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Ascendus

Manufactured by Hitachi
Sourced in Japan

The Ascendus is a laboratory instrument designed for the analysis and separation of complex biological samples. It utilizes advanced chromatography techniques to enable efficient purification and characterization of biomolecules such as proteins, nucleic acids, and other macromolecules. The core function of the Ascendus is to provide accurate, high-performance separation and analysis capabilities to support a wide range of scientific research and development activities.

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10 protocols using ascendus

1

Diagnostic Ultrasound Image Analysis

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In total, 537 ultrasound images from 221 patients in the Picture Archiving and Communication Systems acquired during 2015 to 2018 were retrospectively analyzed (Table 1). The images came from a variety of machines, including Phillips IU22, IE33, or CX50 (Philips Healthcare, Eindhoven, the Netherlands); HITACHI Hi Vision Preirus or Ascendus (Hitachi Ltd, Tokyo, Japan); GE Logiq E9, S6, S8, E6, or E8 (GE Healthcare, Milwaukee, WI); Siemens S1000/S2000 (Siemens Healthineers, Munich, Germany); and Toshiba Aplio 300 or Aplio 500 (Toshiba Medical Systems, Tokyo, Japan). Histopathological examination, including aspiration biopsy and surgery pathology, was used as the reference standard. Images without artifacts were eligible for participation. Nodules larger than the region of interest (ROI), diffuse diseases, and cystic nodules were excluded. Multiple lesions without a separable nodule were excluded as well. Moreover, another set of 85 images from 38 patients were prepared for the initial validation of the CNN-based CAD systems. All images were stored as PNG data. In this study, 30 additional cases were enrolled prospectively to evaluate the value of the separate and combined CAD systems and the ultrasound guidelines. The study was approved by the Ethics Committee of the Third Affiliated Hospital of Guangzhou Medical University.
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2

Breast Lesion Biopsy Training Phantom

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Students practiced the US-guided core-needle biopsy on an in-house-designed training phantom which looked like a “round pie” of black ink colored agar–agar gel, with several green olives floating inside, mimicking breast lesions (Fig. 2). Presence of olive material inside the biopsy needle confirmed a correct biopsy.
The US devices were Hitachi Preirus and Hitachi Ascendus. The biopsies were performed using BARD® MAGNUM® biopsy system.
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3

Unresectable Pancreatic Cancer Protocol

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Patients diagnosed with unresectable pancreatic cancer (locally advanced or metastatic disease) between January 2011 and October 2016, as evaluated by both computed tomography (CT) scan and endoscopic ultrasound (EUS), were eligible for inclusion in this analysis [30 ]. Confirmation of pancreatic adenocarcinoma by cytology or histology after EUS-guided fine needle aspiration (FNA) or fine needle biopsy (FNB) was required for final inclusion. EUS and EUS-guided FNA or FNB was performed in all patients by two experienced endosonographers using Pentax linear echoendoscopes and Hitachi Preirus (2011–2012) or Ascendus (2012–2016) equipment. All FNA and FNB samples were evaluated by a single highly experienced pathologist. Patients who survived less than 30 days after diagnosis, in whom no therapy could be started, and those who underwent neoadjuvant chemotherapy for downstaging, were excluded from the analysis.
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4

University Hospital Ulm Ultrasound Units

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The following ultrasound units were used for examinations performed at university hospital Ulm:

GE Logiq E9 (year launched: 2008–2015; CE marking: 0459);

Siemens Acusion S3000 (year launched: 2012; CE marking: 0123);

Toshiba Aplio 500 (year launched: 2011; CE marking: 0197);

Toshiba Aplio i800 (year launched: 2016; CE marking: 0197);

Mindray TE5 und TE7 (year launched: 2020; CE marking: 0123);

Philips IU22CE (year launched: 2004; CE marking: 0086);

Philips Epiq 7 (year launched: 2013; CE marking: 0086);

Hitachi Ascendus (year launched 2011; CE marking: 0123).

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5

Comprehensive Lower Limb Ultrasound for PE

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Complete lower limb compression ultrasonography was performed within 24h of the diagnosis of PE by the same operator with extensive experience in echo-colour Doppler (7,5 Mhz linear probe, Ascendus, Hitachi, Japan).
In detail, common iliac vein, common femoral vein, superficial femoral vein, saphenofemoral junction, popliteal vein and posterior tibial vein were investigated. Each vein was examined in both longitudinal and cross-section scansions. Ultrasonographic criteria for deep-vein thrombosis were non-compressibility or incomplete compressibility of the vein [14 (link)].
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6

Microwave Ablation of Thyroid Nodules

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The following data were recorded before treatment: three diameters of the nodules (largest diameter, d1 and two perpendicular diameters, d2 and d3); the composition of the nodules (assessed by US examiner subjectively); the cosmetic grading score (CGS; 1: no palpable mass, 2: invisible but palpable mass, 3: visible mass visible only to experienced clinician's eyes, and 4: easily visible mass) [32] ; and the symptomatic score (SS; visual analog scale, 0-10) indicating the distress of patients. The volume (V) of the nodules was calculated using the following equation:
US examination of thyroid nodules was performed before treatment and at each follow-up (1, 3, 6 and 12 months postoperatively and every 6 months thereafter) with a Hitachi Ascendus instrument (L75-type high-frequency linear array, frequency range: 5-18 MHz). The MWA therapy instrument used was a KY-2000 (Kangyou Medical, Nanjing, China) that consists of a microwave generator, a flexible low-loss coaxial cable and a cooled 16-G shaft antenna (a 10-cm shaft coated with polytetrafluoroethylene and a 3-mm narrow radiating segment 3 mm from the tip). The generator can produce 1-100 W of power at 2450 MHz; the energy we used for thyroid ablation was between 30 and 50 W. Cooled MWA was applied to reduce the occurrence of complications [19, 33, 34] .
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7

Ultrasound Imaging with Linear and Convex Probes

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Ultrasound systems with 4.0-8.0 MHz linear transducers and 2.0-5.0 MHz convex array probes were used (Philips IU22, Koninklijke Philips NV, and Hitachi Ascendus). All of the examinations were performed by experienced sonographers (with > 5 years of experience). Training courses on how to collect the standard images and save them to the picture archiving and communication system (PACS) were organized for the sonographers.
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8

Carotid Intima-Media Thickness Measurement

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Using the GE Logiq E9 at a transducer frequency of 6-15 MHz or the Hitachi Ascendus at a transducer frequency of 5-18 MHz, a designated experienced sonographer performed ultrasonography Doppler to measure the intima-media thickness (IMT) of the common carotid artery (CCA). The distance between the first and second echogenic line edges was used to determine the IMT. The mean value of the IMT was computed after three sets of measurements were made. The ankle pressures of both legs were measured and the ABI was calculated.
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9

Comprehensive Carotid Ultrasound Protocol

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CDU along with TCCD or TCD were used in this study and were mandated per protocol. An EPIQ5 (Philips Medical Systems, Bothell, WA, USA The Netherlands) CDU with a 3.0–12.0 MHz linear array transducer or an Ascendus (Hitachi, Tokyo, Japan) CDU with a 4.0–8.0 MHz micro-convex transducer and phased array probe with 1.0–5.0 MHz was used. All CDU examinations were performed by vascular ultrasonography trained doctors with > 5 years of experience. A standardized approach was used, with the patients placed in a supine position. The transducer was placed in a sagittal plane at the mid-cervical region and adjusted to optimize the visualization of the proximal ICA. The ultrasound transducer was adjusted to ⩽ 60° angles to measure PSV and EDV. The negative blood flow signal detected through the temporal acoustic window at the depth of 60~75 mm (related to the biparietal diameter) corresponds to anterior cerebral artery (ACA). When the temporal sound window has poor or no sound transmission, ACA can be checked through the eye window. When the ipsilateral carotid artery is compressed, the direction of ACA blood flow is reversed, which can confirm the accuracy of ACA detection and the existence of ACoA.11
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10

Ultrasound Assessment of Achilles Tendinopathy

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Worst pain and pain during walking was collected with a numerical rating scale going from 0 (indicating no pain) to 10 (worst imaginable pain). For ultrasonographical assessment of the Achilles tendon, we used a Hitachi Ascendus with an 18 Hz linear transducer.
Ultrasonographical measures were collected due to their potential association with patient symptoms (15, 16) . Doppler settings were the same for all patients, with a gain setting just below the noise level and pulse repetition frequency set to 1.0. Tendon thickness was measured at the thickest point in a longitudinal scan perpendicular to the greatest width of the tendon (the true thickness) in accordance with earlier recommendations (17) . All included patients had ultrasonographically determined spindle-shaped thickening, inhomogeneity and hypoechogenicity of the symptomatic tendon with increased Doppler activity. Doppler settings were the same for all patients, with a gain setting just below the noise level and the V scale set to 350. We ranked the colour Doppler activity from grades 0 to 4, where grade 0 = no activity, 1 = single vessel, 2 = Doppler activity in >25%, 3 = Doppler activity in 25% to 50%, and 4 = Doppler activity in > 50% (18) . The same experienced specialist in rheumatology performed both the measurements before and after the surgery and was blinded to the treatment.
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