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Acuson s2000 system

Manufactured by Siemens
Sourced in United States, Germany

The Acuson S2000 system is a diagnostic ultrasound device manufactured by Siemens. It is designed to provide high-quality imaging for various medical applications. The system features advanced technology to generate detailed, real-time images of the body's internal structures.

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11 protocols using acuson s2000 system

1

Carotid Artery Plaque Strain Imaging

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Radio frequency (RF) data were acquired on all patients using a Siemens Acuson S2000 system and an 18L6 transducer (Siemens Medical Solutions, Malvern, PA, USA). Acquisitions over several cardiac cycles were made at the common carotid artery, the carotid bifurcation and internal carotid artery on both left and right carotid arteries for each patient. Plaque in each of the end diastolic frames were manually segmented by an experienced sonographer.
Displacement estimation was performed using a multi-level algorithm [16 (link), 17 (link)] with Bayesian regularization [18 (link)]. Displacement information was used to propagate the manual segmentations from end diastole to other frames over the cardiac cycle. Axial, lateral and shear strain were calculated from accumulated displacement vector estimates. A fast GPU version of the algorithm was used for the estimation reported in this paper [19 ]. Figure 1, shows an example of axial, lateral and shear strain maps obtained. The maximum accumulated strain index (MASI) was calculated from the estimated strain distribution as previously described [5 (link)]. MASI quantifies the strain distribution in a small region of interest with highest strain values over the entire plaque and over a cardiac cycle.
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2

Kidney CEUS Imaging Protocol

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The ultrasonographic device used in this study was an Acuson S2000 system equipped with a C6-2 transducer (Siemens, Erlangen, Germany), with a frequency of 2–6 MHz. The patients lay on their side. The left kidney was displayed to capture its form, echo, and size in the long-axis view. The contrast agent SonoVue (Bracco, Milan, Italy), consisting of sulfur hexafluoride microbubbles, was prepared according to the manufacturer’s instructions. After the CEUS mode was initiated, 0.5 mL of contrast agent was administered through the superficial elbow vein using the bolus injection method, followed by a 5 mL flush with 0.9% saline. Image acquisition was performed by a physician with more than 5 years of CEUS experience. The patients were asked to hold their breath for at least 30 s and then breathe slowly and smoothly for up to 3 min.
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3

Ultrasound Phantom Characterization Experiment

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For our experimental data acquisitions, we utilized two uniformly attenuating TM phantoms that were constructed in our laboratory. Both phantoms consist of microscopic glass beads and graphite powder in an agar gel background. The reference phantom has glass beads with diameters ranging from 5 to 43 μm in concentration of 4 g per liter and a uniform attenuation coefficient of 0.5 dB/cm/MHz (±2%). The sample phantom has glass beads with diameters ranging from 75 to 90 μm in concentration of 2.8 g per liter, and a uniform attenuation coefficient of 0.8 dB/cm/MHz (±2%). Speed of sound for both phantoms was 1540 m/s.
The physical TM phantoms were scanned using an ACUSON S2000 system (Siemens Medical Solutions USA Inc., Mountain View, California) equipped with a 9L4 linear array transducer. The transmit pulse was centered at 6 MHz with a −3dB bandwidth of 50%. Imaging depth was set to 6 cm. Focal depth was at 5 cm. Ten independent frames of RF data were collected by translating the transducer in the elevational direction. As in the simulated case, we vary the processing parameters and compute estimation statistics across all independent frames of RF data. These statistics are plotted against corresponding processing parameters and presented in the “Results” section.
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4

Liver Stiffness Assessment by Ultrasound

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Ultrasound was performed after 8–12 hours of strict fasting. The ultrasound doctor was blinded to the results of the endoscopy. Conventional ultrasound and ARFI imaging were performed using the Siemens Acuson S2000 system. The oblique diameter of the right lobe of the liver, spleen thickness, and spleen diameter (SD) were measured, and the degree of ascites was defined based on recent guidelines (15 (link)). The portal vein system was observed, and the collateral vessels were determined as described in the literature (13 (link)). Successful detection of the LGV was defined as identification of the vein on the B-mode image (8 (link)). The average of 3 valid measurements was considered, and the LGV flow volume (mL/min) was calculated as π × (diameter/2)2 × 60 × velocity. LS and SS were measured by ARFI (m/s). Each parameter was repeatedly measured 10 times, and the average was calculated. Failure of ARFI imaging was defined as absence of valid shots, and unreliable measurements were defined as a median interquartile range greater than 30% or success rate less than 60%.
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5

Fine Needle Aspiration of Cervical Lymph Nodes

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The nature and possible consequences of the fine needle aspiration procedure were explained through informed consent. An ultrasound scan of the neck including Doppler analysis safely identified accessible CLNs (Siemens Acuson S2000 system and 18L6 HD probe). Then, under sterile conditions, level Va/Vb, or Ia/Ib nodes were targeted via rotatory corkscrew motions of a 23G needle and transferred into Dulbecco’s PBS (D-PBS): the procedure was repeated two to three times. Tuerk’s solution was used to estimate mononuclear cell count and the remaining material was centrifuged at 200g for 5 min. The fine needle aspiration pellet was resuspended in D-PBS supplemented with 1% bovine serum albumin, mononuclear cells were separated using Ficoll density gradient solution, washed and then resuspended in D-PBS-1% bovine serum albumin. Aspirate supernatants were removed and stored at −80°C for CXCL13 measurement.
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6

Ultrasound-Based Gastrocnemius Muscle Analysis

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The architecture of the medial gastrocnemius muscle was measured by an ultrasound Acuson S2000 system (Siemens Healthcare, Erlangen, Germany) using an 18L6 HD linear-array transducer (Siemens Medical Solutions) with a range frequency of 6–18 MHz. The probe was placed at the mid-edge medial gastrocnemius muscle belly, which was directly over the tape in the case of the two taping interventions (ST and KT). For all three interventions, the probe position was marked in advance in order to assure the proper placement of the transducer. In addition, a custom-built frame was used to secure the probe in place without applying any additional compression force to the monitored area during MVIC and lunge movement as illustrated in Fig. 4b,c. In order to segment the lunge task for further analysis, the ground reaction force (GRF) was measured by two force platforms (981B, Kistler Instrument Corporation, Amherst, NY, USA) at a sampling rate of 1000 Hz and an eight-camera ExperVision Motion Analysis System which captured 15 standard reflective markers with a diameter of 25 mm attached on the anatomical landmarks of the lower trunk following the modified Helen-Hayes marker set. After post-processing, OrthoTrak 6.6 software was used to get the ankle angle.
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7

Multimodal Imaging Evaluation of Cancer

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CT examinations were performed on dedicated CT scanners (Siemens Flash, Siemens Somatom AS, Siemens Healthineers, Erlangen, Germany). Iodinated contrast medium was administered intravenously 70 s before the scan. CT was acquired using the manufacturer-supplied dose reduction CareKV and CareDose 4D.
Axillary sonography was conducted by experienced gynecologists (A.K.B. and S.M.) with over 10 years of expertise in breast and axillary ultrasound. The following systems and transducers were utilized: an Acuson S2000 system (Siemens Healthcare GmbH, Erlangen, Germany), a SuperSonic Imagine Aixplorer (Toshiba Medical Systems GmbH, Neuss, Germany) and an Aplio MX SSA-780A System (Toshiba Medical Systems GmbH, Neuss, Germany), all equipped with 5 to 12 MHz linear array transducers.
Bone scintigraphy was performed with planar whole-body scans using a dual-headed gamma camera equipped with low-energy high-resolution collimator (Symbia S, Siemens Healthineers). Three hours after intravenous injection of a body-weight-adapted amount of [99mTc]-labeled polyphosphonate (PDP), anterior and posterior view scans were acquired with an acquisition time of 20 to 35 min. In all cases of uncertain radionuclide accumulations in the bone scan, additional target images or SPECT/CT images were acquired.
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8

ARFI Liver Stiffness Measurement Protocol

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ARFI imaging was done with an Acuson S2000 system (Siemens Medical Solutions). Liver stiffness was measured with a standardized protocol at two locations of the right hepatic lobe[12 (link),13 (link)]. The mean of the two locations was used as the final measurement. Most of the studies were done by one senior technician (HTW). Because it is not covered by the Taiwanese National Health Insurance Administration, the charge of ARFI (around 50 United States dollars) was mostly paid by the patients. The exceptions were patients undergoing a liver biopsy study or those participating in clinical trials (around 25%), where the cost was paid for by research grants. The first ARFI study was used in this analysis. The ARFI-estimated fibrosis grades was according to the cutoff values in our previous histology proven study[13 (link)].
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9

Diagnostic Imaging of Budd-Chiari Syndrome

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All examinations were performed by an attending physician with at least 3 years of experience. Doppler ultrasound (DUS) images were acquired with a Siemens Acuson S2000 system (Siemens Medical Solutions, Mountain View, CA, USA), equipped with a C-1 curved array transducer. All patients fasted for 6–8 h before the examination and lay supine with their right arm raised above their head to expand the intercostal space. The portal vein diameter and peak velocity were measured at 1–2 cm from the junction of the superior mesenteric vein and splenic vein; the splenic vein diameter and peak flow velocity were measured at 1–2 cm near the splenic hilum. All measurements were made three times by the same operator. The local stenosis or occlusion of hepatic veins can be seen in DUS with the following characteristics: ① hypoechoic substances fill the veins, ② venous stenosis with upstream dilation, ③ fibrous hyperechoic cords replace the veins, and ④ intraluminal thrombus. The presence of at least one of these imaging features is sufficient for the diagnosis of BCS-HV. The DUS images and reports of all patients were collected retrospectively.
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10

Quantifying Venous Reflux via DUS

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The standardized DUS examination protocol has previously been described in detail elsewhere. 7 In short, an ACUSON S2000 system (Siemens Medical Solutions, Malvern, PA) with 9-and 18-MHz transducers was used to asses reflux in the superficial, perforator, and deep veins. To exclude significant central obstruction, normal phasic flow during breathing in the common femoral vein was mandatory. Distal compression and a following rapid release was carried out with an automatic cuff unit (Ekman Biochemical Data AB, Gothenburg, Sweden) inflated to 100 mm Hg. The first second after release of distal compression was used to classify reflux in the proximal part of the GSV. The above classification is based on data correlating peak flow velocity and volume flow with venous hemodynamics. GSV incompetence was defined as severe (>100 mL/min and/or a maximal flow velocity of >30 cm/s), moderate (30-100 mL/min and/or <30 cm/s) or mild (<30 mL/min). 17 The proximal part of the GSV was used for diameter measurements. At the 1-year follow-up, reflux and incompetent accessory branches in and below the treated area were evaluated.
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