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Echopac bt 11

Manufactured by GE Healthcare
Sourced in Norway

Echopac BT 11.1.0 is a software application developed by GE Healthcare for processing and analyzing ultrasound images. It provides tools for visualizing, measuring, and quantifying various cardiac parameters from echocardiographic data.

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7 protocols using echopac bt 11

1

Echocardiographic Assessment of CRT Outcomes

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Echocardiographic studies (GE Vivid 7 system, Horten, Norway) were analysed (GE EchoPAC BT11, Horten, Norway) by investigators blinded to all other patient data. LV end-diastolic and end-systolic volumes (LVEDV and LVESV) and EF were measured by the biplane Simpson's rule. Dyssynchrony analysis using speckle-tracking echocardiography (STE) was performed as recommended by the American Society of Echocardiography/Heart Rhythm Society.10 (link) Radial strain was obtained from mid-LV short-axis images with endocardial and epicardial regions of interest adjusted for optimal time-strain curves. Radial dyssynchrony was defined as a septal to posterior peak strain opposite wall delay of ≥130 ms.5 (link) Our intraobserver variability is 6±6% and interobserver variability is 8±7%. Changes in EF and LV volumes were determined approximately 1 year after CRT. ECG width and morphology were obtained from automated computer analysis of ECGs and review of electrophysiologist notes prior to CRT implantation. The predefined clinical outcomes were death, transplant or left ventricular assist device (LVAD), and a composite of death or first HF hospitalisation following CRT. Clinical events were adjudicated independently by two investigators blinded to all echocardiographic data.
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2

Assessing Left Ventricular Mechanics

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A short-axis view (mid LV at the level of the papillary muscles) was acquired with a commercial system (5MHz probe Vivid-7, Vingmed- General Electric, Fairfield, CT, USA) during the pacing protocol as described above. Radial strain was acquired from the mid-LV short axis view as previously described to assess LV mechanics8 (link). Briefly, frame rates of 70–90 Hz were used for acquisition and endocardial and epicardial borders were manually traced to create a region of interest which was adjusted and re-drawn on playback if required to accomplish optimal tracking (GE EchoPac BT11, Horton, Norway). QRS-to-peak radial strain (ms) was measured in 6 different LV segments at baseline, and during PACs and PVCs only. LV dyssynchrony in the ectopic beat alone was assessed by the dispersion of QRS-to-peak strain between all segments (earliest – last QRS-to-peak strain). Radial strain analysis was performed in at least one PVC beat by a blinded reader.
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3

Comprehensive Echocardiographic Evaluation

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All echocardiograms were obtained using Vivid E7 and Vivid 9 ultrasound systems (GE Healthcare, Horten Norway) and all images were stored digitally on a central server. All participants were examined with conventional two-dimensional echocardiography, m-mode, pulsed-wave TDI, colour TDI and two-dimensional strain imaging. All the echocardiographic analyses in the present study were performed de novo and offline (blinded to other clinical data) using Echopac BT11 software (GE Healthcare, Horten Norway).
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4

Echocardiography Assessment of Pulmonary Hypertension

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The Doppler echo parameter 'pulmonary artery acceleration time' (PAAT) is negatively correlated with the mean pulmonary arterial pressure (PAP) measured invasively, namely increased pulmonary hypertension or an increase in PAP as judged by a decreased PAAT (28 (link),29 (link)). Therefore, PAAT is considered as an echocardiographic indicator of PH (30 (link)). PH was also assessed using Doppler echocardiography at day 28 of the study. Transthoracic closed-chest echocardiography was performed by an experienced doctor using a Vivid E9 ultrasound system equipped with a 12-MHz transducer (GE Healthcare). Rats were anesthetized by i.p. injection of 3% sodium pentobarbital (40 mg/kg) and placed in a shallow left lateral decubitus position, and an ultrasound gel was applied to the shaved chest. Blood flow through the pulmonary artery and PAAT were measured in the two-dimensional short-axis parasternal view by M-mode and Pulsed-wave Doppler at the level of the pulmonary valve. Papillary muscles were used as the reference point for echocardiography measurements. PAAT was measured from the onset of systolic flow to peak pulmonary outflow velocity according to the American Society of Echocardiography guidelines (31 (link)). The acquisition of Echo images and all the echocardiographic analyses were performed using Echopac BT11 software (v.6.5; GE Healthcare).
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5

Echocardiographic Assessment of Myocardial Strain

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The assessment of the images was executed using a Vivid 7 (General Electric, Horten, Norway) echocardiographic machinery. A frame rate of 60 - 75/s was adopted for obtaining the images. Subsequently, they were digitally transferred to a remote workstation for offline analysis (Echopac BT 11.1.0, General Electric, Horten, Norway). All analyses were made by only one experienced operator who had been kept blinded to clinical and biochemical data concerning the patients. Two-dimensional speckle tracking was executed by means of a semiautomatic algorithm. In short, using manual identification, three reference points (two annular and one apical) were selected in each of the three apical views, so as to enable the software to monitor the myocardium in a semi-automated manner in the course of the cardiac cycle. Each ventricular wall was subsequently subdivided into three segments so as to realize the creation of 17 segments covering the whole myocardium. Accurate manual inspection for tracking purposes was performed, and in the case of unsatisfactory tracking, the segment would have been ousted from the analysis. Longitudinal strain curves were built for each segment and the maximum value was determined. The GLS was then computed as the average of all 17 segments.
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6

Speckle Tracking Echocardiography Evaluation

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The evaluation of the echocardiograms was accomplished by means of a Vivid 7 (General Electric, Horten, Norway) echocardiographic machinery. A frame rate of 60 - 75/s was used for acquiring the images. Then, they were digitally transferred to a remote workstation for offline analysis (Echopac BT 11.1.0, General Electric, Horten, Norway). All analyses were performed by only one experienced operator who had been kept blinded to clinical and biochemical data concerning both the patients, i.e. subjects taking sacubitril/valsartan, and controls. Two-dimensional speckle tracking echocardiography was carried out using a semiautomatic algorithm.
In brief, using manual determination, three reference points (two annular and one apical) were chosen in each of the three apical views, so as to enable the software to monitor the myocardium in a semi-automated manner during the entire course of the cardiac cycle. Each ventricular wall was then splitted into three segments so as to achieve the generation of 17 segments encompassing the entire myocardium. Thorough manual inspection for tracking purposes was carried out, and in the case of imperfect tracking, the segment was removed from the analysis. Longitudinal strain curves were built for each segment and the maximum value was calculated. The GLS was then inferred as the mean of all 17 segments.
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7

Echocardiographic Assessment of LV Function

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Echocardiography was performed within 48 h of admission to the tertiary centre. Three consecutive heart cycles were acquired. All examinations were performed on a Vivid e9 system (General Electric, Horten, Norway). Images were obtained at a frame rate of at least 50 frames/s and analysed offline (Echopac BT 11.1.0, General Electric). All analyses were performed by a single experienced operator (M.E.) who was blinded to follow-up information. Measurements of LV volumes and function, LVEF, LV end-diastolic volume (EDV) and LV end-systolic volume (ESV) were performed using biplane Simpson model.
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