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22 protocols using ge revolution

1

Phantom CT Imaging Protocol Evaluation

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The phantom was scanned on a 16-cm multidetector CT scanner (GE Revolution; GE Healthcare; Milwaukee, WI), with scan parameters listed in Table 1, applying a range of tube currents considered clinically relevant [26] . To increase data for statistical analysis, the phantom was scanned three times for each dose level where inserts were interchanged and rotated freely about the z-axis between these scans to avoid lesion location recall bias among readers. All series were reconstructed with FBP, 50% hybrid IR (IR50; ASiR-V 50%), and DLIR of low strength (DLL; TrueFidelity Low), medium strength (DLM; TrueFidelity Medium) and high strength (DLH; TrueFidelity High) with 2.5 mm slice thickness. For reconstruction of the DLIR images, raw data were sent to the DLIR vendor (GE Healthcare) as the study was initiated prior to clinical implementation of the DLIR algorithm which is now commercially available.

Scan parameters applied in study.

Table 1
Scan parameterData
Detector collimation (mm)80 (128 ×0.625 mm)
Tube potential (kVp)120
Pitch0.5
Rotation speed (seconds)0.5
Tube current-time product (mAs)75, 150, 225, 300 and 375
CT dose index (mGy)5, 10, 15, 20 and 25
Matrix512 × 512
Scan field of viewLarge body
Display field of view (mm)350
Reconstruction kernelStandard kernel

1 Tube potential of 120 kVp chosen based on phantom size and density.

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2

Chest CT Dose Optimization Protocols

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All chest CT examinations were acquired using 256-slice multidetector CT (GE Revolution; General Electric Healthcare, Milwaukee, USA). We first used a usual high-resolution chest CT (CCT) protocol to obtain reference images: 0.5 s gantry rotation time, 120 kVp, 0.984 : 1 beam pitch, 40 mm table feed for gantry rotation, and z-axis tube current modulation.
To obtain LD and ULD acquisitions, the automatic tube current modulation was replaced by manually chosen values of mA, while the other parameters were maintained. For the ULD protocol, kVp was lowered to 80 and mA was set to 30. We decided to experiment with different low-dose protocols to verify how reductions in kV and mA affect the dose and nodule detection, since previous studies show that CT performed for other reasons, like pulmonary embolism, can be performed with lower doses and similar detection rates when those parameters are modified [10 (link)]. For LD protocol A, (lower mA) mA was lowered to 20 and, for LD protocol B (lower kVp), kVp was lowered to 100. LD protocol C (conventional LDCT) followed the AAPM recommendations for lung cancer screening [11 ]. Table 1 specifies the protocols used.
Images were reconstructed at 0.625 mm thickness, 512 × 512 matrix, using iterative reconstruction (ASiR-V™ General Electric Healthcare, Milwaukee, USA).
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3

CT Imaging of Arthroplasty Migration

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CT examinations were performed on 2 CT scanners (GE Revolution, GE Healthcare, Chicago, USA and Siemens SOMATOM Force, Siemens Healthcare GmbH, Erlangen, Germany). Model-based iterative reconstruction algorithms (ADMIRE 2, Siemens and ASiRV50, GE Healthcare) were used, with metal artefact reduction (MAR). The CT protocol parameters were tube voltage 120 kV, tube current 100 mAs, slice thickness 0.625 mm, rotation time 0.5 seconds, pitch 1.0, and field-of-view 200 × 200 mm. These parameters, scan length, CT dose index volume (CTDIvol), and dose length product (DLP) were matched on the CT scanners at a total dose of 6.34 mGy. EDs were estimated by multiplying DLP by the knee conversion factor 0.0004 mSv/(mGy × cm) (17 (link)).
The cadaver was repositioned between each exposure. Scans were analyzed with a commercially available CT migration analysis software (generic name CTRSA), CTMA software (Sectra AB, Linköping, Sweden) (12 (link)). The following steps were performed, as previously described for hip and shoulder arthroplasty (8 (link),9 (link)):
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4

Chest CT Imaging Protocol for Lung Evaluation

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Chest CT scans were performed with different multi-slice CT systems: Aquilion ONE (Toshiba Medical Systems, Otawara, Japan); GE Revolution, GE Discovery CT750 HD, or LightSpeed VCT (GE Healthcare, Milwaukee, WI, USA); and Brilliance iCT (Philips Healthcare, Cleveland, OH, USA). Parameters used for scans without intravenous contrast included a peak x-ray tube voltage of 120 kV, automatic tube current modulation (300–500 mAs), and slice thickness of 0.625 to 1.25 mm. The protocol for contrast-enhanced included a peak x-ray tube voltage of 120 kV, automatic tube current modulation (500–650 mAs), and slice thickness of 0.625 to 1.0 mm. A total of 80–100 ml iodinated contrast material (Iomeron 400, Bracco Imaging SpA, Milan, Italy; or Ominpaque 350, GE Healthcare, United States) was injected intravenously at a rate of 5 ml/s and followed by 20–30ml of saline chaser at a rate of 4–5 ml/s. Images were reconstructed using standard lung filters specific to each CT vendor. All scans were obtained in the supine position during inspiratory breath-hold.
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5

Non-contrast Chest CT Protocol

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The CT scans were performed from the level of the
first rib to the upper renal pole using a 128-detector
CT scanner (GE Revolution, GE, Milwaukee, WI).
Scans were acquired without contrast, utilizing the
following parameters= 100 kV, 110 mAs, a 1.25 mm
slice thickness for volumetric study, a 512 x 512
reconstruction matrix, BonePlus kernel, and an
adaptive statistical iterative reconstruction (ASIR) of
70%, via body filter.
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6

Comprehensive Nanoparticle Characterization Protocol

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The morphology and elemental composition of the nanoparticles were analyzed using a transmission electron microscope (TEM) and a high-resolution TEM (JEM 2100 F, Japan). The surface charge of the nanoparticles was determined using a Zeta PALS system (Brookhaven Instruments, Holtsville, NY, USA). The absorption spectra of the nanoparticles were measured using an ultraviolet-visible spectrophotometer (Agilent Cary 60, USA). The elemental concentration of the nanoparticles was determined using inductively-coupled plasma optical emission spectroscopy (ICP-OES). The imaging performance of the nanoparticles was evaluated using a spectral CT scanner (GE Revolution, USA) and a 3.0T magnetic resonance scanner (Philips Ingenia, the Netherlands).
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7

CT Imaging Protocol for Acute Ischemic Stroke

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CT was performed on a range of scanners from different vendors including Siemens Somatom X.cite, Somatom Definition Flash, Somatom Definition AS+, and Somatom Definition Edge Plus (Siemens, Erlangen, Germany), as well as GE Revolution (General Electric, Boston, MA, USA) and Philips Brilliance iCT 256 (Philips, Amsterdam, The Netherlands). The three-phase CT clinical protocol consists of NCCT, an arterial phase measured with CTA and CTV after intravenous contrast agent injection. Due to the different scanner types and acute setting of AIS, the CTV was timed with a mean delay of 70 ± 28 s after the CTA. A fixed tube voltage of 120 kV for both the unenhanced and venous phases was used.
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8

Non-contrast Chest CT Imaging Protocols

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Noncontrast chest CT scans were performed with different multi-slice CT systems: Aquilion ONE (Toshiba Medical Systems, Otawara, Japan); GE Revolution, GE Discovery CT750 HD, or LightSpeed VCT (GE Healthcare, Milwaukee, WI, USA); and Brilliance iCT (Philips Healthcare, Cleveland, OH, USA). Parameters used for scans included a peak x-ray tube voltage of 120 kV, automatic tube current modulation (300–500 mAs), and slice thickness of 0.625 to 1.25 mm. Images were reconstructed using lung kernels specific for respective scanner vendors. All scans were obtained in the supine position during inspiratory breath-hold.
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9

Contrast-Enhanced Liver CT Protocol

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Contrast-enhanced liver CT was performed using a 256-section (GE Revolution; both GE Healthcare) or a 128-section (Siemens Somatom Definition; Siemens) multidetector CT scanner. The following CT acquisition parameters were used: Tube voltage 120 kVp, tube current 240 mAs, rotation time 0.5 s, matrix size 512 × 512, slice thickness 5 mm. Nonionic contrast agent (300 mg of iodine per milliliter, 3 mL/s, 1.5 mL/kg body weight, Omnipaque, GE Healthcare) was administered as a bolus rapidly via the antecubital vein using a syringe pump. The arterial phase (AP), portal vein phase, and delayed phase images were obtained during suspended respiration at 15 s, 30 s, and 180 s respectively.
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10

CT Diagnosis of Elbow Dysplasia in Dogs

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Dogs presenting to the authors’ institution between September 2019 and September 2020 for unilateral or bilateral thoracic limb lameness and signs of pain on elbow manipulation were included in this study. Dogs not undergoing both CT and elbow arthroscopy were excluded. Elbows were subsequently divided into two groups depending on the presence or absence of HIF on CT imaging. The groups were termed “HIF positive” and “HIF negative.”
Computed tomography (GE Revolution, GE Healthcare, Chalfont St Giles, UK) of both thoracic limbs from the carpi to the shoulders was performed preoperatively with the dog under deep sedation (3‐8 mcg/kg dexmedetomidine and 0.2 mg/kg butorphanol, IV). Dogs were positioned in sternal recumbency, with the elbow joints parallel and extended cranially at approximately 130°‐140° of extension. If CT revealed changes of the humeral condyle compatible with development or presence of HIF (as previously described by Carrera et al.),8 the affected elbow was included in the HIF positive group. All remaining cases that showed no evidence of HIF on preoperative CT examination but where there were other bone changes suggestive of joint pathology (such as fragmented coronoid process, kissing lesions, and medial compartment disease) were included in the HIF negative group.
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