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DOI:10.2214/AJR.07.3740
AJR 2008; 191:W181-W189
© American Roentgen Ray Society


Original Research

Influence of Tagged Fecal Material on Detectability of Colorectal Polyps at CT: Phantom Study

Ayso H. de Vries1, Henk W. Venema1,2, Jasper Florie1, Chung Y. Nio1 and Jaap Stoker1

1 Department of Radiology, Academic Medical Center, University of Amsterdam, Meibergdreef 9, 1105 AZ Amsterdam, The Netherlands.
2 Department of Medical Physics, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.

Received January 28, 2008; accepted after revision April 11, 2008.

 
Address correspondence to A. H. de Vries (Ayso.devries{at}amc.uva.nl).

A grant was received from Philips Healthcare, which was not involved in designing or conducting the study and did not have access to the data. Philips Healthcare was not involved in analyzing the data or writing the manuscript and was not asked for approval.

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Abstract
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
OBJECTIVE. The purpose of this study was to determine the influence of tagged material on the minimal radiation dose needed to detect colorectal polyps at CT.

MATERIALS AND METHODS. The study was conducted in two phases. In the first, three experienced observers determined the visibility of sessile polyps (6 mm) at five contrast levels (300, 480, 790, and 1,040 HU and air) and five tube charge levels (10, 14, 20, 28, and 40 mAs) in an anthropomorphic phantom. Each polyp was present in one of eight possible locations. The mean tube charge threshold for 90% correct responses was determined for each contrast level. Blinded observers performed independent 2D readings. In the second phase of the study, three 150-cm virtual colons were evaluated at two contrast levels (300 and 480 HU) and at five tube charge levels between 20 and 80 mAs. The three colons contained 18 randomly located polyps. The mean tube charge threshold for 90% sensitivity was determined for each contrast level.

RESULTS. In the first phase of the study, the estimated tube charge thresholds for 300, 480, and 790 HU were 24.0, 16.3, and 6.2 mAs. At 1,040 HU and in air, all polyps were detected at the lowest tube charge setting (10 mAs). In the second phase, the tube charge thresholds for 90% sensitivity at 300 and 480 HU were 70 and 35 mAs, respectively.

CONCLUSION. If polyps are covered by fecal material, a considerably higher tube charge setting is needed for adequate visualization than is needed for polyps in a completely cleansed colon, especially when the density of the tagged residue is low.

Keywords: bowel preparation • CT colonography • dose reduction • fecal tagging • phantom study


Introduction
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
CT colonography (CTC) is a promising technique of screening for colorectal cancer and colonic polyps. An important disadvantage of the technique is that many patients consider the bowel preparation burdensome [1]. Labeling fecal material with an oral contrast agent (fecal tagging) enables patients to prepare for CTC with less extensive bowel preparation [2–4]. Minimizing bowel preparation, however, may increase patient compliance [57] but results in a higher amount of residual feces in the colon [8].

Because of reduced contrast (i.e., reduced difference in attenuation) between the polyp and the luminal contents, polyps covered by fecal material are less conspicuous than polyps surrounded by air, even if oral contrast material has been administered. Figure 1A, 1B, 1C, 1D shows that the submerged polyp is less visible than the haustral fold in air at 40 mAs. Another factor that influences polyp conspicuity is radiation dose. Especially in low-dose scan protocols, the noise of CT images is prominent. In Figure 1A, 1B, 1C, 1D, this phenomenon is illustrated by the submerged polyp visible at 40 mAs but hardly visible at 5 mAs.


Figure 1
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Fig. 1A Influence of tagged material on visibility. 75-year-old man with colonic polyp. CT scan (40 mAs; window width, 1,250 HU; level, –50 HU) shows colonic wall and polyp (white arrow). Gray arrow indicates haustral fold in transverse colon surrounded by air.

 

Figure 2
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Fig. 1B Influence of tagged material on visibility. Simulated CT scans at tube charges lower than in A: 20 mAs (B), 10 mAs (C), and 5 mAs (D). White arrow indicates 6-mm polyp submerged in fecal material in descending colon proven at colonoscopy. Polyp is highly visible in A but hardly visible in D. In comparison, haustral fold in transverse colon surrounded by air (gray arrow) remains highly visible in D.

 

Figure 3
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Fig. 1C Influence of tagged material on visibility. Simulated CT scans at tube charges lower than in A: 20 mAs (B), 10 mAs (C), and 5 mAs (D). White arrow indicates 6-mm polyp submerged in fecal material in descending colon proven at colonoscopy. Polyp is highly visible in A but hardly visible in D. In comparison, haustral fold in transverse colon surrounded by air (gray arrow) remains highly visible in D.

 

Figure 4
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Fig. 1D Influence of tagged material on visibility. Simulated CT scans at tube charges lower than in A: 20 mAs (B), 10 mAs (C), and 5 mAs (D). White arrow indicates 6-mm polyp submerged in fecal material in descending colon proven at colonoscopy. Polyp is highly visible in A but hardly visible in D. In comparison, haustral fold in transverse colon surrounded by air (gray arrow) remains highly visible in D.

 
With regard to using CTC for screening, the goal should be the lowest possible patient burden and radiation dose. To our knowledge, the influence of the use of oral contrast material on the minimal radiation dose for qualitatively acceptable CTC has not been determined. We performed a phantom study to determine the magnitude of this effect.


Materials and Methods
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
Study Design
This phantom study consisted of two parts. The aim of the first phase was to determine the detectability of clinically relevant polyps (≥ 6 mm) in tagged material of various densities or in air as a function of the tube charge—that is, the product of tube current and exposure time divided by the pitch—in an idealized setup. We performed the second phase to translate the results of the first phase into clinically applicable performance values, such as sensitivity and number of false-positive findings.

Phantom
A cylindric water-filled polyethylene drum with a diameter of 34 cm was used to mimic the abdomen of a fairly obese patient (Fig. 2). We devised a synthetic colonic segment by placing a cylindric polymethyl methacrylate (PMMA) tube in the center of this drum. We positioned this phantom with the long axis of the tube parallel to the long axis of the drum. The tube contained eight PMMA rings with a thickness of 11 mm and an inner diameter of 50 mm in the order of the diameter of a distended colon segment. Each ring could contain a PMMA hemisphere with a diameter of 6 mm, mimicking a 6-mm sessile polyp. We chose 6 mm because it often is considered the smallest clinically relevant size for polyps [9]. All rings were separated by a thin PMMA ring (inner diameter, 40 mm; thickness, 2 mm), representing an artificial haustral fold.


Figure 5
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Fig. 2 Phantom (width, 1,250 HU; level, –50 HU). CT scan shows water-filled drum (1) with centrally placed polymethyl methacrylate cylinder (2), representing colon. Cylinder is filled with contrast material (3). Contrast between lumen and border is 480 HU. Filling defect represents 6-mm polyp.

 
We use the terms "contrast" and "contrast level" to indicate the difference in attenuation between polyps and contrast material or air in the lumen. The attenuation of PMMA is approximately 120 HU. We used PMMA because it is readily avail able and its attenuation is reasonably close to that of soft tissue. The tube was completely filled with either contrast material or air for each scan. The contrast material was a mixture of iodine (sodium amidotrizoate, 300 mg I/mL, hospital pharmacy) and water. We chose this concentration of contrast material so that the differences in attenuation between the polyp and the lumen would be approximately 300, 500, 800, and 1,000 HU. These attenuation values encompassed the range of contrast measured in tagged CTC examinations performed at our hospital with a regimen of 4 L of polyethylene glycol and 200 mL of 300 mg I/mL of meglumine ioxithalamate (Telebrix, Guerbet). Other regimens with similar attenuation have been described [10, 11].

CT Data and Preprocessing
We obtained scans of this phantom with a 64-MDCT scanner (Brilliance 64, Philips Health care) with the following parameters: 120 kV; collimation, 64; pitch, 1.2. Effective tube charge settings were used in steps of the square root of two from the lowest tube charge value available: 10, 14, 20, 28, 40, 56, and 80 mAs. In this way, the noise in the images decreased by a constant factor between successive values. For the first phase of the study, scans of the phantom filled with the four iodine mixtures and air were obtained with tube charge values increasing from 10 mAs until the value was reached at which all polyps were visible for all observers. Because we expected that the task for the observers would be more difficult for the second phase of the study, higher tube charge values (20–80 mAs) were used in this phase. In the second phase, only the two lowest con centrations were used. For each contrast level, a scan at 300 mAs was made for reference purposes. All images were reconstructed at a slice thickness of 0.9 mm and an increment of 0.45 mm with reconstruction filter C (sharper standard filter). The pixel size was 0.6 mm.

Measurement of Contrast and Noise
Because it is difficult to exactly obtain the intended contrast levels, for each intended contrast level we measured the actual contrast level, that is, the difference in attenuation between the wall of the colonic phantom and its content. We also measured the SD as a measure of noise in the images at the location of the polyps. This measurement of noise also was performed at the same position in a cross section of the drum that contained water only. This approach made it possible to determine the influence of the tagged material on noise. The measuring procedure is described in Appendix 1.

Observer Studies
Scans of the phantom were used to construct virtual colons for the observer studies. These colons consisted of a large number of rings separated by thin PMMA rings mimicking haustral folds. Before images of the virtual colons were presented to the observers, a research fellow assessed the visibility of the polyps for all contrast levels at the lowest tube charge setting (10 mAs). If the polyps could absolutely not be missed, the particular contrast level was not further evaluated by the observers. This measure was taken because a visibility threshold cannot be determined if all polyps are highly visible. For all other contrast levels, the visibility of polyps was determined in the first phase of the study.

Three observers, an experienced abdominal radiologist, a resident in radiology, and a research fellow reviewed all images. All observers had read more than 250 colonoscopic ally verified CTC examinations before this study. The observers reviewed the images using a 2D review method (ViewForum, Philips Healthcare) and indicated the location of the polyp with a cursor. All annotations were digitally stored. Because window and level settings can influence the conspicuity of submerged polyps [12], the window width and level were preset by two researchers at a setting deemed optimal for polyp detection at the given contrast level. These settings varied from 1,000/200 HU for contrast of 300 HU to 2,400/550 HU for contrast of 1,000 HU. The observers, however, were free to adjust the win dow setting to their preference. This procedure is in accordance with that used in the clinical evaluation of CTC scans.


Figure 6
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Fig. 3A Colonic phantom in first phase of study. CT scans (300 mAs; 300 HU; width, 1,000 HU; level, 200 HU) show polyp in one of eight possible locations. Half past one-o'clock position.

 


Figure 7
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Fig. 3B Colonic phantom in first phase of study. CT scans (300 mAs; 300 HU; width, 1,000 HU; level, 200 HU) show polyp in one of eight possible locations. Twelve-o'clock position.

 


Figure 8
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Fig. 3C Colonic phantom in first phase of study. CT scans (300 mAs; 300 HU; width, 1,000 HU; level, 200 HU) show polyp in one of eight possible locations. Half past ten-o'clock position.

 


Figure 9
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Fig. 3D Colonic phantom in first phase of study. CT scans (300 mAs; 300 HU; width, 1,000 HU; level, 200 HU) show polyp in one of eight possible locations. Nine-o'clock position.

 


Figure 10
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Fig. 3E Colonic phantom in first phase of study. CT scans (300 mAs; 300 HU; width, 1,000 HU; level, 200 HU) show polyp in one of eight possible locations. Half past seven-o'clock position.

 


Figure 11
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Fig. 3F Colonic phantom in first phase of study. CT scans (300 mAs; 300 HU; width, 1,000 HU; level, 200 HU) show polyp in one of eight possible locations. Six-o'clock position.

 


Figure 12
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Fig. 3G Colonic phantom in first phase of study. CT scans (300 mAs; 300 HU; width, 1,000 HU; level, 200 HU) show polyp in one of eight possible locations. Half past four-o'clock position.

 


Figure 13
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Fig. 3H Colonic phantom in first phase of study. CT scans (300 mAs; 300 HU; width, 1,000 HU; level, 200 HU) show polyp in one of eight possible locations. Three-o'clock position.

 
First Phase of Study
In the first phase of the study, we determined the visibility of the polyps in an eight-alternative forced-choice paradigm. In this paradigm a polyp always was present in each ring at one of eight possible locations (Fig. 3A, 3B, 3C, 3D, 3E, 3F, 3G, 3H), and the observers had to choose one of the eight locations. With this paradigm we could determine the visibility of polyps in a time-efficient way.

For every contrast level, a virtual colon was composed of 80 rings. Each virtual colon contained rings from scans made at five tube charge levels (10, 14, 20, 28, and 40 mAs), so each observer had to locate 16 polyps at each combination of tube charge and contrast. Each ring was rotated so that the polyp was present in one of eight possible clock-face positions on the phantom wall. The choice of location was made at random (Fig. 3A, 3B, 3C, 3D, 3E, 3F, 3G, 3H).

After the reading by the three observers, a researcher not involved in reading the data assessed the correctness of the annotations. On the basis of these annotations, the number and average percentages of correct responses were determined for every combination of tube charge level and contrast level. Psychometric curves with constant steepness were fitted to this average percentage of correct responses as a function of tube charge [13]. For the fitting we applied a maximum likelihood procedure [14] for every contrast level. At each contrast level we determined the tube charge for 90% correct responses and the SD of this estimate [15].

We also determined whether the number of correctly detected polyps increased significantly with the density of the contrast material. We counted the correctly detected polyps for each virtual colon for each observer and for the three observers combined. A chi-square test (SPSS 15.0, SPSS) was used for the comparison of proportions in two independent groups.

Contrast-to-Noise Ratio
The conspicuity of a polyp of a certain size depends both on the contrast of the polyp to its surroundings and on the noise in the image, quantified by the contrast-to-noise ratio (CNR) [16, 17]. For different contrast levels, the conspicuity at the tube charge for 90% correct responses is by definition the same. The CNRs at these tube charge levels should therefore also be equal. We checked whether this was indeed the case to cross-validate our results.

The SD of the attenuation is used as a measure of noise. The CNR at 90% correct responses was determined by dividing each contrast value by the SD for that contrast value at the tube charge for 90% correct responses. The SD can be considered inversely proportional to the square root of the tube charge [18]. Therefore, the SD at the tube charge for 90% correct responses can be derived from the SD in the 300 mAs reference scan as follows:

Formula
where mAs@90% is the tube charge value for 90% correct responses.

Second Phase of Study
Although in an eight-alternative forced-choice design, the tube charge value for 90% correct responses can be determined efficiently, no clinically applicable measures such as sen sitivity and number of false-positive findings can be determined. In the second phase of the study, these performance values were measured, and the threshold tube charge value for a sensitivity of at least 90% was determined.

The second phase was performed at the two lowest contrast levels, 300 and 480 HU, and scans were obtained at five tube charge levels between 20 and 80 mAs. For each contrast and tube charge level, three virtual colons were composed, each consisting of 120 rings (Fig. 4). Five percent (18 of 360) of these rings contained a polyp. Rings containing polyps were randomly distributed among the three colons. All rings were randomly rotated. Thus the virtual colons in the second phase of the study differed in three important aspects from those of the first phase: The prevalence of polyps was only 5%; in each ring the polyps were situated at any angle along the phantom wall; and colons were composed of rings scanned at the same tube charge levels.


Figure 14
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Fig. 4 Coronal section of part of virtual colon (24 of 120 rings) composed of scans at 80 mAs (width, 1,000 HU; level, 200 HU) for second phase of study. Contrast between colon and its contents is 300 HU. Arrow indicates 6-mm sessile polyp.

 
The same three observers as in the first phase evaluated the virtual colons starting at the level nearest the tube charge value for 90% cor rect responses determined in the first phase. The tube charge was increased until the level was reached at which the average per-polyp sensitivity of the observers was greater than 90%.

The observers knew that the polyps, if present, were of the same size and shape as in the first phase and were in random locations. The observers did not, however, know the polyp prevalence. After the reading, a researcher not involved in interpretation of the data assessed the correctness of the scores by comparing the true polyp locations with the annotations of the observers. For each contrast level, per-polyp sensitivity and the number of false-positive findings were determined for every tube charge value used. The tube charge value for 90% sensitivity was deter mined by linear interpolation.

Also in the second phase, we determined whether the number of correctly detected polyps significantly increased with the density of the tagging material (300 and 480 HU). In this case, we compared the total numbers of correctly detected polyps at 28 and 40 mAs for which data were available for both densities. This procedure was performed for each observer and for the three observers combined. The statistical procedure was the same as that used in the first phase of the study.

Ratio of Thresholds of the First and Second Phases of the Study
The eight-alternative forced-choice task of the first phase of the study was relatively easy. The second phase of the study was performed to obtain results closer to the reality of clinical practice, but the task in this phase was more difficult for the observers. The ratio of the tube charge value for 90% sensitivity (second phase) to the tube charge value for 90% correct responses (first phase) was determined as an indicator of the relative difficulty of detection of polyps in the second versus the first phase of the study. This ratio can be used to translate the thresholds to extrapolate the results of the first phase of the study to those of the more clinically orientated second phase. The significance of this ratio is elucidated in the Discussion section.


Results
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
Measurement of Contrast and Noise
The actual contrast values were close to the intended values. The actual values of contrast and SD are listed in Table 1. Table 1 shows that the SD, which is a measure of the noise at the location of the polyps, increases as the contrast level increases. For the highest contrast level (1,040 HU), the noise is approximately twice as high as for a phantom filled with air (SD, 70 and 33 HU, respectively).


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TABLE 1: Contrast Values and SDs at Locations of Polyps

 

Observer Study
The polyps in the air-filled colon were clearly visible at 10 mAs (Fig. 5). Consequently, this contrast level was not further evaluated.


Figure 15
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Fig. 5 Polymethyl methacrylate colon phantom in center of 34-cm-diameter water-filled drum. CT scan (10 mAs; width, 2,000 HU; level, 0 HU) shows 6-mm polyp (arrow) surrounded by air. Polyp was considered visible beyond doubt.

 
First Phase of Study
With increasing tube charge levels, the number of errors decreased. At contrast levels of 300, 480, and 790 HU, the observers correctly located all polyps at, respectively, 40, 28, and 20 mAs. The tube charges for 90% correct responses for the three observers combined were 24.0, 16.3, and 6.2 mAs for these three contrast levels (Fig. 6). At 790 HU, nearly all polyps were located correctly. The fitting procedure remained valid under these circumstances [14, 15], although the precision of the estimate was impaired. This phenomenon was evidenced by the much higher SD of the estimated threshold (Table 2). At 1,040 HU, all polyps were correctly located at all tube charge levels. Therefore, the tube charge value for 90% correct responses could not be determined for this contrast level.


Figure 16
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Fig. 6 Graph shows percentages of correct responses for each tube charge level for three lowest contrast levels. Data points are mean values for three observers. Ranges from lowest to highest scores are indicated. Curves are psychometric curves fitted to these data points. Dashed line indicates score of 90% correct. • = 300 HU, {blacksquare} = 400 HU, {blacktriangleup} = 790 HU.

 

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TABLE 2: Tube Charges for 90% Correct Responses Determined in First Phase of Study

 

For the 300, 480, and 790 HU contrast levels, the numbers of correctly detected polyps in each virtual colon (i.e., for the five tube charge levels combined) are listed in Table 3. Nearly all differences between contrast levels were significant.


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TABLE 3: Number of Polyps Correctly Detected in First Phase of Study

 

The CNRs at the tube charge value for 90% correct responses varied between 1.7 and 1.9, with an average of 1.8 (Table 2).

Second Phase of Study
Sensitivities and numbers of false-positive findings by the three observers combined at contrast levels of 300 and 480 HU are shown in Figure 7. Sensitivity increased with tube charge level and with the density of the contrast material. The sensitivity at a contrast of 300 HU exceeded 90% at 80 mAs and at a contrast of 480 HU exceeded 90% at 40 mAs. Using linear interpolation, we obtained tube charges for 90% sensitivity of 70 mAs and 35 mAs for 300 HU and 480 HU, respectively. At these tube charge levels, each observer had a maximum of one false-positive finding. For 300 and 480 HU, the total numbers of correctly detected polyps per observer at 28 and 40 mAs are listed in Table 4. All observers detected more polyps in the colon filled with the densest contrast material. This difference was statistically significant for two of the three observers and for all observers combined.


Figure 17
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Fig. 7 Graph shows sensitivity and number of false-positive findings at contrast levels of 300 HU (28–80 mAs) and 480 HU (20–40 mAs). Data points are average values for three observers. Sensitivity ranges from lowest to highest value are indicated. Horizontal dashed line represents 90% sensitivity. {blacksquare} = sensitivity at 480 HU, • = sensitivity at 300 HU, {square} = number of false-positive findings at 480 HU, {circ} = number of false-positive findings at 300 HU.

 

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TABLE 4: Total Number of Correctly Detected Polyps at 28 and 40 mAs Combined in Second Phase of Study

 

Ratio
The ratios of the tube charge for 90% sensitivity (second phase of the study) and the tube charge for 90% correct responses (first phase of the study) were 2.9 for 300 HU and 2.2 for 480 HU, with an average value of 2.5.


Discussion
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
The results of this CTC study show that the minimal radiation dose needed to visualize a 6-mm polyp increases considerably if the contrast between the polyp and its surroundings is reduced. Although all polyps in air were well visible at 10 mAs, approximately 70 mAs was needed to achieve 90% sensitivity at a contrast level of 300 HU.

We determined the minimal tube charge level to visualize a clinically relevant polyp in two study phases. The first phase was performed to obtain the threshold visibility in a simple and time-efficient way. It showed that if contrast was increased from 300 to 790 HU, the tube charge for 90% correct responses decreased from 24 to 6.2 mAs. The CNRs at these tube charge levels were nearly constant. This finding can be expected because the detectability of structures with relatively low contrast, such as polyps, is primarily limited by noise on the images [18]. With a 1.8 mean CNR at the tube charge for 90% correct responses, the tube charge level for 90% correct responses at the highest contrast (1,040 HU) and for air can be estimated to be 4 and 1 mAs, respectively.

We realized that extrapolation to a clinical setting is a problem with phantom studies. Therefore, we performed the second phase of the study to obtain results closer to the reality of clinical practice. Important points of the setup of the second phase are that only a few polyps were present, at uncertain locations, and that measures of practical clinical relevance could be determined. We expected that in this setup, the task for the observers in the second phase of the study would be more difficult than in the first phase. Our expectation turned out to be correct. In the second phase of the study, a sensitivity of 90% at 300 and 480 HU was obtained at, respectively, 70 and 35 mAs, with less than one false-positive finding per observer per tube charge level. Thus, this sensitivity was obtained at tube charge levels approximately 2.5 times higher than the corresponding levels in the first phase of the study.

This ratio depends on factors such as the number of locations in which a polyp can be present (only eight for the first phase of the study and at a large number of locations in the second phase), the certainty or lack of certainty that a polyp is present, and the possibility of choice (forced in the first phase of the study, free in the second phase). Thus this ratio reflects the relative difficulty of the tasks in the two phases, and the ratios can therefore be expected to be similar for each contrast level.

The independence of contrast level was also found by Burgess and Ghandeharian [19], who compared the percentage of correct responses in a two-alternative forced-choice study with those of alternative forced-choice studies with up to 1,800 possible locations. Therefore, we could have estimated this ratio using only one of the contrast levels in the second phase of the study. For cross check and to improve accuracy and precision, we decided to use two contrast levels. We could have performed the second phase of the study with a third contrast level (790 HU). However, we did not do so since nearly all polyps were visible at this contrast level in the first phase of the study. As a consequence, the precision of the threshold for the first phase was rather poor (Table 3). Using the ratio of 2.5, we can estimate that for the second phase of the study, the tube charges for 90% sensitivity should be on the order of 15, 10, and 3 mAs for contrast of 790 and 1,040 HU and for air.

Our results are for data from all three observers combined. Both observer studies showed interobserver variability. This finding is evident from the error bars in Figures 6 and 7. The results in Tables 3 and 4 show that systematic differences were present between observers. Yet the general trend is confirmed by the results for the individual observers, which consistently showed an increase in polyp detectability with an increase in the density of the tagging material. In most cases this increase was significant. We conclude that although individual thresholds may vary, the influence of tagged material on visibility is important.

A number of phantom studies and simulation studies have been conducted to determine optimal scan parameters for CTC [2027]. In all of those studies, the visibility of polyps was investigated in air only. Because of differences in study design and scan parameters, a comparison of these studies is difficult. The main finding is that all polyps 6 mm in diameter or larger are detected, even at the lowest tube charge levels (5 or 10 mAs). These studies are thus in line with our findings on polyps in air.

For this study we used the range of contrast levels measured in tagged CTC examinations at our hospital. Polyp detectability increases with the density of the tagging material. Aiming at even higher densities than used in this study may seem advantageous. It appears, however, that as contrast level increases, image noise increases as well (Table 1). This phenomenon is a consequence of the increased attenuation of x-rays in dense material. The increase in noise, also noted by Zalis et al. [28], counteracts the improved visibility owing to the higher contrast and may eventually lead to streak artifacts in the directions of the highest attenuation of the x-rays. For these reasons, striving for higher densities of tagging material than the ones used in this study may be of limited value.

Many factors contribute to the quality of CT images. In this study we varied the density of the contrast agent and the tube charge level. Other image-quality factors such as tube voltage, pitch, and slice thickness were left constant and were not subject to study. The conspicuity of polyps is also considerably influenced by the size of the patient. In this study we used a water-filled drum with a diameter of 34 cm, mimicking a rather corpulent patient. If we had used a smaller human phantom, the noise would have been lower, and therefore the same visibility of the polyps would have been obtained with lower tube charge values. In state-of-the-art scanners, dose modulation can be used in which the tube current can be automatically adapted to the size of a patient. The results of this study can be used to determine the reference setting for dose modulation.

With regard to ability to generalize our results to other CT scanners, it is important to realize that CT scanners differ in effective dose and image quality when scans are obtained with identical parameter settings. These differences have to be taken into account in translation of our threshold values to other scanners. The conclusion of our study, however, applies to any CT scanner.

The main factor in visibility of a polyp is its size. The size of a polyp correlates with its malignant potential [2931]. Polyps measuring 6–9 mm in diameter, especially polyps 10 mm in diameter and larger, are associated with increased risk of abnormal histologic findings. Polyps smaller than 6 mm can be disregarded because of minimal risk. This policy is endorsed by a CTC consensus proposal by Zalis et al. [9], which defines a normal colon as a colon without polyps larger than 5 mm, and a European Society of Gastrointestinal and Abdominal Radiology consensus statement [32] that a reasonable minimum size for reported polyps is 5 or 6 mm, depending on local preference.

We found that the visibility of polyps is substantially reduced when the polyp is submerged in tagged material with relatively low density. In practice, however, the overall per-polyp sensitivity would be affected less because not all segments are completely filled with tagged material, even if a regimen of reduced bowel preparation is undertaken. Owing to acquisition of prone and supine images, a polyp may not be surrounded by tagged material in both scan positions. We believe, however, that one should aim to visualize all relevant polyps and thus choose the scan parameters to reach this goal. Doing so means that the dose of the scan has to be increased in comparison with that of a scan in which the colon is completely cleansed. The higher dose level also may influence the visibility of extracolonic findings.

This study had limitations. Although the setup in the second phase was chosen to more closely resemble a clinical situation than did the first phase, it still is an idealization of real life. Polyp detection in patients can be more difficult than it was in the second phase of the study. Thus tube charge values needed in practice to adequately visualize 6-mm polyps may be somewhat higher than in the study.

A second limitation was that the colon phantom was made of PMMA. This material has an attenuation of approximately 120 HU, slightly higher than the 40-HU attenuation of colonic wall and polyps in vivo [33]. We reported polyp conspicuity as a function of the contrast, that is, the difference between the attenuation of polyps and that of the luminal content. Our results therefore also apply to these contrast levels in vivo in that each contrast level corresponds to slightly lower attenuation of the tagging material. Because the noise at the location of the polyp depends on the attenuation of the tagging material (Table 1), the noise would also be somewhat lower. One can calculate from the data in Table 1 that this difference is slight ({approx} 4%) and that the main outcome of our study remains unaffected.

A third limitation was that we considered detection of polyps only in a colon completely filled with contrast material. The increase in noise due to increased attenuation in the tagged material would be lower in a smaller lumen or a lumen only partly filled with tagged material. Therefore, in these situations, the visibility of the polyps for the same tube charge level would be somewhat better.

We used a homogeneous iodine solution to mimic colonic content because it completely covered the inner surface of the phantom. It is known, however, that different types of preparation produce tagging with varying degrees of heterogeneity [11]. Therefore, a fourth limitation was that the influence of heterogeneity of fecal material was not evaluated. Heterogeneity may have a negative effect on the visibility of colonic lesions. With inhomogeneous tagging, it can be expected that the tube charge values needed to adequately visualize a 6-mm polyp will have to be somewhat increased.

This phantom study is, to our knowledge, the first to show the negative influence of tagging on the detectability of polyps covered by tagged material. For adequate visualization of these polyps, a considerably higher tube charge level is needed than for polyps in a cleansed colon, especially when the density of the tagging material is low.


Figure 18
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Fig. 8A Measuring contrast level and noise. Graphs show mean (A) and SD (B) of attenuation in regions of interest with shape of concentric rings within lumen of phantom and within polymethyl methacrylate border. Circles indicate measured values; lines, fitted values. Value of contrast and SD at site of polyp was taken as difference between fitted values of contrast and SD for ring with diameter of 47 mm (indicated by dashed vertical line), on which each polyp is centered. SDs for regions of interest at 48 and 52 mm are high because these regions of interest contain pixels of both lumen and border. SD at 50 mm is higher than 100 HU and therefore not shown.

 


Figure 19
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Fig. 8B Measuring contrast level and noise. Graphs show mean (A) and SD (B) of attenuation in regions of interest with shape of concentric rings within lumen of phantom and within polymethyl methacrylate border. Circles indicate measured values; lines, fitted values. Value of contrast and SD at site of polyp was taken as difference between fitted values of contrast and SD for ring with diameter of 47 mm (indicated by dashed vertical line), on which each polyp is centered. SDs for regions of interest at 48 and 52 mm are high because these regions of interest contain pixels of both lumen and border. SD at 50 mm is higher than 100 HU and therefore not shown.

 
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APPENDIX 1: Procedure for Measuring Contrast Level and Noise

 


References
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
 

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