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Discovery rt

Manufactured by GE Healthcare
Sourced in United States, Canada

The Discovery RT is a laboratory equipment product from GE Healthcare. It functions as a real-time PCR (Polymerase Chain Reaction) system used for the amplification and detection of DNA or RNA sequences.

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6 protocols using discovery rt

1

Clinical Manifestations of Systemic Sclerosis

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The clinical data of SSc patients were collected through retrospective medical records. Disease duration, which is the clinical period of the disease, was defined as the period from the first appearance of symptoms and signs to this visit. Esophageal dysfunction was defined as symptoms of acid reflux heartburn or findings of reflux esophagitis on gastrointestinal endoscopy. Cardiovascular diseases were assessed by color Doppler echocardiography (EF, ECO, PHILIPS EPIQ7C). The diagnosis of interstitial lung disease (ILD) was determined by a review of a high-resolution computed tomography scan (HRCT, GE DiscoveryRT). Lung involvement and fibrosis were evaluated using HRCT, which has four features: single ground glass lesions, ground glass lesions and reticular nodular lesions (mixed pattern), single reticular nodular lesions (reticular-nodular), and honeycomb changes. Diagnosed renal involvement with blood pressure exceeding 140/90 mmHg and decreased renal function (Renal dysfunction was defined as an increase in serum creatinine concentration of more than 30% above baseline levels at any study time point). In addition, the presence of joint contractures and Raynaud’s phenomenon were noted.
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2

Micro-CT Imaging of Implant Integration

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Each implant in the sheep model was imaged at day zero using clinical resolution computed tomography (CT) (Discovery RT, GE Healthcare, ON, Canada) for confirmation of appropriate defect fill. Clinical CTs were not recorded for the rabbit model given the smaller implant size rendering the image resolution too low for effective analysis. Following animal sacrifice of both the rabbits and sheep, microCT imaging was performed on a General Electric Medical Systems Locus Explore Scanner at 45-micron isotropic pixel resolution using an 18 min protocol (Kv = 80, mA = 450). Image slices were reconstructed into 3D images after calibration using a hydroxyapatite (HA) phantom and subsequent image analysis was performed using MicroView (Parallax Innovations, version 2.5.1, Ilderton, Ontario, Canada).
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3

IGBT Planning-CT Protocol for Dose Reduction

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Planning-CT images were acquired after ICBT applicator insertion for every IGBT session with LightSpeed VCT (GE Healthcare, Chicago, USA) or discovery RT (GE Healthcare), with a slice thickness of 2.5 mm. The scan area was generally set to include the cranial border at the level of the L5 vertebrae and the caudal border of the perineum. To decrease IGBT doses delivered to the small bowel, the bladder was filled with saline (approximately 100–150 ml).
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4

Evaluating CBCT Stereotactic Accuracy

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The CBCT system is calibrated to use the Leksell Coordinate System (LCS) for stereotactic space definition. In order to test the agreement between the stereotactic reference CBCT and the gold‐standard Frame‐based definition of Leksell stereotactic space, we used a simple tool consisting of five ball‐bearing (BB) fiducial markers (0.5 mm diameter) attached to a taut string hung diagonally along stereotactic frame posts (Fig. 1). The frame was scanned in our CT simulator (Discovery RT, GE, San Diego, CA, USA) with the standard CT fiducial indicator box. The Frame‐based stereotactic coordinates of each BB were determined in the LGP software. The BB coordinates are then compared with coordinates determined from a CBCT scan of the tool. The magnitude of the three‐dimensional (3D) vector difference (r) between the coordinates of Frame‐based and CBCT‐based is calculated as: r=(xFramexCBCT)2+(yFrameyCBCT)2+(zFramezCBCT)2
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5

Evaluating Bone Resorption around GPC Implants

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GPC implants were imaged using clinical (imaging was done on live sheep) resolution computed tomography (CT) (Discovery RT, GE Healthcare, Mississauga, ON, Canada) at Day 0 and also after six- and 12 weeks post-implantation. Moreover, higher resolution micro-CT images (General Electric Medical Systems Locus Explore Scanner, Mississauga, ON, Canada) were obtained at a 45-micron isotropic pixel resolution (Kv = 80, mA = 450). Next, the image data acquired at different angles were reconstructed into a 3D model and analyzed by MicroView (Parallax Innovations, version 2.5.1, Ilderton, ON, Canada).
Bone resorption leads to lysis of cells and appears as radiolucent lines on radiographs [50 ]. Therefore, to detect any sign of bone resorption, clinical CT and micro-CT images were investigated in order to check the existence of radiolucent lines at the implant–bone interface.
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6

Breast Immobilization and Imaging Protocol

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Patients were immobilized using All-in-One immobilization system (Orfit Industries, Belgium) in supine position with both arms raised above the head. The 5° wedge was given to raise the chest, which helps to reduce dose to ipsilateral lung and avoid skin folds. Four-clamp thermoplastic cast (Orfit Industries, Belgium) was prepared in this position. Radiopaque markers were placed around the palpable breast as well as in the inferior, superior, lateral, and medial border of the radiation field. Markers were also placed around the palpable right breast. Computed tomography (CT) images were taken from the mandible to 7 cm below the inframammary fold, with 5-mm slice thickness in CT simulator Discovery RT (GE Medical Systems, Chicago, USA).
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