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207 protocols using aquilion 64

1

Coronary CT Angiography Protocol

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Prior to CT acquisition, patients with a high heart rate, defined as >65 beats per minute, received oral oral β-blockers (metoprolol 50 or 100 mg, single dose, 1 h before examination), if tolerated. Depending on the residual kidney function, pre and post procedural measures were taken in order to prevent further deterioration. These measures included pre and post procedural hydration (dose and route depending on the patients residual kidney function) and moreover in hemodialysis patients the scan was performed on the day prior to the next dialysis session.
Examinations were performed with a 64-detector row CT Scanner (Aquilion 64, Toshiba Medical Systems, Tokyo, Japan) or a 320-detector row CT scanner (Aquilion ONE, Toshiba, Tokyo, Japan) as previously described [11 (link)].
Data analysis was performed by two experienced CT observers (Including JWJ). If there was no consensus between these two reviewers a 3rd independent reviewer was consulted. Data of all major epicardial segments (in the RCA segments 1–3; in the LAD segments 5–8; and in the LCx segments 11 and 13) was analysed as previously described. Significant CAD was defined as coronary luminal narrowing of ≥ 50% [11 (link)].
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2

Whole Lung CT Imaging Protocol

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Whole lung CT scans were obtained with a 32-detector row CT scanner (Aquilion 32, Toshiba Medical Systems) or a 64-detector row CT scanner (Aquilion 64, Toshiba Medical Systems) using the following technique: collimation, 1 mm; rotation time, 0.5 s; reconstruction thickness, 2 mm; and pitch (ratio of table travel per rotation to total beam width), 27 or 53, 120 kV. Automatic tube current modulation (z-axis modulation with the Real E.C. technique, Toshiba Medical Solutions) was used with the noise level set at10 SD. Each CT image was displayed and evaluated using a standard lung window (window width, 1600 HU; window level, −600 HU) and a mediastinal window (window width, 350 HU; window level, 50 HU) on a high-resolution monitor.
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3

Non-Contrast CT Evaluation of Abdominal VAT

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CT examinations were performed using a 64-slice CT scanner (Aquilion 64, Toshiba Medical Systems Co., Ltd., Tochigi, Japan) with a collimation of 64 × 0.5 mm, pixel size of 0.39 × 0.39 mm, gantry rotation time of 350 msec, and tube voltage of 120 kV. The protocol of premedication and CT scan have been described previously [8 (link)]. A noncontrast scan was performed at the level of the umbilicus in order to assess the abdominal VAT area. Only one slice at the umbilical level was captured for the sake of reducing radiation exposure. The reconstructed image data were analyzed by a computer workstation (Ziostation2, Ziosoft Inc., Tokyo, Japan).
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Dynamic CT for Hepatic TACE Guidance

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All 37 patients were examined with dynamic contrast-enhanced CT with a 64-channel MDCT scanner (Aquilion 64, Toshiba, Tochigi, Japan) before TACE. Images were reconstructed in a section thickness of 5 mm with 5-mm intervals.
Non-ionic contrast material, a bolus of 100 ml iopamidol (370 mg I/ml, Iopamiron 370; Bayer Healthcare, Osaka, Japan) was administered intravenously via typically an antecubital vein at a rate of 3 to 4 ml/second with a power injector (Auto Enhance A-60; Nemotokyorindo, Tokyo, Japan).
For setting the adequate starting time of hepatic arterial phase scanning, an automatic bolus-tracking program (Real prep, Toshiba) was used. A circular region of interest (ROI) with an area of 50 pixels was placed in the aorta at the level of the celiac axis. The hepatic arterial phase scan started automatically 22 second after the threshold enhancement of 50 HU was reached in the aorta with the bolus-tracking program. The portal venous phase scan started 75 second just after contrast material injection.
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5

Dynamic CT for Hepatic TACE Guidance

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All 37 patients were examined with dynamic contrast-enhanced CT with a 64-channel MDCT scanner (Aquilion 64, Toshiba, Tochigi, Japan) before TACE. Images were reconstructed in a section thickness of 5 mm with 5-mm intervals.
Non-ionic contrast material, a bolus of 100 ml iopamidol (370 mg I/ml, Iopamiron 370; Bayer Healthcare, Osaka, Japan) was administered intravenously via typically an antecubital vein at a rate of 3 to 4 ml/second with a power injector (Auto Enhance A-60; Nemotokyorindo, Tokyo, Japan).
For setting the adequate starting time of hepatic arterial phase scanning, an automatic bolus-tracking program (Real prep, Toshiba) was used. A circular region of interest (ROI) with an area of 50 pixels was placed in the aorta at the level of the celiac axis. The hepatic arterial phase scan started automatically 22 second after the threshold enhancement of 50 HU was reached in the aorta with the bolus-tracking program. The portal venous phase scan started 75 second just after contrast material injection.
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Noncontrast Lung CT Imaging Protocol

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Preoperatively, Aquilion 16 and Aquilion 64 (Toshiba Medical, Tokyo, Japan) were used to collect all noncontrast 3D CT images in the craniocaudal direction under the following conditions: X-ray tube voltage, 120 kVp; automatic tube current modulation, maximum of 500 mA; gantry rotation speed, 0.5 sec; and beam collimation, 1 mm or 0.5 mm. Using a high-spatial-frequency technique (FC 86 or FC52; Toshiba Medical), whole lung axial thin-section multidetector CT scans were reconstructed at the same increment with a section thickness of 1 or 0.5 mm.
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Cardiovascular CT Protocol for Imaging

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Data acquisitions were performed with a 64-detector row CT scanner (Aquilion 64, Toshiba Medical Systems, Tokyo, Japan) or 320-detector row CT scanner (Aquilion One, Toshiba Medical Systems, Tokyo, Japan) according to a previous described protocol [21 (link)]. In short, if the heart rate was higher than 65 beats per minute, oral or intravenous β blockers were administered, if not contra-indicated. In total, 60–110 mL non-ionic contrast material (Iomeron 400, Bracco, Milan, Italy or Ultravist 370, Bayer Schering Pharma AG Berlin, Germany) was administered followed by a saline flush with a flow rate of 5 mL/second. Thereafter, images were reconstructed at the best phase of the R–R interval. The average image size and voxel size of the datasets were 512 × 512 × 512 and 0.307 × 0.307 × 0.25 mm, respectively.
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8

Preoperative Pulmonary Vasculature Mapping

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Patients underwent CT pulmonary arteriography/venography (CTPA/V) using a 64-slice multi-detector CT (MDCT) unit (Aquilion-64, Toshiba Medical Systems, Tokyo, Japan) with injection of contrast medium (iodixanol, Visipaque 320, GE Healthcare, Cork, Ireland) after admission. Image data in DICOM format were imported into the Exoview system to complete the 3D reconstruction, with pulmonary bronchi, arteries, veins, and tumors marked out with different colors (Figure 2). Detailed parameters and procedures have been reported in our previous article (13 (link)). For each individual, careful preoperative planning was carried out by surgeons on the basis of the 3D reconstruction images to reduce the risk of unplanned injury of aberrant anatomical structures. Additionally, we briefly defined several variations of pulmonary vessels.
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9

CT-Guided Aspiration and Drainage

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After written informed patient consent, CT-guided aspiration or drainage of potentially infectious foci were performed on both inpatients and outpatients. Aspirations of thoracic, abdominal or musculoskeletal localization that yielded no fluid or less than 5 mL were not included. All CT studies were performed on a 64-slice CT-machine (Toshiba Aquilion 64, Toshiba, Neuss, Germany). Depending on clinical conditions, iomeprol (Imeron 400, 400 mg/mL Bracco Imaging, Konstanz, Germany) was injected at a flow rate of 2.5 mL/s. Thereafter, 40 mL saline solution was injected using the same flow rate. CT data acquisition was started in the portal-venous phase of enhancement. Image reconstruction was carried out at a slice thickness of 0.5 mm.
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Detailed CT Angiography Protocol

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Scanning and reconstruction protocol: All patients were scanned with 64-row multislice computed tomography system (Toshiba Aquilion 64; Toshiba Medical Systems; Japan). The imaging parameters were 120 kVp, 250 mA, 125 mAs with a collimation of 64 x 0.5 mm, and a rotation time of 0.5 seconds. Image reconstruction parameters were as follows: section thickness of 0.5 mm, overlapping steps of 0.3 mm, and field of view (FOV) of 120 mm 2 . After brain scanning without contrast administration, all patients were scanned with intravenous contrast application for enhancing intracranial vessels. An iodine contrast medium of 100 mL with a concentration of 300 mg Iodine per mL (Omnipaque® 300mg I/ml, Amersham health, Ireland) was used. Infusions were performed with an automatic injector system (Mallinckrodt automatic injector). The infusion rate was adjusted as 4 mL/sec. A bolus tracking method was used for synchronization of contrast medium and scanning time.
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