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Automatic bolus tracking program

Manufactured by Canon
Sourced in Japan

The Automatic bolus-tracking program is a software tool designed to automatically track and monitor the injection of contrast media during medical imaging procedures. It provides real-time data on the timing and distribution of the contrast agent within the patient's body, enabling healthcare professionals to optimize the imaging process.

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2 protocols using automatic bolus tracking program

1

Abdominal MDCT Contrast Protocol

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All examinations were performed on an MDCT scanner (Aquilion 64, Canon medical systems, Ohtawara, Tochigi, Japan) using the following parameters: 1-mm section thickness and interval, 0.5 s rotation time (fixed), 120 kVp tube voltage, and under automatic exposure control with a noise index of 10. Nonionic contrast medium containing an iodine concentration of 300 mg/mL (Omnipaque 300; Daiichi Sankyo, Tokyo, Japan) at a dose of 2 mL per kg of BW was injected into the antecubital vein using a power injector (Nemoto DUAL SHOT Type D, Tokyo, Japan) with a fixed injection duration of 30 s. The scan delay for arterial and portal venous phase imaging were determined using an automatic bolus-tracking program (Canon medical systems). Scanning for the arterial and portal venous phases was started automatically 20 and 60 s, respectively, after the trigger threshold (100 HU) was reached at the level immediately above the celiac trunk. Pre-contrast images and equilibrium phase images were also obtained for all patients; for the equilibrium phases, a fixed-time delay of 180 s was applied. However, pre-contrast and equilibrium phase images were not evaluated in this study.
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2

Low-Radiation Abdominal CT Imaging Protocol

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All scans were performed using a 320 row multidetector CT scanner (Aquilion ONE PRISM; Canon Medical Systems, Otawara, Japan) with the following parameters: 80 row × 0.5 mm, pitch of 0.813, 0.6 s rotation time (fixed), 120 kVp tube voltage, and automatic exposure control with a noise index of 20. The standard care of abdominal CT in our hospital is the MBIR protocol (FIRST BODY Mild), which is designed for low exposure, with a mean volume CT dose index (CTDIvol) of 7.9 mGy. This value was obtained by retrospectively evaluating the doses of 125 consecutive patients prior to the start of this study. Iohexol (Omnipaque 300; Daiichi-Sankyo, Tokyo, Japan), iomeprol (Iomeron 350; Eisai, Tokyo, Japan), or iopamidol (Iopamiron 370; Nihon Schering, Osaka, Japan) was administered via an antecubital vein using a 20-gauge catheter at a dose of 600 mgI/kg; the injection procedure was standard across all patients. The scan delays for arterial and portal venous phase imaging were determined using an automatic bolus-tracking program (Canon Medical Systems). The region of interest (ROI) cursor was placed in the aorta at the level of the diaphragmatic dome, and scanning for the arterial and portal venous phases began automatically at 20 and 60 s, respectively, after the trigger threshold of 100 Hounsfield Units was reached.
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