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Ge lightspeed scanner

Manufactured by GE Healthcare
Sourced in Germany, Japan

The GE Lightspeed Scanner is a high-performance computed tomography (CT) imaging system designed for medical diagnostic applications. It utilizes advanced technology to capture detailed images of the body's internal structures, enabling healthcare professionals to make informed clinical decisions.

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2 protocols using ge lightspeed scanner

1

Radiological Evaluation of Pulmonary Lesions

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In all the 105 patients, chest X-rays (CXRs) were taken and repeated; 84 patients underwent chest spiral computed tomography (CT) examinations and repeated in most of them. CT scans were performed with different scanner types, but with similar CT protocols. The CT scanners included a Somatom Plus 4 CT Scanner (Siemens, Erlangen, Germany), a GE Lightspeed Scanner (GE Medical Systems, Milwaukee, USA). Chest CT scans of the entire lungs were obtained while the patients were in a supine position at the end of inspiration. The scanning parameters included 120 kV, 150–350 mAs, 5 mm collimation, and a pitch of 1 or 1.5. All scans were viewed at standard lung window settings (level − 700 HU, width 1500 HU).
The CXR and chest CT images were retrospectively reviewed by two independent diagnostic radiologists who were experienced in the interpretation of thoracic radiological images. They reached a consensus decision regarding the findings. We used a standard glossary of radiological images definitions to describe the pulmonary lesions.[10 (link)]
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2

Natural Course of Asymptomatic OPLL

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The study was approved by the IRB of the Clinical Research Support Center of the University of Tokyo Hospital. Written informed consent was obtained from all subjects. The subjects in this study comprised healthy individuals who had undergone whole-body CT scans for cancer screening at our institution between September 2007 and December 2011. All CT volumes were scanned by a GE Light Speed Scanner (GE Healthcare Japan; 120 kV, 80 mA, 512 × 512 matrix). We retrospectively reviewed axial CT images of 2585 subjects in the bone window with automatic adjustment. The diagnosis of OPLL was established by two experienced spine surgeons (T.D. and S.H.). OPLL was defined as ossification of the posterior longitudinal ligament with more than a 2-mm thickness 6, 23 from the atlas to the pelvis. Among subjects who were diagnosed with OPLL, we selected those who underwent follow-up CT at least 5 years after the initial examination. Subjects who underwent surgical treatment for OPLL during the follow-up period were excluded because this study focused on the natural course of OPLL mass in asymptomatic subjects.
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