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205 protocols using acuson s2000

1

Brachial Artery Diameter and Flow Measurement

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The FMD measurements were performed with patients in the supine position. Patients were instructed to avoid caffeine-, nicotine- and alcohol-containing products for at least 12 h before measurements. A blood pressure cuff was placed around the upper arm distal to the brachial artery segment that was explored. Ultrasound images were acquired using a commercially available ultrasound system with an 18 MHz high-resolution linear-array transducer (Acuson S2000, Siemens Healthcare, Erlangen, Germany). The cuff was continuously inflated 50 mmHg above the patient’s systolic blood pressure for 5 min. Brachial artery diameter and flow velocity were recorded using 2D echography prior to cuff inflation, at deflation and after deflation at 1 min intervals for 5 min. The probe was angulated at 90° for optimal morphologic B-mode imaging and <60° for optimal velocity acquisition. Diameter measurements were made with electronic calipers at the end of ventricular diastole (Fig. 1).

Ultrasound in M-mode (Acuson S2000 @18 MHz 18L6 40 frames/s, Siemens Medical, Erlangen, Germany) illustrates cross-sectional imaging of the brachial artery. The vessel diameter is determined according to the orthogonal distance between the intima reflexion zone (double arrow = 4.9 mm; longitudinal scale 25 mm)

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2

Liver Assessment via Multimodal Imaging

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Liver status was assessed under fasting conditions by qualified staff at the Clinic University of Navarra. The presence of hepatic steatosis was determined by means of Ultrasonography (Siemens ACUSON S2000 and S3000) in accordance with previously described methodology [6 (link)]. In addition, liver stiffness was evaluated by Acoustic Radiation Force Impulse (ARFI) elastography (Siemens ACUSON S2000 and S3000) and transient elastography through FibroScan® (Echosens, Paris, France). Ten valid ARFI measurements were performed in each patient [22 (link)] to estimate the median value of liver stiffness. The same qualified radiologist from the department of Ultrasonography and Radiology executed all the ultrasonographic evaluations. In order to quantify the fat and iron content of the liver as well as the hepatic volume, a Magnetic Resonance Imaging (MRI) (Siemens Aera 1.5 T) was also performed to each participant following standardized procedures [6 (link)]. The MRI assessment of liver fat and iron content was performed through the Dixon method.
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3

Comprehensive Liver Ultrasound Assessment Protocol

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A detailed description of the liver ultrasound scans has been published previously [20 (link)].
Briefly, upper abdominal USS was completed by one of four trained sonographers using a Siemens Acuson S2000 USS system, with the participant at rest in the dorsal decubitus position. Echogenicity (a marker of liver fat) was assessed during deep inspiration and recorded as present, absent or uncertain according to established protocols using the right kidney as the reference organ [21 (link)].
Acoustic radiation force impulse-imaging (ARFI) of the right lobe of the liver was used to measure liver stiffness (or fibrosis), using standard protocols [22 (link), 23 (link)] and this was used as our main indicator of liver fibrosis. The right lobe of the liver was viewed through the intercostal space such that the pulse wave was traversing an area of at least 6 cm and was not traversing any major vascular structures and the right lobe was clearly viewed.
Estimated liver volume was assessed by three transversely (lateral to medial), from diaphragm down to the inferior pole of the liver (cranio-caudal) and back to front (posterior to anterior) sweeps through the liver.. These produced distances, which were used to calculate liver volume with the Siemens Acuson S2000 system software.
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4

Standardized Ultrasound Examination for Breast Evaluation

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All women in our second-level centre undergo a standardized ultrasound examination if referred for (1) routine or screening mammography in cases of breast density ACR C or D, or in case of (2) a suspicious finding upon mammography, (3) referral due to a suspicious finding upon clinical examination, or (4) referral from an extramural radiology practice due to suspicious imaging findings. Examinations were performed on an Acuson Sequoia, Acuson S2000 or S3000 Evolution US scanner with an 18–6 or 13.5 MHz high-resolution probe (Siemens, Erlangen, Germany) encompassing a systematic scanning of the axillary and breast regions. Focal lesions were documented in two perpendicular planes to determine the relation to surrounding tissue, size, B-mode, and Doppler properties. SE was performed by repeated controlled compression of the tumour and the surrounding tissue. Compression quality was assessed by visual inspection and by the vendor-specific quality index. Only SE images with a high quality index (>90 on Acuson S2000 or S3000, >65 on Acuson Sequoia) were used for further analysis. In addition, special attention was paid to ensure that the elastographic ROI was no more than a quarter in the chest wall in order to avoid any artefacts. Based on previously published criteria, lesions were graded according to U.S. BI-RADS criteria [19 ].
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5

Breast Tumor Ultrasound Segmentation Protocol

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Breast ultrasound examinations were carried out by sonographers with more than 5 years of experience in breast ultrasound imaging, within 2 weeks before surgical resection. Ultrasound was performed using the LOGIQ E9 ultrasound system with a 6–15 L linear array probe and the Siemens Acuson S2000 with a 6–18 L linear array probe with radial, transverse, and longitudinal scanning on both breasts. The imaging parameters were consistent among patients: gain was about 50%; image depth was about 3.0 cm to 5.0 cm; and focus paralleled the lesion. The ultrasound image was 1164 × 873 pixels and 1024 × 768 pixels in size on the LOGIQ E9 and Siemens Acuson S2000 devices, respectively. The image of the largest section of the breast tumor with the clearest imaging was saved in the format of Digital Imaging and Communications in Medicine to maximize the preservation of the image information. Manual segmentation was performed on gray-scale ultrasound images of breast lesions. Sonographer 1 (with more than 5 years of experience in breast ultrasound imaging) with no information about the patient’s clinical history selected the largest plane of each breast lesion and drew an outline of the region of interest (ROI) by using ITK-SNAP software (version 3.4.0).
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6

Breast Lesion Stiffness Evaluation by Ultrasound

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B-mode US images of the lesions were acquired with a Siemens Acuson S2000 device (Siemens Medical Solutions, Mountain View, CA, USA), using an 18 L6 HD (5.5–18 MHz) linear transducer. To evaluate the stiffness of lesions, SE was performed using a Siemens Acuson S2000 device (Siemens Medical Solutions, Mountain View, CA, USA) with a 9L4 (4–9 MHz) linear transducer. When performing SE, the freehand compression method described by Itoh et al. [1] was used. With the patient in supine position, the US transducer was positioned parallel to the breast lesion. To achieve appropriate contact with the skin, slight pressure was applied through the transducer over the breast tissue, resulting in its displacement by 1-2 mm posteriorly, and coming back to its initial location, and elastography images were acquired. The compression sufficiency was adjusted according to quality factor 60 and higher as an adequate value. A region of interest (ROI) box was placed on the targeted lesion, and another ROI box was placed on reference tissue determined to be adjacent fat tissue, to measure strain ratio. Strain ratio was calculated by comparing the strain value of the reference tissue with that of the targeted lesion.
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7

Siemens Ultrasound Elastographic Evaluation

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All US and ARFI elastographic examinations were performed using Siemens Acuson S2000, Acuson S3000 and Acuson Sequoia (Siemens Medical Solutions, Erlangen, Germany) by two independent, qualified investigators (ESZ, AA) under the supervision and active participation of a German Society for Ultrasound in Medicine (DEGUM) Level III qualified examiner (CG, internal medicine) with more than 35 years of US experience.17 (link) With the patient laying supine, the curvilinear transducer (6C1) was placed gently on an area of the abdomen where the OM was optimally visualised. Focus and gain were adjusted as needed. The echogenicity of the lesion was classified as hypoechoic or isoechoic/hyperechoic compared with that of the spleen as an in vivo reference. Both echogenicity, and thickness of the of the OM (largest diameter in cm), as well as the presence of ascites were evaluated on B-mode US.
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8

Standardized Thyroid Nodule Ultrasound Protocol

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US examinations were performed according to a standard protocol that includes grayscale and color Doppler US assessment of the thyroid bed and cervical lymph nodes in all neck compartments. US reports include information about size, location, and structure of thyroid nodules and cervical lymph nodes. Size was defined as the largest diameter among the 3 dimensions observed. The US studies were performed with Siemens Acuson S2000 or SEQUOIA (Siemens Medical Solutions, Mountain View, CA), or the GE Logiq 9 (GE Healthcare, Little Chalfont, UK) units, using 8- to 15-MHz linear transducers.
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9

Ultrasound Diagnosis of Cervical Lymphatic Malformation

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A high-resolution ultrasound system, equipped with a 4–15 MHz transducer (Acuson S2000; Siemens, Hamberg, Germany), was used to diagnose cervical lymphatic malformation. Patients in whom the relationship between the lesion and adjacent structures was not clear by ultrasonography because of individual cysts < 1 mm in diameter underwent further evaluation by magnetic resonance imaging (MRI) (Signa; GE Medical Systems, Milwaukee, WI, USA) or contrast-enhanced computed tomography (CT). All patients underwent colour Doppler and power Doppler ultrasonography. Ultrasonographic diagnosis and differential diagnosis were based on the intracystic fluid echo, thickness of cyst wall, cyst location, and colour flow signal distribution. The macrocystic (cysts > 1 cm in diameter), microcystic (individual cysts < 1 cm in diameter), and mixed types were classified according to the cyst diameter. Cervical lymphatic malformation was diagnosed with haemorrhage, infection, and/or calcification according to increased cyst diameter (compared with prior size) and intracyst fine spot echo, local pain, increased temperature and abnormal blood test results, and calcified plaque in cyst before treatment, respectively.
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10

Carotid Plaque Assessment Protocol

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Carotid artery two‐dimensional grey scale images were examined using a standardised protocol with a Siemens Acuson S2000 ultrasound scanner equipped with a 9L4 linear transducer (Siemens, Forchheim, Germany) and interpreted by regularly trained operators.19 (link) Carotid plaque was defined in accordance with the Mannheim consensus.30 (link) Common carotid, bulb and internal carotid arteries were examined, and participants without valid readings in both right and left carotid arteries were excluded for the analysis. Participants were classified as having either no plaque, unilateral plaque/s or bilateral carotid plaques.31 (link) For splines analysis, a carotid plaque score was calculated as follows: no plaque=0, unilateral plaque/s=1 and bilateral plaques=2.
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