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Variability of CT Attenuation Measurements in Virtual Unenhanced Images Generated Using Multimaterial Decomposition from Fast Kilovoltage-switching Dual-energy CT

Rationale and Objectives

To compare Hounsfield unit (HU) data obtained from true-unenhanced (TUE) and virtual-unenhanced (VUE) imaging obtained with a fast kv-switching dual-energy computed tomography (CT) scanner using multimaterial decomposition algorithm.

Materials and Methods

In this Institutional Review Board-approved, Health Insurance Portability and Accountability Act-compliant, retrospective cohort study, CT scans of 19 patients undergoing multiphasic renal protocol abdominal CT on a fast kv-switching dual-energy CT scanner were reviewed. CT numbers were measured on the matched TUE and VUE generated using a multimaterial decomposition algorithm with selective iodine suppression, and postcontrast images at predefined locations in seven organs. Six hundred sixty regions of interest were placed at 132 locations. Agreement was assessed with paired t test, Pearson’s correlation, and Bland-Altman analysis.

Results

Mean TUE and VUE measurements were not significantly different in the corticomedullary ( P = 0.25) or nephrographic ( P = 0.10) phases. There was a strong correlation between TUE and VUE CT numbers (corticomedullary: r = 0.90, nephrographic: r = 0.90, each P < 0.001). Discrepancies ≥5 HU occurred 46 times (35%, 46 of 132) in the corticomedullary phase and 44 times (33%, 44 of 132) in the nephrographic phase. Discrepancies ≥10 HU occurred in 7% (9 of 132 in both corticomedullary and nephrographic phases). Interphase, intrasubject VUE CT numbers were strongly correlated ( r = 0.93, P < 0.001), but discrepancies ≥5 HU (22% [29 of 132]) and ≥10 HU (2% [3 of 132]) occurred. There was no significant correlation between the true postcontrast CT number and the magnitude of VUE-TUE discrepancy ( r = −0.04, P = 0.6).

Conclusion

CT numbers on VUE images generated from fast kv-switching dual-energy CT scans strongly correlate with TUE CT numbers on a population basis, but commonly vary 5–9 HU on a per-patient basis.

Introduction

One of the principal advantages of dual-energy computed tomography (DECT) is its ability to derive material-specific information using material decomposition algorithms that analyze the change in attenuation of tissues between the low and high-energy scans . This enables differentiation of materials with a high atomic number (eg, iodine) from those with a low atomic number (eg, soft tissue, water). With fast kv-switching DECT, a “basis material decomposition algorithm” is used to generate material-specific information that enables selective identification of iodine on contrast-enhanced DECT and generation of virtual unenhanced (VUE) images . However, unlike with dual-source DECT, in which material decomposition is performed in image space, material decomposition with fast kv-switching DECT is performed in projection space, which has limited the ability of users to translate the VUE data into Hounsfield units (HU) .

An advanced material analysis algorithm known as multimaterial decomposition (MMD) has recently been made available for clinical use, and extends the material discrimination capability of fast kv-switching DECT to more than two materials . As opposed to VUE images generated using an iodine:water material basis pair, in which the image pixels containing iodine are removed, with MMD algorithm image voxels of iodine are replaced by voxels simulating the same volume and attenuation of blood that would have been displaced by the iodine . These images are referred to as material suppressed iodine (MSI) images, and they enable measurement of HU in the VUE images . If accurate, they would allow the translation of these virtual HU data into commonly used attenuation-based diagnostic algorithms (eg, renal mass and adrenal nodule characterization) that rely on specific HU criteria to discriminate benign from potentially malignant pathology .

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Materials and Methods

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Study Subjects

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CT Technique

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Image Analysis

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Effective Dose Estimation

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Statistical Analysis

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Results

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Table 1

Mean CT Numbers and Standard Deviations of TUE and VUE Data From Fast kv-Switching Dual-energy CT Using a Multimaterial Decomposition Algorithm

Organ TUE HU±SD Corticomedullary

VUE HU±SD_P_ Value Nephrographic

VUE HU±SD_P_ Value Aorta ( n = 19) 36.4 ± 6.1 36.7 ± 3.4 0.84 30.8 ± 3.6 0.002 \* Erector spinae ( n = 19) 42.0 ± 7.6 38.8 ± 7.4 0.19 39.5 ± 8.1 0.33 Kidney ( n = 19) 30.5 ± 3.3 29.7 ± 4.8 0.53 29.2 ± 3.8 0.24 Liver ( n = 19) 54.0 ± 7.1 49.3 ± 7.2 0.05 51.1 ± 5.6 0.18 Portal vein ( n = 19) 32.2 ± 6.6 31.8 ± 6.2 0.88 30.8 ± 5.7 0.51 Pancreas ( n = 19) 28.1 ± 9.3 27.7 ± 8.1 0.89 27.5 ± 7.6 0.82 Spleen ( n = 18) 44.1 ± 5.1 43.2 ± 4.4 0.58 43.6 ± 3.4 0.70 All organs ( n = 132) 38.1 ± 10.7 36.7 ± 9.4 0.25 36.0 ± 9.9 0.10

CT, computed tomography; HU, Hounsfield unit; SD, standard deviation; TUE, true unenhanced; VUE, virtual unenhanced.

P values are repeated univariate comparisons of TUE and VUE data.

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Table 2

Rate of Discrepancies of HU Measurements Between TUE and VUE Data, and Between Different Phases of Examination Derived From Fast kv-Switching Dual-energy CT Using a Multimaterial Decomposition Algorithm

Discrepancies < 5 HU Discrepancies ≥ 5 HU – < 10 HU Discrepancies ≥ 10 HU TUE vs VUE corticomedullary 58% (77/132) 35% (46/132) 7% (9/132) TUE vs VUE nephrographic 60% (79/132) 33% (44/132) 7% (9/132) VUE corticomedullary vs VUE nephrographic 76% (100/132) 22% (29/132) 2% (3/132)

CT, computed tomography; HU, Hounsfield unit, TUE, true unenhanced, VUE, virtual unenhanced.

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Table 3

Mean Differences (ie, Bias), Standard Deviations (±), and Limits of Agreement Between True Unenhanced and Virtual Unenhanced Data From Fast kv-Switching Dual-energy CT Using a Multimaterial Decomposition Algorithm

Organ Corticomedullary Phase Nephrographic Phase Mean Difference ±SD_P_ Value Limits of Agreement (Mean Bias with 95% CI) Mean Difference ±SD_P_ Value Limits of Agreement (Mean Bias with 95% CI) Aorta 0.6 ± 5.8 0.67 (-10.7, 11.9) 6.2 ± 6.0 <0.001 \* (-5.6, 18.0) Erector spinae 3.3 ± 6.0 0.02 \* (-8.5, 15.1) 2.3 ± 5.8 0.10 (-9.0, 13.6) Kidney 0.8 ± 3.2 0.29 (-5.4, 7.0) 1.3 ± 2.5 0.04 \* (-3.6, 6.1) Liver 4.3 ± 4.3 <0.001 \* (-4.2, 12.8) 2.8 ± 3.3 0.001 \* (-3.6, 9.3) Portal vein 0.3 ± 3.9 0.73 (-7.3, 7.9) 1.3 ± 4.8 0.24 (-8.0, 10.7) Pancreas 0.6 ± 5.6 0.66 (-10.4, 11.5) 0.8 ± 5.2 0.95 (-9.4, 11.1) Pancreas (LOG) \\ 0.003 ± 0.08 0.85 (0.7, 1.4) 0.004 ± 0.07 0.80 (0.7, 1.4) Spleen 1.1 ± 4.3 0.38 (-7.3, 9.6) 0.9 0.29 (-7.4, 9.2)

CI, confidence interval; CT, computed tomography; SD, standard deviation.

P values represent the statistical significance of mean differences.

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Table 4

Determination of Systematic Bias by Bland-Altman Approach: Correlation Between Absolute Differences and Average Hounsfield Unit Measurements Between True Unenhanced and Virtual Unenhanced Data Generated From Fast kv-Switching Dual-energy CT Using a Multimaterial Decomposition Algorithm

Organ Corticomedullary Nephrographic Aorta 0.41 0.08 Erector spinae 0.94 0.61 Kidney 0.71 0.48 Liver 0.73 0.22 Portal vein 0.58 0.15 Pancreas 0.004 \* 0.02 \* Pancreas (LOG) 0.34 \\ 0.06 \\ Spleen 0.06 0.37

CT, computed tomography;

Data are P values from Pearson correlation statistics.

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Figure 1, Bland-Altman plots in the corticomedullary (a) and nephrographic (b) phases.

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Discussion

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Acknowledgements

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