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Aquilion one 320 row

Manufactured by Toshiba
Sourced in Japan

The Aquilion One 320-row is a computed tomography (CT) scanner manufactured by Toshiba. It features a 320-row detector array that allows it to capture volumetric images of the entire organ in a single rotation. The Aquilion One provides high-resolution imaging capabilities for diagnostic purposes.

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3 protocols using aquilion one 320 row

1

Cardiac CT Imaging Protocol with Contrast

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Computed tomography was performed using an Aquilion One 320-row multi-detector computed tomography scanner (Toshiba Medical Systems, Japan). Imaging was triggered manually during the arterial phase and scan parameters were as follows: detector collimation 320 × 0.5 mm; tube current between 300 and 500 mA depending on BMI; tube voltage 100–120 kV; gantry rotation time 270 or 350 ms; and temporal resolution 135 or 175 ms. A 55 ml bolus of 100% iohexol 56.6 g/75 ml (Omnipaque 350) was injected at a rate of 5 ml per second into the antecubital vein, followed by a 20 ml bolus of a 30:70 mixture of contrast medium and saline, followed by a 30 ml bolus of saline. All patients underwent were prospective electrocardiogram gated scans. After image acquisition, raw data was exported, postprocessed, and analysed on a dedicated workstation (Vitrea Fx 6.6.2, Vital Images, USA).
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2

Optimizing Cranial CT Image Quality

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The patients were examined by the Toshiba Aquilion™ ONE 320-row helical CT machine (Toshiba Corp., Tokyo, Japan). The parameters of group A were set as 120 kV and 300 mA, group B as 100 kV and automatic milliamperes, and group C as 80 kV and automatic milliamperes. Iopamidol injection (Iopamidol) (Patheon Italia S.p.A., Ferentino, Italy; sub-packaging: BRACCO; approval no. NMPN J20150090) was used as the contrast agent. The concentration used was 370 mg iodine/ml, 25 ml of 0.9% sodium chloride was injected with an injection rate of 5 ml/sec. Scanning mode: Helical acquisition. The patient was guided to stay in the supine position with both hands naturally falling on both sides of the body; then the CT scan was performed for the patient's neck and head, from the level of the aortic arch to the level of the top of the head.
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3

MRgFUS for Painful Osteoid Osteoma

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We retrospectively evaluated patients treated with MRgFUS for superficial painful osteoid osteoma or osteoblastoma at our musculoskeletal interventional center between January 2012 and February 2021. Inclusion criteria were the procedural and clinical success and availability of pre- and post-procedural CT examinations performed at our musculoskeletal center. CT examinations were carried out using a 640-slice CT (Toshiba Aquilion ONE 320-row detector of 0.5 mm each), before and after treatment, during the regularly scheduled follow-up. Exclusion criteria were: (1) unavailability of CT images during follow-up at our Institution; (2) disease recurrence or MRgFUS procedural failure, due to an inadequate acoustic window.
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