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Original Research |
1 Department of Radiology and Center for Imaging Science, Samsung Medical
Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
2 Department of Radiology, Seoul National University Hospital, 101 Daehangno,
Jongno-gu, Seoul 110-744, South Korea.
3 Institute of Radiation Medicine, Seoul National University Hospital, Seoul,
South Korea.
4 Department of Radiology, Konkuk University School of Medicine, Konkuk
University Hospital, Seoul, South Korea.
5 Interdisciplinary Program in Radiation Applied Life Science, Seoul National
University College of Medicine, Seoul, South Korea.
OBJECTIVE. The objective of our study was to compare the diagnostic performances of two commercial computer-aided detection (CAD) systems and a CAD system developed in our laboratory, which we refer to as an "academic CAD system," for polyp detection on CT colonography (CTC) and to assess the detection characteristics of the CAD systems.
MATERIALS AND METHODS. One hundred three polyps (48 polyps < 6 mm
and 55 polyps
6 mm; 45 sessile, 33 flat, and 25 pedunculated polyps) were
created. Each CTC data set was analyzed using two commercial CAD systems
(Computer Assisted Reader [CAR] and Polyp Enhanced View [PEV]) and one Hessian
matrix–based academic CAD system. Per-polyp sensitivities according to
polyp size and shape were compared among the three CAD systems. The average
number and causes of false-positives (FPs) were analyzed and compared.
RESULTS. Per-polyp sensitivity for all polyps was significantly
better for the academic CAD system (83.5%) than for both commercial CAD
systems (64.1%) (p < 0.01). However, the difference in per-polyp
sensitivity for polyps
6 mm was not significant (p > 0.017).
According to morphology, per-polyp sensitivities as determined with the CAR,
PEV, and academic CAD systems for flat, sessile, and pedunculated polyps were
51.5%, 57.6%, and 81.8%; 60.0%, 62.2%, and 84.4%; 88.0%, 76.0%, and 84.0%,
respectively. The average number of FPs was not significantly different
(p > 0.05); however, the distribution of the causes of FPs for the
three systems was significantly different (p < 0.001).
CONCLUSION. For polyps
6 mm, the three CAD systems showed
comparable perpolyp sensitivities. Although the number of FPs was not
significantly different, the distribution of the causes of FPs for each of the
CAD systems was significantly different.
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