|
|
||||||||
Original Research |
1 Department of Radiology, Mayo Clinic Rochester, 200 First St. SW, Rochester,
MN 55905.
2 Department of Radiology, National Institutes of Health, Bethesda, MD
20892.
Received November 15, 2004;
accepted after revision January 4, 2005.
R. L. Summers has patents pending and awarded in the subject area of this
article.
Abstract
|
|
|---|
MATERIALS AND METHODS. A colon phantom containing 144 polyps of
varying sizes (5-12 mm) and shapes (flat, sessile, pedunculated) was scanned.
Polyp shape and distortion at virtual dissection were categorized as flame,
club, pea, or bizarre. Haustral fold distortion was graded. The CT
colonography examinations in 20 consecutive patients (colonoscopically proven
normal findings, n = 5; polyps
1 cm, n = 17 in 15
patients) were blindly reviewed by three radiologists using the virtual
dissection technique. The added benefits of double interpretation and
computer-aided diagnosis were tabulated.
RESULTS. Sessile polyps appeared flame (35/48 [73%]) or pea (11/48 [23%]) in shape. Flat polyps appeared flame-shaped (31/47 [66%]) or pea-shaped (16/47 [34%]). Pedunculated polyps were flame (15/45 [33%]), club (20/45 [44%]), or pea (6/45 [13%]) in shape. Axial distortion occurred along the longitudinal axis. The sensitivities of the three observers for polyps of 1 cm or more were 16/17 (94%), 14/17 (82%), and 15/17 (88%). The specificities were 5/5 (100%), 5/5 (100%), and 4/5 (80%). Sensitivities after double interpretation and computer-aided diagnosis improved but did not reach statistical significance.
CONCLUSION. Although distortion of colonic structures exists at virtual dissection, it does so in recognizable patterns, so that sensitivity for polyp detection is not compromised.
Keywords: colon polyps CT colonography virtual dissection
|
|
|---|
Virtual dissection is a new 3D rendering technique that draws a midline trace through the colon and displays the entire luminal surface of the colon as a flattened 2D image. The image produced is similar to a Mercator map and resembles the pathologic display of a resected colon specimen. Using this interpretation paradigm, the number of images required to view the luminal surface of the colon is dramatically reduced to a few images (depending on the preferred length of the colon displayed). Unlike conventional-perspective volume-rendered 3D endoluminal images, a tedious centimeter-by-centimeter fly-through is not required. Rather, the colonic lumen is viewed by sequentially looking at the colon segment by segment, similar to a barium enema. Furthermore, computer-aided diagnosis (CAD) can be applied to the same data set, potentially improving polyp detection. Double interpretation has also been proven to reduce interobserver variability associated with conventional CT colonography interpretation methods [6].
|
|
|
|
|---|
The CT data set of a previously studied colon phantom [6] was evaluated using virtual dissection software (Virtual Dissection, version 3.0.64q, GE Healthcare). The phantom is constructed of glass and contains 144 soft-tissue-attenuation polyps of different sizes (5, 7, 10, and 12 mm), shapes (flat, sessile, and pedunculated), and locations (on the fold, on the tip of the fold, on the base of the fold, and on the wall). The phantom was placed in a water bath simulating the body cavity and was scanned using a LightSpeed Ultra-8 CT scanner (GE Healthcare). Scanning parameters were 8 x 1.25 mm detector configuration, 2.5-mm slice thickness, 1.25-mm reconstruction interval, 120 kVp, 130 mA, 65 mAs, 13.5 mm/rotation table speed, and 0.5-sec tube rotation time. This technique is identical to our clinical CT colonography technique. The CT data were sent to a workstation (ADW 4.2, dual monitors, GE Healthcare) and viewed using the virtual dissection software. This requires a midline trace that is performed automatically with manual confirmation of its accuracy. If the midline trace is not accurately mapped, manual seed placement occurs.
Three-hundred-sixty degree virtual dissection images of the phantom (Figs. 1A and 1B) were assessed in an unblinded fashion for the presence and morphologic appearance of each polyp. On the basis of preliminary review, 3D polyp morphology was classified as having a flame, club, pea, or bizarre shape (Figs. 2A, 2B, 2C, and 2D). Haustral fold distortion was also noted as none, mild, moderate, or severe. The direction of distortion (axial, longitudinal, or both) in reference to the midline trace and the degree of distortion (none, mild, moderate, and severe) were recorded.
|
|
|
|
Three radiologists who had extensive experience with CT colonography (each having interpreted > 750 cases) reviewed the images in a blinded fashion using 360° virtual dissection software as the primary interpretation method; they noted the presence, size, and location of any lesions. Two-dimensional axial and multiplanar images and 3D endoluminal views were used for problem solving and to improve reviewer confidence. To evaluate the effectiveness of double interpretation, the individual interpretations of each radiologist were paired with those of each of the other two radiologists. Consensus interpretation was not used.
|
|
|
|---|
Table 1 summarizes the locations and amounts of haustral fold distortion. Mild haustral fold distortion usually occurred along the superior (top) and inferior (bottom) aspects of the virtual dissection image. Severe distortion (marked widening and contour irregularity) was most likely to occur in the middle of the haustral fold. Haustral distortion occurred more frequently and to a greater degree at a colonic bend or flexure. Nearly all folds (90%) had at least mild distortion along the longitudinal (midline trace) axis of the colon. No axial (perpendicular to the midline) distortion was observed.
|
Human Study
Sensitivities of the three radiologists for detecting the 17 proven
colorectal polyps or cancers of 1 cm or larger were 16/17 (94%), 14/17 (82%),
and 15/17 (88%), with specificities of 5/5 (100%), 5/5 (100%), and 4/5 (80%).
For the 20 polyps of 5 mm in diameter or larger, the sensitivities were 17/20
(85%), 15/20 (75%), and 17/20 (85%) with specificities of 5/5 (100%), 5/5
(100%), and 4/5 (80%).
|
|
|
|
|
|
|
|
Sensitivities using CAD alone for polyps of 1 cm or greater and 5 mm or greater were 12/17 (71%) and 13/20 (65%), respectively. False-positives existed in all cases; therefore, the specificity was 0. There were 1.3 false-positive findings per patient. The added benefit of using CAD combined with each of the three reviewers improved the sensitivity for a single reviewer from 14/17 (82%) to 16/17 (94%) for polyps 1 cm or larger. Two of three reviewers benefited from CAD for detecting lesions 5 mm or greater, with sensitivities improving 5-15% to 18/20 (90%), 18/20 (90%), and 17/20 (85%). One reviewer found no additional polyps (Fig. 6). The improved performance was not statistically significant.
|
|
|---|
When a proven phantom with optimal preparation (no stool, fluid, or motion artifacts and full distention) is used, polyps are detectable at virtual dissection. Image distortion occurs at virtual dissection because a 3D cylindric and curved structure is mapped as a 2D straight image. Polyps are distorted into recognizable patterns: flame, club, pea, or bizarre. Haustral folds are distorted least along the superior and inferior aspects of the virtual dissection image display. Haustral folds in the middle aspect of the image often appear enlarged and bulbous. Distortion occurs solely along the longitudinal axis of the colon. The phantom study indicates the high potential of this technique. Like all 3D endoluminal renderings, the usefulness of this technique likely depends on ideal preparation of the colon.
In patients, polyps 5 mm or larger in diameter were detected with a sensitivity of 75-85%. This detection rate is not significantly different from those in reports using conventional CT colonography interpretation methods [1, 9-11]. As an early feasibility study, these results are encouraging because a totally different paradigm for image review is required at virtual pathology. It is possible that with additional experience, diagnostic performance might improve.
The causes for error were investigated. All polyps were found in retrospect. This indicates a high potential for virtual dissection. An incomplete midline trace through the cecum accounted for one third of the false-negative examinations. Since the completion of our study the manufacturer has addressed this problem, and the midline trace nearly always extends the full distance of the colon automatically. In rare instances in which the trace is not extended to the base of the cecum, all the colonic mucosa should be manually reviewed.
Perceptive error accounted for two additional cecal errors. In one patient a cecal polyp was believed to be the ileocecal valve. This type of error occurred with conventional CT colonography interpretation methods early in the development of that technique. The normal valve will probably be readily recognized with more experience or by correlation with multiplanar reformatted 2D images. Another cecal polyp hidden behind a haustral fold was also overlooked. Careful inspection of each haustral fold must be performed to detect flat lesions and those that do not project markedly into the lumen. A diminutive polyp was overlooked in a partially collapsed cecum in a single patient. A single flat polyp in the sigmoid was difficult to identify.
Although interpretation times were not formally documented by all reviewers in this study, they were considered by our group to be highly variable. For those times recorded, interpretation times varied between 5 and 32 min. We believe that this was probably because of unfamiliarity with this technique, despite reviewer training. It is common that interpretation times can be long until confidence with the technique is gained.
Virtual dissection does require user input at two stages. The first stage is confirmation of the midline trace. If this is done automatically, it is quick and adds little extra time to the evaluation. However, if manual tracing is required and the colon is suboptimally distended, tracing can require considerable effort and time. For this reason, we elected to train registered technologists to trace the colons before interpretation. In this way, the radiologist can more rapidly assess the image for abnormalities.
Virtual dissection shows great promise in reducing the number of images to be interpreted. Cotton et al. [2] showed that 3D endoluminal images can increase the sensitivity for colorectal lesions at CT colonography by approximately 12%. Virtual dissection provides a parody for examining the colonic lumen, with only a few images that display entire colonic segments, dramatically reducing the time it takes to view 3D images of the colonic lumen. This markedly decreases the difficulty inherent in reviewing CT colonography examinations.
In summary, CT colonography using virtual dissection image display is a feasible and promising technique. Polyps and normal colonic anatomy are distorted but can be recognized with training. Virtual dissection addresses a fundamental problem of conventional CT colonography by reducing the number of images to review. Even at this early stage of its development, the estimated performance of virtual dissection is similar in sensitivity and specificity to in reports of conventional CT colonography. Polyp detection can be improved with the use of either double interpretation or CAD. Further study of this technique in larger in vivo studies should be encouraged.
|
|
|---|
This article has been cited by other articles:
![]() |
D. Hock, R. Ouhadi, R. Materne, A.-S. Aouchria, I. Mancini, T. Broussaud, P. Magotteaux, and A. Nchimi Virtual Dissection CT Colonography: Evaluation of Learning Curves and Reading Times with and without Computer-aided Detection Radiology, September 1, 2008; 248(3): 860 - 868. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. D. Johnson, J. G. Fletcher, R. L. MacCarty, J. N. Mandrekar, W. S. Harmsen, P. J. Limburg, and L. A. Wilson Effect of Slice Thickness and Primary 2D Versus 3D Virtual Dissection on Colorectal Lesion Detection at CT Colonography in 452 Asymptomatic Adults Am. J. Roentgenol., September 1, 2007; 189(3): 672 - 680. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. H. Kim, J. M. Lee, H. W. Eun, M. W. Lee, J. K. Han, J. Y. Lee, and B. I. Choi Two- versus Three-dimensional Colon Evaluation with Recently Developed Virtual Dissection Software for CT Colonography Radiology, September 1, 2007; 244(3): 852 - 864. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. H. Park, E. K. Choi, S. S. Lee, J.-S. Byeon, J.-Y. Jo, Y. H. Kim, K. H. Lee, H. K. Ha, and J. K. Han Polyp Measurement Reliability, Accuracy, and Discrepancy: Optical Colonoscopy versus CT Colonography with Pig Colonic Specimens Radiology, July 1, 2007; 244(1): 157 - 164. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. S. WERDERMAN CT Colonography Radiol. Technol., March 1, 2007; 78(4): 309CT - 324CT. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Mang, A. Maier, C. Plank, C. Mueller-Mang, C. Herold, and W. Schima Pitfalls in Multi-Detector Row CT Colonography: A Systematic Approach RadioGraphics, March 1, 2007; 27(2): 431 - 454. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. C. Silva, C. V. Wellnitz, and A. K. Hara Three-dimensional Virtual Dissection at CT Colonography: Unraveling the Colon to Search for Lesions RadioGraphics, November 1, 2006; 26(6): 1669 - 1686. [Abstract] [Full Text] [PDF] |
||||
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |