Acceptance Test and Clinical Commissioning of CT S
Acceptance Test and Clinical Commissioning of CT S
Acceptance Test and Clinical Commissioning of CT S
Received 13 December 2019 This study examined the clinical use of two newly installed computed tomography (CT) simulators
Revised 17 December 2019 in the Department of Radiation Oncology. The accreditation procedure was performed by the
Accepted 18 December 2019 Korean Institute for Accreditation of Medical Imaging. An Xi R/F dosimeter was used to measure
the CT dose index for each plug of the CT dose index phantom. Image qualities such as the
Corresponding author Hounsfield unit (HU) value of water, noise level, homogeneity, existence of artifacts, spatial
Minsoo Chun resolution, contrast, and slice thickness were evaluated by scanning a CT performance phantom.
([email protected]) All test items were evaluated as to whether they were within the required tolerance level. CT
Tel: 82-2-2072-4151 calibration curves━the relationship between CT number and relative electron density━were
Fax: 82-2-765-3317 obtained for dose calculations in the treatment planning system. The positional accuracy of the
lasers was also evaluated. The volume CT dose indices for the head phantom were 22.26 mGy and
23.70 mGy, and those for body phantom were 12.30 mGy and 12.99 mGy for the first and second
CT simulators, respectively. HU accuracy, noise, and homogeneity for the first CT simulator were
一0.2 HU, 4.9 HU, and 0.69 HU, respectively, while those for second CT simulator were 1.9 HU,
4.9 HU, and 0.70 HU, respectively. Five air-filled holes with a diameter of 1.00 mm were used for
assessment of spatial resolution and a low contrast object with a diameter of 6.4 mm was clearly
discernible by both CT scanners. Both CT simulators exhibited comparable performance and are
acceptable for clinical use.
accuracy, low-contrast resolution, image uniformity, and institute for CT simulation for radiotherapy. The accredita-
volume CT dose index (CTDIvol) are assessed in the ac- tion procedures were performed by the KIAMI during the
creditation process. The acceptance criteria for CTDIvol are acceptance testing stage of the CT simulators.
80 mGy and 30 mGy for adult head and abdominal scans,
respectively.7) In Europe, a reference level of 60 mGy for 1. S
can parameters and computed tomography
weighted CTDI was proposed for a routine head protocol.8) dose index
A similar accreditation program is performed in South
Korea by the Korean Institute for Accreditation of Medical The scan parameters were evaluated to confirm whether
Imaging (KIAMI). For this program, spatial resolution, low the kV and mAs set by users are appropriately and accu-
contrast resolution, linearity, image noise, and the pres- rately delivered by the CT simulators. An Xi R/F detector
ence of artifacts are evaluated along with CTDI for each (Unfors RaySafe AB, Billdal, Sweden) capable of measur-
9)
plug position. The CTDI acceptance criterion for each ing tube potential, dose, dose rate, pulse, pulse rate, dose/
plug position is much stricter in South Korea than those frame, time, half-value layer, and total filtration simultane-
stated by international guidelines. Although CTDIvol does ously was used for this purpose. Scan parameters are listed
10,11)
not imply the actual patient dose, CTDIvol can be used in Table 1, and the tolerance limits for the measurements
7-9)
for the verification and monitoring of imaging doses. were ±7% and ±10% for kVp and mAs, respectively. CTDI
Although several studies insist that noise is the primary was measured with dedicated a head and body CTDI
variable affecting image quality and diagnostic perfor- phantom (Fluke Corporation, Everett, WA, USA). An Xi CT
12,13)
mance, other quality indices should also be examined detector (Unfors RaySafe AB) and a black piranha Qual-
5,14)
for CT scanner assessment. ity Assurance (QA) meter (RTI Electronics AB, Moelndal,
Recently, two CT simulators were newly installed in our Sweden) were used. CTDIs for each plug position were
institute. The aim of this study was thus to evaluate the im- evaluated as to whether the measurement was within the
age quality and radiation dose of these CT simulators, and acceptable range (Table 2).
to ensure their clinical acceptance for use in radiotherapy
planning. 2. Image quality
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162 Hyun Joon An, et al:ATP and Commissioning of CT Simulator
slice thickness insert. The phantom was scanned with 120 as the standard deviation of HU for 4 ROIs and should be
kVp, 250 mAs, and a slice thickness of 10 mm, and was less than 5 HU. The existence of artifacts was subjectively
reconstructed with a standard reconstruction algorithm. evaluated by determining if reviewers could identify any
The Hounsfield unit (HU) of water, noise level, homogene- visible artifacts. In the image of the spatial resolution insert
ity, presence of artifacts, spatial resolution, contrast, and (Fig. 1c) where eight sets of five air-filled holes are imaged
slice thickness were evaluated in the reconstructed im- (with diameters of 1.75, 1.5, 1.25, 1.00, 0.75, 0.61, 0.5, and
2
ages. The mean and standard deviation of 4×4 cm regions 0.4 mm), reviewers should be able to discern all five holes
of interest (ROI) drawn in water were defined as the HU of each set at least 1.00 mm diameter in order to pass the
of water and noise level, respectively. The HU of water spatial resolution test. Six pairs of the low contrast inserts
should be between –7 HU and 7 HU, and the noise level (Fig. 1d) with diameters of 25.4, 19.1, 12.7, 9.5, 6.4, and 3.2
should be less than 7 HU. Homogeneity was calculated mm were filled with dextrose or sodium chloride solutions
of various densities with 2%–3% differentials in density be-
tween cavities. Reviewers must be able to identify the two
Table 2. CTDI measured with an Xi CT detector 6.4 mm spheres in the image in order to pass the low con-
Acceptable CTDI (mGy)
Phantom Location trast resolution test. The slice thickness as determined by
range CT SIM1 CT SIM2
measuring the distance of the aluminum strips should be
Head Center 24.8 mGy±35% 21.059 21.867
accurate within ±1 mm to pass the slice thickness test (Fig.
0° (12 o’clock) 28.7 mGy±35% 24.713 25.886
1e). Complete assessments were performed independently
90° (3 o’clock) 27.3 mGy±35% 23.079 24.597
180° (6 o’clock) 25.8 mGy±35% 21.146 22.633 by two KIAMI-trained reviewers.
270° (9 o’clock) 27.4 mGy±35% 22.520 25.375
Body Center 8.7 mGy±35% 7.362 7.383 3. Hounsfield unit curves and laser position
0° (12 o’clock) 18.4 mGy±35% 16.336 16.745
90° (3 o’clock) 18.5 mGy±35% 15.144 15.957
An electron density phantom (Model 62M; CIRS Inc.,
180° (6 o’clock) 18.1 mGy±35% 12.326 13.647
270° (9 o’clock) 16.3 mGy±35% 15.274 16.802 Norfolk, VA, USA) was used to acquire the HU value cor-
Both scans were taken with 120 kVp, 250 mAs, and 2.4 cm of slice responding to each tissue-equivalent insert. The phantom
thickness. Values are presented as mean±standard deviation. was scanned with a body scan protocol of 120 kVp, 213
CTDI, computed tomography dose index; CT, computed tomo
graphy; SIM1, the first CT simulator; SIM2, the second CT sim mAs, and 2 mm slice thickness. The acquired HU to elec-
ulator. tron density curve and the acquired HU to physical density
0.40 mm
Ave: 1.3 HU
SD: 4.0 HU 0.50 mm
0.61 mm
0.75 mm
1.00 mm
1.25 mm
Ave: 1.1 HU Ave: 1.1 HU 1.50 mm
SD: 3.9 HU SD: 3.9 HU
1.75 mm
Ave: -0.2 HU
SD: 4.9 HU b c
3.2 mm
6.4 mm
9.5 mm
12.7 mm
9.08 cm
19.1 mm
25.4 mm
a d e
Fig. 1. (a) A modular 76-410 AAPM computed tomography (CT) Performance Phantom (Fluke Corporation, Everett, WA, USA); CT slices
of (b) water Hounsfield unit (HU), noise level, homogeneity evaluation, (c) spatial resolution, (d) low contrast resolution insert, and (e)
slice thickness. Ave, average; SD, standard deviation.
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Progress in Medical Physics Vol. 30, No. 4, December 2019 163
Table 3. Physical characteristics and HU acquired during the clinical commissioning stage
Physical density Electron density Relative electron density
Plug bar description HU for CT SIM1 HU for CT SIM2
(g/mL) (×1023 electrons/mL) (relative to H2O)
Lung inhale 0.20 0.634 0.190 −795.3 −792.1
Lung exhale 0.50 1.632 0.489 −457.2 −458.8
Adipose 0.96 3.171 0.949 −65.2 −67.4
Breast (50% gland/50% adipose) 0.99 3.261 0.976 −33.3 −31.6
Muscle 1.06 3.483 1.043 50.6 50.2
Liver 1.07 3.516 1.052 56.3 59.2
Trabecular bone (200 mg/mL) 1.16 3.730 1.117 213.1 216.4
Solid dense bone (800 mg/mL) 1.53 4.862 1.456 867.8 868.2
HU, Hounsfield unit; CT, computed tomography; SIM1, the first CT simulator; SIM2, the second CT simulator.
curve were imported to the treatment planning system for and the homogeneity were –0.2 HU, 4.9 HU, and 0.69 HU,
dose calculation. respectively, for CT SIM1. These parameters for CT SIM2
A DORADOnova 3 laser system (LAP GmbH Laser Ap- were 1.9 HU, 4.9 HU, and 0.70 HU, respectively. All review-
plications, Lüneburg, Germany) along with a CARINAnav ers agreed that there were no visible artifacts as shown in
smart control system (LAP GmbH Laser Applications) Fig. 1b. Five air-filled holes with a diameter of 1.00 mm
for patient alignment were installed. A Wilke phantom and a low contrast object with a diameter of 6.4 mm were
was aligned using the DORADOnova 3 laser system, and clearly discernible for both CT simulators as shown in Fig.
scanned with 120 kV, 200 mAs, and a slice thickness of 1.25 1c, d, respectively. Thus, the CT simulators passed the
mm. The accuracy of the laser system was analyzed using spatial resolution assessment. The slice thicknesses for the
the tumorLOC program (Philips Medical System). aluminum strip were 8.9 mm and 9.1 mm, for CT SIM1 and
CT SIM2, respectively. All testing parameters were within
Results the required tolerance level (Fig. 1e).
1. Verification of scan parameters and computed 3. Hounsfield unit curves and verification of laser
tomography dose index position
The scan parameters set by users were correctly mea- The phantom manufacturer provided the physical den-
sured, showing average discrepancies of –1.28% and sity as well as the electron density for the designated mate-
–1.67% in kV, and –0.39% and –1.06% in mAs, for the first rials. The average HU values for each ROI according to the
CT simulator (CT SIM1) and the second CT simulator (CT material were comparable for both scanners. A relatively
SIM2), respectively. As shown in Table 1, the results of the large HU difference for the lung inhale insert (3.2 HU) and
scan parameter verification were tolerable for both CT sim- at the trabecular bone insert (3.3 HU) was observed, and
ulators as they were within the tolerance levels of ±7% and the complete results are summarized in Table 3. The aver-
±10% for kVp and mAs, respectively. The CTDI measure- age of HU values corresponding to each relative electron
ments are provided in Table 2. The head and body CTDIs density (RED) were imported into the treatment planning
for each chamber position were all within the tolerance system. The laser position was verified in three directions
limit for both CT simulators. as shown in Fig. 2. The difference between the laser posi-
tion and the groove center shown in the images was less
2. Image quality than 0.1 mm for both scanners.
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164 Hyun Joon An, et al:ATP and Commissioning of CT Simulator
a b c
Fig. 2. (a) Wilke phantom, (b) an axial slice, and (c) a coronal slice. The deviations between laser position and groove position in the
images are marked.
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Progress in Medical Physics Vol. 30, No. 4, December 2019 165
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166 Hyun Joon An, et al:ATP and Commissioning of CT Simulator
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