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Aquilion one 64

Manufactured by Toshiba
Sourced in Japan

The Aquilion One-64 is a computed tomography (CT) scanner manufactured by Toshiba. It is designed to capture high-resolution, three-dimensional images of the human body. The core function of the Aquilion One-64 is to provide healthcare professionals with detailed diagnostic information to support medical decision-making.

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3 protocols using aquilion one 64

1

Chest CT Scanning Protocol

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Chest CT was performed using four different CT scanners: Aquilion One-64 (Toshiba Medical Systems), Somatom Sensation-16 and Dual-energy Force (Siemens Medical Solutions), and Discovery HD 750 (GE Medical Systems). The scanning parameters were as follows: 120 kVp; 80–200 mAs; rotation time, 0.5 sec; field of view, 350×350 mm; detector collimation, 64×0.625 mm or 16×0.6 mm; and matrix, 512×512. Two different slice thicknesses of 3.0 mm (n=164) and 2.5 mm (n=15) were obtained, and the corresponding images were reconstructed using soft-tissue and lung kernels, respectively.
CT scanning was conducted during a single deep breath-hold, with the patient in a supine position. The scanning field extended from the level of the thoracic inlet to the level of the adrenal glands. First, a conventional plain CT scan was obtained, and then, an iodinated contrast agent was injected into the antecubital vein of the patient (Ultravist, Bayer Schering Pharma; dose, 1.5 ml/kg; injection rate, 3.5–4.5 ml/sec). Enhanced CT scans in the arterial and venous phases were obtained at 30 and 60 sec, respectively, after the injection of the contrast material.
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2

Abdominal Contrast-Enhanced CT Imaging Protocol

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Abdominal contrast-enhanced CT was performed using one of the following CT scanners: Toshiba Aquilion One-64 (Toshiba Medical Systems, Otawara, Japan) and Somatom Force CT Scanner (Siemens Healthcare). The scanning parameters were as follows: tube voltage, 120 kv; tube current, auto; detector collimation, 64 × 0.625 mm and 192 × 0.625 mm, respectively; field of view, 350 mm × 350 mm; pitch, 0.656 and 0.7, respectively; rotation time, 0.5 s; matrix, 512 × 512; slice interval, 3 mm; slice thickness, 3 mm; reconstructed section thicknesses, 3 mm. Triple-phase CT, which included a plain scan, arterial phase, and portal venous phase, was performed for each patient. The arterial and portal venous phase images were acquired at 30 s and 60 s, respectively, after the injection of contrast agent (1.5 mL/kg, 3.0–3.5 mL/s, Ultravist, Bayer Schering Pharma, Berlin, Germany) via a pump injector.
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3

Retrospective Study of Elective EVAR

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From January 2010 to December 2019, 1,523 patients with infrarenal AAAs who underwent elective EVAR at our single center were retrospectively reviewed. Patients with preoperative and postoperative CTA were enrolled in this study. The exclusion criteria were abdominal aortic dissecting aneurysm, ruptured AAA, isolated iliac artery aneurysm, history of aortic surgery, fenestration, and chimney technique. A total of 979 patients were included in this study. Ethical approval was obtained from the ethics committee of our hospital (B2021-063). The need to obtain informed consent from patients was waived due to the retrospective nature of the study.
Contrast-enhanced computed tomography (CT) was performed using Toshiba Aquilion One-64 (Version 3.1; Toshiba Medical Systems, Otawara, Japan) with 1-mm thickness slices. Triple-phase CT was performed, which included a plain scan, arterial phase, and portal venous phase. Arterial phase images were acquired 20–30 s after injection of contrast agent (Ultravist, Bayer Schering Pharma, Berlin, Germany).
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