In protocol B, ATCM was activated. To investigate the effect of ATCM on radiation dose and image noise, consecutive acquisitions were performed with the NI ranging from 3 to 8 for head and 9 to 15 for thorax and abdomen/pelvis. In protocol C, ATVS was additionally activated. To investigate the effect of clinical mode on radiation dose and image contrast, acquisitions were performed at all clinical modes. Besides, at each clinical mode, consecutive acquisitions were performed with the NI ranging from 3 to 8 for head and 9 to 15 for thorax and abdomen/pelvis.
Three cylindrical plastic vials (diameter, 10 mm; volume, 5 mL) containing iodine contrast (Iopamiro 370; Bracco Imaging, Italy) diluted with pure water at 2.5, 5, and 10 mg I/mL were prepared. These vials along with one vial containing pure water were accommodated at the posterior surface of each phantom at the level of the eyes for head, heart for thorax, and middle abdomen for abdomen/pelvis (Fig. 3).
Quantitative Image Quality Assessment
Circular regions of interest (ROIs) were manually drawn on uniform brain-equivalent areas for head, and soft tissue-equivalent areas for torso. Regions of interest were also drawn on bone-equivalent areas (Fig. 3). Regions of interest were drawn at the axial level superior to eyes for head, the middle heart level for thorax, and the middle abdomen level for abdomen/pelvis. The mean Hounsfield unit (HU) value obtained from each ROI was recorded. Image noise was measured as the standard deviation (SD) of the mean HU. Mean HU and SD were recorded from acquisitions performed with protocols A, B at all NIs, and C at all clinical modes and NIs. To reduce measurement error, each parameter was measured 3 times on 3 consecutive image slices.
The CNR of iodine (CNRI) was calculated as: CNRI = (HUI − HUST)/SDST, where HUI is the mean HU measured in 3 iodinated vials, HUST is the mean HU in brain or soft tissue equivalent areas, and SDST is corresponding image noise. The CNR of bone (CNRB) was calculated as: CNRB = (HUB − HUST)/SDST, where HUB is the mean HU in bone equivalent areas. The CNR of soft tissue (CNRST) was calculated as: CNRST = (HUST − HUw)/SDw, where HUw is the mean HU in the pure water vial, and SDw is the corresponding image noise. Quantitative image analysis was performed using the ImageJ image analysis software (1.52d; National Institutes of Health, Maryland).
Protocol B: The Effect of ATCM on Reference NI, Reference CNR, and Reference Radiation Dose
To investigate the effect of user-defined NI on image noise, NI versus image noise linear fits were generated. The fitting parameters were used to estimate the NI that generates images at a noise equal to images obtained with protocol A. This NI is designated hereafter as ATCM-reference NI (
CNRI, CNRB, and CNRST were calculated at all NIs. Polynomial fits of CNRI, CNRB, and CNRST versus NI were generated. The fitting parameters were used to estimate the CNRI, CNRB, and CNRST values for the
determined previously. These values are designated hereafter as
To calculate the percent radiation dose difference between protocols A and B (%DAB), the following equation was applied:
where ACTDIvol is the CTDIvol value prescribed by protocol A, and
is the CTDIvol prescribed by protocol B at
Protocol C: The Effect of ATVS on Reference NI and Reference Radiation Dose
CNRI versus NI in CTA, CNRB versus NI in BONE, CNRI versus NI in C+, and CNRST versus NI in C− were calculated at all NIs. Polynomial fits of NI versus CNRI, CNRB, and CNRST were generated. The fitting parameters were used to estimate the NI for the
values described previously. These NIs are designated hereafter as ATVS-reference NI for “CTA” (
), “Bone” (
), “C+” (
), and “C−” (
At each clinical mode, polynomial fits of CTDIvol versus NI were generated. The fitting parameters were used to estimate the CTDIvol at the ATVS-reference NI values described previously.
To calculate the percent dose difference between protocols A and C (%DAC), the following equation was applied:
is the CTDIvol prescribed by protocol C at the ith clinical mode, and kVp,
values that generate images of a similar CNR to images with protocol A.
Noise Index was linearly correlated to image noise. Association between CNR and NI and between CTDIvol and NI was determined using polynomial fitting. Correlation coefficients and P values were used to evaluate goodness of fit. All statistical computations were processed using MedCalc software package (Med-Calc Software, Ostend, Belgium).
Measured image noise in acquisitions with protocol A ranged across phantoms from 3.93 to 7.08 for head, 6.55 to 10.95 for thorax, and 6.82 to 10.56 for abdomen/pelvis. ACTDIvol ranged from 15.12 mGy to 46.26 mGy for head, 1.89 mGy to 4.53 mGy for thorax, and 3.21 mGy to 5.22 mGy for abdomen/pelvis (Table 3).
Measured image noise correlated strongly with NI across all phantoms and anatomical regions (Fig. 4, Table S1, Supplemental Digital Content, http://links.lww.com/RLI/A419). However, image noise tended to be lower than NI. This trend was more pronounced for thorax and abdomen. Typically, at NI equal to 15, image noise was 8.98 for thorax and 11.31 for abdomen/pelvis for neonate. Calculated
values in protocol B that generate images of similar noise to images in protocol A ranged from 3.86 to 5.81 for head, 10.74 to 13.11 for thorax, and 10.63 to 12.46 for abdomen/pelvis (Table 4). B(CTDIvol)NIRef recorded from acquisitions performed at
, ranged from 12.24 mGy to 57.59 for head, 1.58 mGy to 2.76 mGy for thorax, and 1.88 mGy to 3.49 mGy for abdomen/pelvis (Table 4).
CNRI, CNRB, and CNRST correlated strongly and decreased with NI (Fig. 5, Table S2, Supplemental Digital Content, http://links.lww.com/RLI/A419).
, estimated using the aS, bS fitting parameters of Table S2, Supplemental Digital Content, http://links.lww.com/RLI/A419, are reported in Table 5.
Percent dose difference (%DAB) between protocols A and B, across all phantoms and anatomical regions, are reported in Table 6.
User-selected NI in protocol C correlated strongly and decreased with CNRI, CNRB, and CNRST at all clinical modes, and across all phantoms and anatomical regions (Fig. 6 and Table S3, Supplemental Digital Content, http://links.lww.com/RLI/A419). Calculated
values that generate images of similar contrast to corresponding acquisitions of protocol B, are reported in Table 7. These values were calculated using the aK, bK, fitting parameters of Table S3, Supplemental Digital Content, http://links.lww.com/RLI/A419, and the
values of Table 5.
The ATVS-recommended kVp at each clinical mode varied on the user-selected NI. The ATVS-recommended kVp at the
values of Table 7 are reported in Table 8. In neonate, 80 kVp was recommended at all clinical modes and anatomical regions. In 1-year-old, 80 kVp was recommended most often, whereas 100 kVp was recommended in C+ and C− of head and abdomen/pelvis. In 5-year-old, 100 kVp was recommended most often, whereas 120 kVp was recommended in C+ and C− of head. In 10-year-old, 100 kVp was recommended in CTA, BONE, and C+ of thorax and abdomen/pelvis, and 120 kVp was recommended at all clinical modes of head and C− of thorax and abdomen/pelvis.
CTDIvol in protocol C correlated strongly and decreased with NI at all clinical modes, and across all phantoms and anatomical regions (Fig. 7 and Table S4, Supplemental Digital Content, http://links.lww.com/RLI/A419). These aM, bM fitting parameters were used to calculate the
at the ATVS-reference NI (Table 9). In CTA, calculated
ranged from 7.86 to 33.54 mGy for head, 0.61 to 1.26 mGy for thorax, and 0.87 to 2.67 mGy for abdomen/pelvis. In BONE, calculated
ranged from 11.79 to 52.27 for head, 0.88 to 1.69 mGy for thorax, and 0.69 to 2.21 mGy for abdomen/pelvis. In C+, calculated
ranged from 10.66 to 33.07 mGy for head, 0.54 to 1.47 mGy for thorax, and 0.85 to 2.57 mGy for abdomen/pelvis. In C−, calculated
ranged from 15.87 to 55.97 mGy for head, 1.57 to 3.71 mGy for thorax, and 1.67 to 3.86 mGy for abdomen/pelvis.
Percent dose difference (%DAC) between protocols A and C, across all phantoms and anatomical regions, are reported in Table 10.
This work presents data on radiation dose when modern ATCM and ATVS systems are activated in routine head and torso pediatric CT examinations. Our results on activation of ATCM demonstrate a dose reduction of up to 24% for head, 39% for thorax, and 41% for abdomen/pelvis compared with the REPs. Furthermore, our results on the additional activation of ATVS demonstrate a dose reduction, which varied on the clinical diagnostic task. CTA resulted to the highest dose reduction, which was up to 70% for head, 77% for thorax, and 76% for abdomen/pelvis compared with the REPs. This is owing to the increased iodine contrast at lower kVp. The increased contrast allows for higher noise levels to be tolerated, which in turn enable a substantial dose reduction. BONE resulted to a dose reduction, which was up to 22% for head, 66% for thorax, and 85% for abdomen/pelvis. C+ resulted to a dose reduction of up to 46% for head, 71% for thorax, and 79% abdomen/pelvis. In contrast-enhanced soft tissue examinations, such as chest or portal venous phase abdominal CT, detection and characterization of tissue lesions require a lower noise level compared with CTA studies. C− resulted to a dose increase of up to 21% for head and a dose reduction of up to 34% for thorax and 48% for abdomen/pelvis. In noncontrast examinations, the tolerated image noise might be even less compared with contrast-enhanced studies. Thus, the kVp and NI settings recommended by the ATVS system for thorax and abdomen/pelvis result to a lower dose reduction compared with contrast-enhanced studies. It is not known, however, why dose was increased in head acquisitions. Possible explanation might be that increased modulated mA values are required in that clinical mode to counterbalance the low inherent
in the brain. This merits further clinical investigation into whether ATVS might be applicable to pediatric noncontrast head CT examinations.
Several studies have demonstrated the advantages of using ATVS in body CT examinations of adult patients. Spearman et al15 on a multicenter study have shown that ATVS reduces radiation exposure by up to 56% in temporal bone CT and that dose reduction is profound in CT angiographic studies. Layritz et al17 have shown that the use of ATVS in coronary CTA reduces radiation dose by 39%, and Lee et al21 have reported that the use of ATCM and ATVS in contrast-enhanced liver CT of adults reduce radiation dose by up to 31%. In a study performed by Siegel et al22 on the effect of ATVS on radiation dose in pediatric contrast-enhanced thoracoabdominal CT, a dose reduction of 27% has been reported. Furthermore, Siegel et al23 have used 3 small-sized semianthropomorphic phantoms to investigate the effect of ATVS on radiation dose in pediatric abdominal CTA examinations. Radiation dose was reduced by 31%, 36%, and 44% for the small, medium, and large phantoms, respectively. The above studies have been reporting results using an ATVS system available from a single only vendor (Siemens Healthcare). To our knowledge, scarce data are available on the use of ATVS used by other CT vendors. Li et al14 have recently shown that ATVS in contrast-enhanced adult chest CT examinations results to a dose reduction of 31% without affecting image quality. Another important approach to reduce pediatric radiation dose is tin filtering. Weis et al24 have suggested that the use of additional tin filtering at 100 kVp significantly reduces radiation dose compared with 70 kVp and therefore should be preferred in non–contrast-enhanced pediatric chest CT, particularly when the main focus is evaluation of lung parenchyma.
A major contribution of this work is that we have determined the
values in ATCM-activated acquisitions that produce images of comparable noise to the images derived from the REPs (Table 4). To our knowledge, there is no published data on the effect of ATCM, which is based on the NI concept, on radiation dose, and image quality in pediatric CT. In NI-based ATCM, a higher NI will generate images of more noise, and CT acquisition will be performed at a lower mA, whereas a lower NI will generate images of less noise, and CT acquisition will be performed at a higher mA compared with the REP. Computed tomography operators may use the
values of Table 4 to generate images at a comparable noise and at a substantially reduced dose compared with the corresponding REP (Table 6).
One further major contribution of this work is that we have determined the
in ATVS-activated acquisitions that produce images of comparable CNR to the images derived from the REPs (Table 7).
values are proposed for each clinical imaging diagnostic task. When CT operators are asked to activate ATVS for a specific diagnostic task, they should input a
value. To our knowledge, there is no published data on what NI values should operators use in ATVS-activated acquisitions of pediatric CT. Moreover, there is no published data on the effect of
on radiation dose and image quality for different clinical diagnostic tasks. Computed tomography operators may use the
(Table 7) to generate images at a comparable CNR and at substantially reduced dose compared with the REP (Table 10).
One limitation of this study was that we did not verify our results in the clinical practice. However, it is not feasible to perform repetitive exposures to the same patient because of ethical issues. Moreover, a large number of patients are required to cover ages from newborns to adolescents to make interindividual comparisons. The physical anthropomorphic phantoms used herein facilitate the investigation of the effect of acquisition parameters on image quality and radiation dose in the same subject without considering ethical issues. Moreover, image quality was assessed only on the basis of objective quality measures. A subjective evaluation of the image quality from experienced radiologists would add useful input on the verification of the proposed
values. Scanning at 70 kVp has also been shown to reduce pediatric radiation dose compared with 80 kVp.25 However, the technology of the scanner used herein did not allow acquisition at this tube potential. The results presented herein refer to a single vendor and 4 clinical diagnostic tasks. It would be very interesting to apply the methodology presented in this study on scanners developed by other CT manufacturers and on more clinical diagnostic settings.
In conclusion, we have shown that the use of ATCM in pediatric head and torso CT reduces radiation dose without impairing image noise. The use of ATVS for a specified clinical diagnostic task reduces further radiation dose without impairing CNR. We suggest that ATCM should be activated in all pediatric examinations. Moreover, ATVS should be activated in all but head noncontrast examinations. The current results highlight the importance of using the ATCM and ATVS tools in the clinical routine for dose optimization in pediatric CT.
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optimization in CT; pediatric head and body CT; automatic tube current modulation; automatic tube voltage selection; image quality
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