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Dual Energy Versus Single Energy MDCT Measurement of Radiation Dose Using Adult Abdominal Imaging Protocols

Rationale and Objectives

The aim of this study was to measure the radiation dose of dual-energy and single-energy multidetector computed tomographic (CT) imaging using adult liver, renal, and aortic imaging protocols.

Materials and Methods

Dual-energy CT (DECT) imaging was performed on a conventional 64-detector CT scanner using a software upgrade (Volume Dual Energy) at tube voltages of 140 and 80 kVp (with tube currents of 385 and 675 mA, respectively), with a 0.8-second gantry revolution time in axial mode. Parameters for single-energy CT (SECT) imaging were a tube voltage of 140 kVp, a tube current of 385 mA, a 0.5-second gantry revolution time, helical mode, and pitch of 1.375:1. The volume CT dose index (CTDI vol ) value displayed on the console for each scan was recorded. Organ doses were measured using metal oxide semiconductor field-effect transistor technology. Effective dose was calculated as the sum of 20 organ doses multiplied by a weighting factor found in International Commission on Radiological Protection Publication 60. Radiation dose saving with virtual noncontrast imaging reconstruction was also determined.

Results

The CTDI vol values were 49.4 mGy for DECT imaging and 16.2 mGy for SECT imaging. Effective dose ranged from 22.5 to 36.4 mSv for DECT imaging and from 9.4 to 13.8 mSv for SECT imaging. Virtual noncontrast imaging reconstruction reduced the total effective dose of multiphase DECT imaging by 19% to 28%.

Conclusion

Using the current Volume Dual Energy software, radiation doses with DECT imaging were higher than those with SECT imaging. Substantial radiation dose savings are possible with DECT imaging if virtual noncontrast imaging reconstruction replaces precontrast imaging.

Dual-energy computed tomographic (DECT) imaging is a computed tomographic (CT) imaging technique that uses two different kilovoltage energies nearly simultaneously during the same imaging session. Scanning at two different tube voltages has the potential to improve the characterization of various tissues because of the inherent changes in CT absorption parameters at different kilovoltage energies. Several applications for DECT scans in abdominal imaging are currently under investigation. DECT imaging has the potential to improve the detection of malignant liver tumors , enable the determination of urinary stone composition in vivo , and expedite the postprocessing of cardiac and abdominal CT angiography . Another potential application of DECT imaging is the capability to generate virtual noncontrast images reconstructed from postcontrast images by using iodine-subtraction techniques . Replacing the precontrast phase of a multiphase imaging protocol with a virtual noncontrast image reconstruction has the potential to reduce radiation dose effects as well as decrease imaging time.

The performance of DECT scans is currently vastly different for the various manufacturers of CT scanners . Volume Dual Energy (VDE) (GE Healthcare, Milwaukee, WI) is an investigative software package that can be added to an existing single-energy 64-detector CT scanner (LightSpeed VCT; GE Healthcare) and allow it to perform both single-energy CT (SECT) and DECT imaging without any additional hardware changes. This software enables a conventional (single-source) 64-detector CT scanner to produce two different kilovoltage energies nearly simultaneously during a single imaging acquisition. VDE works by rapidly switching between 80 and 140 kVp with each gantry rotation, while operating in axial cine mode.

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Materials and methods

CT Scanner and Imaging Protocols

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Imaging Protocols

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Table 1

Liver, Renal, and Aortic Imaging Protocols and Console Radiation Dosimetry for SECT Imaging

Liver Renal Aortic Parameter Precontrast Arterial Phase Portal Phase Delayed Precontrast Nephrographic Excretory Precontrast Arterial Phase Peak kilovoltage (kVp) 140 140 140 140 140 140 140 140 140 Amperage (mA) 385 385 385 385 385 385 385 385 385 Gantry revolution time (s) 0.5 0.5 0.5 0.5 0.5 0.5 0.5 0.5 0.5 Detector configuration 64 × 0.625 64 × 0.625 64 × 0.625 64 × 0.625 64 × 0.625 64 × 0.625 64 × 0.625 64 × 0.625 64 × 0.625 Longitudinal table coverage (cm) 20 20 20 20 28 12 28 32 32 Pitch 1.375 1.375 1.375 1.375 1.375 1.375 1.375 1.375 1.375 Field of view 50 50 50 50 50 50 50 50 50 CTDI vol (mGy) 16.19 16.19 16.19 16.19 16.19 16.19 16.19 16.19 16.19 DLP (mGy · cm) 420.4 420.4 420.4 420.4 549.9 290.9 549.9 614.6 614.6

CTDI vol , volume computed tomographic dose index; DLP, dose-length product; SECT, single-energy computed tomographic.

Table 2

Liver, Renal, and Aortic Imaging Protocols and Console Radiation Dosimetry for DECT Imaging

Liver Renal Aortic Parameter Precontrast Arterial Phase Portal Phase Delayed Precontrast Nephrographic Excretory Phase Precontrast Arterial Phase Peak kilovoltage (kVp) 140 140 80 140 140 140 140 140 80 140 140 80 Amperage (mA) 385 385 675 385 385 385 385 385 675 385 385 675 Gantry revolution time (s) 0.5 0.8 0.8 0.5 0.5 0.5 0.5 0.8 0.8 0.5 0.8 0.8 Detector configuration 64 × 0.625 64 × 0.625 64 × 0.625 64 × 0.625 64 × 0.625 64 × 0.625 64 × 0.625 64 × 0.625 64 × 0.625 64 × 0.625 64 × 0.625 64 × 0.625 Longitudinal table coverage (cm) 20 20 20 20 20 28 12 28 28 32 32 32 Pitch 1.375 1 1 1.375 1.375 1.375 1.375 1 1 1.375 1 1 CTDI vol (mGy) 16.19 35.61 13.82 16.19 16.19 16.19 16.19 35.61 13.82 16.19 35.16 13.82 DLP (mGy · cm) 420.4 712.2 276.9 420.4 420.4 549.9 549.9 997.1 387.1 614.6 1139.5 442.4

CTDI vol , volume computed tomographic dose index; DLP, dose-length product; DECT, dual-energy computed tomographic.

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Organ Dose Determination

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SECT Organ Dose Determination

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DECT Organ Dose Determination

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Effective Dose Determination

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Noise Analysis and Image Quality Measurements

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Results

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Table 3

Liver, Renal, and Aortic Protocols: Individual-Phase Effective Doses for SECT and DECT Imaging

DECT Imaging Protocol SECT Imaging (mSv) 140 kVp (mSv) 80 kVp (mSv) 80 and 140 kVp Together (mSv) Liver 9.4 ± 0.7 17.5 ± 0.6 5.1 ± 0.3 22.5 ± 0.6 Renal 13.1 ± 0.6 26.5 ± 0.5 7.6 ± 0.5 34.0 ± 0.7 Aortic 13.8 ± 0.7 28.5 ± 1.3 7.9 ± 0.4 36.4 ± 1.4

DECT, dual-energy computed tomographic; SECT, single-energy computed tomographic.

Figure 1, Bar graph shows organ dose values for dual-energy multidetector computed tomographic (DECT) imaging (black bars) and single-energy multidetector computed tomographic (SECT) imaging (gray bars) for organs with the highest dose values from an individual phase of the liver protocol. Numbers above each column represent absorbed doses; error bars are for 1 standard deviation; SECT and DECT organ doses for thyroid, thymus, bone marrow (BM)/ribs, lungs, BM/thoracic spine, esophagus, ascending colon, descending colon, BM/pelvis, uterus, and ovaries were <0.65 cGy.

Figure 2, Bar graph shows organ dose values for dual-energy multidetector computed tomographic (DECT) imaging (black bars) and single-energy multidetector computed tomographic (SECT) imaging (gray bars) for organs with the highest dose values from an individual phase of the renal protocol. Numbers above each column represent absorbed doses; error bars are for 1 standard deviation; SECT and DECT organ doses for right breast, thyroid, thymus, bone marrow (BM)/ribs, lungs, BM/thoracic spine, and esophagus were <0.03 cGy.

Figure 3, Bar graph shows organ dose values for dual-energy multidetector computed tomographic (DECT) imaging (black bars) and single-energy multidetector computed tomographic (SECT) imaging (gray bars) for organs with the highest dose values from an individual phase of the aortic protocol. Numbers above each column represent absorbed doses; error bars are for 1 standard deviation; SECT and DECT organ doses for right breast, thyroid, thymus, bone marrow (BM)/ribs, lungs, BM/thoracic spine, and esophagus were <0.12 cGy.

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Discussion

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Figure 4, Images obtained in a 52-year-old man with hepatitis C cirrhosis and hepatocellular carcinoma using a preset soft tissue window (window width, 350 Hounsfield units; window level, 40 Hounsfield units). Transverse, contrast-enhanced computed tomographic scans obtained of the liver during the late hepatic arterial phase at (A) 140 kVp and (B) 80 kVp demonstrate increased conspicuity of the tumor (curved arrow) on the 80-kVp image. This improved lesion detection comes at the cost of greater image noise at 80 kVp compared to 140 kVp. (C) Corresponding dual-energy virtual noncontrast image reconstruction. Additional transverse, contrast-enhanced computed tomographic scans obtained of the liver at the level of the portal vein demonstrate decreased enhancement of the portal vein (straight arrows) and decreased image noise at (D) 140 kVp compared to (E) 80 kVp. (F) Corresponding dual-energy virtual noncontrast image reconstruction.

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Conclusions

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Acknowledgment

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