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Ultravist 300 mg ml

Manufactured by Bayer
Sourced in Germany

Ultravist 300 mg/mL is a non-ionic, water-soluble, low-osmolar iodinated contrast agent used in diagnostic imaging procedures. It contains 300 mg of iodine per milliliter.

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4 protocols using ultravist 300 mg ml

1

Doxorubicin-Loaded DC Beads for DEB-TACE

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TACE was implemented using local analgesia, heparin (5000 IU), antibiotic prophylaxis (cephalosporin), and antiemetic (granisetron) drugs. Angiography was performed according to a standardized protocol prior to intervention. Superselective catheterization of the hepatic artery and the artery supplying the tumor was performed using a 2.7-F microcatheter (Progreat; Terumo Corp., Tokyo, Japan) in all cases. DEB-TACE was then applied to the feeding vessel with a combination of DC beads (Biocompatibles; Terumo Corp., Tokyo, Japan) loaded with doxorubicin (Fig. 1). The microsphere size (100–300 μm and 300–500 μm) of the beads was chosen according to the size of the tumor. DC beads 100–300 µm and/or 300–500 µm in size were used for lesions >6 cm, while beads 100–300 μm in size were used for lesions <6 cm in size. Doxorubicin was administered in a maximum dose of 150 mg per embolization contingent on the tumor size. After loading the beads, the fluid was removed from the suspension and the beads were diluted in 15 mL contrast material (Ultravist 300 mg/mL; Bayer AG, Leverkusen, Germany). The intervention was terminated when imaging confirmed no contrast agent drainage into the tumor and appropriate blood flow blockage.
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2

Chest CT Imaging with Contrast

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A CT scanner with 64 rows of detectors (LightSpeed 64; GE Healthcare, Milwaukee, WI, USA) was used to perform the chest CT scans. Plain CT scan was carried out from apex pulmonis to the diaphragm dome (collimation: 0.625 mm, peak tube voltage: 120 kVp, tube current-time product: automatic). Next, 80 mL of a non-ionic contrast medium (Ultravist 300 mg/mL; Bayer, Munich, Germany) was administered intravenously at a rate of 3 mL/s with an automatic injector. The contrast-enhanced scan began 40 seconds after injection of the contrast medium.
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3

Coronary CT Angiography Protocol

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For cCTA a dual-source 2 × 192-slice multidetector CT scanner (Siemens Somatom Force, Erlangen, Germany) was used from November 2015. Before 2015, the cCTA images were acquired using a 64-slice CT scanner (Philips, Brilliance64). For both scanners a prospective ECG-triggered step-and-shoot protocol was used and images were reconstructed with a slice-thickness of 0.6 and 0.9 mm, respectively. Contrast medium (Ultravist 300 mg/ml, Bayer Healthcare Pharmaceuticals) was administered intravenously. The total iodine dose and iodine delivery rate were adjusted for body weight. The scan delay was determined using a test bolus, after which 4 s were added for the scan delay of the main bolus. A multidisciplinary team including a radiologist, cardiologist, pediatric cardiologist, and pediatric immunologist (with expertise in KD) discussed the results, as reported previously (4 (link)).
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4

Coronary CT Angiography Protocol

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From June 2015, a third generation dual source CT-scanner (Siemens Somatom Force, Germany) was used for cCTA in our hospital. A prospective ECG-triggered high-pitch spiral scan sequence was applied for patients in sinus rhythm and a heartrate below 70 beats per minute. A prospective ECG-triggered sequential step and shoot sequence was used for patients with an irregular heartrate or heartrate above 70 beats per minute. The lowest feasible tube voltage was selected by using care-kV (range 70-120 kV). Intravenous iodine-based contrast medium (Ultravist 300 mg/ml, Bayer Healthcare Pharmaceuticals, Berlin, Germany) was administered via venous access at the antecubital fossa with an injection speed adjusted to body weight and ranging from 0.3 (0.5 kg body weight) tot 4 ml/s (44 kg body weight). Scans were analyzed and reported by an experienced cardiovascular radiologist using dedicated coronary post-processing software (SyngoVia, Siemens). Coronary anatomy, vessel wall irregularities by calcified plaque, mixed plaque or non-calcified plaque and luminal stenosis was assessed.
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