The largest database of trusted experimental protocols

Brilliance 64 slice

Manufactured by Philips
Sourced in Italy

The Philips Brilliance 64-slice is a computed tomography (CT) imaging system that captures high-resolution, three-dimensional images of the body. It features a 64-slice detector configuration, enabling rapid data acquisition and image reconstruction.

Automatically generated - may contain errors

12 protocols using brilliance 64 slice

1

Chest CT and CTA Imaging Protocol

Check if the same lab product or an alternative is used in the 5 most similar protocols
All examinations were performed with 64 slice MDCT scanner (Philips brilliance 64 slice). Noncontrast chest CT scan was performed with a collimation of 64 × 0.625 and reconstruction thickness of 1 mm with an increment of 0.2. A voltage of 120 kv and 100 mA was used with scan thickness 0.9 mm. For CT angiogram, the locator and tracker were placed in the right ventricle with minimum delay of 3.2 s. A voltage of 120 kv and 350–400 mA exposure was used for contrast study. The resolution was standard, the pitch was 0.2, the field of view (FOV) was 250, the filter was cardiac sharp, rotation time was 0.4 s and window was 150–850. Trigger density threshold was 150 and postthreshold delay was 150. Non-ionic contrast medium was used - ultravist molecule – Iopromide - concentration of 769 mg/ml. Contrast medium was administered via the peripheral venous cannula using an automated pressure injector pump. The volume of the nonionic contrast was 1.5 ml/kg administered at a rate of 2.5 ml/s with 325 psi pressure.
+ Open protocol
+ Expand
2

Evaluating Bony Ingrowth in Implants

Check if the same lab product or an alternative is used in the 5 most similar protocols
The primary endpoint was visible bony ingrowth on six and twelve -month CT scans. CT scans to determine the presence of bone ingrowth into implant tread openings or central cavity were performed at two weeks, six and twelve months post-operatively. In order to be categorized as having bony ingrowth, a subject must have bone ingrowth of 4% or greater compared with baseline in the volume of the screw.
The patients were scanned in a supine position in a multislice CT-scanner (Brilliance 64-slice, Philips Medical Systems, Cleveland, OH). Axial slices were made starting from the joint-space level to one centimeter distal to the cap of the screw. The scans were performed in high resolution with collimating on 64 × 0.625 mm, slice thickness 0.9 mm. Reformatting was performed a with C-filter resulting in a slice thickness of 0.5 mm and 1.0 mm spacing.
+ Open protocol
+ Expand
3

Pulmonary Embolism Diagnosis via CTPA

Check if the same lab product or an alternative is used in the 5 most similar protocols
The thoracic CT scans were performed using a 64-detector multi-sectional CT scanner (Brilliance 64-slice; PHILIPS, Amsterdam, Netherlands) with an intravenously injected contrast agent. Scanned with multi-slice spiral CT, collimation of 0.6, rotation time of 0.5 s, slice thickness of 5 mm, and pitch of 1.0, contrast agent (100 ml) was injected at 4 ml/s. CTPA results were categorized as positive for PE if an intraluminal filling defect was observed within a pulmonary arterial vessel and were considered negative if no filling defect was seen. Scans were considered technically inadequate only if main or lobar pulmonary vessels were not visualized.
+ Open protocol
+ Expand
4

CT Protocol for Liver Metastasis Evaluation

Check if the same lab product or an alternative is used in the 5 most similar protocols
The CT examination of thorax, abdomen and pelvis were performed on Philips Brilliance Premium 64 slice, Philips Brilliance 64 slice, or Philips MX 8000 IDT (16 slice) machines (Brilliance; Philips Healthcare, DA Best, the Netherlands). Intravenous contrast, Iomeprol 350 mgI/ml, according to bodyweight, was injected prior to the examination. The examination was performed at 60–70 s timed delay to obtain the portovenous contrast phase. The department’s usual technical parameters were used for the examination; 120 kV and 300 mAs, with 64 × 0.625 mm or 16 × 1.5 mm collimation, reconstructed to 3 mm in axial, coronal and sagittal plane. Hypodense lesions in the parenchyma which showed no sign of being a cyst or haemangioma in the portal-venous phase of a contrast enhanced CT were considered liver metastases. Finding of metastatic lesions were documented and recorded by the size and segmental location in the liver.
+ Open protocol
+ Expand
5

3D Printed Uncemented Humeral Prosthesis Reconstruction

Check if the same lab product or an alternative is used in the 5 most similar protocols
Between March 2018 and July 2019, seven patients (two females and five males) with humeral malignant tumors received 3D printed uncemented prosthesis reconstructions in our institution. The average age was 19.25 years (range, 16–24 years). All the patients received preoperative radiographic assessments, including x-rays, 3D computed tomography (CT) scans (Philips Brilliance 64 Slice, thickness: .4 mm), magnetic resonance imaging (MRI) scans, and bone scans (SPECT) or positron emission tomography/computerized tomography (PET/CT) scans (Figure 1). A preoperative biopsy was performed for all patients. An Enneking surgical staging system was used to evaluate the surgical stage (Enneking, 1986 (link)). Tumor locations were classified with reference to the epiphyseal plate proposed by Kumta et al. (Kumta et al., 1999 (link)). Neoadjuvant chemotherapy was performed for patients with high-grade sarcoma according to the NCCN guidelines for bone cancer. The detailed characteristics of the patients are summarized in Table 1.
This study was performed in accordance with the Declaration of Helsinki as revised in 2008 and was approved by the Ethics Committee of the West China Hospital. All patients signed an informed consent form before surgery and provided consent to publish and report individual clinical data.
+ Open protocol
+ Expand
6

Non-Contrast CT and CTA Imaging

Check if the same lab product or an alternative is used in the 5 most similar protocols
Unenhanced CT and CTA images were obtained using either a Philips Brilliance 64-slice or iCT 256-slice CT scanner (Philips Healthcare, Best, The Netherlands) at 80–120 kVP and 250 mAs (adjusted based on patient body composition).
+ Open protocol
+ Expand
7

Catphan Phantom CT Scan Protocols

Check if the same lab product or an alternative is used in the 5 most similar protocols
CT scans of the Catphan phantom were acquired with a Philips Brilliance 64 slice CT simulator (Philips Healthcare, Cleveland, OH). All CT acquisition and reconstruction parameters were selected to mimic routine clinical protocols at our institution. The phantom was scanned with two tube potential settings (120 and 140 kVp) and two fixed tube current values (250 and 500 effective mAs). Other scan parameters included: 64×0.625mm collimator setting, 0.5 s rotation time, pitch 0.638, and standard resolution, which for Philips scanners refers to the sampling frequency of the CT detectors. For each scan, volumetric images were reconstructed using a conventional FBP algorithm and the iDose4 algorithm with 3 mm slice thickness setting, as well as three different reconstruction filters: A (smooth), B (standard), and C (sharp). In order to analyze the effect of pixel dimension on the calculated NPS (Eq. (3)), images were reconstructed using two fields of view (FOV): 350 mm and 500 mm. Using a 512×512 data matrix, this resulted in pixel sizes of 0.6836mm×0.6836mm and 0.9766mm×0.9766mm, respectively.
+ Open protocol
+ Expand
8

Thoracic CT Scans for Pulmonary Embolism

Check if the same lab product or an alternative is used in the 5 most similar protocols
The thoracic CT scans were performed using a 64-detector multisectional CT scanner (Brilliance 64-slice; PHILIPS, Amsterdam, The Netherlands) with an intravenously injected contrast agent while the patients held their breath. For multidetector scans, 100 ml of contrast was injected at 4 mm/s and 1.25-mm images were obtained at 1.2-mm intervals using a pitch of 1.0:1.0. CTPA results were categorized as positive for pulmonary embolism if an intraluminal filling defect was seen within a pulmonary arterial vessel and were considered negative if no filling defect was observed. Scans were considered technically inadequate only if main or lobar pulmonary vessels were not visualized.
+ Open protocol
+ Expand
9

Multimodal Fusion Imaging Technique

Check if the same lab product or an alternative is used in the 5 most similar protocols
The fusion images technique was done and the images were acquired from all patients who were operated in Fujita Health University – Banbuntane Hotokukai Hospital, Japan. Fusion images were made and acquired in Imai Clinic, Nagoya, Japan. To acquire fusion images, in our institution, patients have to had brain magnetic resonance imaging (MRI) (Phillips Intera©, 1.5 Tesla) and computed tomography (CT) angiography (Philips Brilliance© 64 slices), and then the data in Digital Imaging and Communications in Medicine are fused in a workstation (Fujifilm© Vincent© Ver. 3.0) [Figure 1]. The use of fusion images was described in illustrative cases.
+ Open protocol
+ Expand
10

Contrast-Enhanced CT Imaging Protocol

Check if the same lab product or an alternative is used in the 5 most similar protocols
A CT scanner (Brilliance 64 slices; Philips Medical Systems, Best, The Netherlands) with a 64  0.625 detector configuration was used, with the following settings: rotation time, 0.75 s; section thickness and intersection gap, 0.7 mm and 0.3, respectively; helical pitch, 0.609; scan field of view, 50 cm; x-ray tube voltage, 120 kV; and x-ray tube current, 300 mA. All patients were administered nonionic iodine contrast material containing 350 mg I/ml (Iomeron; Bracco Imaging Italia srl) or 370 mg I/ml (Ultravist; Bayer Spa) using a double-syringe power injector (Stellant D; MedRad, Pittsburgh, PA, USA) at a rate of 4 ml/s through an at least 20-gauge angiocatheter placed in an antecubital vein. A bolus-tracking program was used to monitor the contrast enhancement after the injection of contrast medium before starting the diagnostic scans. Different scan delays for the three phases (arterial, nephrographic, and delayed phases) were set at 7 s, 70 s, and at least 10 min, respectively.
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!