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Ie elite

Manufactured by Philips
Sourced in United States

The Philips IE Elite is a laboratory equipment designed for precise and reliable analysis. It features advanced technology to deliver accurate and consistent results. The core function of the IE Elite is to provide high-performance laboratory testing capabilities.

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15 protocols using ie elite

1

Perimembranous VSD Diagnosis and Factors

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Philips IEElite advanced cardiac color Doppler ultrasound and Philips IE33 advanced cardiac color Doppler ultrasound systems were used for VSD diagnosis. The frequency of the probe was 3-5 MHz, and they could display the location, size, and the base, width, depth of the perimembranous aneurysm, and the width of the breach in multiple sections, angles, and directions. If there were multiple breaches, it was calculated by the sum of all breach widths

Determination of inflammatory factors in aneurysmal perimembranous tissue: aneurysmal perimembranous tissue with a size of 3 mm × 3 mm was taken from the breaches from all children with APVSD during the operation. The tissue was minced and ground sufficiently, and the suspension was collected by centrifugation. The levels of IL-1β, IL-6, TGF-β, and TNF-α were determined by ELISA.

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2

Carotid Plaque in Ischemic Stroke

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The present study recruited 218 patients with ischemic stroke from the Department of Neurology, Second Hospital of Jilin University, Changchun, China between November 2015 and March 2017. Their demographic information and clinical characteristics were detailed in our previous publications (14 (link), 15 (link)). All patients had atherosclerotic carotid plaques and the carotid intima-media thickness (CIMT) was measured via the examination with a diagnostic ultrasound system (iE ELite, Philips, Franklin, TN, USA). These patients aged 61.2 ± 0.8 years included 127 males and 91 females. A total of 198 healthy subjects aged 61.1 ± 0.8 years were simultaneously recruited as controls from local communities and well-matched for ethnicity, age and sex. The participants who had history of any types of malignant tumors or autoimmune disorders, such as autoimmune thyroid disease, pernicious anemia, multiple sclerosis, type I diabetes, celiac disease, systemic lupus erythematosus, and inflammatory bowel disease, were excluded from this study. All eligible participants were of Chinese Han origin and they all gave informed consent to take part in this study as approved by the Ethics Committee of the Second Hospital of Jilin University, Changchun, China (IRB#: SHJU2017-099), and conformed to the requirements of the declaration of Helsinki.
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3

Ultrasound Imaging with SonoVue Contrast

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A Philips IE Elite ultrasound diagnostic instrument with an S5-1 probe at 2.5 to 3.5 MHz was used in this study, and the data analysis was completed using offline Q-Lab 9.0 software. The ultrasound contrast agent used was SonoVue (Bracco, Italy).
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4

Atherosclerosis Biomarker Plasma Study

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Plasma samples were collected from patients with atherosclerosis who were
admitted to the Department of Neurology, Second Hospital of Jilin University,
Changchun between November 2015 and March 2017. All patients showed
atherosclerotic carotid plaques and carotid intima–media thickness was analyzed
using a diagnostic ultrasound system (iE Elite, Philips, Franklin, TN, USA).
Participants who had suffered from any type of malignancy or autoimmune
disorders such as autoimmune thyroid disease, pernicious anemia, type 1
diabetes, celiac disease, multiple sclerosis, systemic lupus erythematosus and
inflammatory bowel disease were excluded. Because most patients with
atherosclerosis were taking lipid-lowering drugs at the time of sampling,
information regarding circulating lipid levels was not collected. This study was
approved by the Ethics Committee of the Second Hospital of Jilin University and
was performed in accordance with the ethical guidelines of the Declaration of
Helsinki. All participants were of Chinese Han descent and all provided written
informed consent for use of their blood samples in this study. All samples were
anonymized prior to analysis, so the identities of participants could not be
ascertained in any way.
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5

Echocardiography Data Acquisition Protocol

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Each echocardiographic examination was acquired through standard methods. Videos from three standard apical views were include in this study: apical 4-chamber (A4C), apical 2-chamber (A2C), and apical long axis (ALX). Images were acquired from a diverse array of standard echocardiography machine manufacturers including Phillips EPIQ 7C and iE-elite with S5-1 and X5-1 transducers (Phillips, Andover, MA, United States), and Vivid E95 (General Electric, Fairfield, CT, United States) and portable bedside machines including Philips CX50 and Mindray M9cv with transducer SP5-1s (Mindray, Shenzhen, Guangdong, China). All images were stored with a standard Digital Imaging and Communication in Medicine (DICOM) format according to the instructions from each manufacturer.
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6

Postnatal Echocardiography Procedure

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Postnatal echocardiography was performed with a Philips EPIQ 7C and IE Elite ultrasound diagnostic instrument, with the probe frequency set at 3.0–8.0 MHz. According to the American Society of Echocardiography (ASE) pediatric echocardiography guidelines (17 (link)), the heart was comprehensively scanned by segmental analysis to observe the origin, internal diameter, and blood flow of the pulmonary artery and its branches. The development of other cardiovascular structures was also evaluated.
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7

Echocardiographic Assessment of Ventricular Function

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Echocardiography was performed routinely at hospital admission. Digital echocardiograms were analyzed on the EchoPAC workstation (Philips IE Elite). Left ventricular end-diastolic and -systolic volumes were obtained using Simpson’s method of discs in the apical 4- and 2-chamber views as recommended by the American Society of Echocardiography [22 (link)]. Left ventricular ejection fraction (LVEF) was calculated using left ventricular volumes and the formula: [(end-diastolic volume − end-systolic volume)/end-diastolic volume] × 100%.
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8

Echocardiographic Evaluation of Right Ventricular Function

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Echocardiography was used to evaluate the structure and function of RV at the end of the experiment. Echocardiographic evaluation was measured by transthoracic echocardiography using a 15 MHz phased array transducer (Philips IE Elite). The indicators of diastolic and systolic thickness of the RV, and tricuspid annular plane systolic excursion (TAPSE) were measured as previously described (2 (link)).
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9

Ultrasound Imaging with Philips iE Elite

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A Philips iE Elite color Doppler ultrasound diagnostic equipment, equipped with 2D phased array probe s5-1 (frequency 2.0–3.5 MHz), real-time three-dimensional probe x5-1 (frequency 1.0–3.0 MHz) was used.
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10

Measuring Radial Artery Diameter by Ultrasound

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All measurements were performed in an air-conditioned room with constant temperature. Before the examination, patients were requested to rest for at least 15 min and to not ingest caffeine or tobacco during the previous 24 h. The images were acquired using an ultrasound system with a 5.0–12.0 MHz linear transducer (Philips iE-elite, Amsterdam, Netherlands). A schematic representation of measuring RA by ultrasound is shown in Fig. 1. The diameter of the distal RA was measured at a landmark 2–3 cm above the styloid process using ultrasound to evaluate the radial sheath insertion point. Similarly, the diameter of the proximal RA was measured at 2 cm below the cubital fossa to evaluate the outlet of radial sheath where there was no sheath protection. Measurements were taken across the three timepoints (preoperative baseline, 24 h, and 48 h after the procedure). At each timepoint, we assessed the distal and proximal of right RA (cannulated) functions as well as left RA (noncannulated) functions using flow-mediated dilation (FMD) and nitroglycerin-mediated dilation (NMD).
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