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Aortic Pressure

Aortic Pressure: The pressure within the aorta, the largest artery in the body.
Aortic pressure is an important indicator of cardiovascular health and can provide insights into conditions like hypertension, atherosclerosis, and aortic stenosis.
Researchers can leverage AI-driven tools like PubCompare.ai to optimize their research on aortic pressure, locating relevant literature, pre-prints, and patents, and conducting AI-driven comparisons to streamline their research process and improve the quality of their findings.
This MeSH term offers a concise, informative overview of this critical cardiovascular measurment.

Most cited protocols related to «Aortic Pressure»

The ARCSolver method aims to be a novel method for the determination of the aSBP and AIx based on oscillometric blood pressure measurement with a common cuff. The method16 has been developed by the Austrian Institute of Technology, Vienna, Austria. The method uses the pulse waves assessed at A. brachialis. The recordings are carried out at diastolic pressure level for approximately 10 s using a conventional blood pressure cuff for adults available in two sizes (24–34 and 32–42 cm) and a high fidelity pressure sensor (MPX5050, Freescale Inc., Tempe, AZ, USA). The sensor is connected to a 12 bit A/D converter by means of an active analogue band bass filter (0<>25 Hz). After digitalization, the signal processing is performed using a three level algorithm. In a first step, the single pressure waves are verified for their plausibility by testing the position of minima and the corresponding wavelengths. During the second stage, all single pressure waves are compared with each other to recognize artifacts. Thereafter, an aortic pulse wave is generated by the means of a generalized transfer function. The idea behind a transfer function is the modification of a certain frequency range within the acquired pulse signal to get the aortic pressure wave. Modulus and phase characteristics of the ARCSolver transfer function are illustrated in Figure 1a. Compared with data published by Karamanoglu et al.17 (link) similar parameters have been obtained.18 (link) The first positive zero crossing of the fourth-order time derivative of the generated aortic pulse wave represents the desired inflection point.19 (link) Finally, the coherence of the measured parameters is verified. Therefore, the inflection point of each single pulse wave is compared with the mean inflection point. The determination of aSBP and AIx is carried out in the same way as in SphygmoCor (see Figure 1b).
Publication 2010
Adult Aorta Aortic Pressure Bass Blood Pressure Determination, Blood Pressure Oscillometry Pressure Pressure, Diastolic Pulse Rate Tempeh
Sm22αCre, Brg1F/F,
Mef2cCre, R26R and
Tnnt2-rtTA;Tre-Cre mice have been described23 (link), 24 (link),
27 (link), 31 (link), 38 (link). Immunostaining, RNA in
situ hybridization, quantitative RT-PCR, and whole embryo culture were performed as
described23 (link), 26 (link). TAC was modified from previous descriptions20 (link). The pressure load caused by TAC was
verified by the pressure gradient across the aortic constriction measured by
echocardiography. Only mice with a pressure gradient > 30 mmHg were analyzed
for cardiac hypertrophy and gene expression. Curve modeling was performed with the
Levenburg-Marquardt non-linear regression method and XLfit software. Detailed
methods can be found in the Supplementary Information.
Publication 2010
Aortic Pressure Aortic Valve Stenosis Cardiac Hypertrophy Embryo Gene Expression In Situ Hybridization Mice, Laboratory Pressure Reverse Transcriptase Polymerase Chain Reaction Stenosis
Recordings were made in deeply anesthetized and laparatomized rats, with a cannula (BD Neoflon™ Cannula) connected to a pressure transducer (78534C MONITOR/ TERMINAL; Hewlett Packard, United States) inserted into the portal vein, inferior vena cava and abdominal aorta at the level of the bifurcation at 15 min, 24 h or 48 h post-ligation. Each recording lasted five minutes, being assessed in one minute intervals.
Notably, normal rats exhibited a portal pressure of 3–5 mmHg[25 (link)] similar to that of the inferior vena cava, though with at least 1 mmHg higher values in the portal vein. By contrast, abdominal aorta blood pressure values were 100–120 mmHg at the level of the bifurcation[21 (link)].
Publication 2020
Abdomen Aortas, Abdominal Aortic Pressure Cannula Ligation Portal Pressure Rattus norvegicus Transducers, Pressure Veins, Portal Vena Cavas, Inferior
Reservoir pressure (figure 2) was calculated from the ensemble averaged radial tonometric waveforms recorded by the Sphygmocor device without the application of a generalized transfer function. In brief, sphygmocor *.txt files were saved and data subsequently imported into Matlab (Mathworks, Inc, Natick, Massachusetts, USA) for analysis using customised programs based on (10 (link);21 (link)). Further details are provided in Supplementary data. Reservoir pressure is assumed to vary temporally in the same way throughout aorta and large elastic arteries, but with a time lag that depends on the location and wave propagation characteristics of the arteries (13 (link)). Mass conservation in an arterial system containing N vessels requires
Q0(t)=nNCndP¯(tτn)dt+nNP¯(tτn)PRn
where Q0(t) is the volume flow rate at the aortic root, Cn is the compliance of the vessel segment n, P¯(t) is the reservoir pressure at the aortic root, P¯(tτn) is the reservoir pressure in vessel n, Rn is the resistance of vessel n, τn is the time it takes for a wave to travel from the aortic root to vessel n and P is the pressure at zero flow.
Excess pressure in vessel n (XSPn) is defined as the difference between the measured pressure Pn(t) and the reservoir pressure
XSPn(t)=Pn(t)P¯(tτn)
Hydraulic work done by the ventricle (W) depends on the volume flow rate Qot and the pressure in the aortic root
W=0τP¯(t)Q0(t)dt
where t corresponds to the cardiac period. This work can be separated into reservoir and excess work
W=0τP¯(t)Q0(t)dt+0τXSP0(t)Q0(t)dtW¯+XSW
where reservoir work (W¯) is the hydraulic work done by the ventricle against the reservoir pressure and the excess work (XSW) is the work done against the excess pressure at the aortic root. For a given flow, Qo(t) the integral of the excess pressure (XSPI) is therefore an index of the excess work done by the ventricle.
Publication 2014
Aorta Aortic Pressure Aortic Root Arteries Blood Vessel Heart Heart Ventricle Medical Devices Plant Roots Pressure Tonometry, Ocular Vascular Resistance
The model of left ventricular wall mechanics is incorporated in lumped parameter models for the coronary and systemic circulation (Fig. 2). The aortic (AV) and mitral valve (MV) are modeled as an ideal diode. Vessels are modeled with constant resistances R, inertances L and capacitances C. The pressure drop Δp across each of these components is given by
with V the volume in the capacitance and q the flow through a resistance or an inertance. The pressure–volume relation of the capacitance represents a linearization around the physiologic working point, V0 representing the volume at zero pressure. Values of parameters in the circulation model were based on literature (Table 2).

Reference settings for parameters in the circulation model; coronary resistance values in parentheses represent maximum vasodilation.

Systemic circulationCoronary circulation
ParameterValueUnitParameterValueUnit
Rart5106 Pa s m−3Rart,c700 (200)106 Pa s m−3
Rper120106 Pa s m−3Rmyo,1900 (100)106 Pa s m−3
Rven5106 Pa s m−3Rmyo,2900 (100)106 Pa s m−3
Cart2010−9 m3 Pa−1Rven,c200106 Pa s m−3
Cven80010−9 m3 Pa−1Cart,c0.0310−9 m3 Pa−1
Vart,050010−6 m3Cmyo,c1.410−9 m3 Pa−1
Vven,0300010−6 m3Cven,c0.710−9 m3 Pa−1
Lart60103 Pa s m−3Vart,c0610−6 m3
Lven60103 Pa s m−3Vmyo,c0710−6 m3
Vblood500010−6 m3Vven,c01010−6 m3
The connection between the model of LV mechanics and the coronary circulation model is made through the intramyocardial pressure, that acts on the myocardial capacitance Cmyo,c. The values of the coronary capacitances were based on measurements by Spaan et al.:23 (link) 0.0022, 0.091 and 0.045 ml mm Hg−1 100 g−1 LV in large coronary arteries, myocardial coronary bed, and coronary veins, respectively. Zero pressure volumes were chosen such that under normal physiological conditions, time-averaged coronary volume was about 15 ml 100 g−1 of LV tissue, distributed over arterial, myocardial and venous vessels in a ratio of 1:2:2.23 (link)
In the coronary circulation, resistance values during normoxia and hyperemia were derived from Chilian et al.7 (link) In that study, total coronary resistance under normal and vasodilated conditions was measured to be 66 and 14 mm Hg min g ml−1, respectively. Distribution of resistance over the arterial, myocardial and venous compartment was measured to be 25, 68 and 7% under normal conditions, and 42, 27 and 31% under maximal vasodilation.
Systemic parameters are chosen to yield representative function curves for a 70 kg adult, at a heart rate of 75 bpm. LV wall volume was set to 200 ml, and cavity volume at zero pressure was set to 30% of this volume. The arterial load was modeled by a three-element windkessel model, consisting of a characteristic aortic impedance Rart, an arterial compliance Cart, and a peripheral resistance Rper. The peripheral resistance was chosen to yield realistic time-averaged values of aortic pressure and aortic flow. Next, arterial capacitance was chosen to yield realistic values of minimum and maximum aortic pressure. Total blood volume was set to 5000 ml. The blood volume at which mean systemic pressure is zero was assumed to be equal 70% of total blood volume, about 85% of which is contained in the venous system. Venous capacitance was chosen such that the additional 30% of blood volume leads a mean systemic pressure of about 2 kPa.
Publication 2006
Adult Aorta Aortic Pressure Arteries Artery, Coronary Blood Vessel Blood Volume Cardiac Volume CART protein, human Coronary Circulation Coronary Veins Dental Caries Heart Hyperemia Left Ventricles Mechanics Mitral Valve Myocardium Pressure Rate, Heart SERPINA3 protein, human Tissues Total Peripheral Resistance Vasodilation Veins

Most recents protocols related to «Aortic Pressure»

In the time domain, features can be calculated from the timing and amplitude of several fiducial points. The starting point of the pulse wave indicates the beginning of a pulse cycle and the end of the previous one. The time of the inflection point marks the arrival of the Pb (O'Rourke and Yaginuma, 1984 (link)). The notch is caused by aortic valve closure and blood reflux, representing the transition between the systolic and diastolic phases (Hartmann et al., 2019 (link)). The pulse wave systolic period is the duration between the starting point and the dicrotic notch point of the pulse wave, followed by the pulse wave diastolic period. Usually, the local maxima of the second derivative of the pulse waveforms are utilized to extract inflection points and dicrotic notch points (as in Figure 2 (Vlachopoulos et al., 2011 (link))).
For some participants (e.g., those with severe atherosclerosis), the inflection point of the aortic pulse wave is difficult or even impossible to extract. In order to make this pulse wave decomposition method more practical, it has been proposed to use 30% of the systolic time as the location of the inflection point (Miyashita et al., 1994 (link); Westerhof et al., 2006 (link)). In this paper, for pulse wave with inconspicuous inflection point, 30% of ejection time (ET) is used as the location of the inflection point to calculate the relevant features of pulse wave decomposition. The beginning of the pulse wave systole indicates the time of aortic valve opening and the start of ejection, and the notch time of the pulse wave is the time of aortic valve closure and the end of ejection. ET represents the systolic time of the pulse wave, which is determined by subtracting the beginning time from the end time of aortic flow (as in Figure 3).
In the arterial system, both aortic pressure and flow waveforms consist of forward waves (Pf, Qf) and backward waves (Pb, Qb). The CAPW mainly comprises forward and lower limb reflection waves (Westerhof et al., 1972 (link)). As shown in Figure 4, CAPW equals the sum of the Pf and Pb; and the flow wave equals the difference between the Qf and Qb, (as shown in Eq. 1, 2). P=Pf+Pb
Q=Qf+Qb
The basic principle of pulse wave decomposition is as follows (Westerhof et al., 1972 (link)): Pf=P+Zc×Q2
Pb=PZc×Q2 where, Q = U*A represents aortic flow; U is the flow velocity; A is blood vessels cross-sectional area; Zc is the characteristic impedance.
Since the pulse waveform is not affected by the Pb in the early systolic phase, Zc equals the ratio of blood pressure to flow (Li, 1986 (link); Khir et al., 2001 (link)), and Zc can also be calculated by high-frequency input impedance (Murgo et al., 1981 (link); Miyashita et al., 1994 (link)). The input impedance (Zin) is defined as follows: Zinw=Pw/Qw where P(w) and Q(w) are pressure and flow frequency components.
RI is the amplitude ratio of Pb to the sum of Pb and Pf, and the amplitude ratio of Pb to Pf is RM (Hametner et al., 2013 (link)). RM and RI are defined as follows: RM=PbPf
RI=PbPb+Pf
PTT can be determined by pulse wave decomposition, an important index to assess arterial stiffness in the young and old (Qasem and Avolio, 2008 (link)). PTT can be calculated as half the time difference between Pf and Pb (Tfb), as in Eq. 8. PTT=Tfb/2
Qasem and Avolio calculated the cross-correlation coefficient of Pf and Pb to determine Tfb (Qasem and Avolio, 2008 (link)). The time of maximum cross-correlation coefficient is the Tfb between Pf and Pb (as in Figure 5).
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Publication 2023
Aorta Aortic Pressure Arterial Stiffness Arteries Atherosclerosis BLOOD Blood Pressure Blood Vessel Diastole Lower Extremity Pressure Pulse Rate Reflex Systole Valves, Aortic
A biventricular test loop created HF scenarios utilizing dual pneumatic pumps (Abiomed AB5000™, Danvers, MA, USA) controlled by a double output driver. Inflows for one CFTAH (Figures 3A, B) and two UVADs (Figures 4A, B) were configured for both atrial and ventricular cannulations (15 (link)). Assessing BVADs occurred on a static test loop, which resulted in the generation of pressure-flow curves from several pump speeds. For each trial, the BVAD was operated over its entire range (i.e., device-specific motor speeds, aortic pressure ranging from 20 to 120 mm Hg), data was recorded, and pressure differentials were monitored and measured throughout the device.
In our feasibility study, the cannula had a longer length and smaller diameter, which resulted in an increase in flow resistance, requiring the pump to be operated at higher speeds than are typically used in a clinical setting. Ventricular cannulation was verified by measuring device inlet pressures with cannulae clamped proximally. Via fluid-filled pressure lines, hemodynamic data were recorded from both outflow cannulae. From fixed points on the outflow cannulae, near both pump outlets, total cardiac output was recorded.
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Publication 2023
Aortic Pressure Cannula Cannulation Cardiac Output Heart Atrium Heart Ventricle Hemodynamics Medical Devices Pressure
Continuous tracking of the brachial artery pressure waveform was obtained with standard methodology (41 (link)), and the average of 2 or more recorded profiles was used for PWA as previously reported (13 (link)). The AIx was calculated from the aortic pressure waveform as the difference in height between the first and the second systolic peaks that were expressed as a percentage of the pulse pressure. The intraobserver coefficient of variation of the AIx was 8.4%.
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Publication 2023
Aortic Pressure Brachial Artery Pressure Pulse Pressure Systole
The two Aims of this work are summarized in Fig 1. In Aim 1, we performed multiscale CFD simulations of patient-specific post-CABG models (including the native coronary artery stenoses) under computationally hyperemic conditions. Then, we compared the computational FFR in the grafted LAD derived from CFD with the angiographic FFR (CAAS vFFR, Pie Medical Imaging, Maastricht, Netherlands). The angiographic FFR was used as a surrogate for the invasive wire-based FFR [25 (link)]. In Aim 2(i), we 3D reconstructed post-CABG anatomies from CCTA and computationally created focal lumen stenoses with four degrees of severity (mild, moderate, severe, critical) in the LAD (proximal to the LIMA anastomosis; Fig 2). The stenosis of the LAD arteries of Aim 2 was less than 70%, thus exerting minimal impact. Then, in each post-CABG model with the computationally created LAD stenosis, we computationally removed all bypass grafts to reproduce the pre-CABG coronary artery anatomy (Fig 2). Using the computational framework of Aim 1, we compared the local hemodynamics [resting distal coronary pressure to aortic pressure ratio (Pd/Pa) and FFR] in the LAD before and after the LIMA grafting under computational resting and hyperemic conditions. In Aim 2(ii), we used the same post-CABG models as in Aim 2(i) and studied the impact of four different degrees of LAD stenosis on the flow in the LAD and LIMA under computational resting and hyperemic conditions. In total, in each patient of Aim 2, we computationally simulated 16 different conditions, i.e., 4 degrees of stenosis severity (mild, moderate, severe, critical) x 2 hemodynamic conditions (rest and hyperemia) x 2 CABG conditions (pre-CABG and post-CABG).
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Publication 2023
Angiography Aortic Pressure Arteries Artery, Coronary AURKB protein, human Coronary Artery Bypass Surgery Coronary Stenosis Heart Hemodynamics Hyperemia Patients Patient Simulation Pressure Stenosis Surgical Anastomoses
The CFD-derived FFR in the native LAD distal to the LIMA anastomosis was compared to the reference angiography-derived FFR. The angiographic FFR was calculated with the CAAS software (CAAS vFFR, Pie Medical Imaging, Maastricht, Netherlands). Briefly, the LIMA-LAD were semi-automatically segmented in two perpendicular angiographic projections and 3D reconstructed. The systemic aortic pressure was used as input for the automatic calculation of the angiographic FFR. Notably, the post-CABG CCTA and invasive angiogram were acquired within fewer than two months to minimize the effect of disease progression on the calculated hemodynamics with different imaging modalities.
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Publication 2023
Angiography Aortic Pressure Coronary Artery Bypass Surgery Disease Progression Hemodynamics Surgical Anastomoses

Top products related to «Aortic Pressure»

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The SphygmoCor is a non-invasive medical device developed by AtCor Medical. Its core function is to measure and analyze the arterial pulse wave, providing insights into the cardiovascular system's health and function.
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The SphygmoCor system is a non-invasive diagnostic device used to measure arterial stiffness and central blood pressure. It utilizes applanation tonometry to capture pressure waveforms from the radial artery, which are then analyzed to derive various parameters related to cardiovascular function.
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MATLAB is a high-performance programming language and numerical computing environment used for scientific and engineering calculations, data analysis, and visualization. It provides a comprehensive set of tools for solving complex mathematical and computational problems.
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The 78534C MONITOR/ TERMINAL is a display device that can be used as a monitor or a terminal for computing applications. It provides visual output for computer systems.
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PowerLab is a data acquisition system designed for recording and analyzing physiological signals. It provides a platform for connecting various sensors and transducers to a computer, allowing researchers and clinicians to capture and analyze biological data.
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The SphygmoCor XCEL is a medical device designed for the non-invasive measurement of central blood pressure and arterial stiffness. It utilizes applanation tonometry technology to capture peripheral pulse waveforms, which are then analyzed to derive central hemodynamic parameters.
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The SphygmoCor device is a non-invasive diagnostic tool designed to measure central blood pressure and arterial stiffness. It utilizes applanation tonometry technology to assess the mechanical properties of the cardiovascular system.
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The SPC-301 is a benchtop spectrophotometer designed for accurate absorbance and transmittance measurements. It features a wavelength range of 190 to 1100 nanometers, a spectral bandwidth of 1 nanometer, and a photometric range of -0.3 to 3.0 absorbance units. The SPC-301 is a versatile instrument suitable for a variety of applications.
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The SphygmoCor XCEL system is a noninvasive device that measures central blood pressure and arterial stiffness. It uses applanation tonometry to capture arterial pressure waveforms, providing objective data on cardiovascular health.
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The Vevo 2100 is a high-resolution, real-time in vivo imaging system designed for preclinical research. It utilizes advanced ultrasound technology to capture detailed images and data of small animal subjects.

More about "Aortic Pressure"

Aortic pressure, also known as central blood pressure or aortic systolic pressure, is a crucial cardiovascular measurement that provides valuable insights into an individual's overall health.
This parameter represents the pressure within the aorta, the largest artery in the body, and serves as an important indicator of cardiovascular wellbeing.
Researchers and clinicians can leverage advanced tools like the SphygmoCor system, powered by MATLAB, to accurately measure aortic pressure and gain a deeper understanding of conditions such as hypertension, atherosclerosis, and aortic stenosis.
The SphygmoCor device, also referred to as the SPC-301 or SphygmoCor XCEL system, is a widely used solution for non-invasive assessment of central hemodynamics, including aortic pressure.
This technology, along with the Vevo 2100 imaging system, allows researchers to optimize their research protocols and enhance the reproducibility of their findings on aortic pressure.
By utilizing AI-driven platforms like PubCompare.ai, researchers can streamline their literature search and analysis processes, identifying relevant publications, pre-prints, and patents related to aortic pressure.
This tool enables AI-driven comparisons, helping researchers improve the quality and efficiency of their research, ultimately leading to better understanding and management of cardiovascular conditions.
Accurate measurement and analysis of aortic pressure, facilitated by the SphygmoCor system and complementary technologies, is crucial for clinicians and researchers alike.
These insights can inform treatment decisions, monitor disease progression, and support the development of novel therapeutic strategies to address cardiovascular health challenges.
With the aid of innovative tools and AI-driven research optimization, the study of aortic pressure continues to advance, promoting improved patient outcomes and advancements in the field of cardiovascular medicine.