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Brilliance ict 256 scanner

Manufactured by Philips
Sourced in United States

The Philips Brilliance iCT 256 is a computed tomography (CT) scanner that features a 256-slice detector configuration. It is designed to capture high-resolution images of the body's internal structures. The core function of the Brilliance iCT 256 is to provide detailed imaging data for medical professionals to support diagnostic and treatment-planning decisions.

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6 protocols using brilliance ict 256 scanner

1

CT Grading of Urinary Calculi

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Immediately after undergoing ultrasonography, all patients were examined using noncontrast helical computerized tomography (NCHCT) with a Philips Brilliance iCT 256 scanner (Philips Healthcare, Cleveland, OH). The CT value of each calculus was generated, as follows: Hounsfield units were measured for 3 different 0.02 cm2 regions of interest on each calculus. The average of the 3 measurements was used as the final CT value for each specific calculus. The CT values of the calculi were classified into 4 grades: below 400 Hu was grade 1, between 400 and 800 Hu was grade 2, between 800 and 1200 Hu was grade 3, and over 1200 Hu was grade 4.
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2

Trauma CT Scans for Hip Morphology

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A previously described cohort of 400 patients undergoing whole-body trauma computed tomography scans was retrospectively included [15 (link)]. All CT scans were screened for inclusion and exclusion criteria. Here, the presence of fractures, deformities, implants, and immature skeleton served as exclusion criteria. Patients were stratified for further analysis into four groups consisting of 100 scans (200 hips) each: (A) male under 60 years of age, (B) male over 59 years of age, (C) female under 60 years of age, and (D) female over 59 years of age. A detailed description of the cohort has been published previously [15 (link), 16 (link)].
Computed tomography scans were acquired using a Brilliance iCT 256 scanner (Philips Healthcare, Cleveland, OH, USA) and a standardized trauma-scan protocol was used. Radiographic data was deposited in a picture archiving and communication system (PACS) and analyzed using a PACS client (IMPAX EE; AGFA HealthCare GmbH, Bonn, Germany). Two independent observers performed radiologic measurements after a training-series of 10 cases. In 10% of all cases repeated measurements were performed by observer one and two 3 months after the first analysis, blinded to the previous results; intra- and interrater reliabilities were calculated.
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3

Cardiac-Gated CT Angiography Protocol

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All scans were acquired with a 256-slice CT scanner (Brilliance iCT 256 scanner, Philips Healthcare, Eindhoven, The Netherlands). A total of 100 mL of contrast agent was intravenously administered at 5 mL/s. Scan acquisition was performed during the arterial phase, using bolus triggering at a threshold of 150 Hounsfield units in the distal descending thoracic aorta during a single inspiration breath hold after performing a standard breathing exercise. Scan parameters were as follows: tube voltage, 100–120 kV; current time product, 157–1551 mA∙s; slice thickness, 0.9–1.5 mm; slice increment, 0.4–1.0 mm; rotation time, 0.27–0.33 s; collimation, 128 × 0.625; pitch factor of 0.18 or 0.30, reconstruction matrix 512 × 512 pixels (iDose).
By means of retrospective gating, 8 or 10 equally sized phases of the cardiac cycle were obtained from 0% to 87.5% (12.5% intervals) or 0% to 90% (10% intervals) of the RR interval, respectively. Previous investigation has shown that displacement quantification on ECG-gated CT scans of 8- and 10-phase reconstructions can be accurately compared with an accuracy of 0.05 mm and interobserver variability of median 0.00 mm (−0.03 to 0.03 mm, intraclass correlation coefficient, ICC 0.839 p < 0.01) and an intraobserver variability of median 0.00 mm (−0.02 to 0.02 mm, ICC 0.853 p < 0.01) [15 (link),24 (link),28 ].
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4

Laryngeal CT Imaging Protocol for Tumor Profiling

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Laryngeal CT images were acquired rapidly during a single breath-hold in the craniocaudal direction. All patients were scanned using a Philips Brilliance-iCT256 scanner. The scanning parameters were as follows: tube voltage, 120 kV; tube current, 250mA; field of view (FOV), 500 mm; matrix, 512 × 512 mm; and scan thickness, 0.9 mm. For the enhancement scan, 60–80 mL of non-ionic contrast agent was injected through the elbow vein using a high-pressure syringe (iodixanol, 320 mg/ml, Byer, 1.5 mL/kg and 2 mL/s). A free-hand, phase-based, individualized ROI outlining the whole tumor profile was manually and independently drawn on contrasted images by two radiologists, and the CT value was automatically generated. In this study, the metastatic lymph nodes were not included in ROI.
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5

Chest CT Imaging with Contrast

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The Philips Brilliance 256 iCT scanner was used for chest scans without and with contrast for all 27 patients. Scan parameters include tube voltage 120 kVp, automatic tube current modulation, 1.0–1.5 mm thickness thin layer reconstruction. Lung window: window width 1600HU, window level -600HU; mediastinum window: window width 400HU, window level 40HU. The scan with the contrast used a nonionic contrast medium, i.e. 70-90ml of iohexol or iopromide (300 mgI/mL), the velocity at 3.5 ml/s, and scans for the arterial phase and the venous phase was performed 25–30s and 60–65s respectively after injection of the contrast medium.
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6

CT Imaging Protocol for Thoracic Assessment

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CT images were acquired using a TOSHIBA Aquilion 4-row spiral CT scanner and a Philips Brilliance 256 iCT scanner. Unenhanced and enhanced examinations were performed. During unenhanced CT scanning, the patients held their breath after deep inspiration. The scanning parameters were as follows: pitch of screw 1, slice thickness and layer distance 1–2 mm, matrix 512 × 512, tube voltage 120 kV, tube current 300 mA, and scanning range from the apex pulmonis to below the diaphragm. In enhanced scanning, a contrast agent (Ultravist solution, 150, 300, 300 mgI/ml) was injected through the hand dorsal vein or ulnar vein at a dose of 1.5 ml/kg of body weight with an injection rate of 3–3.5 ml/s by a power injector (Medrad VCT610, Kanggao Industrial Co., Ltd., USA or YOUWO Bliztwing, Guangzhou Youwo Medical Co., Ltd., China). Imaging of the arterial phase was acquired by a 25-second delay from the beginning of contrast agent injection, and imaging of the venous phase was acquired by a 75-second delay. A filter backprojection algorithm was used for imaging reconstruction. A high-resolution algorithm was used in the lung window, with a window width of 1,250 HU and a window level of 500 HU. A standard algorithm was used in the mediastinal window, with a window width of 250 HU and a window level of 40–60 HU.
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