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Eub 8500

Manufactured by Hitachi
Sourced in Japan

The EUB-8500 is a compact and versatile ultrasound system designed for a wide range of clinical applications. It features a high-resolution display, intuitive user interface, and advanced imaging capabilities. The EUB-8500 is intended for use by healthcare professionals in diagnostic and treatment settings.

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5 protocols using eub 8500

1

Contrast-enhanced Ultrasound Imaging Protocol

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The contrast agent used in CEUS was SonoVue (Bracco SpA, Milan, Italy). The agent consisted of microbubbles containing sulfur hexafluoride (SF 6) encapsulated in phospholipids. The microbubbles had a mean diameter of 2.5 μm and pH values of 4.5–7.5. The SonoVue powder was thoroughly dissolved in 5 mL normal saline; then, 2.4 mL of the solution was injected into the bolus through the cubital vein.
The ultrasound devices used included Aplio500 (TOSHIBA CORPORATION, Tokyo, Japan), LOGIQ E9 GE (General Electric Company, Boston, MA, USA), EPIQ7 (Philips Electronic N.V, Amsterdam, The Netherlands), EUB-8500 (HITACHI, Tokyo, Japan), and Aixplorer (SuperSonic Imagine, Aix-en-Provence, France). The CEUS function was available on all these devices. A linear array probe was selected with a frequency of 5.0–12.0 MHz for small masses, while an abdominal convex array probe was used with a frequency of 3.0–5.0 MHz for large masses, as the linear array probe may not be fully displayed.
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2

Achilles Tendon Evaluation through Strain-Elastography

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All patients underwent an exam of both Achilles tendons with real-time tissue S-ELA procedure (Hitachi system EUB-8500, with L54 M transducer, frequency 6–13 MHz) and gray-scale sonographic findings performed simultaneously (B mode) [9 (link), 10 (link)].
Longitudinal and axial scans in three areas of Achilles tendon (in the proximal area near the myotendinous junction, in the middle, and in the distal area of the insertion of the tendon in the calcaneus bone) enabled the assemblage of several integrated images to evaluate its morphological structure, as well as its stiffness and to classify it using a semi-quantitative score of different colors to represent stiff tissue (blue, grade 1) to more soft tissue (green-yellow, grade 2) and (yellow-red, grade 3) [9 (link)] (see Fig. 1).

Strain-Elastography. a Normal stiffness. b Abnormal elasticity greater deformability. Red color. c Morphological and stiffness alteration

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3

Contrast-Enhanced Ultrasound Imaging Protocol

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The contrast agent used in CEUS was SonoVue (Bracco SpA, Milan, Italy). The agents were microbubbles of the phospholipids microencapsulated sulfur hexafluoride (SF 6). The microbubbles had an average diameter of 2.5 μm and pH values of 4.5–7.5. After the SonoVue powder was thoroughly dissolved in 5 mL of normal saline, 2.4 mL of the solution was injected into the bolus through the cubital vein.
The ultrasound devices used included the Aplio500 (TOSHIBA CORPORATION, Tokyo, Japan), LOGIQ E9 GE (General Electric Company, Boston, Massachusetts, USA), EPIQ7 (Philips Electronic N.V, Amsterdam, The Netherlands), EUB-8500 (HITACHI, Tokyo, Japan), and Aixplorer (SuperSonic Imagine, Aix-en-Provence, France). The CEUS function was available on all of these devices. A linear array probe was used (frequency 5.0 -12.0 MHz).
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4

Infrarenal Aortic Diameter Measurement

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The abdominal aorta was scanned from proximal of the superior mesenteric artery in distal direction by Ultrasound (Hitachi EUB 8500). The maximum infrarenal aortic diameter above aortic bifurcation was recorded. Diameters were traced from wall to wall of the aorta in both transverse and anterior–posterior directions. We chose the diameter values in anterior–posterior direction. All measurements were performed by professional technicians under a standard protocol.
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5

Ultrasound Evaluation of Thyroid Nodules

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Baseline clinicopathological information comprised sex, age, ultrasonographic appearance (largest nodule diameter, location), and pathological results. The included ultrasound images were collected using the Esaote Mylab Class_C (Esaote Group, Genoa, Italy, shallow probe) and the HITACHI EUB-8500 (Hitachi, Tokyo, Japan, shallow probe) ultrasound equipment. The dynamic images and the maximum-diameter tomographic images of the nodules when scanning the lesions were retained and were stored in the picture archiving and communication system workstation for later measurements and evaluations by the doctors. The TI-RADS scoring items comprise composition, echo, shape, margin, and calcification. Two senior radiologists with >8 years of work experience from each hospital measured and scored the lesions in all patients. The four doctors were unaware of other assessments and pathological results, and any differences were resolved through negotiation to ensure the reliability of the data. Any histological and pathological findings of unclear significance were discarded, and only accurate and undisputed reports were used.
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