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Synapse workstation

Manufactured by Fujifilm
Sourced in United States

The Synapse Workstation is a digital imaging and information management solution designed for healthcare organizations. It provides tools for viewing, manipulating, and managing medical images and patient data. The workstation offers features for image processing, report generation, and data storage and retrieval.

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Lab products found in correlation

4 protocols using synapse workstation

1

Pediatric ACL Reconstruction with Hamstring Autograft

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All patients who had undergone primary ACLR from January 2017 to December 2018 were identified. The inclusion criteria were patients younger than 18 years who underwent surgery using a quadrupled hamstring autograft. Patients were excluded if their preoperative knee MRI scans were not available for viewing on the Synapse picture archiving and communication system (Synapse Workstation, version 4.4.210; FujiFilm Medical Systems USA, Stamford, CT). Additionally, patients were excluded from the study if they underwent a previous ACLR or ipsilateral knee operation or were aged 18 years or older. In all patients, the indication for surgery was symptomatic knee instability with an MRI-confirmed ACL tear.
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2

Spinal Anatomy Measurements Protocol

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Measurements of the C2 spine parameters, including width, height, length, and angle of the pedicle and lamina, were performed using the PACS program (Synapse Workstation FUJIFILM Medical Systems Stamford Connecticut USA, Inc., version 4.3.221). The measurements were recorded as millimeters and degrees by a single author. The measurements were repeated two times.
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3

Radiographic and MRI Evaluation of Lumbar Spine

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All individuals underwent anteroposterior and lateral lumbar X-ray radiography, as well as magnetic resonance imaging (MRI). Film viewing and parameter measurements were performed using the Picture Archiving and Communication System (PACS), specifically Fujifilm's Synapse Workstation (Version 3.2.1).
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4

Optimizing Imaging Protocols: Evaluating Dose and Quality

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We collected data for a 2-month period after implementing the new imaging protocol. The mean DLPs were compared before and after the implementation using the Wilcoxon rank-sum test. We also assessed any change in the prevalence of significant findings (category 3 or 4) by the Cochran-Armitage test. In addition, patients who underwent two non-contrast head CTs before and after the protocol change were selected to evaluate subjective imagequality parameters: noise (1, severely degraded images; 2, moderately degraded images; 3, minimally degraded images), severity of artifacts (1, severe artifacts affecting interpretation; 2, artifacts are present but do not negatively affect the interpretation; 3, no artifacts), and gray-white matter differentiation (1, unable to assess; 2, detectable; 3, well-visualized). Radiologists with 9 and 14 years of experience were blinded to the acquisition parameters, and they visually evaluated all 30 CT studies independently by reviewing axial images on ordinary workstations (Synapse workstation, Fujifilm Medical Systems, Japan). Subjective image quality parameters were scored and compared before and after the change in protocol by means of the Wilcoxon rank-sum test.
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