance experiments.


    Footnotes
 
Abbreviations: Az = area under the receiver operating characteristic curve CD = contrast diameter product SNR = signal-to-noise ratio

Author contributions: Guarantors of integrity of entire study, E.S., M.J.F., W.R.E.; study concepts and design, E.S., M.J.F.; definition of intellectual content, E.S., M.J.F.; literature research, E.S., W.R.E.; experimental studies, E.S.; data acquisition and analysis, E.S.; statistical analysis, E.S.; manuscript preparation, E.S., W.R.E.; manuscript editing and review, E.S., W.R.E., M.J.F.


    References
 TOP
 Abstract
 Introduction
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 Appendix 1
 References
 

  1. Guiss LW, Kuenstler P. A retrospective view of survey photofluorocarbons of persons with lung cancer. Cancer 1960; 13:91-95.
  2. Muhm JR, Miller WE, Fontana RS, Sanderson DR, Uhlenhopp MA. Lung cancer detected during a screening program using four-month chest radiographs. Radiology 1983; 148:609-615.[Abstract/Free Full Text]
  3. Stitik FP. Chest radiology. In: Miller AB, eds. Screening for cancer. Orlando, Fla: Academic Press, 1985; 163-191.
  4. Heelan RT, Flehinger BJ, Melamed MR, Zaman MB, Perchick WB. Nonsmall-cell lung cancer: results of the New York screening program. Radiology 1984; 151:289-293.[Abstract/Free Full Text]
  5. Gavelli G, Giampalma E. Sensitivity and specificity of chest x-ray screening for lung cancer. Proceedings of the International Conference on Prevention and Early Diagnosis of Lung Cancer. Varese, Italy: , 1998; 103-108.
  6. Burgess AE, Wagner RF, Jennings RJ. Human signal detection performance for noisy medical images. IEEE Computer Soc Int Workshop Med Imaging 1982; 99-105.
  7. Rose A. The sensitivity performance of the human eye on an absolute scale. J Opt Soc Am 1948; 38:196-208.
  8. Greening RG, Pendergrass PE. Postmortem roentgenography with particular emphasis upon the lung. Radiology 1954; 62:720-724.
  9. Boynton RM, Bush WR. Recognition of forms against a complex background. J Opt Soc Am 1956; 46:758-764.[Medline]
  10. Smith MJ. Error and variation in diagnostic radiology Springfield, Ill: Thomas, 1967.
  11. Revesz G, Kundel HL, Graber MA. The influence of structured noise on the detection of radiologic abnormalities. Invest Radiol 1974; 9:479-486.[Medline]
  12. Neitzel U, Pralow T, Schaefer-Prokop C, Prokop M. Influence of scatter reduction on lesion signal-to-noise ratio and lesion detection in digital chest radiography. SPIE Med Imaging 1998; Vol 3336:337-346.
  13. Barrett HN. Objective assessment of image quality: effects of quantum noise and object variability. J Opt Soc Am A 1990; 7:1266-1278.[Medline]
  14. Ruttimann UK, Webber RL. A simple model combining quantum noise and anatomical variation in radiographs. Med Phys 1984; 11:50-60.[Medline]
  15. Kundel HL, Nodine CF, Thickman D, Carmody D, Toto L. Nodule detection with and without a chest image. Invest Radiol 1985; 20:94-99.[Medline]
  16. Matsuda T, Arakawa S, Kohda K, Torii S, Nakajima N. New technological developments in the FCR9000: Fuji computed radiography, technical review 2 Tokyo, Japan: Fuji Photo Film, 1993.
  17. Nakajima N, Takeo H, Ishida M, Nagata T. Automatic setting functions for image density and range in the FOR system: Fuji computed radiography, technical review 3 Tokyo, Japan: Fuji Photo Film, 1994.
  18. Tucker DM, Rezentes PS. The relationship between pixel value and beam quality in photostimulable phosphor imaging. Med Phys 1997; 24:887-893.[Medline]
  19. Samei E, Flynn MJ, Beute GH, Peterson E. Comparison of observer performance for real and simulated nodules in chest radiography. SPIE Med Imaging 1996; Vol 2712:60-70.
  20. Samei E, Flynn MJ, Eyler WR. Simulation of subtle lung nodules in projection chest radiography. Radiology 1997; 202:117-124.[Abstract/Free Full Text]
  21. Samei E. The performance of digital x-ray imaging systems in detection of subtle lung nodules [dissertation] Ann Arbor, Mich: University of Michigan, 1997.
  22. Lusted LB. Receiver operating characteristic analysis of radiologic images. In: Perkins WJ, eds. Biomedical computing. Baltimore, Md: University Park Press, 1977; 183-197.
  23. Metz CE. ROC methodology in radiologic imaging. Invest Radiol 1986; 21:720-733.[Medline]
  24. Egan JP. Signal detection theory and ROC analysis New York, NY: Academic Press, 1975.
  25. Swets JA, Pickett RM. Evaluation of diagnostic systems: methods from signal detection theory New York, NY: Academic Press, 1982.
  26. Dorfman DD, Alf E. Maximum likelihood estimation of parameters of signal detection theory and determination of confidence intervals: rating method data. J Math Psychol 1969; 6:487-496.
  27. Grey DR, Morgan BJT. Some aspects of ROC curve-fitting: normal and logistic models. J Math Psychol 1972; 9:128-139.
  28. Rolland JPY. Factors in influencing lesion detection in medical imaging [dissertation] Tuscon, Arizona: University of Arizona, 1990.
  29. Burgess AE. Statistically defined backgrounds: performance of a modified nonprewhitening observer model. J Opt Soc Am A 1994; 11:1237-1242.[Medline]
  30. Schiffman HR. Sensation and perception: an integrated approach New York, NY: Wiley, 1990; 6-16.
  31. Burgess AE, Wagner RF, Jennings RJ, Barlow HB. Efficiency of human visual signal discrimination. Science 1981; 214:93.[Abstract/Free Full Text]
  32. Judy PF, Kijewski MF, Fu X, Swensson RG. Observer detection efficiency with target size uncertainty. SPIE Med Imaging 1995; Vol 2436:10-17.
  33. Zwirewich CV, Vedal S, Miller RR, Muller NL. Solitary pulmonary nodule: high-resolution CT and radiologic-pathologic correlation. Radiology 1991; 179:469-476.[Abstract/Free Full Text]
  34. Hartman TE, Muller NL, Primack SL, et al. Metastatic pulmonary calcification in patients with hypercalcemia: findings on chest radiographs and CT scans. AJR 1994; 162:799-802.[Abstract/Free Full Text]
  35. Samei E, Flynn MJ, Reimann DA. A method for measuring the presampled MTF of digital radiographic systems using an edge test device. Med Phys 1998; 25:102-113.[Medline]
  36. Samei E, Flynn MJ. Physical measures of image quality in photostimulable phosphor radiographic systems. SPIE Med Imaging 1997; Vol 3032:328-338.



This article has been cited by other articles:


Home page
RadiologyHome page
J. Vikgren, S. Zachrisson, A. Svalkvist, A. A. Johnsson, M. Boijsen, A. Flinck, S. Kheddache, and M. Bath
Comparison of Chest Tomosynthesis and Chest Radiography for Detection of Pulmonary Nodules: Human Observer Study of Clinical Cases
Radiology, December 1, 2008; 249(3): 1034 - 1041.
[Abstract] [Full Text] [PDF]


Home page
Radiat Prot DosimetryHome page
M. J. Tapiovaara
Review of relationships between physical measurements and user evaluation of image quality
Radiat Prot Dosimetry, March 1, 2008; 129(1-3): 244 - 248.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Roentgenol.Home page
E. Samei, S. A. Stebbins, J. T. Dobbins III, and J. Y. Lo
Multiprojection Correlation Imaging for Improved Detection of Pulmonary Nodules
Am. J. Roentgenol., May 1, 2007; 188(5): 1239 - 1245.
[Abstract] [Full Text] [PDF]


Home page
RadiologyHome page
E. Samei, R. S. Saunders Jr, J. A. Baker, and D. M. Delong
Digital Mammography: Effects of Reduced Radiation Dose on Diagnostic Performance
Radiology, May 1, 2007; 243(2): 396 - 404.
[Abstract] [Full Text] [PDF]


Home page
RadiologyHome page
H. P. McAdams, E. Samei, J. Dobbins III, G. D. Tourassi, and C. E. Ravin
Recent Advances in Chest Radiography
Radiology, December 1, 2006; 241(3): 663 - 683.
[Abstract] [Full Text] [PDF]


Home page
RadiologyHome page
L. J. M. Kroft, W. J. H. Veldkamp, B. J. A. Mertens, J. P. A. van Delft, and J. Geleijns
Detection of simulated nodules on clinical radiographs: dose reduction at digital posteroanterior chest radiography.
Radiology, November 1, 2006; 241(2): 392 - 398.
[Abstract] [Full Text] [PDF]


Home page
RadiologyHome page
C. L. Hoe, E. Samei, D. P. Frush, and D. M. Delong
Simulation of Liver Lesions for Pediatric CT
Radiology, December 21, 2005; (2005) 2381050477.
[Abstract] [Full Text]


Home page
Radiat Prot DosimetryHome page
M. Bath, M. Hakansson, S. Borjesson, S. Kheddache, A. Grahn, M. Ruschin, A. Tingberg, S. Mattsson, and L. G. Mansson
Nodule detection in digital chest radiography: introduction to the RADIUS chest trial
Radiat Prot Dosimetry, May 17, 2005; 114(1-3): 85 - 91.
[Abstract] [Full Text] [PDF]


Home page
Radiat Prot DosimetryHome page
M. Hakansson, M. Bath, S. Borjesson, S. Kheddache, A. A. Johnsson, and L. G. Mansson
Nodule detection in digital chest radiography: effect of system noise
Radiat Prot Dosimetry, May 17, 2005; 114(1-3): 97 - 101.
[Abstract] [Full Text] [PDF]


Home page
Radiat Prot DosimetryHome page
M. Bath, M. Hakansson, S. Borjesson, S. Kheddache, A. Grahn, F. O. Bochud, F. R. Verdun, and L. G. Mansson
Nodule detection in digital chest radiography: part of image background acting as pure noise
Radiat Prot Dosimetry, May 17, 2005; 114(1-3): 102 - 108.
[Abstract] [Full Text] [PDF]


Home page
Radiat Prot DosimetryHome page
E. Samei, J. T. Dobbins III, J. Y. Lo, and M. P. Tornai
A framework for optimising the radiographic technique in digital X-ray imaging
Radiat Prot Dosimetry, May 17, 2005; 114(1-3): 220 - 229.
[Abstract] [Full Text] [PDF]


Home page
Radiat Prot DosimetryHome page
M. Bath, M. Hakansson, J. Hansson, and L. G. Mansson
A conceptual optimisation strategy for radiography in a digital environment
Radiat Prot Dosimetry, May 17, 2005; 114(1-3): 230 - 235.
[Abstract] [Full Text] [PDF]


Home page
Radiat Prot DosimetryHome page
M. Bath, M. Hakansson, A. Tingberg, and L. G. Mansson
Method of simulating dose reduction for digital radiographic systems
Radiat Prot Dosimetry, May 17, 2005; 114(1-3): 253 - 259.
[Abstract] [Full Text] [PDF]


Home page
Radiat Prot DosimetryHome page
J. Hansson, M. Bath, M. Hakansson, H. Grundin, E. Bjurklint, P. Orvestad, A. Kjellstrom, H. Bostrom, M. Jonsson, K. Jonsson, et al.
An optimisation strategy in a digital environment applied to neonatal chest imaging
Radiat Prot Dosimetry, May 17, 2005; 114(1-3): 278 - 285.
[Abstract] [Full Text] [PDF]


Home page
Radiat Prot DosimetryHome page
L. G. Mansson, M. Bath, and S. Mattsson
Priorities in optimisation of medical X-ray imaging--a contribution to the debate
Radiat Prot Dosimetry, May 17, 2005; 114(1-3): 298 - 302.
[Abstract] [Full Text] [PDF]


Home page
Br. J. Radiol.Home page
D G W Onnasch, A Schemm, and H-H Kramer
Optimization of radiographic parameters for paediatric cardiac angiography
Br. J. Radiol., June 1, 2004; 77(918): 479 - 487.
[Abstract] [Full Text] [PDF]


Home page
J Ultrasound MedHome page
S. R. Turner, E. Samei, B. S. Hertzberg, D. M. DeLong, R. Vargas-Voracek, A. Singer, C. H. Maynor, and M. A. Kliewer
Sonography of Fetal Choroid Plexus Cysts: Detection Depends on Cyst Size and Gestational Age
J. Ultrasound Med., November 1, 2003; 22(11): 1219 - 1227.
[Abstract] [Full Text] [PDF]


Home page
RadiologyHome page
E. Samei, M. J. Flynn, E. Peterson, and W. R. Eyler
Subtle Lung Nodules: Influence of Local Anatomic Variations on Detection
Radiology, July 1, 2003; 228(1): 76 - 84.
[Abstract] [Full Text] [PDF]


Home page
RadiologyHome page
J. T. Dobbins III, E. Samei, H. G. Chotas, R. J. Warp, A. H. Baydush, C. E. Floyd Jr, and C. E. Ravin
Chest Radiography: Optimization of X-ray Spectrum for Cesium Iodide-Amorphous Silicon Flat-Panel Detector
Radiology, January 1, 2003; 226(1): 221 - 230.
[Abstract] [Full Text] [PDF]


This Article
Right arrow Abstract Freely available
Right arrow Figures Only
Right arrow Full Text (PDF)
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Samei, E.
Right arrow Articles by Eyler, W. R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Samei, E.
Right arrow Articles by Eyler, W. R.


HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
RADIOLOGY RADIOGRAPHICS RSNA JOURNALS ONLINE