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Epic7g

Manufactured by Philips
Sourced in Norway

The Epic7G is a high-performance lab equipment product designed for precise and efficient analysis. It features advanced analytical capabilities to support various research and testing applications. The core function of the Epic7G is to provide reliable and accurate data measurements, enabling researchers to make informed decisions. Further details on the intended use of this product are not available.

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5 protocols using epic7g

1

Comprehensive Echocardiographic Evaluation of Cardiac Chambers

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Comprehensive transthoracic two-dimensional and Doppler echocardiographic examination were performed using a commercially available ultrasound system (iE33 or Epic7G, Philips Medical System, Andover, Massachusetts; Vivid E95, GE Healthcare, Horten, Norway).
3DE was performed according to guidelines of the American Society of Echocardiography (ASE) using an iE33, Epic7G, or Vivid E95 equipped with a 3DE transducer (X5-1, Philips Medical System, Andover, Massachusetts; 4V or 4Vc, GE Healthcare, Horten, Norway) (3 (link)). 3DE datasets that focused on the left heart chamber were acquired from the apical approach in one- or multi-beat acquisition mode. In addition, 3DE datasets that focused on the right heart chamber were acquired from more lateral transducer positions. In order to increase the volume rate, the width of the image sector size was reduced as narrow as possible, keeping orthogonal 2D echocardiographic images encompassing the entire right ventricle. Datasets were transferred to a separate workstation for off-line analysis.
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2

Echocardiographic Imaging Database for Cardiac Disease

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Echocardiograms of patients with congenital and structural heart disease were selected retrospectively from the routine clinical imaging database of the Department of Cardiology III—Adult Congenital and Valvular Heart Disease at the University Hospital Muenster. Echocardiograms were chosen for diversity of underlying disease etiology (see Table 1), comprehensiveness of echocardiographic views and quality of acquired loops. In addition, echocardiograms of patients without a cardiac abnormality were prospectively included according to the aforementioned criteria. The examinations were performed on different echocardiography machines from different vendors (especially GE Vivid E9, Vivid E95, Vivid 7; Philips EPIC 7C, EPIC 7G, iE33). Two-dimensional (2D) echocardiographic studies performed according to current guideline recommendations [1 (link)] were anonymized, exported and converted into individual frames in a PNG format for automated analysis. In total, individual frames of 17 separate TTE views were obtained. Figure 1 details the utilized echocardiography views.
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3

Comprehensive Cardiac Assessment via 3D Echocardiography

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3DE was performed immediately after standard transthoracic 2D echocardiography (2DE) and Doppler echocardiography. 3DE images were acquired using an apical approach and commercially available ultrasound machines (iE33 or Epic7G, Philips Healthcare, Andover, MA; Vivid7 or Vivid E95, GE Healthcare, Horten, Norway) equipped with a 3DE transducer (X3-1 or X5-1, Philips Healthcare, Andover, MA; 4V, GE Healthcare, Horten, Norway). Trans-mitral flow velocity was recorded at the coaptation point of both leaflets. Mitral annular velocities were recorded at septal and lateral sides of the mitral annulus, and average e' was calculated. Peak aortic flow velocity was recorded in multiple transducer positions, and the highest value was used for the measurements of the mean pressure gradient (PG) and velocity-time integral (VTI). RV fractional area change (RVFAC) was calculated by standard formula. 2DE RV speckle tracking analysis was performed using commercially available, vendor-independent, fully automated strain analysis software (AutoStrain RV, TomTec Imaging Systems, Unterschleissheim, Germany). The software automatically determined the RV endocardial border and performed speckle tracking analysis during a single cardiac cycle. The endocardial border was manually corrected as required. RV free-wall longitudinal strain (RVfwLS) and global longitudinal strain (RVGLS) were calculated.
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4

Comprehensive Abdominal Ultrasound Evaluation in Cats

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Cats were scanned using an Epic 7G or an iU22, with a curvilinear 8–5 MHz, or linear 12–5 MHz or 18–5 MHz transducer (Phillips). Images, video clips and reports were reviewed by a board-certified radiologist (DP) and a diagnostic imaging resident (TM).
The presence, echogenicity, amount of peritoneal/retroperitoneal effusion and mesenteric fat echogenicity were evaluated. Evaluation of abdominal LNs included thickness, echogenicity and margination. LNs >5 mm thick were considered enlarged.16
Hepatobiliary assessment included subjective liver size, echotexture and echogenicity, focal lesions (number and size), common bile duct dilation (>4 mm), and gallbladder wall thickening (>1 mm) and contents.17
GI tract evaluation included wall thickness, layering, and extent and distribution of lesion(s). Wall thickness was considered normal if it was 2–4 mm for the stomach, up to 2.5 mm for the duodenum and jejunum, 2.8 mm for the ileum and 1.5 mm for the colon.18 (link)
The splenic size was considered normal if the mean thickness was ⩽1 cm, as previously described.19 (link)
Splenic echogenicity and echotexture were subjectively assessed. Renal evaluation included size, shape, echogenicity, presence of focal lesions, subcapsular rim and pyelectasia. Urinary bladder wall thickness and contents were reported if abnormal.
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5

Comprehensive Echocardiographic Assessment

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Comprehensive transthoracic 2DE and Doppler echocardiography were performed according to guidelines from the American Society of Echocardiography [8] , using a commercially available ultrasound system and transducer (X5-1, iE33 or Epic7G, Philips Medical Systems, Andover, MA, USA). LV inflow velocity was recorded at the tip of the mitral leaflet using pulsed-wave Doppler echocardiography, and mitral annular velocity at both sides of the mitral annulus was recorded with tissue Doppler echocardiography. Systolic pulmonary arterial pressure was determined using the formula [4 * (peak tricuspid regurgitation velocity) 2 + right atrial pressure]. Subsequently, 3DE datasets aimed at the left heart chambers were acquired using an apical approach in either multibeat or one-beat acquisition mode (HMQ). All 3DE datasets were transferred to a separate workstation for off-line analysis.
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