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Imeron 400 mct

Manufactured by Bracco
Sourced in Germany, Italy

Imeron 400 MCT is a contrast agent used in medical imaging procedures. It is a water-soluble, iodinated compound that enhances the visibility of specific areas or structures within the body during diagnostic imaging tests, such as computed tomography (CT) scans.

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16 protocols using imeron 400 mct

1

Contrast-Enhanced CT Angiography Protocol

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CTPA was performed on a 128-slice CT scanner (Ingenuity 128, Philips, Hamburg, Germany). Intravenous administration of an iodine-based contrast medium (60 mL Imeron 400 MCT, Bracco Imaging Germany GmbH, Konstanz, Germany) was given at a rate of 4.0 mL/s via a peripheral venous line. Automatic bolus tracking was performed in the pulmonary trunk with a trigger of 100 Hounsfield units (HU). Typical imaging parameters were: 100 kVp; 125 mAs; slice thickness = 1 mm; and pitch = 0.9. CTPA was performed in every case in deep inspiration level.
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2

CTPA Imaging Protocol with Contrast

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CTPA was performed on a 128-slice CT scanner (Ingenuity 128, Philips, Hamburg,
Germany). Intravenous administration of an iodine-based contrast medium
(60 ml Imeron 400 MCT, Bracco Imaging Germany GmbH, Konstanz, Germany)
was given at a rate of 4.0 ml s−1 via a peripheral
venous line. Automatic bolus tracking was performed in the pulmonary trunk with
a trigger of 100 Hounsfield units (HU). Typical imaging parameters were: 100
kVp; 125 mAs; slice thickness, 1 mm; pitch, 0.9. In every case, CTPA was
performed in deep inspiration level.
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3

Evaluation of Contrast Agents for Imaging

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The following five fluids were used as contrast agents:

NaCl 5.85%; ready-to-use hypertonic (1 mmol/mL) sodium-chloride solution, clinically used for the substitution of sodium (Natriumchlorid 5.85% Braun Mpc, B. Braun Melsungen AG, Melsungen, Germany).

NaBic (sodium-bicarbonate) 8.4%, ready-to-use hypertonic buffer solution, clinically used for correction of the acid-base balance (Natriumhydrogencarbonat 8.4%, B. Braun Melsungen AG, Melsungen, Germany).

Jonosteril; ready-to-use iso-tonic, balanced crystalloid solution, clinically used for intravascular volume replacement (Jonosteril®, Fresenius Kabi, Bad Homburg, Germany).

Glucose 5%; ready-to-use ion-free isotonic glucose solution, clinically used as carrier solution for intravenous drug administration (Glucose 5%, B. Braun Melsungen AG, Melsungen, Germany).

Iomeprol 400 mg/mL; ready-to-use non-ionic but iodinated X-ray contrast medium, clinically used for angiography (Imeron® 400 MCT, Bracco Imaging Deutschland GmbH, Konstanz, Germany).

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4

Comprehensive Cardiac Imaging for Ablation

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Prior to the ablation procedure, all patients underwent transthoracic and transesophageal echocardiography to exclude possible LA thrombus formation. Additionally, individual left atrial anatomy was revealed using a 64‐slice CT scanner (Brilliance 64, Philips Medical Systems, Cleveland, OH, USA) with retrospective electrocardiography (ECG) gating and 3D reconstruction prior to the procedure. Scanning was performed at 120 kVp, with an effective tube current of 600 mAs. The slice collimation was 64 × 0.625 mm, with a gantry rotation time of 0.4 s and a pitch of 0.2. Images were reconstructed at 0.9 mm slice thickness at increments of 0.45 mm. Contrast enhancement with 80 ml of contrast agent (Imeron 400 MCT, Iomeprol 81.65 g/100 ml, Bracco, Konstanz, Germany) was injected at a flow rate of 5 ml/s and followed by a 50‐ml saline flush. A blinded observer (JP) analyzed, segmented, and measured each CCTA image visually and quantitatively with regard to the defined parameters and the morphological classification of the LAA using EnSite Precision™ (Abbott Medical GmbH, Eschborn, Germany). Multiplan volume‐rendered post‐processing was used to acquire a 3D perspective. After anatomical segmentation into PV, LA, and LAA, all 2‐dimensional (2D) and 3D measurements were conducted.
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5

Late Arterial Phase CT Imaging Protocol

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Contrast-enhanced CT was performed in a clinical setting using a 128-slice CT scanner (Ingenuity 128, Philips). Iodine-based contrast medium (90 mL Imeron 400 MCT, Bracco Imaging Germany GmbH) was administered intravenously at a rate of 2-4.0 mL/s. Automatic bolus tracking was performed in the descending aorta with a trigger of 100 Hounsfield units. CT images were obtained in the late arterial phase in every case. Typical imaging parameters were as follows: 100 kVp; 125 mAs; slice thickness, 1 mm; and pitch, 0.9. The CT covered the head to the upper thighs.
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6

Chest CT Imaging Protocol for Arterial and Venous Phases

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All patients underwent a chest plain scan and enhanced scan by using the conventional mode of DLCT (iQon, Phillips). Contrast agent (Iomeprol, Imeron 400 MCT, 400 mg/mL; Bracco Imaging Deutschland GmbH) was administered intravenously at a dose of 1.2 ml/kg at a flow rate of 2 to 2.5 mL/s, and then injected 30 mL normal saline at the same flow rate. The scan delay time after the contrast agent injection is 35 s and 65 s, which are considered to be the arterial and venous phase scans respectively. Scanning parameters: 120 kVp; automatic tube current (37−84 mAs); matrix 512 × 512; collimation 64 × 0.625 mm; reconstruction thickness and interval 0.9 mm/0.9 mm. Regular and spectral images were reconstructed using iDose4 and spectral level 6 (Philips Healthcare) reconstruction algorithms. The average volume-weighted CT dose index and dose length product are 4.4 mGy and 180 mGy*cm, respectively, corresponding to an effective dose of 2.5 mSv (conversion coefficient: 0.014). The scanning range is from the apex of the lungs to the level of the septal muscles, and the patient is asked to complete it under breath-holding. All patients had signed an informed consent form before undergoing enhanced scanning.
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7

Contrast-Enhanced CT Imaging Protocol

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CT was performed with a 128-slice CT scanner (Ingenuity 128, Philips, Hamburg, Germany). In n = 38 cases (42% of patients), intravenous iodine-based contrast medium (60 mL Imeron 400 MCT, Bracco Imaging Germany GmbH, Konstanz, Germany) was injected at a rate of 4.0 mL/s via a peripheral venous line. Automatic bolus tracking was performed in the aorta descenders with a trigger of 100 Hounsfield units (HU). Typical imaging parameters were: 100 kVp; 125 mAs; slice thickness,1 mm; pitch, 0.9.
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8

Dual-Source CT Lung Perfusion Imaging Analysis

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The acquisitions were performed on a dual-source CT-scanner (SOMATOM Force, Siemens Healthcare). A test bolus slice was scanned with intravenous injection of 10 ml contrast medium (400 mg iodine/ml; Imeron 400 MCT, Bracco Imaging) followed by 30 ml of normal saline at 4 ml/s. Time to peak (TTP) opacification in the left ventricle was identified from the test bolus time-density curve and set as a fixed delay for the following main acquisition. This timepoint was chosen according to the work from Masy et al. [15 (link)] so that lung parenchyma is expected to have an optimal contrast enhancement. The DECT scan was obtained using 150Sn/90 kVp and 0.6 mm collimation with injection of 50 ml contrast medium followed by 50 ml of normal saline flush at 4 ml/s. The tube current was modulated as a function of angle and position along the Z-axis (CARE Dose 4D, Siemens Healthcare). Scan direction was caudocranial with coverage from diaphragm to lung apex in held gentle inspiration (to avoid Valsalva maneuver). Reconstructions used a 1 mm slice thickness with a QR40 convolution kernel.
Lung PBV quantification (derived iodine maps) was performed using syngo.CT DE Lung Analysis (syngo Multimodality Workplace, Siemens Healthcare). In order to minimize noise artefacts, a 3D Gaussian-smoothing filter (standard deviation of 2) was applied to CT-PBV maps using MATLAB (R2018b, MathWorks).
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9

Spectral CT Imaging Protocol for Abdominal Scans

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CT images were acquired with one DLCT scanner (IQon Spectral CT, Philips Healthcare). For all scans, a routine abdominal CT protocol was used with a tube voltage of 120 keV. Non-contrast-enhanced (NE) scans had an exposure of 107 ± 49 mAs (mean ± SD) and a mean CT dose index (CTDIvol) of 9.7 ± 4.5 mGy; contrast-enhanced (CE) scans had an exposure of 110 ± 43 mAs and a mean CTDIvol of 10.0 ± 3.9 mGy.
CE scans were performed using iomeprol, a non-ionic iodinated contrast agent for intravenous application (Imeron 400 MCT, Bracco Imaging Deutschland GmbH). Per routine clinical protocol and depending on the clinical situation, a volume of 50 to 70 ml was administered with a flow rate of 3 ml/s. Arterial phases were triggered when the average CT numbers of a volume of interest (VOI) in the descending thoracic aorta exceeded a threshold value of 150 HU. The portal-venous phases started 70 s after contrast administration.
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10

Biphasic Contrast CT for Head and Neck

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All CT examinations were performed on an 80-slice CT scanner (Aquilion PRIME, Canon Medical Systems, Otawara, Japan). A biphasic contrast administration protocol was used. The first bolus of a 50 mL contrast agent (Imeron 400 MCT, Bracco) was followed by a 50 mL flush of saline. After 55 sec, the second bolus of 30 mL contrast agent was followed by a 40 mL saline flush to differentiate arterial vessels in the H&N area. After 18 s, a helical scan covering the entire neck from the frontal sinus to the aortic arch was acquired. Routinely, iterative reconstruction (AIDR3D, standard level) was applied. In those cases, where metal dental restorations were detected on the scout view, an additional dataset using Single-Energy Metal Artifact Reduction (SEMAR) was reconstructed. Scan parameters were: Auto-kV and Auto-mA with an SD of 7.5, 0.75 sec rotation time, 80 × 0.5 mm collimation, and pitch factor of 0.813.
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