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Epiq 7c system

Manufactured by Philips
Sourced in United States

The EPIQ 7C system is a diagnostic ultrasound device manufactured by Philips. It is designed to provide high-quality imaging for a variety of clinical applications. The system features advanced imaging technologies and tools to assist healthcare professionals in making informed clinical decisions.

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6 protocols using epiq 7c system

1

Echocardiographic Assessment of Intracardiac Thrombus

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Transthoracic echocardiography was performed on patients at their admission. Two‐dimensional and targeted M‐mode echocardiography with Doppler colour flow mapping were performed by Philips EPIQ7C system (Philips Ultrasound, Bothell, WA, USA). Routine parameters, including LVEF, LVEDD, and left atrial diameter, were measured by echocardiograph according to the American Society of Echocardiography and the European Association of Cardiovascular Imaging guidelines. LVEF is calculated via biplane modified Simpson's method. Intracardiac thrombus was confirmed by echocardiography. The presence of an echo‐dense mass protruding into the atrial and/or ventricular chamber with margins distinct from the atrial and/or ventricular wall, endocardium, and papillary muscles was identified as intracardiac thrombus (Figure 2). To avoid as far as possible the artefacts or potential false positive findings, multiple views, including apical four‐chamber view and left parasternal long‐axis view, were explored. Each echocardiographic image was read and checked by at least two experienced echocardiographic cardiologists for internal controls.
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2

Contrast-Enhanced Transthoracic Echocardiography

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The cTTE study was performed using a Philips Epiq7c system fitted with an S5–1 probe (1–5 MHz). The TTE test was routinely performed to rule out cardiac shunt due to other reasons before the injection of mixture solution. The apical four-chamber view was used to record the count of microbubbles continuously. Following recordings in basal condition, it was repeated during a VM. The VM was performed by the patients blowing into a plastic tube connected to the manometer device [15 (link)]. We asked patients to carry out the VM a few seconds before the contrast injection and maintain until the right atrium was filled with the contrast agent. If the testing results with or without VM were positive, two more operations were needed to assess its reproducibility. The maximum number of bubbles recorded from the left ventricle was regarded as the ultimate result.
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3

Echocardiographic Assessment of Pressure Gradients

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All subjects underwent TTE using an EPIQ 7C system (Philips Medical System, Andover, MA, USA), equipped with X5-1 matrix transducer. The 2D grey-scale images were acquired over three heart cycles and analysed using QLab software (version 10.0 Philips Medical System, Andover, MA, USA) by one of four experienced echocardiographers, blinded to the CT data. Transaortic peak and mean pressure gradients were derived using the simplified Bernoulli equation (Table 1). Change in mean pressure gradient was defined as the difference between the pressure gradient values measured pre-procedurally and during follow-up.
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4

Comprehensive Cardiac Assessment Protocol

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In the medical examination, the presence of ischemic heart disease, arterial hypertension, and diabetes mellitus was accurately recorded; moreover, cardiovascular drugs taken, weight, height, and systolic and diastolic arterial pressure were recorded. Heart rhythm and heart rate were assessed using a 12-lead electrocardiogram. History of chronic heart failure (CHF) was defined based on the current European Society of Cardiology criteria [6 (link)].
Echocardiographic images were obtained using an echocardiography EPIQ 7C system (Philips, Amsterdam, Netherlands) equipped with a 5-MHz probe. Left and right systolic functions were assessed by measuring the left ventricular ejection fraction (LVEF) (Simpson rule) and the systolic peak of the tricuspid annular plane excursion [7 (link)]. Mitral regurgitation (MR) and tricuspid regurgitation (TR) were semi-quantitatively evaluated using color Doppler, with arbitrary units ranging from 0 to 4. Dilatation of the inferior vena cava and its collapsibility during inspiration were evaluated to establish a central venous pressure (CVP) > 5 mmHg. Finally, pulmonary arterial systolic pressure (PASP) was evaluated based on the peak velocity of TR and estimation of the CVP [7 (link)].
Blood samples were taken to evaluate serum creatinine (mg/dL) and hemoglobin (g/dl) levels. The baseline GFR was calculated using the EPI formula [8 (link)].
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5

Echocardiographic Evaluation of Mitral Valve

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The measurements were performed echocardiographically using the Philips Epiq 7c system. All the parameters were taken by a single person to avoid observer bias. The area of mitral valve was calculated using 2D planimetric method. Continuous-wave Doppler was used to measure the gradients across the mitral valve and pulmonary artery systolic pressure.
Post-BMV mitral valve area, pulmonary artery pressure, mean mitral gradient, and global LA strain were measured 24–48 h after procedure. Delta (Δ) was used to define the absolute changes in the valve area and gradients across the mitral valve pre- and post-BMV.
ΔMitral valve area=postBMVMVAvaluepreBMVMVAvalueΔMean mitral gradient=postBMVMMGvaluepreBMVMMGvalue
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6

Echocardiography Protocol for Analyzing Left Ventricular Strain

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Echocardiography was performed in accordance with current guidelines, using two machines: between 2009 and 2019 a Philips iE33 system, equipped with a S5-1 transducer, and, since 2019, a Philips EPIQ 7C system (both Philips, Amsterdam, The Netherlands), equipped with a X5-1 transducer. Left ventricular wall thickness was measured on 2D B-mode end-diastolic images. Wall thickness was defined as the average of the septal and posterior wall thickness. For strain analysis, we used QLab 10.5 software, (Philips, Amsterdam, The Netherlands). For the analysis of the regional strain differences (to find the so called apical sparing or “cherry on top” sign), we followed the method originally described by Phelan et al. [7 (link)], and used the following equation: relative apical LS (longitudinal strain) = average apical LS/(average basal LS + average mid LS). All measurements were performed by a single experienced echocardiographer.
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