US20170354331A1 - Blood Pressure and Arterial Compliance Estimation from Arterial Segments - Google Patents
Blood Pressure and Arterial Compliance Estimation from Arterial Segments Download PDFInfo
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Definitions
- the disclosure relates to methods for at least one of blood pressure and arterial compliance estimation from arterial segments.
- the pulse wave generated by left ventricular ejection, propagates at a velocity that has been identified as an important marker of atherosclerosis and cardiovascular risk.
- Increased pulse wave velocity indicates an increased risk of stroke and coronary heart disease. This velocity is considered a surrogate marker for arterial compliance, is highly reproducible, and is widely used to assess the elastic properties of the arterial tree.
- research shows that measurement of pulse wave velocity as an indirect estimate of aortic compliance could allow for early identification of patients at risk for cardiovascular disease. The ability to identify these patients would lead to better risk stratification and earlier, more cost-effective preventative therapy.
- LVET left ventricular ejection time
- a method for determining material characteristics for an artery including providing at least three values for each of blood pressure, internal radius, and external radius of an arterial segment or segments of a subject; applying a base model of fluid-structure interaction incorporating conservation of mass and momentum for the fluid, and non-linear elasticity of the structure; and running a mathematical optimization on the base model to provide a calibrated model to determine material characteristics of the arterial segment or segments.
- a method for determining at least one of a blood pressure and an arterial compliance parameter of a subject including providing a value for pulse wave velocity within an arterial segment or segments of a subject; providing a value for flow velocity within the arterial segment or segments of the subject; providing a value for blood density of the subject; providing the material characteristics of an artery; and applying a calibrated model of fluid-structure interaction incorporating conservation of mass and momentum for the fluid, and non-linear elasticity of the structure, to calculate at least one of blood pressure and an arterial compliance parameter of the subject using the provided values.
- FIG. 1 is a diagram on the longitudinal cross section of the arterial wall at diastolic ( 10 ) and systolic ( 11 ) pressure;
- FIG. 2 is a graph of the dependence of distensibilty on transmural pressure and a flow velocity
- FIG. 3 is a flowchart depicting creation of a blood pressure and distensibility lookup table
- FIG. 4 is a format of a lookup table for blood pressure and distensibility
- FIG. 5 is a flowchart depicting a method for determining blood pressure of a subject based on a PWV measure using a lookup table
- FIG. 6 is a flowchart depicting a method for determining arterial compliance of a subject based on a PWV measure using a lookup table
- FIG. 7 is an illustration of pressure pulse measurement on two locations in the same artery for determination of a systolic and diastolic PWV;
- FIG. 8 is a flowchart depicting a method for determining the material characteristics of an arterial segment.
- a fully nonlinear model of pressure and flow propagation in arterial segments is disclosed that enables determination of blood pressure and arterial compliance based on measures of pulse wave velocity and flow velocity following a calibration.
- the approach allows for determination of systolic and diastolic blood pressure.
- the approach allows for determination of a systolic and diastolic aortic compliance.
- a noninvasive method for monitoring the blood pressure and arterial compliance of a patient based on measurements of a flow velocity and a pulse wave velocity is described.
- An embodiment uses a photoplethysmograph and includes a method to monitor the dynamic behavior of the arterial blood flow, coupled with a hemodynamic mathematical model of the arterial blood flow motion in a fully nonlinear vessel.
- a derived mathematical model creates the patient specific dependence of a blood pressure versus PWV and blood flow velocity, which allows continuous monitoring of arterial blood pressure.
- the calibrated mathematical model presents an arterial compliance and a distensibility as a clinical marker of arterial stiffness.
- the disclosure is applicable for fully nonlinear elastic vessels that are commonly found in the major arteries, as well as smaller vessels that operate closer to the linear elastic regime.
- the disclosure includes a fully nonlinear basic model for blood pressure wave propagation in compliant arteries.
- a nonlinear traveling wave model was used to investigate mechanisms underlying the effects of pressure, ejection time, ejection volume, geometric, and physical properties on PWV.
- a patient calibration procedure was developed that involves measurement of blood pressure and arterial dimensions (internal and external radii).
- An embodiment includes blood pressure prediction using the model, per patient calibration, and the measurement of flow velocity and pressure wave velocity.
- An embodiment includes arterial compliance determination using the model, per patient calibration, and the measurement of flow velocity and pressure wave velocity.
- a basic mathematical fluid-structure interaction model for pulse wave velocity (PWV) propagation incorporates the dynamics of incompressible flow in a compliant vessel.
- This one dimensional model simulating blood flow in arteries effectively describes pulsatile flow in terms of averages across the section flow parameters. Although it is not able to provide the details of flow separation, recirculation, or shear stress analysis, it accurately represents the overall and average pulsatile flow characteristics, particularly PWV.
- t time
- z the axial coordinate shown in FIG. 1
- ⁇ is blood density
- Equation (5) indicates sensitivity of pressure with respect to the wall normal deflection, and has a clear interpretation as tangent (incremental) moduli in finite strain deformation.
- equation (5) is supplemented by appropriate constituent equations for a hyperelastic anisotropic arterial wall, accounting for finite deformation.
- R, Z, H an internal radius, axial coordinate and a wall thickness in a stress free configuration
- r,z,h internal radius, axial coordinate and a wall thickness in a physiologically loaded configuration
- the Green-Lagrangian strain components relate to the principal stretch ratios of Eq. 12 by
- Arterial stiffness, or its reciprocals, arterial compliance and distensibility may provide indication of vascular changes that predispose to the development of major vascular disease.
- compliance is defined as a change of a volume V for a given change of a pressure, and distensibilty as a compliance divided by initial volume.
- distensibilty is defined as a compliance divided by initial volume.
- the local (tangent) compliance C and distensibility D are defined as
- Equations (14) determine arterial wall properties as local functions of transmural pressure.
- FIG. 2 illustrates the dependency of distensibility on pressure and flow velocity. Since PWV is monotonically increasing with pressure, distensibility is a decreasing function. Unlike the classical Bramwell-Hill model, which being linked to the Moens-Korteweg wave speed predicts arterial distensibility as a constant irrespective to the pressure level, the present model predicts distensibility as a function of PWV, pressure and a blood flow.
- a circumferential stress is a function of a circumferential strain and two material constants, a and c
- ⁇ ⁇ ac ⁇ ⁇ ⁇ ⁇ 2 ⁇ e aE ⁇ 2 ⁇ E ⁇ ( 18 )
- Q aE ⁇ 2 ( 19 )
- a a 11 - a 12 2 a 22 ( 20 )
- p is the transmural pressure
- r i is the internal radius
- r o is the outer radius
- h is the wall thickness.
- r m is the mid radius of a loaded vessel
- R m is the mid radius for a stress free vessel. Measuring r i and r o corresponding to the pressure p leaves us with three unknowns (a, c, R m ) which need to be determined as a part of a calibration procedure.
- the calibration provides a calibrated model which can be individualized for each subject.
- An embodiment of the calibration includes the use of published values for a population or segment of a population. Referenced values for material constants c, a 11 , a 12 , a 22 can be used to calculate the material constant a based on equation (20). The material constant c is used directly. A reference value for the mid radius in the stress free state (R m ) is used along with a reference value for the arterial wall thickness (h) and associated mid radius (r m ) for the loaded wall.
- the material parameters (a, c, R m ) along with the product of wall thickness and mid radius for the loaded wall (hr m ) can then be used to determine at least one of blood pressure and arterial compliance, e.g., distensibility, of a subject by measuring PWV and flow velocity.
- the following nonlinear calibration method describes one approach that may be completed to determine arterial constants.
- tonometry could be used to measure a continuous blood pressure to create the array of blood pressures
- Doppler speckle ultrasound could be used to measure artery radii to create the corresponding array of r ik , r ok .
- Step 2 Run a least square minimization as in equation (23) to identify the three constants (two material constants a, c and the mean radius R m , in a load free condition). Substituting ⁇ ⁇ in equation (23) with equation (18) results in
- LS is a function of measured parameters p k, r ik, r mk, h k and unknown properties (a,c,R m ), determined from the minimization procedure. Since we have 3 unknowns, at least 3 sets of pressure and associated outer and inner radii are required.
- a calibrated model can be used to determine at least one of blood pressure and arterial compliance, e.g., distensibility, of a subject by measuring PWV and flow velocity.
- a blood pressure may be estimated based on the equilibrium equation (21) rearranged to
- the circumferential strain (E ⁇ ) can be defined in terms of ⁇
- Equation (5) for PWV in arterial tissues can be re-arranged
- a lookup table can be created for convenience to enable determination of a blood pressure and distensibility based on the 4 arterial parameters (can be subject specific) and measurement of PWV and flow velocity.
- a blood density ⁇ is either measured or a value is assumed based on age and gender.
- the steps to create the blood pressure and distensibility lookup table are as follows:
- equation (31) Using equation (31) and the array of values for ⁇ and p n calculate a 1D array for p ⁇ (1+ ⁇ ).
- FIG. 4 An example resultant array is shown in FIG. 4 .
- This row also contains other relevant arterial parameters such as E ⁇ , ⁇ ⁇ , h, and r, which can be extracted for that individual based on the measured PWV f . Note that for determination of a systolic blood pressure and distensibility, a systolic PWV and a maximum flow velocity is used to calculate PWV f .
- a diastolic PWV and a minimum (or zero) flow velocity is used to calculate PWV f .
- Intermediate values of blood pressure and distensibility may also be determined based on the associated intermediate values of PWV f and flow velocity.
- a method for monitoring a blood pressure of a subject is disclosed.
- the model is calibrated for the subject (or population) by a non-linear calibration.
- a non-linear calibration as illustrated in FIG. 3 can be performed.
- a patient specific lookup table can be formed for convenience as described in FIG. 3 and as shown in FIG. 4 .
- the method for monitoring a subject's real time blood pressure is shown in FIG. 5 .
- An ECG measurement can be made for use as a timing reference for start of the pulse wave transit time, or to be used as a reference for determining acceptance time windows for other waveform features, or for averaging waveforms.
- An arterial flow velocity is measured providing minimum and maximum flow velocities, although a minimum could be assumed to be zero.
- An average flow velocity can also be measured.
- the flow velocity can also be estimated based on other measures or as a percentage of PWV.
- the pulse wave velocity is measured, ideally providing both a systolic and diastolic PWV.
- the subject (or population based) blood density ⁇ are then used with the lookup table of FIG. 4 to estimate blood pressure.
- the arrays of associated blood pressure (p), PWV f and distensibility (D) can also be used directly or with interpolation to estimate p and D based on the PWV f measure.
- the systolic PWV and the peak flow velocity are used to estimate a systolic blood pressure, while a diastolic PWV and the minimum flow velocity are used to estimate a diastolic blood pressure.
- PWV can be measured at the foot and the systolic flow velocity (u) can be added to it as an estimate of systolic PWV f .
- Other empirical or relational estimates for the systolic and diastolic PWV f can also be used.
- Determination of PWV includes measurement of the transit time of the pulse wave between two points, and a measure or estimate of the distance traveled.
- the PWV is the distance travelled divided by the time difference. This can be done by extracting the foot ( FIG. 1 , item 12 ) or peak ( FIG. 1 , item 13 ) of the pressure wave in two locations (proximal, distal) of the same artery, calculating the time difference between these two extracted features, and measuring the distance between these two measurement points. In one embodiment, this is done in the radial artery as shown in FIG. 7 with measurements items 80 (proximal) and 81 (distal).
- the PWV can also be measured using the heart as the proximal measurement point with an electrocardiogram feature (e.g., the ECG r-wave) as the first time point, or by sensing when the aortic valve opens using a feature on measured waveforms or images such as the ballistocardiogram (BCG), ultrasound imaging, Doppler ultrasound, impedance plethysmography (IPG), or photoplethysmography (PPG) on the chest over the aorta.
- BCG ballistocardiogram
- IPG impedance plethysmography
- PPG photoplethysmography
- the distal pressure wave is then used as above to extract a second time point.
- the arterial distance between the aortic root and the distal measurement point is used in the calculation of PWV. This can be measured or estimated, and may be based on subject characteristics such as height, weight age and gender.
- the distal pressure wave can be measured using sensors such as tonometry, an arterial c
- the wave will propagate across multiple arterial segments between the proximal and distal points of pressure measurement.
- This measurement can be used in at least two ways.
- average properties of the vessel segments, radius, and modulus will be considered so that the result corresponds to bulk average of the segment.
- the properties of individual arterial segments are determined.
- use the model to determine the relative transit time through each sequential arterial segment based on geometrical properties of each segment and assuming a similar pressure within all segments.
- a solution method such as minimization of a least squares or another method, solve for the PWV within each segment by recognizing that the total transit time (measured) is the sum of the transit time through each segment.
- Measurement of flow velocity can be done using Doppler ultrasound, an inductive coil, MRI or CT scan with contrast agents.
- Left ventricular ejection time (LVET) can be measured or estimated using a number of sensors (e.g.
- the measure of LVET is the length of time from the foot of the PPG wave ( FIG. 1 item 12 ) to the dicrotic notch (item 14 ).
- heart sound LVET is the time between the first and second heart sound.
- Ejection volume can be based on direct measurement for the subject (e.g. ultrasound, thermal dilution, etc) at rest and at exercise with subsequent scaling based on heart rate.
- the cross-sectional area can be directly measured by ultrasound imaging, MRI, or CT scans.
- EV and CA can also be based on subject specific parameters such as age, gender, height and weight. EV can also be measured or estimated using features from the BCG such as the amplitude of the j-wave or m-wave.
- An estimate of flow velocity in the periphery can be made based on scaling of the blood volume in that arterial tree branch, and relative arterial size as compared to the aorta. Although a direct measurement of flow velocity or an estimate based on PWV is preferred in the periphery.
- Pressure can be measured using any approved technique, for example, brachial cuff, tonometry, or intra-arterial catheter.
- a continuous method e.g., tonometry, intra-arterial
- PWV measures e.g. via ECG
- serial measures can also be used.
- the pressure p can be systolic, diastolic, or any intermediate pressure (e.g., mean pressure) when coupled with the appropriate flow velocity (u).
- systolic pressure could be associated with the peak flow velocity
- diastolic pressure could be associated with the lowest (or zero) flow velocity
- an average pressure could be associated with an average flow velocity.
- ECG ECG
- Other locations are also possible such as ear lobes, behind the ears, buttocks, thighs, fingers, feet or toes.
- PPG can be measured at the chest or wrist.
- Other locations such as the ear lobes, fingers, forehead, buttocks, thighs, and toes also work.
- Video analysis methods examining changes in skin color can also be used to obtain a PPG waveform.
- Flow velocity can be measured at the chest or wrist. Other locations for flow velocity measure are also possible such as the neck, arm and legs.
- the pulse transit time is measured based on aortic valve opening determined by the J-wave of the BCG waveform, and a PPG foot measured (e.g., FIG. 1 , item 12 ) from the thigh.
- the ECG r-wave may be used as a reference for determining acceptance windows for BCG and PPG feature delineations, or as a starting point for a PWV measure.
- the aorta distance is estimated from aortic root along the path of the aorta to the femoral artery at the thigh PPG measurement location.
- the PWV is calculated by dividing the aorta distance by the measured time difference (BCG J-wave to PPG foot).
- the minimum and maximum flow velocity is measured by ultrasound Doppler at the aortic root.
- a blood density ⁇ is assumed based on age and gender of the subject.
- the lookup table of FIG. 4 is used to determine the associated pressure.
- the minimum measured flow velocity can be used in combination with an estimate of diastolic PWV, where diastolic PWV is calculated based on the BCG J-wave to PPG foot time difference.
- the peak flow velocity or a percentage of the peak flow velocity can be used in combination with an estimate of systolic PWV, where the systolic PWV is calculated based on the peak flow velocity time point to the PPG peak time difference.
- diastolic flow velocity can be assumed to be 0, while systolic flow velocity can be estimated as a percentage of PWV (e.g ⁇ 20%).
- the pulse transit time is measured from the carotid artery using tonometry, to the pressure pulse measured at thigh with a thigh cuff.
- the arterial distance is estimated from aortic root along the path of the aorta to the femoral artery at the thigh cuff measurement location.
- the PWV is calculated by dividing the arterial distance by the measured time difference.
- the foot to foot timing on the measured pressure pulses (e.g., FIG. 7 items 801 and 810 ) is used to determine a diastolic pulse transit time and to calculate a diastolic PWV.
- the peak to peak timing (e.g., FIG.
- items 802 and 811 is used to determine a systolic pulse transit time and to calculate a systolic PWV.
- the peak flow velocity is estimated at 20% of the systolic PWV while the minimum flow velocity is estimated at zero.
- a blood density ⁇ is assumed based on age and gender of the subject.
- the lookup table of FIG. 4 is used to determine the associated pressure.
- p d the minimum measured flow velocity can be used in combination with the diastolic PWV.
- p s the peak flow velocity is used in combination with the systolic PWV.
- a method for monitoring an arterial compliance of a subject is disclosed.
- the model is calibrated for the subject (or population) by a non-linear calibration.
- a non-linear calibration as illustrated in FIG. 8 can be performed.
- a patient specific lookup table can be formed for convenience described in FIG. 3 and as shown in FIG. 4 .
- the method for monitoring a subject's arterial compliance is shown in FIG. 6 .
- An optional ECG measurement can be made for use as a timing reference for start of the pulse wave transit time, or to be used as a reference for determining acceptance time windows for other waveform features, or for averaging waveforms.
- An arterial flow velocity is measured providing minimum and maximum flow velocities, although a minimum could be assumed to be zero.
- An average flow velocity can also be measured.
- the flow velocity can also be estimated based on other measures or as a percentage of PWV.
- the pulse wave velocity is measured, ideally providing both a systolic and diastolic PWV.
- the subject (or population based) blood density ⁇ is then used with the patient specific lookup FIG. 4 , to determine compliance as shown in FIG. 6 and equation 16.
- the systolic PWV and the peak flow velocity are used to determine a systolic distensibility, while a diastolic PWV and the minimum flow velocity are used to estimate a diastolic distensibility. Although other estimates and combinations may be used to determine the subject distensibility parameter.
- the pulse transit time is measured based on aortic valve opening determined by the J-wave of the BCG waveform, and a PPG foot measured (e.g., FIG. 1 , item 12 ) from the thigh.
- the aorta distance is estimated from aortic root to femoral artery at the thigh PPG measurement location.
- the PWV is calculated by dividing the aorta distance by the measured time difference (BCG J-wave to PPG foot).
- the minimum flow velocity is assumed to be zero, enabling distensibility calculation without a direct flow measurement.
- a blood density ⁇ is assumed based on age and gender of the subject with the patient specific lookup FIG. 4 to determine compliance as shown in FIG. 6 and equation 16. Measures of a systolic PWV, peak flow velocity, may also be used to determine D.
- the pulse transit time is measured from the carotid artery using tonometry, to the pressure pulse measured at thigh with a thigh cuff.
- the arterial distance is estimated from aortic root along the path of the aorta to the femoral artery at the thigh cuff measurement location.
- the PWV is calculated by dividing the arterial distance by the measured time difference.
- the foot to foot timing on the measured pressure pulses (e.g., FIG. 8 items 801 and 810 ) are used to determine a diastolic pulse transit time and to calculate a diastolic PWV.
- the peak to peak timing (e.g., FIG.
- items 802 and 811 is used to determine a systolic pulse transit time and to calculate a systolic PWV.
- the peak flow velocity is estimated at 20% of the systolic PWV while the minimum flow velocity is estimated at zero.
- a blood density p is assumed based on age and gender of the subject with the patient specific lookup FIG. 4 to determine compliance as shown in FIG. 6 and equation 16.
- the pulse transit time is measured based on time synchronized tonometry at the carotid artery and at the femoral artery, each providing a pressure pulse waveform.
- the equivalent aortic distance between the two measurement points is measured at for example 1.0 m.
- the foot to foot time difference between the two tonometry waveforms is measured at for example 200 nis.
- the arterial compliance parameter distensibility (D) is determined from the systolic and diastolic PWV f measures and the associated array elements. In this paper example the diastolic distensibility is identified as
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Abstract
Description
- This application claims the benefit of the filing date of U.S. Provisional Patent Application Ser. No. 62/080,740, filed Nov. 17, 2014, and U.S. Provisional Patent Application Ser. No. 62/080,738, filed Nov. 17, 2014, each of which are hereby incorporated by reference in their entirety.
- The disclosure relates to methods for at least one of blood pressure and arterial compliance estimation from arterial segments.
- The pulse wave, generated by left ventricular ejection, propagates at a velocity that has been identified as an important marker of atherosclerosis and cardiovascular risk. Increased pulse wave velocity (PWV) indicates an increased risk of stroke and coronary heart disease. This velocity is considered a surrogate marker for arterial compliance, is highly reproducible, and is widely used to assess the elastic properties of the arterial tree. Research shows that measurement of pulse wave velocity as an indirect estimate of aortic compliance could allow for early identification of patients at risk for cardiovascular disease. The ability to identify these patients would lead to better risk stratification and earlier, more cost-effective preventative therapy. Several studies have shown the influence of blood pressure and left ventricular ejection time (LVET) on pulse wave velocity.
- Over the past decades, there has been ongoing research for better theoretical prediction of PWV. The clinical relationship between PWV and arterial stiffness is often based on classic linear models or the combination of the linear models, and measured results with an incorporated correction factor. Whereas linear models predict PWV as a function of only geometric and physical properties of the fluid and the wall, there is strong empirical evidence that PWV is also correlated to pressure and ejection time.
- There exist no models that accurately describe PWV and flow accounting for the nonlinearities in an arterial segment. A model that would enable solution of the inverse problem of determination of blood pressure and aortic compliance for a PWV measure has yet to be developed.
- In accordance with one aspect of the present invention, there is provided a method for determining material characteristics for an artery, the method including providing at least three values for each of blood pressure, internal radius, and external radius of an arterial segment or segments of a subject; applying a base model of fluid-structure interaction incorporating conservation of mass and momentum for the fluid, and non-linear elasticity of the structure; and running a mathematical optimization on the base model to provide a calibrated model to determine material characteristics of the arterial segment or segments.
- In accordance with another aspect of the present invention, there is provided a method for determining at least one of a blood pressure and an arterial compliance parameter of a subject, the method including providing a value for pulse wave velocity within an arterial segment or segments of a subject; providing a value for flow velocity within the arterial segment or segments of the subject; providing a value for blood density of the subject; providing the material characteristics of an artery; and applying a calibrated model of fluid-structure interaction incorporating conservation of mass and momentum for the fluid, and non-linear elasticity of the structure, to calculate at least one of blood pressure and an arterial compliance parameter of the subject using the provided values.
- These and other aspects of the present disclosure will become apparent upon a review of the following detailed description and the claims appended thereto.
-
FIG. 1 is a diagram on the longitudinal cross section of the arterial wall at diastolic (10) and systolic (11) pressure; -
FIG. 2 is a graph of the dependence of distensibilty on transmural pressure and a flow velocity; -
FIG. 3 is a flowchart depicting creation of a blood pressure and distensibility lookup table; -
FIG. 4 is a format of a lookup table for blood pressure and distensibility; -
FIG. 5 is a flowchart depicting a method for determining blood pressure of a subject based on a PWV measure using a lookup table; -
FIG. 6 is a flowchart depicting a method for determining arterial compliance of a subject based on a PWV measure using a lookup table; -
FIG. 7 is an illustration of pressure pulse measurement on two locations in the same artery for determination of a systolic and diastolic PWV; and -
FIG. 8 is a flowchart depicting a method for determining the material characteristics of an arterial segment. - A fully nonlinear model of pressure and flow propagation in arterial segments is disclosed that enables determination of blood pressure and arterial compliance based on measures of pulse wave velocity and flow velocity following a calibration. The approach allows for determination of systolic and diastolic blood pressure. The approach allows for determination of a systolic and diastolic aortic compliance.
- A noninvasive method for monitoring the blood pressure and arterial compliance of a patient based on measurements of a flow velocity and a pulse wave velocity is described. An embodiment uses a photoplethysmograph and includes a method to monitor the dynamic behavior of the arterial blood flow, coupled with a hemodynamic mathematical model of the arterial blood flow motion in a fully nonlinear vessel. A derived mathematical model creates the patient specific dependence of a blood pressure versus PWV and blood flow velocity, which allows continuous monitoring of arterial blood pressure. The calibrated mathematical model presents an arterial compliance and a distensibility as a clinical marker of arterial stiffness. The disclosure is applicable for fully nonlinear elastic vessels that are commonly found in the major arteries, as well as smaller vessels that operate closer to the linear elastic regime.
- The disclosure includes a fully nonlinear basic model for blood pressure wave propagation in compliant arteries. A nonlinear traveling wave model was used to investigate mechanisms underlying the effects of pressure, ejection time, ejection volume, geometric, and physical properties on PWV. A patient calibration procedure was developed that involves measurement of blood pressure and arterial dimensions (internal and external radii). An embodiment includes blood pressure prediction using the model, per patient calibration, and the measurement of flow velocity and pressure wave velocity. An embodiment includes arterial compliance determination using the model, per patient calibration, and the measurement of flow velocity and pressure wave velocity.
- A basic mathematical fluid-structure interaction model for pulse wave velocity (PWV) propagation incorporates the dynamics of incompressible flow in a compliant vessel. This one dimensional model simulating blood flow in arteries effectively describes pulsatile flow in terms of averages across the section flow parameters. Although it is not able to provide the details of flow separation, recirculation, or shear stress analysis, it accurately represents the overall and average pulsatile flow characteristics, particularly PWV.
- Conservation of mass and momentum results in the following system of one dimensional equations
-
- where t is time, z is the axial coordinate shown in
FIG. 1 , A=A (z,t) is the arterial cross-sectional area, u=u(z,t) is the blood flow velocity, ρ is blood density, p=p(z,t) is blood pressure. - For an impermeable thin walled membrane, neglecting inertia forces, the vessel pressure-strain relationship is maintained by equilibrium condition as a function p=p(η), based on relevant constitutive relations where 11 is the circumferential strain (ratio of wall deflection to zero stress arterial radius (R)). Noting that A=πR2(1+η)2, and assuming that transmural pressure is a smooth function of a wall normal deflection (derivative pη=∂p/∂η exists at any point), the total system of equations can be presented in the following non-conservative form
-
- We find the eigenvalues of H(U) to be real and distinct. PWV is associated with the forward running wave velocity, i.e., the largest eigenvalue, hence it is identified as
-
- The partial derivative pii indicates sensitivity of pressure with respect to the wall normal deflection, and has a clear interpretation as tangent (incremental) moduli in finite strain deformation. In the general case, equation (5) is supplemented by appropriate constituent equations for a hyperelastic anisotropic arterial wall, accounting for finite deformation.
- It is assumed that arterial wall is hyperelastic, incompressible, anisotropic, and undergoing finite deformation. After a few original loading cycles (preconditioning) the arterial behavior follows some repeatable, hysteresis free pattern with a typical exponential stiffening effect regarded as pseudo elastic. The strain energy density function W for the pseudo elastic constitutive relation may be presented in the form
-
W=½c(e Q−1) (6) - where c is a material coefficient, and Q is the quadratic function of the Green-Lagrange strain components. For the finite inflation and extension of a thin walled cylindrical artery the following strain energy function is used
-
Q=a 11 E θ 2+2a 12 E θ E z +a 22 E z 2 (7) - where c, a11, a12, a22 are material constants. The Cauchy stress components in circumferential and axial directions are:
-
- With the geometry of the reference state determined, we define R, Z, H—as an internal radius, axial coordinate and a wall thickness in a stress free configuration, r,z,h—internal radius, axial coordinate and a wall thickness in a physiologically loaded configuration. The corresponding principal stretch ratios are
-
λθ =r/R,λ z =dz/dZ,λ r =h/H (9) - Assuming isochoric deformation incorporate the incompressibility condition as
-
λzλθλr=1 (10) - The Green-Lagrangian strain components relate to the principal stretch ratios of Eq. 12 by
-
E i=½(λi 2−1), (i=θ, z, r) (11) - For the membrane thin walled cylindrical artery undergoing finite inflation and axial deformation, the load-stress relations follow from the static conditions
-
- where F is the axial pretension force and f is the axial pre-stress per unit of cross section area of a load free vessel. A substitution back into equation (8) yields the desired relations:
-
- The solution of equations (13), (11), (7) results in a load-strain relations, which with account of the identity
-
- converts into the p=p(η) function, required by (5) to predict a wave front speed of propagation, i.e., PWV.
- Arterial stiffness, or its reciprocals, arterial compliance and distensibility, may provide indication of vascular changes that predispose to the development of major vascular disease. In an isolated arterial segment filled with a moving fluid, compliance is defined as a change of a volume V for a given change of a pressure, and distensibilty as a compliance divided by initial volume. As functions of pressure the local (tangent) compliance C and distensibility D are defined as
-
- Equations (14) determine arterial wall properties as local functions of transmural pressure.
- We present equations (14) in the following equivalent form
-
- The classical results are generalized for the case of a hyperelastic arterial wall with account of finite deformation and flow velocity. To proceed, determine pη from Equation (5) and substitute in Equation (15), arriving at the following relations
-
-
FIG. 2 illustrates the dependency of distensibility on pressure and flow velocity. Since PWV is monotonically increasing with pressure, distensibility is a decreasing function. Unlike the classical Bramwell-Hill model, which being linked to the Moens-Korteweg wave speed predicts arterial distensibility as a constant irrespective to the pressure level, the present model predicts distensibility as a function of PWV, pressure and a blood flow. - Arterial constants can be defined based on the developed mathematical model. The Cauchy stress components based on Fung's energy are presented in equations (6), (7), and (8). Neglecting longitudinal stress (σ=0) in equation (8), we obtain
-
- where the ratio
-
- is a counterpart of a Poisson coefficient in a linear isotropic elasticity.
- It follows from Equations (7), (17) that a circumferential stress is a function of a circumferential strain and two material constants, a and c
-
- The governing equation specifies an equilibrium condition
-
- where p is the transmural pressure, ri is the internal radius, ro is the outer radius, and h is the wall thickness. Let us define rm as the mid radius of a loaded vessel, and Rm as the mid radius for a stress free vessel. Measuring ri and ro corresponding to the pressure p leaves us with three unknowns (a, c, Rm) which need to be determined as a part of a calibration procedure. The calibration provides a calibrated model which can be individualized for each subject.
- An embodiment of the calibration includes the use of published values for a population or segment of a population. Referenced values for material constants c, a11, a12, a22 can be used to calculate the material constant a based on equation (20). The material constant c is used directly. A reference value for the mid radius in the stress free state (Rm) is used along with a reference value for the arterial wall thickness (h) and associated mid radius (rm) for the loaded wall. The material parameters (a, c, Rm) along with the product of wall thickness and mid radius for the loaded wall (hrm) can then be used to determine at least one of blood pressure and arterial compliance, e.g., distensibility, of a subject by measuring PWV and flow velocity.
- Another embodiment of the calibration is disclosed as follows and described in
FIG. 8 . Assuming we have k measurements of the radius and pressure during a cardiac cycle or cycles, the following four variables are defined (rik , rok , rmk , pk). By using these sampled variables circumferential stress can be presented as a function of three unknowns -
σθ=σθ(a, c, R m) (22) - Now using a mathematical optimization, e.g., a least square (LS) minimization technique identifies (a, c,Rm)
-
- The following nonlinear calibration method describes one approach that may be completed to determine arterial constants.
- Step 1: Obtain k measurements, k≧3, for blood pressure-pk, internal radius-rik; outer radius-rok, calculate mean radii rmk=0.5(rik+rok) and wall thicknesses hk=rok−rik. example, tonometry could be used to measure a continuous blood pressure to create the array of blood pressures, and Doppler speckle ultrasound could be used to measure artery radii to create the corresponding array of rik, rok.
- Step 2: Run a least square minimization as in equation (23) to identify the three constants (two material constants a, c and the mean radius Rm, in a load free condition). Substituting σθ in equation (23) with equation (18) results in
-
- where
-
- LS is a function of measured parameters pk, rik, rmk, hk and unknown properties (a,c,Rm), determined from the minimization procedure. Since we have 3 unknowns, at least 3 sets of pressure and associated outer and inner radii are required.
- In an embodiment, a calibrated model can be used to determine at least one of blood pressure and arterial compliance, e.g., distensibility, of a subject by measuring PWV and flow velocity.
- With the three material properties (a,c,Rm) and the constant product (hrm) a blood pressure may be estimated based on the equilibrium equation (21) rearranged to
-
- where the stretch ratio (λθ) can be defined in terms of η
-
- The circumferential strain (Eθ) can be defined in terms of η
-
E θ=(λθ 2−1)/2=η(η+2)/2 (27) - Wall thickness follows from incompressibility conditions
-
hrm=hkrmk (28) - where from
-
- Internal Radius
-
r i =r m−0.5h=λ θ R m−0.5h=(η+1)R m−0.5h (30) - These formulations provide a relationship between pressure (p), circumferential strain (η), two arterial material parameters (a and c) and two arterial geometric parameters (Rm and the constant product hkrmk).
- Equation (5) for PWV in arterial tissues can be re-arranged
-
p η(1+η)=2ρ*PWVf 2 (31) - where a flow corrected PWV (PWVf) has been introduced (PWVf=PWV-u).
- This relation can be used in combination with equation (16) to define distensibility D in terms of the pη
-
D= 2/pη (32) - In an embodiment, a lookup table can be created for convenience to enable determination of a blood pressure and distensibility based on the 4 arterial parameters (can be subject specific) and measurement of PWV and flow velocity. A blood density ρ is either measured or a value is assumed based on age and gender. As illustrated in an embodiment shown in
FIG. 3 , the steps to create the blood pressure and distensibility lookup table are as follows: - Set η=0.
- Using equation (26) calculate circumferential stretch ratio λθ.
- Using equation (27) calculate circumferential strain Eθ.
- Using equation (29) and any hkrmk product from the calibration, calculate wall thickness h.
- Using equation (30) calculate the internal radius ri.
- Using equation (25) calculate pressure p.
- While η<0.5, η=η+0.005, go back to calculation of the circumferential stretch ratio or else continue.
- Calculate the array for pn using the slope of the (p,η) curve.
- Using equation (31) and the array of values for η and pn calculate a 1D array for pη(1+η).
- Using equation (31) and the array of pη, calculate D for each value of η.
- An example resultant array is shown in
FIG. 4 . This lookup table enables determination of a subject blood pressure and distensibility by measuring PWVf and identifying the row (either directly or by interpolation) where pη(1+η)=2ρ*PWVf 2. This row also contains other relevant arterial parameters such as Eθ, λθ, h, and r, which can be extracted for that individual based on the measured PWVf. Note that for determination of a systolic blood pressure and distensibility, a systolic PWV and a maximum flow velocity is used to calculate PWVf. For determination of a diastolic blood pressure and distensibility, a diastolic PWV and a minimum (or zero) flow velocity is used to calculate PWVf. Intermediate values of blood pressure and distensibility may also be determined based on the associated intermediate values of PWVf and flow velocity. - A method for monitoring a blood pressure of a subject is disclosed. The model is calibrated for the subject (or population) by a non-linear calibration. For example, a non-linear calibration as illustrated in
FIG. 3 can be performed. Once the calibration is complete, a patient specific lookup table can be formed for convenience as described inFIG. 3 and as shown inFIG. 4 . The method for monitoring a subject's real time blood pressure is shown inFIG. 5 . An ECG measurement can be made for use as a timing reference for start of the pulse wave transit time, or to be used as a reference for determining acceptance time windows for other waveform features, or for averaging waveforms. An arterial flow velocity is measured providing minimum and maximum flow velocities, although a minimum could be assumed to be zero. An average flow velocity can also be measured. The flow velocity can also be estimated based on other measures or as a percentage of PWV. The pulse wave velocity is measured, ideally providing both a systolic and diastolic PWV. The subject (or population based) blood density ρ are then used with the lookup table ofFIG. 4 to estimate blood pressure. The arrays of associated blood pressure (p), PWVf and distensibility (D) can also be used directly or with interpolation to estimate p and D based on the PWVf measure. The systolic PWV and the peak flow velocity are used to estimate a systolic blood pressure, while a diastolic PWV and the minimum flow velocity are used to estimate a diastolic blood pressure. Although other estimates and combinations may be used to estimate an average or systolic or diastolic blood pressure. PWV can be measured at the foot and the systolic flow velocity (u) can be added to it as an estimate of systolic PWVf. Diastolic pressure could use the raw PWV measured at the foot and use either the minimum flow velocity or assume u=0. Other empirical or relational estimates for the systolic and diastolic PWVf can also be used. - Determination of PWV includes measurement of the transit time of the pulse wave between two points, and a measure or estimate of the distance traveled. The PWV is the distance travelled divided by the time difference. This can be done by extracting the foot (
FIG. 1 , item 12) or peak (FIG. 1 , item 13) of the pressure wave in two locations (proximal, distal) of the same artery, calculating the time difference between these two extracted features, and measuring the distance between these two measurement points. In one embodiment, this is done in the radial artery as shown inFIG. 7 with measurements items 80 (proximal) and 81 (distal). Use of the foot location on the pressure or PPG waveform (items 801 and 810) will correlate to a diastolic PWV, while use of the peak location (items 802 and 811) will correlate to a systolic PWV. Two different arteries can also be used with a measurement or estimate of the arterial path distance between the two measurement points. The PWV can also be measured using the heart as the proximal measurement point with an electrocardiogram feature (e.g., the ECG r-wave) as the first time point, or by sensing when the aortic valve opens using a feature on measured waveforms or images such as the ballistocardiogram (BCG), ultrasound imaging, Doppler ultrasound, impedance plethysmography (IPG), or photoplethysmography (PPG) on the chest over the aorta. The distal pressure wave is then used as above to extract a second time point. The arterial distance between the aortic root and the distal measurement point is used in the calculation of PWV. This can be measured or estimated, and may be based on subject characteristics such as height, weight age and gender. The distal pressure wave can be measured using sensors such as tonometry, an arterial cuff, ultrasound, RF based arterial wall tracking, and PPG. - In some embodiments, the wave will propagate across multiple arterial segments between the proximal and distal points of pressure measurement. This measurement can be used in at least two ways. In the first form, average properties of the vessel segments, radius, and modulus will be considered so that the result corresponds to bulk average of the segment. In the second, the properties of individual arterial segments are determined. First, use the model to determine the relative transit time through each sequential arterial segment based on geometrical properties of each segment and assuming a similar pressure within all segments. Then using a solution method, such as minimization of a least squares or another method, solve for the PWV within each segment by recognizing that the total transit time (measured) is the sum of the transit time through each segment.
- Measurement of flow velocity can be done using Doppler ultrasound, an inductive coil, MRI or CT scan with contrast agents. The flow velocity can be captured as a continuous wave, as a peak value, or a minimum value (including u=0). It is also possible to estimate flow velocity using related measures or with a scale factor. For example PWV can be measured using previously described techniques and flow velocity is then estimated as a percentage of PWV (for example u=0.2 PWV). Aortic flow velocity can be estimated through left ventricular ejection time (LVET), ejection volume (EV), and aortic cross-sectional area (CA) where u=EV/(LVET*CA). Left ventricular ejection time (LVET) can be measured or estimated using a number of sensors (e.g. PPG, heart sound). Using PPG for example, the measure of LVET is the length of time from the foot of the PPG wave (
FIG. 1 item 12) to the dicrotic notch (item 14). Using heart sound, LVET is the time between the first and second heart sound. Ejection volume can be based on direct measurement for the subject (e.g. ultrasound, thermal dilution, etc) at rest and at exercise with subsequent scaling based on heart rate. The cross-sectional area can be directly measured by ultrasound imaging, MRI, or CT scans. EV and CA can also be based on subject specific parameters such as age, gender, height and weight. EV can also be measured or estimated using features from the BCG such as the amplitude of the j-wave or m-wave. An estimate of flow velocity in the periphery can be made based on scaling of the blood volume in that arterial tree branch, and relative arterial size as compared to the aorta. Although a direct measurement of flow velocity or an estimate based on PWV is preferred in the periphery. - Pressure can be measured using any approved technique, for example, brachial cuff, tonometry, or intra-arterial catheter. Ideally a continuous method (e.g., tonometry, intra-arterial) is used with a method of time synchronization to the flow and PWV measures (e.g. via ECG). However serial measures can also be used. Here the pressure p can be systolic, diastolic, or any intermediate pressure (e.g., mean pressure) when coupled with the appropriate flow velocity (u). For example, systolic pressure could be associated with the peak flow velocity, and diastolic pressure could be associated with the lowest (or zero) flow velocity, or an average pressure could be associated with an average flow velocity.
- An optional ECG can be measured across the chest or wrists. Other locations are also possible such as ear lobes, behind the ears, buttocks, thighs, fingers, feet or toes. PPG can be measured at the chest or wrist. Other locations such as the ear lobes, fingers, forehead, buttocks, thighs, and toes also work. Video analysis methods examining changes in skin color can also be used to obtain a PPG waveform. Flow velocity can be measured at the chest or wrist. Other locations for flow velocity measure are also possible such as the neck, arm and legs.
- In one embodiment, the pulse transit time is measured based on aortic valve opening determined by the J-wave of the BCG waveform, and a PPG foot measured (e.g.,
FIG. 1 , item 12) from the thigh. The ECG r-wave may be used as a reference for determining acceptance windows for BCG and PPG feature delineations, or as a starting point for a PWV measure. The aorta distance is estimated from aortic root along the path of the aorta to the femoral artery at the thigh PPG measurement location. The PWV is calculated by dividing the aorta distance by the measured time difference (BCG J-wave to PPG foot). The minimum and maximum flow velocity is measured by ultrasound Doppler at the aortic root. A blood density ρ is assumed based on age and gender of the subject. Using the measured PWVf as shown inFIG. 5 the lookup table ofFIG. 4 is used to determine the associated pressure. To calculate pd the minimum measured flow velocity can be used in combination with an estimate of diastolic PWV, where diastolic PWV is calculated based on the BCG J-wave to PPG foot time difference. To calculate ps the peak flow velocity or a percentage of the peak flow velocity can be used in combination with an estimate of systolic PWV, where the systolic PWV is calculated based on the peak flow velocity time point to the PPG peak time difference. Under conditions where flow velocity is not measured, diastolic flow velocity can be assumed to be 0, while systolic flow velocity can be estimated as a percentage of PWV (e.g ˜20%). - In another embodiment, the pulse transit time is measured from the carotid artery using tonometry, to the pressure pulse measured at thigh with a thigh cuff. The arterial distance is estimated from aortic root along the path of the aorta to the femoral artery at the thigh cuff measurement location. The PWV is calculated by dividing the arterial distance by the measured time difference. The foot to foot timing on the measured pressure pulses (e.g.,
FIG. 7 items 801 and 810) is used to determine a diastolic pulse transit time and to calculate a diastolic PWV. The peak to peak timing (e.g.,FIG. 7 ,items 802 and 811) is used to determine a systolic pulse transit time and to calculate a systolic PWV. The peak flow velocity is estimated at 20% of the systolic PWV while the minimum flow velocity is estimated at zero. A blood density ρ is assumed based on age and gender of the subject. Using the measured PWVf, as shown inFIG. 5 , the lookup table ofFIG. 4 is used to determine the associated pressure. To calculate pd the minimum measured flow velocity can be used in combination with the diastolic PWV. To calculate ps the peak flow velocity is used in combination with the systolic PWV. - A method for monitoring an arterial compliance of a subject is disclosed. The model is calibrated for the subject (or population) by a non-linear calibration. For example, a non-linear calibration as illustrated in
FIG. 8 can be performed. Once the calibration is complete, a patient specific lookup table can be formed for convenience described inFIG. 3 and as shown inFIG. 4 . The method for monitoring a subject's arterial compliance is shown inFIG. 6 . An optional ECG measurement can be made for use as a timing reference for start of the pulse wave transit time, or to be used as a reference for determining acceptance time windows for other waveform features, or for averaging waveforms. An arterial flow velocity is measured providing minimum and maximum flow velocities, although a minimum could be assumed to be zero. An average flow velocity can also be measured. The flow velocity can also be estimated based on other measures or as a percentage of PWV. The pulse wave velocity is measured, ideally providing both a systolic and diastolic PWV. The subject (or population based) blood density ρ is then used with the patient specific lookupFIG. 4 , to determine compliance as shown inFIG. 6 and equation 16. - The systolic PWV and the peak flow velocity are used to determine a systolic distensibility, while a diastolic PWV and the minimum flow velocity are used to estimate a diastolic distensibility. Although other estimates and combinations may be used to determine the subject distensibility parameter.
- In one embodiment, the pulse transit time is measured based on aortic valve opening determined by the J-wave of the BCG waveform, and a PPG foot measured (e.g.,
FIG. 1 , item 12) from the thigh. The aorta distance is estimated from aortic root to femoral artery at the thigh PPG measurement location. The PWV is calculated by dividing the aorta distance by the measured time difference (BCG J-wave to PPG foot). The minimum flow velocity is assumed to be zero, enabling distensibility calculation without a direct flow measurement. The flow corrected PWV is calculated (in this embodiment PWVf=PWV since u=0). A blood density ρ is assumed based on age and gender of the subject with the patient specific lookupFIG. 4 to determine compliance as shown inFIG. 6 and equation 16. Measures of a systolic PWV, peak flow velocity, may also be used to determine D. - In another embodiment, the pulse transit time is measured from the carotid artery using tonometry, to the pressure pulse measured at thigh with a thigh cuff. The arterial distance is estimated from aortic root along the path of the aorta to the femoral artery at the thigh cuff measurement location. The PWV is calculated by dividing the arterial distance by the measured time difference. The foot to foot timing on the measured pressure pulses (e.g.,
FIG. 8 items 801 and 810) are used to determine a diastolic pulse transit time and to calculate a diastolic PWV. The peak to peak timing (e.g.,FIG. 7 ,items 802 and 811) is used to determine a systolic pulse transit time and to calculate a systolic PWV. The peak flow velocity is estimated at 20% of the systolic PWV while the minimum flow velocity is estimated at zero. A blood density p is assumed based on age and gender of the subject with the patient specific lookupFIG. 4 to determine compliance as shown inFIG. 6 and equation 16. - The disclosure will be further illustrated with reference to the following specific examples. It is understood that these examples are given by way of illustration and are not meant to limit the disclosure or the claims to follow.
- Paper Example, Blood Pressure and Distensibility
- This paper example uses referenced values for an aorta c=120123 Pa, a11=0.320, a12=0.068, a22=0.451. The reduced constant ‘a’ is calculated based on equation 20 (a=0.31). In addition reference values were used for the mid radius for the stress free vessel Rm=0.009 m, the aortic wall thickness h=0.00211 m, and the mid radius of the loaded wall rm=0.011. A computer routine executed the functions outlined in
FIG. 3 to calculate an array of pη(1+η), D, and the associated pressures (p) for each value of η. Equation (31) was then used along with a reference value of blood density ρ=060 kg/m3 to create an array of associated PWVf for each value of η. The pulse transit time is measured based on time synchronized tonometry at the carotid artery and at the femoral artery, each providing a pressure pulse waveform. The equivalent aortic distance between the two measurement points is measured at for example 1.0 m. The foot to foot time difference between the two tonometry waveforms is measured at for example 200 nis. The diastolic PWV is then calculated as 1.0 m/200 ms=0.5 m/s. From the same tonometry waveforms the peak to peak time difference is measured at for example 140 ms. The systolic PWV is then calculated as 1.00 m/140 ms=7.14 m/s. Flow velocity is measured using Doppler ultrasound at the aortic root, with the minimum taken as the diastolic flow velocity ud=0.00 m/s, and the maximum taken as the systolic flow velocity us=1.10 m/s. A flow corrected PWV is calculate at systolic blood pressure (PWVf=7.14 m/s−1.10 m/s=6.04 m/s) with the associated systolic blood pressure determined from the array as ps=138 mmHg. A flow corrected PWV is calculate at diastolic blood pressure (PWVf=5.0 m/s−0.0 m/s=5.0 m/s) with the associated diastolic blood pressure determined from the array as pd=84 mmHg. The arterial compliance parameter distensibility (D) is determined from the systolic and diastolic PWVf measures and the associated array elements. In this paper example the diastolic distensibility is identified as -
- and the systolic distensibility is identified as
-
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US11622730B2 (en) | 2014-11-17 | 2023-04-11 | Rochester Institute Of Technology | Pulse wave velocity, arterial compliance, and blood pressure |
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US11957504B2 (en) | 2017-06-23 | 2024-04-16 | Stryker Corporation | Patient monitoring and treatment systems and methods |
US12178553B2 (en) | 2018-12-18 | 2024-12-31 | Koninklijke Philips N.V. | Control unit for deriving a measure of arterial compliance |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
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EP3073400B1 (en) * | 2015-03-25 | 2022-05-04 | Tata Consultancy Services Limited | System and method for determining psychological stress of a person |
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Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5565466A (en) * | 1993-08-13 | 1996-10-15 | Zonagen, Inc. | Methods for modulating the human sexual response |
US6575969B1 (en) * | 1995-05-04 | 2003-06-10 | Sherwood Services Ag | Cool-tip radiofrequency thermosurgery electrode system for tumor ablation |
US20050090720A1 (en) * | 2003-10-22 | 2005-04-28 | Hsien-Tsai Wu | Pulse analyzing apparatus |
US20120190967A1 (en) * | 2010-12-23 | 2012-07-26 | Werner Nahm | Arrangement and method for quantitatively determining the blood flow within blood vessels |
Family Cites Families (45)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2658505A (en) * | 1949-03-08 | 1953-11-10 | Sheer Charles | Arterial pulse wave velocity meter |
US4799491A (en) | 1986-11-06 | 1989-01-24 | Sri International | Blood pressure monitoring method and apparatus |
DE59107232D1 (en) | 1990-07-18 | 1996-02-22 | Avl Medical Instr Ag | Device and method for measuring blood pressure |
US5687731A (en) | 1992-09-10 | 1997-11-18 | Mti, Ltd. | Oscillometric method for determining hemodynamic parameters of the arterial portion of patient's circulatory system and a measuring system for its realization |
US5743856A (en) | 1995-11-06 | 1998-04-28 | Colin Corporation | Apparatus for measuring pulse-wave propagation velocity |
EP0832604A1 (en) * | 1996-09-30 | 1998-04-01 | Koninklijke Philips Electronics N.V. | Method and device for measuring the elasticity of an artery by ultrasonic echography |
DE19746377C1 (en) | 1997-10-21 | 1999-07-01 | Fresenius Medical Care De Gmbh | Blood treatment device with a device for continuous monitoring of the patient's blood pressure |
US6413223B1 (en) | 1999-06-01 | 2002-07-02 | Massachussetts Institute Of Technology | Cuffless continuous blood pressure monitor |
US6984207B1 (en) * | 1999-09-14 | 2006-01-10 | Hoana Medical, Inc. | Passive physiological monitoring (P2M) system |
AU766952B2 (en) * | 1999-10-07 | 2003-10-30 | Alexander K. Mills | Device and method for noninvasive continuous determination of physiologic characteristics |
EP1251775A1 (en) | 2000-01-26 | 2002-10-30 | VSM Medtech Ltd. | Continuous blood pressure monitoring method and apparatus |
US6647287B1 (en) | 2000-04-14 | 2003-11-11 | Southwest Research Institute | Dynamic cardiovascular monitor |
US6890303B2 (en) | 2001-05-31 | 2005-05-10 | Matthew Joseph Fitz | Implantable device for monitoring aneurysm sac parameters |
US7192403B2 (en) | 2001-08-17 | 2007-03-20 | Russell Ted W | Methods, apparatus and articles-of-manufacture for noninvasive measurement and monitoring of peripheral blood flow, perfusion, cardiac output biophysic stress and cardiovascular condition |
US6990222B2 (en) | 2001-11-21 | 2006-01-24 | Arnold Ben A | Calibration of tissue densities in computerized tomography |
AU2003227359A1 (en) | 2002-04-24 | 2003-11-10 | Colin Corporation | Pulse wave analyzing method, pulse wave analyzing software, and so forth |
US20040088123A1 (en) | 2002-11-01 | 2004-05-06 | Zhong Ji | Method for real-time monitoring of cardiac output and blood flow in arteries and apparatus for implementing the same |
US20140296677A1 (en) | 2003-09-18 | 2014-10-02 | New Paradigm Concepts, LLC | Method of measuring total vascular hemoglobin mass |
US7318804B2 (en) | 2003-12-09 | 2008-01-15 | The Regents Of The University Of Michigan | Methods and systems for measuring mechanical property of a vascular wall and method and system for determining health of a vascular structure |
US7179228B2 (en) | 2004-04-07 | 2007-02-20 | Triage Wireless, Inc. | Cuffless system for measuring blood pressure |
US7672706B2 (en) | 2004-08-23 | 2010-03-02 | Boston Scientific Scimed, Inc. | Systems and methods for measuring pulse wave velocity with an intravascular device |
US7621876B2 (en) | 2005-03-17 | 2009-11-24 | Ge Medical Systems Information Technologies, Inc. | Continuous, non-invasive technique for determining blood pressure using a transmission line model and transcutaneous ultrasound measurements |
US7674231B2 (en) | 2005-08-22 | 2010-03-09 | Massachusetts Institute Of Technology | Wearable pulse wave velocity blood pressure sensor and methods of calibration thereof |
US20070163353A1 (en) * | 2005-12-07 | 2007-07-19 | Drexel University | Detection of blood pressure and blood pressure waveform |
US8684900B2 (en) * | 2006-05-16 | 2014-04-01 | Bao Tran | Health monitoring appliance |
WO2008057478A2 (en) | 2006-11-03 | 2008-05-15 | The Regents Of The University Of Michigan | Method and system for determining volume flow in a blood conduit |
JP5297593B2 (en) | 2007-03-07 | 2013-09-25 | 国立大学法人 東京大学 | Synthesis method of polymer complex crystals |
US20110144967A1 (en) | 2008-08-12 | 2011-06-16 | Lev Adirovich | System and method for dynamic cardiac analysis, detection, prediction, and response using cardio-physiological mathematical modeling |
CN102123659B (en) | 2008-08-19 | 2014-07-23 | 皇家飞利浦电子股份有限公司 | Monitoring the blood pressure of a patient |
US20100081946A1 (en) | 2008-09-26 | 2010-04-01 | Qualcomm Incorporated | Method and apparatus for non-invasive cuff-less blood pressure estimation using pulse arrival time and heart rate with adaptive calibration |
CN102170821B (en) * | 2008-10-01 | 2013-08-07 | 株式会社Irumedi | Cardiovascular analysis system |
US20100106016A1 (en) * | 2008-10-23 | 2010-04-29 | Skeletal Dynamics Llc | Non-Invasive Blood Pressure Monitoring Device and Method |
WO2010099016A1 (en) * | 2009-02-25 | 2010-09-02 | Worcester Polytechnic Institute | Automatic vascular model generation based on fluid-structure interactions (fsi) |
US8313439B2 (en) * | 2009-03-20 | 2012-11-20 | Massachusetts Institute Of Technology | Calibration of pulse transit time measurements to arterial blood pressure using external arterial pressure applied along the pulse transit path |
JP5615073B2 (en) * | 2010-07-20 | 2014-10-29 | オムロンヘルスケア株式会社 | measuring device |
EP2667769B1 (en) | 2011-01-27 | 2020-07-22 | The Board of Trustees of the Leland Stanford Junior University | Systems for monitoring the circulatory system |
ES2656222T3 (en) * | 2011-02-17 | 2018-02-26 | Qualcomm Incorporated | A procedure and a system for determining a cardiovascular magnitude of a mammal |
US20120215117A1 (en) * | 2011-02-23 | 2012-08-23 | Pacesetter, Inc. | Systems and methods for estimating central arterial blood pressure of a patient |
TW201309263A (en) | 2011-08-19 | 2013-03-01 | 中原大學 | Measurement device and measurement method thereof for image-type pulse wave transduction velocity |
WO2013110929A1 (en) | 2012-01-26 | 2013-08-01 | King's College London | Aortic pulse wave velocity measurement |
CN104883967A (en) | 2012-11-08 | 2015-09-02 | 勒·泰 | Improved blood pressure monitor and method |
JP2014100249A (en) | 2012-11-19 | 2014-06-05 | Toshiba Corp | Blood vessel analysis device, medical image diagnostic device, blood vessel analysis method, and blood vessel analysis program |
US20150164351A1 (en) | 2013-10-23 | 2015-06-18 | Quanttus, Inc. | Calculating pulse transit time from chest vibrations |
US9396642B2 (en) | 2013-10-23 | 2016-07-19 | Quanttus, Inc. | Control using connected biometric devices |
EP3220812B1 (en) | 2014-11-17 | 2023-10-25 | David A. Borkholder | Pulse wave velocity, arterial compliance, and blood pressure |
-
2015
- 2015-11-17 EP EP15861809.0A patent/EP3220812B1/en active Active
- 2015-11-17 WO PCT/US2015/061190 patent/WO2016081519A1/en active Application Filing
- 2015-11-17 US US15/527,467 patent/US20170354331A1/en not_active Abandoned
- 2015-11-17 WO PCT/US2015/061188 patent/WO2016081517A2/en active Application Filing
- 2015-11-17 EP EP15860209.4A patent/EP3220811B1/en active Active
- 2015-11-17 US US15/527,412 patent/US11622730B2/en active Active
-
2023
- 2023-02-27 US US18/114,585 patent/US20240023898A1/en not_active Abandoned
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5565466A (en) * | 1993-08-13 | 1996-10-15 | Zonagen, Inc. | Methods for modulating the human sexual response |
US6575969B1 (en) * | 1995-05-04 | 2003-06-10 | Sherwood Services Ag | Cool-tip radiofrequency thermosurgery electrode system for tumor ablation |
US20050090720A1 (en) * | 2003-10-22 | 2005-04-28 | Hsien-Tsai Wu | Pulse analyzing apparatus |
US20120190967A1 (en) * | 2010-12-23 | 2012-07-26 | Werner Nahm | Arrangement and method for quantitatively determining the blood flow within blood vessels |
Cited By (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US11622730B2 (en) | 2014-11-17 | 2023-04-11 | Rochester Institute Of Technology | Pulse wave velocity, arterial compliance, and blood pressure |
US12089958B2 (en) * | 2014-12-16 | 2024-09-17 | Lmd Ip, Llc | Personal health data collection |
US11412987B2 (en) * | 2014-12-16 | 2022-08-16 | Leman Micro Devices Sa | Personal health data collection |
US20220395231A1 (en) * | 2014-12-16 | 2022-12-15 | Leman Micro Devices Sa | Personal health data collection |
US11957504B2 (en) | 2017-06-23 | 2024-04-16 | Stryker Corporation | Patient monitoring and treatment systems and methods |
US12089985B2 (en) * | 2017-06-23 | 2024-09-17 | Stryker Corporation | Patient monitoring and treatment systems and methods |
US11311236B2 (en) * | 2018-02-27 | 2022-04-26 | Boe Technology Group Co., Ltd. | Device for determining location of blood vessel and method thereof |
US12178553B2 (en) | 2018-12-18 | 2024-12-31 | Koninklijke Philips N.V. | Control unit for deriving a measure of arterial compliance |
CN112512413A (en) * | 2019-04-12 | 2021-03-16 | 北京顺源开华科技有限公司 | Blood pressure measurement |
WO2020207446A1 (en) * | 2019-04-12 | 2020-10-15 | Beijing Shunyuan Kaihua Technology Co., Ltd. | Blood pressure measurement |
US20210137393A1 (en) * | 2019-11-07 | 2021-05-13 | The Curators Of The University Of Missouri | Systems and methods to improve management and monitoring of cardiovascular disease |
US12102415B2 (en) * | 2019-11-07 | 2024-10-01 | The Curators Of The University Of Missouri | Systems and methods to improve management and monitoring of cardiovascular disease |
CN112842287A (en) * | 2021-01-05 | 2021-05-28 | 清华大学 | Device and method for measuring vascular sclerosis parameters |
CN113706984A (en) * | 2021-08-06 | 2021-11-26 | 西安交通大学 | Synchronous analog calibration device and method for blood pressure and reflection type photoelectric accumulated wave |
US20230142080A1 (en) * | 2021-08-18 | 2023-05-11 | Second Medical Center Of Chinese Pla General Hospital | Glove for detecting multiple physiological parameters and system for detecting risk of hypertension disease |
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EP3220811A4 (en) | 2018-07-25 |
EP3220812B1 (en) | 2023-10-25 |
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EP3220812A2 (en) | 2017-09-27 |
US20190083045A1 (en) | 2019-03-21 |
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US20240023898A1 (en) | 2024-01-25 |
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US11622730B2 (en) | 2023-04-11 |
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