Lin Zhang1,2, Gert Jan Pelgrim3, Jing Yan4, Hao Zhang1, Rozemarijn Vliegenthart3, Xueqian Xie1. 1. Radiology Department, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China. 2. Radiology Department, Shanghai General Hospital of Nanjing Medical University, Shanghai, China. 3. Department of Radiology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands. 4. Siemens Healthcare Ltd, Shanghai, China.
Abstract
PURPOSE: To investigate image quality and bronchial wall quantification in low- and ultralow-dose third-generation dual-source computed tomography (CT). METHODS: A lung specimen from a formerly healthy male was scanned using third-generation dual-source CT at standard-dose (51 mAs/120 kV, CTDIvol 3.41 mGy), low-dose (1/4th and 1/10th of standard dose), and ultralow-dose setting (1/20th). Low kV (70, 80, 90, and Sn100 kV) scanning was applied in each low/ultralow-dose setting, combined with adaptive mAs to keep a constant dose. Images were reconstructed at advanced modeled iterative reconstruction (ADMIRE) levels 1, 3, and 5 for each scan. Bronchial wall were semi-automatically measured from the lobar level to subsegmental level. Spearman correlation analysis was performed between bronchial wall quantification (wall thickness and wall area percentage) and protocol settings (dose, kV, and ADMIRE). ANOVA with a post hoc pairwise test was used to compare signal-to-noise ratio (SNR), noise and bronchial wall quantification values among standard- and low/ultralow-dose settings, and among ADMIRE levels. RESULTS: Bronchial wall quantification had no correlation with dose level, kV, or ADMIRE level (|correlation coefficients| < 0.3). SNR and noise showed no statistically significant differences at different kV in the same ADMIRE level (1, 3, or 5) and in the same dose group (P > 0.05). Generally, there were no significant differences in bronchial wall quantification among the standard- and low/ultralow-dose settings, and among different ADMIRE levels (P > 0.05). CONCLUSION: The combined use of low/ultralow-dose scanning and ADMIRE does not influence bronchial wall quantification compared to standard-dose CT. This specimen study suggests the potential that an ultralow-dose scan can be used for bronchial wall quantification.
PURPOSE: To investigate image quality and bronchial wall quantification in low- and ultralow-dose third-generation dual-source computed tomography (CT). METHODS: A lung specimen from a formerly healthy male was scanned using third-generation dual-source CT at standard-dose (51 mAs/120 kV, CTDIvol 3.41 mGy), low-dose (1/4th and 1/10th of standard dose), and ultralow-dose setting (1/20th). Low kV (70, 80, 90, and Sn100 kV) scanning was applied in each low/ultralow-dose setting, combined with adaptive mAs to keep a constant dose. Images were reconstructed at advanced modeled iterative reconstruction (ADMIRE) levels 1, 3, and 5 for each scan. Bronchial wall were semi-automatically measured from the lobar level to subsegmental level. Spearman correlation analysis was performed between bronchial wall quantification (wall thickness and wall area percentage) and protocol settings (dose, kV, and ADMIRE). ANOVA with a post hoc pairwise test was used to compare signal-to-noise ratio (SNR), noise and bronchial wall quantification values among standard- and low/ultralow-dose settings, and among ADMIRE levels. RESULTS: Bronchial wall quantification had no correlation with dose level, kV, or ADMIRE level (|correlation coefficients| < 0.3). SNR and noise showed no statistically significant differences at different kV in the same ADMIRE level (1, 3, or 5) and in the same dose group (P > 0.05). Generally, there were no significant differences in bronchial wall quantification among the standard- and low/ultralow-dose settings, and among different ADMIRE levels (P > 0.05). CONCLUSION: The combined use of low/ultralow-dose scanning and ADMIRE does not influence bronchial wall quantification compared to standard-dose CT. This specimen study suggests the potential that an ultralow-dose scan can be used for bronchial wall quantification.
computed tomographychronic obstructive pulmonary diseaseas‐low‐as‐reasonably achievablekilovoltiterative reconstructionadvanced modeled iterative reconstructionsignal‐to‐noise ratioCT volume dose indexwall area percentagewall thicknessregion of interest
INTRODUCTION
Airway quantification on computed tomography (CT) provides an estimate of bronchial remodeling and inflammation, which is associated with physiological parameters and symptoms in chronic obstructive pulmonary disease (COPD).
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The increasing concern on radiation exposure in clinical practice stimulates the new techniques to decrease radiation dose,
like peak kilovolt (kV) reduction and iterative reconstruction (IR).
Iterative reconstruction has been widely used for reducing radiation dose while improving image quality.
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Recently, due to the technical advances and natural tissue contrast between lung parenchyma and airway, the radiation dose of chest CT is possible to closer to that of chest x‐ray (approximately < 0.1 mSv).
,Whether the lower radiation dose affects the evaluation of COPD compared with conventional‐dose CT has become an important issue in COPD studies. Some studies showed no significant side effect of dose reduction on emphysema evaluation.
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For example, ultralow‐dose CT at a radiation dose equivalent to 5% of the standard dose (2.33 ± 1.54 mSv), although increasing the percentage of low attenuation area, was strongly correlated with standard‐dose CT, thus could be used to evaluate lung volume and density.
However, the reduction in radiation dose decreases the ability to display distal bronchi. Kirby et al. showed that the spatial resolution of 1‐2 mm in low‐dose CT (about 1.5 mSv) could identify the bronchi with an inner diameter greater than 2.5 mm.
While CT examination at higher radiation dose (11.2 mSv) could show small airways with a diameter of 0.8 mm.
In an ex vivo porcine lung specimen study when radiation dose decreased, the number of evaluable bronchial branches decreased, but measurement variability increased.
To the best of our knowledge, there are few studies investigating bronchial wall quantification using low/ultralow‐dose CT in the human lung.Low kV settings and advanced modeled iterative reconstruction (ADMIRE) have been recently introduced, available on third‐generation dual‐source CT systems.
Therefore, this study aimed to comprehensively validate the correlation between bronchial wall quantification and low/ultralow‐dose CT techniques, using an ex vivo human lung specimen.
MATERIALS AND METHODS
Specimen
An ex vivo lung from a formerly healthy nonsmoking male was used to evaluate the accuracy of bronchial measurements. The specimen size was about 19.5 cm long, 9.5 cm wide, and 7.5 mm high. The anatomy department of the medical school provided the specimen for research purposes.
CT protocols
We used a third‐generation dual‐source CT (SOMATOM Force, Siemens Healthineers) for noncontrast single energy scanning. This study evaluated four different acquisition protocols with an estimated CT volume dose index (CTDIvol) ranging from 3.41 to 0.17 mGy. In the standard‐dose protocol, 120 kV and 110 mAs/51 mAs (target/effective mAs) were applied in accordance with standard clinical practice,
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resulting in CTDIvol of 3.41 mGy. Three low/ultralow‐dose settings were used according to the pre‐defined CTDIvol, that is, 0.84 mGy (low‐dose: 1/4th of the standard dose), 0.33 mGy (low‐dose: 1/10th), and 0.17 mGy (ultralow‐dose: 1/20th). In each low‐ and ultralow‐dose setting, low kVs (70, 80, 90, and Sn100 kV) were applied. The Sn setting involves the prefiltration of the X‐ray beam by using a tin filter. This filter limits the range of the X‐ray energy spectrum reaching the scanned object.
The tube current was adjusted to fit the predefined CTDIvol for each tube voltage (Table 1). Other settings were kept constant across standard‐ and low/ultralow‐dose scans: matrix size 512 × 512, CARE Dose4D on, detector collimation 192 × 0.6 mm, rotation time 0.5 s (a slower gantry rotation speed for higher image quality),
slice thickness 0.6 mm, and field of view 177 mm (cover all the specimen). All the images were reconstructed using Qr40 kernel (a kernel especially for quantitative analysis) with ADMIRE levels 1, 3, and 5, including the full‐dose scan. We repeated each scan five times and performed a small translocation and rotation of the specimen in between to simulate variability among repeated clinical scans. Due to certain differences between the specimen and human lung, a few of the scans could not be reconstructed by software, therefore, airway data of the corresponding repeated scan were excluded from the analysis, while SNR and noise data were retained.
Table 1
Predefined CTDIvol and the corresponding multiple low‐kV and mAs settings.
Because of the limitation of scanning parameter setting of Force CT, the minimum target mAs under 90 kV can only be set to 10 mAs, and the corresponding CTDIvol was 0.26 mGy, which cannot reach 1/20th low‐dose setting, so we excluded the 90 kV at 1/20th low‐dose setting.
Predefined CTDIvol and the corresponding multiple low‐kV and mAs settings.CTDIvol denotes computed tomography volume dose index.Because of the limitation of scanning parameter setting of Force CT, the minimum target mAs under 90 kV can only be set to 10 mAs, and the corresponding CTDIvol was 0.26 mGy, which cannot reach 1/20th low‐dose setting, so we excluded the 90 kV at 1/20th low‐dose setting.
Evaluation method
A semi‐automated software (Thoracic VCAR, Advanced workstation 4.6, GE Healthcare) was used to perform bronchial wall measurement. A radiologist of 14 yr of experience who was unaware of the scan purpose and settings analyzed all images. The analyzing time interval between repeated scans was at least 15 days to avoid reader bias. We chose two points from the bronchial tree (the left main bronchus, and the distal of the posterobasal segmental lower lobe bronchus) to obtain a straightened image of the bronchus [Fig. 1(a)]. Then we selected seven points representing different diameters to outline the contour of the bronchus in the cross‐sectional images, and the cross‐section of the measured bronchus should be close to a round shape. B1 was in the left lower lobe bronchi, B2 in the next generation one third of the proximal bronchi, and so on. We marked the location of B1‐B7 in Fig. 1(b). The software automatically measured average wall thickness (WT) and wall area percentage (%WA). %WA was defined as (wall area)/(wall area + lumen area) × 100%. We showed multiple representative cross‐sectional images explaining how to segment and measure the bronchial wall in Fig. 2.
Fig. 1
(a) Three‐dimensional reconstructed image illustrating the bronchial tree of the posterobasal segment lower lobe bronchus with the centerline. (b) Straightened rendering image along the centerline. B1 is the proximal section of the left lower lobe bronchus. B2–B7 are the proximal measurable sections of each successive segment downward bronchi of the posterobasal segment of the left lower lobe.
Fig. 2
Measurement points of B1–B7 cross‐sectional images explained how the software segmented and measured wall thickness (WT) and wall area percentage (%WA).
(a) Three‐dimensional reconstructed image illustrating the bronchial tree of the posterobasal segment lower lobe bronchus with the centerline. (b) Straightened rendering image along the centerline. B1 is the proximal section of the left lower lobe bronchus. B2–B7 are the proximal measurable sections of each successive segment downward bronchi of the posterobasal segment of the left lower lobe.Measurement points of B1–B7 cross‐sectional images explained how the software segmented and measured wall thickness (WT) and wall area percentage (%WA).The measurement points across different scans were the same distance between the point and the left main bronchus bifurcation. Background signal‐to‐noise ratio (SNR) and noise were measured by placing a circular region of interest (ROI; area of 20 mm2) in the lumen of the left main bronchus.
Statistical analysis
The relationship between measurement values (SNR, noise, WT, and %WA) and protocol settings was evaluated by Spearman correlation analysis. The protocol settings consisted of radiation dose levels (3.41, 0.86, 0.33, and 0.17 mGy), kV settings (70, 80, 90, and Sn100 kV), and ADMIRE levels (1, 3, and 5). Image SNR and noise among the standard‐ and three low/ultralow‐dose settings, among different kV settings, and among different ADMIRE levels were compared using multivariate ANOVA. The difference of bronchial measurements (WT and %WA) among dose settings, kV settings, and ADMIRE levels were pairwisely evaluated using the Student–Newman–Keuls post hoc test. Agreement between each of the low/ultralow‐dose settings and the standard‐dose setting was evaluated using Bland–Altman analysis, in which the value of the standard‐dose setting was subtracted from the low/ultralow‐dose setting and then divided by the mean. Two statistical analysis packages were used (MedCalc 15.8, MedCalc Software and SPSS 19.0, IBM). A value of P < 0.05 was considered statistically significant.
RESULTS
Overview
In total, 108 sets of image reconstruction were accomplished. All the images did not show blocky pixelated at any ADMIRE level (Fig. 3). The semi‐automated software accurately segmented the external and internal contours of the bronchial wall, without the need for manual editing. From the proximal to the distal airway, mean WT decreased from 2. 0 to 1.3 mm and mean %WA increased from 49.8% to 81.3%.
Fig. 3
Axial images of the lung specimen. (a) Standard‐dose 120 kV/51 mAs, advanced modeled iterative reconstruction (ADMIRE) level 3. (b) 1/20 low‐dose Sn100 kV/47 mAs, ADMIRE 1. (c) 1/20 low‐dose Sn100 kV/47 mAs, ADMIRE 3. (d) 1/20 low‐dose Sn100 kV/47 mAs, ADMIRE 5. In these images, no blocky appearance in the high ADMIRE‐level image. The 1/20 low‐dose setting significantly increased the background noise compared to the standard dose. By using a higher ADMIRE level, the image noise was greatly compensated.
Axial images of the lung specimen. (a) Standard‐dose 120 kV/51 mAs, advanced modeled iterative reconstruction (ADMIRE) level 3. (b) 1/20 low‐dose Sn100 kV/47 mAs, ADMIRE 1. (c) 1/20 low‐dose Sn100 kV/47 mAs, ADMIRE 3. (d) 1/20 low‐dose Sn100 kV/47 mAs, ADMIRE 5. In these images, no blocky appearance in the high ADMIRE‐level image. The 1/20 low‐dose setting significantly increased the background noise compared to the standard dose. By using a higher ADMIRE level, the image noise was greatly compensated.
Influential factors on SNR, image noise, and bronchial wall quantification
SNR was significantly correlated with dose level, and ADMIRE level (correlation coefficient 0.716 and 0.546, respectively, P < 0.001), but not with kV (0.219, P = 0.003). Image noise was significantly correlated with dose level, and ADMIRE level (−0.716 and −0.546, P < 0.001), but not with kV (−0.215, P = 0.004). WT and %WA had generally no correlation with dose level, kV, or ADMIRE level (the absolute values of correlation coefficients < 0.3), and the details are shown in Table S1.
Pairwise comparisons of SNR and noise between dose settings, tube voltage settings, and ADMIRE levels
SNR and noise showed no statistically significant differences at different kV in the same ADMIRE level (1, 3, or 5) and in the same dose group (all P > 0.05). Details are shown in Tables S2 and S3.Pairwise comparisons of SNR and noise of the four dose settings are shown in Table 2, where measures of kV settings in the same low/ultralow‐dose scans without significant difference in variance homogeneity were pooled. Compared with the standard‐dose, SNR reduction was significant in 1/4th, 1/10th, and 1/20th dose setting (all P < 0.001). However, the SNR difference between 1/10th and 1/20th dose group was not significant at ADMIRE 3 and 5 (P = 0.058 and P = 0.116, respectively). There was a significant noise increase with decreasing CT dose (P < 0.001), the only exception being between standard‐dose and 1/4th dose setting at ADMIRE level 5 (P = 0.062).
Table 2
Pairwise comparisons of signal‐noise‐ratio (SNR) and noise for low/ultralow‐dose settings versus standard‐dose setting
ADMIRE level
Mean ± SD
P‐value
Standard dose
1/4th dose
1/10th dose
1/20th dose
Standard vs 1/4th
Standard vs 1/10th
Standard vs 1/20th
1/4th vs 1/10th
1/4th vs 1/20th
1/10th vs 1/20th
SNR
ADMIRE 1
121.13 ± 16.26
74.99 ± 13.13
45.56 ± 8.24
37.19 ± 7.08
<0.001
<0.001
<0.001
<0.001
<0.001
0.025
ADMIRE 3
167.57 ± 32.98
104.55 ± 19.93
62.08 ± 14.25
50.30 ± 12.31
<0.001
<0.001
<0.001
<0.001
<0.001
0.058
ADMIRE 5
242.02 ± 60.76
153.82 ± 34.03
91.21 ± 23.58
74.24 ± 22.19
<0.001
<0.001
<0.001
<0.001
<0.001
0.116
NOISE
ADMIRE 1
8.24 ± 1.09
13.45 ± 2.23
22.10 ± 3.48
27.17 ± 4.54
0.003
<0.001
<0.001
<0.001
<0.001
<0.001
ADMIRE 3
6.05 ± 1.17
9.70 ± 1.79
16.43 ± 3.08
20.41 ± 4.10
0.016
<0.001
<0.001
<0.001
<0.001
<0.001
ADMIRE 5
4.28 ± 1.13
6.66 ± 1.42
11.32 ± 2.49
14.15 ± 3.66
0.062
<0.001
<0.001
<0.001
<0.001
0.002
Results are described as mean ± SD and P‐value.
SNR represents signal‐to‐noise ratio; ADMIRE represents advanced modeled iterative reconstruction; and SD represents standard deviation
Pairwise comparisons of signal‐noise‐ratio (SNR) and noise for low/ultralow‐dose settings versus standard‐dose settingResults are described as mean ± SD and P‐value.SNR represents signal‐to‐noise ratio; ADMIRE represents advanced modeled iterative reconstruction; and SD represents standard deviationSNR showed significant differences between ADMIRE 1 and 5 (P = 0.001), between ADMIRE 3 and 5 (P = 0.023), but not between ADMIRE 1 and 3 (P = 0.170; Fig. 4). Noise showed significant differences between ADMIRE 1 and 5 (P < 0.001), between ADMIRE 3 and 5 (P = 0.029), and between ADMIRE 1 and 3 (P = 0.014; Fig. 5). Details are shown in Appendix Table 4.
Fig. 4
Signal‐to‐noise ratio (SNR) among different kV/mAs settings at advanced modeled iterative reconstruction (ADMIRE) levels 1, 3, and 5. SNR in ADMIRE 5 increased for all the kV/mAs settings. Using ADMIRE 5, Sn setting increased SNR in a low‐dose protocol (0.84 and 0.33 mGy), but reduced SNR in ultralow‐dose setting (0.17 mGy).
Fig. 5
Image noise for different kV/mAs settings at advanced modeled iterative reconstruction (ADMIRE) levels 1, 3, and 5. Using ADMIRE 5, image noise was lower than that in ADMIRE 1 and 3. Using tin filtration increased image noise for 1/20th dose scans, while combined with higher mAs and higher ADMIRE level decreased in image noise.
Table 4
Agreement of wall thickness (WT) and wall area percentage (%WA) between each of low/ultralow‐dose settings and standard‐dose setting evaluated by Bland–Altman analysis
Plot differences as %
Arithmetic mean
1.96SD
95% CI
Plots outside the interval/total plots
%WA 1/4
−0.0263
−5.4, 5.3
−0.365, 0.313
13/252
%WA 1/10
0.316
−5.4, 6.0
−0.0446, 0.677
10/252
%WA 1/20
0.538
−5.1, 6.1
0.128, 0.949
13/189
WT 1/4
−0.457
−12.0, 11.1
−1.185, 0.272
9/252
WT 1/10
0.367
−11.5, 12.2
−0.383, 1.117
11/252
WT 1/20
0.686
−14.2, 15.6
−0.408, 1.779
7/189
WT represents wall thickness; %WA represents wall area percentage; SD represents standard deviation; and CI represents confidence interval.
Signal‐to‐noise ratio (SNR) among different kV/mAs settings at advanced modeled iterative reconstruction (ADMIRE) levels 1, 3, and 5. SNR in ADMIRE 5 increased for all the kV/mAs settings. Using ADMIRE 5, Sn setting increased SNR in a low‐dose protocol (0.84 and 0.33 mGy), but reduced SNR in ultralow‐dose setting (0.17 mGy).Image noise for different kV/mAs settings at advanced modeled iterative reconstruction (ADMIRE) levels 1, 3, and 5. Using ADMIRE 5, image noise was lower than that in ADMIRE 1 and 3. Using tin filtration increased image noise for 1/20th dose scans, while combined with higher mAs and higher ADMIRE level decreased in image noise.
Pairwise comparisons of bronchial wall quantification in different dose settings
There were no significant differences in WT and %WA between each of the low/ultralow‐dose settings and standard‐dose setting or in pairwise comparison for the different low/ultralow‐dose settings (all P > 0.05; Table 3).
Table 3
Pairwise comparisons of wall thickness (WT) and wall area percentage (%WA) for dose settings
kV settings
Mean ± SD
P‐value
Standard dose
1/4th dose
1/10th dose
1/20th dose
Standard vs 1/4th
Standard vs 1/10th
Standard vs 1/20th
1/4th vs 1/10th
1/4th vs 1/20th
1/10th vs 1/20th
WT (mm)
70kV
1.71 ± 0.26
1.68 ± 0.25
1.70 ± 0.26
1.73 ± 0.29
0.463
0.815
0.664
0.617
0.243
0.505
80kV
1.71 ± 0.27
1.73 ± 0.26
1.71 ± 0.29
1.000
0.793
0.974
0.793
0.974
0.819
90kV
1.71 ± 0.25
1.73 ± 0.29
—
0.948
0.669
—
0.622
—
—
Sn100kV
1.72 ± 0.28
1.72 ± 0.27
1.74 ± 0.28
0.844
0.844
0.624
1.000
0.769
0.769
%WA
70kV
62.37 ± 11.43
62.04 ± 11.23
62.45 ± 11.37
62.53 ± 11.25
0.869
0.969
0.939
0.839
0.809
0.970
80kV
62.53 ± 11.10
62.49 ± 11.34
62.65 ± 11.06
0.939
0.955
0.890
0.984
0.951
0.935
90kV
62.34 ± 11.43
62.68 ± 11.15
—
0.989
0.880
—
0.869
—
—
Sn100kV
62.40 ± 11.24
62.54 ± 11.07
62.79 ± 11.17
0.989
0.934
0.837
0.945
0.847
0.902
Results were described as mean ± SD and P‐value.
WT denotes wall thickness; %WA denotes wall area percentage; SD denotes standard deviation
Pairwise comparisons of wall thickness (WT) and wall area percentage (%WA) for dose settingsResults were described as mean ± SD and P‐value.WT denotes wall thickness; %WA denotes wall area percentage; SD denotes standard deviation
Agreement of bronchial wall quantifications between standard‐ and each of low/ultralow‐dose settings
Agreement of bronchial quantifications (WT and %WA) between standard‐dose and each low‐dose settings (1/4th, 1/10th, and 1/20th low‐dose) is shown in Table 4 by Bland–Altman analysis. For WT, the mean difference (95% CI) was −0.456% (−1.185%, 0.272%), 0.367% (−0.383%, 1.117%), 0.686% (−0.408%, 1.779%), respectively. For %WA, the mean difference was −0.026% (−0.365%, 0.313%), 0.316% (−0.045%, 0.677%), and 0.538% (−0.128%, 0.949%), respectively.Agreement of wall thickness (WT) and wall area percentage (%WA) between each of low/ultralow‐dose settings and standard‐dose setting evaluated by Bland–Altman analysisWT represents wall thickness; %WA represents wall area percentage; SD represents standard deviation; and CI represents confidence interval.
Pairwise comparisons of bronchial quantification in kV settings
There was no significant differences in WT and %WA in pairwise comparisons of the four kV settings, at the same low‐dose and same ADMIRE level (all P > 0.05). The detailed table is not shown because bronchial wall values did not correlate with kV settings.
Pairwise comparisons of bronchial quantification at the three ADMIRE levels
In pairwise comparisons of WT, generally, no significant difference was observed, except for bronchus B2 between ADMIRE 1 and 5 (P = 0.019). In pairwise comparisons of %WA along B1 to B7 bronchi at ADMIRE levels 1, 3, and 5, no significant difference was observed, except for bronchus B2 and B6 between ADMIRE 1 and 5 (P < 0.05). There was no significant differences in WT and %WA between ADMIRE 1 and 3 or between ADMIRE 3 and 5 (all P> 0.05). Measures at different doses and kV settings were pooled.
DISCUSSION
Low‐dose chest CT has been clinically implemented for more than 20 yr.
Recently introduced ultralow‐dose CT with a radiation dose similar to chest X‐ray (approximately 0.15 mGy or 0.06 mSv) has been applied to pulmonary diseases.
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Studies for low/ultralow‐dose CT mainly focused on validation of image quality,
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disease detection, and dose reduction.
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Its application in thoracic imaging mainly on diagnostic confidence and detectability of pulmonary nodules,
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only a few on interstitial pulmonary disease,
pulmonary inflammation,
emphysema evaluation
, and airway assessment.
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The growing morbidity and mortality of COPD has given rise to suggestions for screening using low/ultralow‐dose CT in the at‐risk population for preventive treatment,
and to identify specific subgroups and exacerbation which may be amenable to therapy.
Therefore, we studied the image quality using low/ultralow‐dose CT, low kV settings, and ADMIRE levels, and analyzed the impact on bronchial wall quantification. We found that SNR and noise were significantly influenced by dose levels and ADMIRE levels, but not significantly influenced by kV settings. Dose, kV settings, and ADMIRE levels showed no obvious influence on bronchial wall quantification.Radiation dose, image quality, and diagnostic accuracy in low/ultralow‐dose CT need to be balanced. There is a disagreement on whether low/ultralow‐dose scanning affects CT measurements such as emphysema index,
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related to reduced image quality. A recent study showed that advanced CT techniques like tin filtration and IR were able to generate CT images with acceptable noise for quantification at ultralow‐dose (CTDIvol of 0.15 mGy) in COPDpatients.
For airway measurements, an ex vivo study showed that a low radiation dose (minimum of 0.25 mGy) did not influence measured airway parameters using IR.
An in vivo large animal study showed that ultralow‐dose CT protocols had small measurement differences of %WA and WT in small airways.
In our study, similar to previous results,
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%WA and WT were not significantly influenced by dose reduction, although the variability of measurements slightly increased. Due to acceptable image quality in ultralow‐dose setting, good contrast between the bronchial wall and adjacent lung tissue could help to obtain airway measurements close to the standard dose. Very few outliers may be explained by a lack of good tissue contrast affecting image segmentation in the proximal bronchus.ADMIRE allows to decrease radiation exposure by retrospectively eliminating increased image noise, and therefore retaining image quality.
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The ADMIRE level mainly controls the strength of noise reduction. Therefore, an increasing ADMIRE level should allow higher radiation dose reduction.
In our study, ADMIRE 5 resulted in improved SNR and lower noise in comparison to ADMIRE 1 and 3 with the same radiation dose, which confirms results from previous studies.
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Although the ADMIRE strength of 5 possibly had a higher amount of noise reduction, blocky appearance (losing detail in the image) of higher strength IR
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was not observed in our study, which may due to ADMIRE’s excellent noise reduction potential, the technology adopts a "statistical model" and iterative decoding chip to integrate the statistical data of virtual data domain, image domain, and model domain efficiently.
Through multiple iterations, the artifact was removed and the noise was reduced to achieve real‐time high‐definition iterative imaging.
Similar results could be found in the latest IR reconstruction studies of other venders.
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According to our results, interestingly, the higher ADMIRE level was associated with higher image SNR and lower image background noise. For the measurement of the airway, we found that the ADMIRE level had no significant influence on the measured values, which were in accordance with Leutz‐Schmidt’s study.
Furthermore, the measurement variability of %WA and WT was acceptable in the three low/ultralow‐dose settings.Low kV and spectral filtration allow dose reduction, but their effect on image quality and bronchial wall measurements need to be studied. Different kVp selection in low/ultralow‐dose chest CT can be used, namely 70 kV,
,
80 kV,
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90 kV,
Sn100 kV,
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and Sn150 kV.
A previous study showed that an Sn100kV setting yielded better image quality in comparison with 70 to 90 kV protocols at similar dose levels in the parasinal region.
In another anthropomorphic chest phantom study, Sn100 kV was found to be better than 70 kV for nodule detection and noise reduction in low/ultralow‐dose CT using ADMIRE 3 and 5.
A study of 1/10 dose (0.32 mSv) using Sn100 kV showed that subjective image quality was not statistically significantly different from the standard 3 mSv dose group.
In our study, image SNR and noise values and airway quantification values showed no obvious changes among kV settings at the same dose and the same ADMIRE level, although Fig. 4 showed a slight noise reduction in the 1/20 ultralow‐dose using Sn100kV and ADMIRE 5. In terms of diagnosis, low kV showed no significant difference from the standard dose in the bronchial wall measurement. We speculated that the result may be related to the scanned object.This study has limitations. First, although the ex vivo lung lacks radiation absorption by the thoracic cage, similar human lung specimens for structural evaluation have proved its usability for research.
We used CARE Dose4D to adjust tube current, and thus, exposure dose. Second, the measurements using standard dose were considered as the reference standard because it was impossible to dissect the lung specimen to obtain true values of the bronchial. Third, CTDIvol is an indirect measure but a surrogate indicating the radiation output of the CT system.
Fourth, our results need to be confirmed in clinical patient studies with regard to the impact on quantitative emphysema assessment before implementation in COPDpatients.
CONCLUSION
Ultralow‐dose settings increased image noise and slightly increased measurement variability, combined higher ADMIRE compensated for the increased noise caused by low‐dose while did not significantly influence the bronchial measurements. This specimen study suggests that an ultralow‐dose scan as low as 0.17 mGy is useful for bronchial wall quantification. If a patient study confirms these findings, ultralow‐dose settings could be used in COPDpatients.
AUTHOR CONTRIBUTION STATEMENT
Lin Zhang MD PhD made substantial contributions to the conception of the work, acquisition, analysis, interpretation of data, and drafting the work. Gert Jan Pelgrim MD PhD revised it critically for important intellectual content. Jing Yan PhD offered important technical support on the scanning. Hao Zhang MD PhD gave important suggestion of the manuscript. Rozemarijn Vliegenthart MD PhD gave important suggestion on statistics, and revised it critically for important intellectual content. Xueqian Xie MD PhD made final approval of the version to be published, and agreed to be accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.
CONFLICT OF INTEREST
The authors of this manuscript declare that they have no conflict of interest related to this study.
Informed Consent and Ethical Approval
Written informed consent was waived by the Institutional Review Board. Institutional Review Board approval was obtained.Data S1. Online supplementary.Click here for additional data file.
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