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Iopamiron

Manufactured by Bayer
Sourced in Japan, Germany

Iopamiron is a radiographic contrast agent used in medical imaging procedures. It contains the active ingredient iopamidol, which is a non-ionic, water-soluble iodinated contrast medium. Iopamiron is designed to enhance the visibility of certain structures or areas within the body during radiographic imaging examinations.

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13 protocols using iopamiron

1

Cardiac CTP Acquisition Protocol

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The cardiac field of view (FOV) in the craniocaudal direction was determined on the
basis of CACS. The 320-row scanner uses a collimation of 320 × 0.5-mm detector row
and a gantry rotation of 350 ms, providing up to 16 cm of z-axis coverage in a single
tube rotation, enough to capture the entire heart.
The stress scan was initiated 2 min after the end of an intravenous dipyridamole
infusion (0.56 mg/kg), which was given through the right antecubital vein for 4 min.
Real-time bolus tracking was performed, adjusting a region of interest (ROI) to a
threshold of 210 HU (Hounsfield Unit) in the descending aorta. CTP acquisition was
always performed within one heartbeat, including systolic and diastolic phases
(40-80% R-R interval), after an infusion of 70 mL of intravenous contrast medium
Iopamidol (Iopamiron 370 mg/mL; Bayer Schering Pharma, Berlin, Germany) at a rate of
5 ml/s, followed by 30 mL of a saline flush. The tube voltage (kV) and tube current
(mA) were pre-determined according to the patient’s BMI (Table 1). During dipyridamole infusion symptoms, blood pressure
and electrocardiographic parameters were continuously monitored.
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2

Standardized CECT Imaging Protocol

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All CECT examinations were performed using a 64 multidetector CT scanner (Light Speed V CT, GE Healthcare, Tokyo, Japan), and cephalocaudal images were obtained with section thicknesses of 3 mm and pitch 1.3, with intravenous bolus injection of non-ionic contrast material (90 mL of 300 mgI/dL; Iopamiron®, Bayer Schering Pharma, Osaka, Japan) at 3 mL/s via an antecubital vein. The scanning delay set for arterial phase and equilibrium phase was 30–40 s and 120–150 s, respectively.
The portal venous phase on CECT could not be obtained in 2/39 lesions (5.1%) in this study due to imaging errors. Therefore, the standard CT protocol not including the portal venous phase is described for all lesions.
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3

Coronary CT Angiography and SPECT Imaging Fusion

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Patients were assessed by CCTA using SOMATOM Definition Flash (Siemens Healthcare, Erlangen, Germany; Siemens Japan, Tokyo, Japan), a 128-section, dual X-ray source CT scanner. Images were acquired using CCTA after ~ 60 mL of contrast medium (Iopamidol 370 mg/mL, Iopamiron 370 mg/mL; Bayer Yakuhin, Ltd., Osaka, Japan) was administered at a flow rate of 4 mL/s followed by a 40 mL saline flush at the same rate. The scanning parameters were as follows: collimation, 128 × 0.6 mm; gantry rotation, 280 ms; step-and-shoot mode; tube voltage, 120 kV; tube current of 340 mAs/rotation; and a 220-mm field of view. Axial images were reconstructed with a slice thickness of 0.75 mm and a reconstruction kernel of B35f (Heart View medium). All data were transferred to an Advantage Workstation 4.6 (GE Healthcare, Chicago, IL, USA; GE Healthcare Japan, Tokyo, Japan) and then manual registration of the CCTA and MP-SPECT images proceeded using pixel-shifting.
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4

Contrast Media Usage in CT Scans

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In our hospital, high-osmolality contrast media (HOCM) is no longer used, and all contrast-enhanced CT are performed using low-osmolality contrast media (LOCM).
We use four kinds of iodinated contrast media. They are Iopamidol (Iopamiron; Bayer Co. Ltd., Osaka, Japan), Iomeprol (Iomeron; Eisai Co. Ltd., Tokyo, Japan), Iohexial (Omnipaque; Daiichi-Sankyo Co. Ltd., Tokyo, Japan), and Ioversol (Optiray; Daiichi-Sankyo Co. Ltd., Tokyo, Japan).
Three kinds of gadolinium contrast media are used, which are Gadoterate meglumine (Magnescope; Terumo Co. Ltd., Tokyo, Japan), Gadteridol (ProHance; Eisai Co. Ltd., Tokyo, Japan), and Gadopentetate dimeglumine (Magnevist; Bayer Co. Ltd., Osaka, Japan). Selection of contrast media was based on the purpose of the examination and the patient’s weight. Although there are few data to support changing the contrast media to decrease the likelihood of a subsequent reaction in patients with a history of prior allergic-like reactions to iodinated contrast media, we usually change the contrast media administered in such cases.
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5

Multimodal CT Imaging for Liver Tumor Assessment

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Because we used a retrospective design, various types of CT scanners and different CT protocols had been used. Dynamic CT studies were performed with a 4-slice (Aquilion: Toshiba Medical Systems, Tokyo: n = 9; or Somatom Plus 4 Volume Zoom: Siemens-Asahi Medical Technologies, Tokyo: n = 2), 64-slice (Aquilion: Toshiba Medical Systems: n = 16; or Brilliance 64: Philips, Cleveland OH, United States: n = 5), 256-slice (Brilliance iCT: Philips: n = 4) or 320-slice (Aquilion One: Toshiba Medical Systems: n = 2) MDCT scanner. Each patient received intravenous nonionic contrast material containing 300 mgI/mL or 370 mgI/mL iopamidol (Iopamiron; Bayer, Osaka, Japan) by an automated power injector, and the portal phase was acquired. The details of the CT protocols are shown in Table 1. The interval between the preoperative MDCT study and the biopsy or surgery ranged from 1 to 244 d (mean ± SD, 44.0 ± 56.7 d).
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6

Cardiac CT Angiography Protocol

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We used the following protocol with the same CT scanner as in the phantom study and prospective ECG-gating axial scans: 320 rows × 0.5-mm collimation, rotation time 0.275 sec, tube voltage 120 kVp, tube current 220–300 mA (automatic exposure control). Each patient received the beta blocker (6–12.5-mg landiolol hydrochloride) and sublingual nitroglycerin (0.3 mg) 5 min before data acquisition. The high-concentration iodinated contrast agent (Iopamiron 370 mgI/mL, Bayer, Osaka, Japan) was delivered via a 20-gauge intravenous catheter placed in an antecubital vein. The amount of contrast agent was tailored according to the patient body weight (300 mgI/kg), and it was injected over 12 s, immediately followed by a 40-mL saline flush at the same rate using a dual-head power injector (Dual Shot-Type GX7; Nemoto Kyorindo, Tokyo, Japan). Synchronization between the flow of the contrast agent and the CT acquisition was achieved using a computer-assisted bolus tracking system. The trigger threshold was set at 200 HU for the ascending aortic region of interest. CT data acquisition commenced 6 s after the trigger.
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7

Dynamic Contrast-Enhanced CT Imaging Protocol

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The protocol of dynamic contrast-enhanced CT is shown in Table 2. We used a 64-row CT scanner, the Light Speed VCT (GE Healthcare, Little Chalfont, UK). Pre-contrast phase and 9 phases after intravenous contrast agent injection were scanned: 7 at 6-second intervals beginning at 22 seconds after injection, and 1 each at 90 and 210 seconds after injection. Scan parameters were as follows: the range was caudal 25 cm from the upper level of the diaphragm; the tube voltage was 120 kVp; the tube current was 300 mA (2 nd through 8 th , and 10 th , phases), or 500 mA (1 st and 9 th phases); the matrix was 512 x 512 pixels; the field of view was 320 x 320 mm; the size of collimation was 0.625 mm; the reconstruction thickness was 2.5 mm.
The median (interquartile range) effective dose was 48.9 mSv (48.2-48.9). A nonionic iodinated contrast agent (Iopamiron 370 mg/mL, Bayer Healthcare, Berlin, Germany) was administered intravenously through a 22-gauge catheter in the median cubital vein. The total dose was 100 mL, and the rate of injection was 3 mL/s. This CT protocol was adopted, instead of angiography, CT during arterioportography, or CT during hepatic arteriography, for preoperative mapping of vascular anatomy and detection of small lesions.
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8

Cardiac CT Angiography Protocol

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We used a 256-slice (128 multi-detector row) CT scanner (Brilliance iCT; Philips Healthcare, Cleveland, Ohio, USA). All patients received 0.6 mg of nitroglycerin (Myocor; Astellas Pharma, Tokyo, Japan), and intravenous beta-blocker (Corebeta; landiolol hydrochloride, 0.125 mg/kg, Ono Pharmaceutical Co., Ltd., Tokyo, Japan), 5 min prior to the timing bolus scan, to reduce heart rate if the heart rate was > 75 beats per minutes, in the absence of contraindication. CorCTA was performed with iohexol (Omnipaque; 350 mg iodine/mL; Daiichi Sankyo, Tokyo, Japan) or with iopamidol (Iopamiron; 370 mg iodine/mL; Bayer Yakuhin, Osaka, Japan) at an injection rate of 5.0–5.5 mL/s for 10 s, followed by a saline flush (20 mL, 5.0–5.5 mL/s). The scan parameters were as follows: retrospective ECG-gated mode (heart rate > 60 beats/min) or prospective ECG-gated mode (heart rate ≤ 60 beats/min); tube voltage, 120 kV; effective tube current time-product, 800–1300 mAs/rotation with dose modulation; gantry rotation time, 0.27 s/rotation; collimation, 2 × 128 × 0.625 mm with a dynamic z-focal spot; 250-mm display field-of-view; 0.8/0.4-mm slice thickness/overlap; and 512 × 512 image matrix.
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9

Multiphasic Liver CT Imaging Protocol

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Intravenous multiphasic contrast-enhanced CT including the whole liver was performed using a 64-row CT scanner (Light Speed VCT; GE Healthcare Japan, Tokyo, Japan) at precontrast and 22, 28, 34, 40, 46, 52, 58, 90, and 210 s after the start of an injection of 370 mgI/mL iodine contrast agent (Iopamiron; Bayer Healthcare, Tokyo, Japan) (100 mL) at 3 mL/s through a 22-gauge catheter in the median cubital vein. Scan parameters were as follows: scan range, 25 cm caudal from the upper diaphragm; tube voltage, 120 kVp; tube current, 300 mA (22 s through 58 s, and 210 s) or 500 mA (precontrast and 90 s); matrix, 512 × 512 pixels; field of view, 320 × 320 mm; and reconstruction thickness, 2.5 mm. The median (interquartile range) effective dose was 48.9 mSv (range, 48.2-48.9). This IV-CT protocol was similar to the one described in a previous report 19 .
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10

Coronary Stent Restenosis Grading

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All patients were scanned with a 64-slice scanner (Discovery CT 750HD). A β-blocker (oral or i.v. propranolol 10-20 mg) was used if the heart rate was ≥65 beats/min. Nitroglycerin was administered to all patients before scanning. A bolus of contrast medium (iopamiron, 370 mg iodine/ml, Bayer, Tokyo, Japan) was injected into the right antecubital vein with an eration with significant restenosis (≥50% narrowing); grade 4, neointimal proliferation with severe stenosis or total occlusion (≥75% narrowing or occlusion). Two skilled observers evaluated the grades of all images while blinded to ICA and each other's data. Significant ISR was defined as grade 3 or 4.
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